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20 pages, 4670 KiB  
Article
Nutraceutical Potential of Djulis (Chenopodium formosanum) Hull: Phytochemicals, Antioxidant Activity, and Liver Protection
by Yu-Chen Huang, Chun-Liang Tung, Shang-Tse Ho, Wei-Sung Li, Shiming Li, Yu-Tang Tung and Jyh-Horng Wu
Antioxidants 2024, 13(6), 721; https://doi.org/10.3390/antiox13060721 - 13 Jun 2024
Cited by 1 | Viewed by 853
Abstract
Djulis (Chenopodium formosanum), a traditional Taiwanese crop enriched with phenolic compounds and betalain pigments, is associated with various health benefits, including antioxidant and hepatoprotective effects. This study analysed the phytochemical content and antioxidant capacity of extracts from both the hull and [...] Read more.
Djulis (Chenopodium formosanum), a traditional Taiwanese crop enriched with phenolic compounds and betalain pigments, is associated with various health benefits, including antioxidant and hepatoprotective effects. This study analysed the phytochemical content and antioxidant capacity of extracts from both the hull and kernel of Djulis. The hull extract, which contained higher levels of flavonoids and exhibited superior antioxidant activity compared to the kernel extract, was selected for further in vivo studies. These experiments showed that oral administration of the Djulis hull crude extract significantly mitigated lipopolysaccharide (LPS)-induced acute liver injury (ALI) in mice by increasing the activity of the antioxidant enzyme glutathione peroxidase (GPx), reducing plasma levels of pro-inflammatory cytokine interferon gamma (IFN-γ), and enhancing liver levels of the anti-inflammatory cytokine interleukin-4 (IL-4). Additionally, the extract demonstrated potential in inhibiting the TLR4/NF-κB pathway, a critical signalling pathway in inflammation and apoptosis, offering insights into its protective mechanisms. These findings underscore Djulis hull’s potential as a functional food ingredient for ALI prevention and propose a valuable application for agricultural by-products. Full article
(This article belongs to the Section Natural and Synthetic Antioxidants)
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Figure 1

Figure 1
<p>The component analysis of three strains of Djulis hull and kernel crude extracts using UPLC-MS/MS. (<b>A</b>) Molecular networking of three strains of Djulis hull and kernel crude extracts. <b>12</b>, <b>18</b>, and <b>20</b> belong to the flavonoid group. (<b>B</b>) Differences in flavonoids in Djulis hull and kernel crude extracts. (<b>C</b>) Differences in flavonoids in three strains of Djulis hull crude extracts. The widths and shades of connecting lines represent the similarity between connected nodes (Edge Score), while the sizes of circular nodes represent the total spectra number for each compound (spectra number). The numbers in the figures corresponded to the compound name, parent mass, and spectra number, as detailed in <a href="#app1-antioxidants-13-00721" class="html-app">Supplementary Tables S1–S3</a>.</p>
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<p>(<b>A</b>) Total phenolic contents, (<b>B</b>) total flavonoid contents, (<b>C</b>) DPPH radical scavenging activity, and (<b>D</b>) half maximal inhibitory concentrations of three strains of Djulis hull and kernel crude extracts. DPPH, 1,1-diphenyl-2-picrylhydrazyl. The statistics were determined by one-way ANOVA with Tukey’s multiple comparisons test. Values are represented as the mean ± SD (<span class="html-italic">n</span> = 3), and different letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effects of Djulis hull and kernel crude extracts on (<b>A</b>) body weight, (<b>B</b>) body weight change, (<b>C</b>) relative liver weight, and (<b>D</b>) white blood cell type of mice in LPS-induced acute liver injury. The arrow represents the time point induced by LPS. A one-tailed Mann-Whitney U test was used for statistical analysis. Values are represented as the mean ± SEM (<span class="html-italic">n</span> = 6), where <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 and <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 compared with the control group.</p>
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<p>Effects of Djulis hull and kernel crude extracts on the (<b>A</b>) liver histopathology and Suzuki scores of mice with an LPS-induced acute liver injury, including (<b>B</b>) vacuolation, (<b>C</b>) necrosis, (<b>D</b>) congestion, and (<b>E</b>) the total score. H&amp;E staining (200×). Solid arrows represent vacuolization, * represents necrosis, and hollow arrows represent congestion. A one-tailed Mann-Whitney U test was used for statistical analysis. Values are represented as the mean ± SEM (<span class="html-italic">n</span> = 6), where <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 and <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 compared with the control group, and * <span class="html-italic">p</span> &lt; 0.05 compared with the water group.</p>
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<p>Effects of Djulis hull and kernel crude extracts on the activities of liver antioxidant enzymes, including (<b>A</b>) SOD, (<b>B</b>) GPx, and (<b>C</b>) CAT, as well as the (<b>D</b>) TBARS content of mice in LPS-induced acute liver injury. SOD, superoxide dismutase; GPx, glutathione peroxidase; CAT, catalase; TBARS, thiobarbituric acid reactive substances. A one-tailed Mann-Whitney U test was used for statistical analysis. Values are represented as the mean ± SEM (<span class="html-italic">n</span> = 6), where <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 and <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 compared with the control group, and * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 compared with the water group.</p>
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<p>Effects of Djulis hull and kernel crude extracts on plasma pro-inflammatory cytokines (<b>A</b>) IFN-γ, (<b>B</b>) IL-6, and (<b>C</b>) TNF-α and liver pro-inflammatory cytokines (<b>D</b>) IFN-γ, (<b>E</b>) IL-1β, (<b>F</b>) IL-6, and (<b>G</b>) TNF-α and liver anti-inflammatory cytokines (<b>H</b>) IL-4 and (<b>I</b>) IL-10 in mice with LPS-induced acute liver injury. IFN-γ, interferon gamma; IL-6, interleukin-6; TNF-α, tumour necrosis factor alpha; IL-1β, interleukin-1 beta; IL-4, interleukin-4; IL-10, interleukin-10. A one-tailed Mann-Whitney U test was used for statistical analysis. Values are represented as the mean ± SEM (<span class="html-italic">n</span> = 6), where <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 and <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 compared with the control group, and * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 compared with the water group.</p>
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<p>(<b>A</b>) Effects of Djulis hull and kernel crude extracts on the protein expression levels of (<b>B</b>) MyD88 and (<b>C</b>) IκBα in the TLR4/NF-κB pathway, (<b>D</b>) HO-1 in the Nrf2/HO-1 pathway, and (<b>E</b>) BAX, (<b>F</b>) cleaved caspase-8, and (<b>G</b>) cleaved caspase-3 in the apoptotic pathway in the livers of mice with LPS-induced acute liver injury. MyD88, myeloid differentiation primary response protein 88; IκBα, nuclear factor-kappa B inhibitor alpha; HO-1, haem oxygenase-1; BAX, Bcl2-associated X protein. A one-tailed Mann-Whitney U test was used for statistical analysis. Values are represented as the mean ± SEM (<span class="html-italic">n</span> = 6), where <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 and <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01 compared with the control group.</p>
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<p>Mechanisms underlying the effects of Djulis hull crude extract on the LPS-induced acute liver injury model in mice (created with BioRender.com). Red solid arrows indicate a significant increase; red dotted arrows indicate a potential increase; blue solid arrows indicate a significant decrease; blue dotted arrows indicate a potential decrease [<a href="#B11-antioxidants-13-00721" class="html-bibr">11</a>,<a href="#B12-antioxidants-13-00721" class="html-bibr">12</a>,<a href="#B13-antioxidants-13-00721" class="html-bibr">13</a>,<a href="#B14-antioxidants-13-00721" class="html-bibr">14</a>,<a href="#B49-antioxidants-13-00721" class="html-bibr">49</a>,<a href="#B52-antioxidants-13-00721" class="html-bibr">52</a>,<a href="#B53-antioxidants-13-00721" class="html-bibr">53</a>].</p>
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27 pages, 3703 KiB  
Article
Utilization of Rhodopseudomonas palustris in Crop Rotation Practice Boosts Rice Productivity and Soil Nutrient Dynamics
by Laurence Shiva Sundar, Kuei-Shan Yen, Yao-Tsung Chang and Yun-Yang Chao
Agriculture 2024, 14(5), 758; https://doi.org/10.3390/agriculture14050758 - 13 May 2024
Cited by 1 | Viewed by 1529
Abstract
Using beneficial microorganisms, such as purple non-sulfur bacteria (PNSB), has shown enormous potential for improving plant growth and agricultural production. However, the full extent of their benefits and interactions with agricultural practices is yet to be fully understood. The present study aimed to [...] Read more.
Using beneficial microorganisms, such as purple non-sulfur bacteria (PNSB), has shown enormous potential for improving plant growth and agricultural production. However, the full extent of their benefits and interactions with agricultural practices is yet to be fully understood. The present study aimed to investigate the use of PNSB in crop rotation practice, focusing on its impact on rice growth and yield. The experiment was conducted over two rice cropping seasons, with djulis grown between the rice as a rotation crop. The study shows that PNSB treatment increased the concentration of 5-aminolevulinic acid (5-ALA) in plants, indicating enhanced photosynthesis. Moreover, when combined with crop rotation, PNSB remarkably improved soil fertility. These combined benefits resulted in substantial increases in tiller numbers (163%), leaf chlorophyll content (13%), and lodging resistance (66%), compared to the untreated plants. The combined treatment also resulted in higher productive tillers per hill (112%), average grain per hill (65%), and grain fertility (26%). This led to increased grain yield (65%), shoot dry weight (15%), and harvest index (37%). The findings clearly suggest that the incorporation of PNSB in crop rotation strategies can significantly augment the growth and yield of rice crops. These insights, pivotal for sustainable rice cultivation, hold the potential to simultaneously tackle the pressing issues of global food security and climate change. Full article
(This article belongs to the Section Crop Production)
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Figure 1

Figure 1
<p>Enhancement of rice growth and yield through incorporation of purple non-sulfur bacteria (PNSB) in rice-djulis rotation practice. (<b>a</b>) Depiction of the rice fields utilized in this study, where djulis was cultivated as a rotational crop within the same field and (<b>b</b>) a schematic representation of the experimental design implemented in this study.</p>
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<p>Comparison of above-ground environmental conditions between Trial 1 and Trial 2, including (<b>a</b>) air temperature patterns and (<b>b</b>) relative humidity variations. * denotes significant differences (<span class="html-italic">p</span> ≤ 0.05) based on an independent sample <span class="html-italic">t</span>-test (<span class="html-italic">n</span> = 7).</p>
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<p>Variations observed for (<b>a</b>) light intensity and (<b>b</b>) sunshine hours in Trial 1 and Trial 2. * denotes significant differences (<span class="html-italic">p</span> ≤ 0.05) based on an independent sample <span class="html-italic">t</span>-test (<span class="html-italic">n</span> = 7).</p>
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<p>Variations in soil fertility parameters, including pH, organic matter (OM), manganese (Mn), copper (Cu), and zinc (Zn), in (<b>a</b>) untreated and (<b>b</b>) purple non-sulfur bacteria (PNSB) treated fields. Additionally, the levels of other essential soil elements such as phosphorus (P), potassium (K), calcium (Ca), magnesium (Mg), iron (Fe), and sodium (Na) content in soil are shown for (<b>c</b>) untreated and (<b>d</b>) PNSB-treated fields. The means followed by the same letter(s) are not significantly different (<span class="html-italic">p</span> ≤ 0.05) based on Duncan’s multiple range test (<span class="html-italic">n</span> = 3).</p>
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<p>Changes in below-ground environmental conditions during Trial 2, including (<b>a</b>) soil temperature fluctuations and (<b>b</b>) variations in soil electrical conductivity (EC). PNSB: purple non-sulfur bacteria; * denotes significant differences (<span class="html-italic">p</span> ≤ 0.05) based on an independent sample <span class="html-italic">t</span>-test (<span class="html-italic">n</span> = 7).</p>
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<p>Variations in 5-aminolevulinic acid (5-ALA) concentration between purple non-sulfur bacteria (PNSB) inoculated and uninoculated plants. The means followed by the same letter(s) are not significantly different (<span class="html-italic">p</span> ≤ 0.05) based on Duncan’s multiple range test (<span class="html-italic">n</span> = 4).</p>
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<p>The changes in plant height until the reproductive stage in (<b>a</b>) Trial 1 and (<b>b</b>) Trial 2 under different treatments. PNSB: purple non-sulfur bacteria; * denotes significant differences (<span class="html-italic">p</span> ≤ 0.05) based on an independent sample <span class="html-italic">t</span>-test (<span class="html-italic">n</span> = 10).</p>
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<p>Variation in leaf chlorophyll content observed until the reproductive stage in (<b>a</b>) Trial 1 and (<b>b</b>) Trial 2 under different treatments. PNSB: purple non-sulfur bacteria; * denotes significant differences (<span class="html-italic">p</span> ≤ 0.05) based on an independent sample <span class="html-italic">t</span>-test (<span class="html-italic">n</span> = 10).</p>
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<p>Comparison of tiller number until the reproductive stage in (<b>a</b>) Trial 1 and (<b>b</b>) Trial 2 under the different treatments. PNSB: purple non-sulfur bacteria; * denotes significant differences (<span class="html-italic">p</span> ≤ 0.05) based on an independent sample <span class="html-italic">t</span>-test (<span class="html-italic">n</span> = 10).</p>
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<p>Differences in the lodging resistance of rice crop plants under various treatments. The means followed by the same letter(s) are not significantly different (<span class="html-italic">p</span> ≤ 0.05) based on Duncan’s multiple range test. PNSB: purple non-sulfur bacteria (<span class="html-italic">n</span> = 10).</p>
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<p>Synergistic effects of crop rotation and purple non-sulfur bacteria (PNSB) inoculation on soil nutrients and rice crop productivity. PGPS: plant growth-promoting substances; 5-ALA: 5-aminolevulinic acid; IAA: indole-3-acetic acid; NUE: nutrient use efficiency.</p>
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16 pages, 6543 KiB  
Article
Development of Chinese-Style Sausage Enriched with Djulis (Chenopodium formosanum Koidz) Using Taguchi Method: Applying Modern Optimization to Indigenous People’s Traditional Food
by Pei-Ling Chung, Ku-Sang Lufaniyao and Mohsen Gavahian
Foods 2024, 13(1), 91; https://doi.org/10.3390/foods13010091 - 26 Dec 2023
Viewed by 1511
Abstract
Djulis (Taiwanese quinoa) has gained popularity among researchers due to its biological characteristics and rich nutritional value. Incorporating Djulis is expected to enhance the sausage’s texture, flavor, and storage stability due to the presence of antioxidants and nutritional components. However, limited studies focus [...] Read more.
Djulis (Taiwanese quinoa) has gained popularity among researchers due to its biological characteristics and rich nutritional value. Incorporating Djulis is expected to enhance the sausage’s texture, flavor, and storage stability due to the presence of antioxidants and nutritional components. However, limited studies focus on product development based on this emerging health-promoting ingredient in the food industry. This study aims to develop Chinese-style sausage enriched with Djulis using the Taguchi L9(34) orthogonal matrix methodology and evaluate the influence of four factors, including un-hulled to hulled Djulis ratios of 0, 50, 100% (A), backfat-to-lean meat ratios of 0/100, 30/70, 50/50% (B), cooking temperature of 55, 75, 95 °C (C), and nitrite content of 0.03, 0.05, 0.07 g/kg (D) on products’ sensory and physicochemical properties. The optimal Taguchi formulation was then verified and compared with conventionally formulated sausage (original sausage) in terms of hardness, springiness, gumminess, CIE color values, and peroxide value (POV). The optimal formulation was A3B2C2D3, which consisted of 16.8% hulled Djulis, 30/70 backfat-to-lean meat ratio, 75 °C cooking temperature, and 0.03 g/kg nitrite content. The most influential independent parameters were identified as B > A > C > D, placing Djulis incorporation as the first runner-up, just after the backfat-to-lean meat ratio. Optimized condition verification identified the Signal-to-Noise ratio (S/N) of 16.63. Comparing the optimized Djulis-enriched sample and the original sausage indicated similar CIE L*, a*, b*, hardness, and springiness but different gumminess according to Texture Profile Analysis (TPA). The Djulis-enriched sausage at the optimized formulation had a significantly lower POV compared to the control sample (4.65 vs. 9.64 meq/kg), which was found to be correlated with Djulis antioxidant effects with 2,2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) free radical antioxidant activity of 62.37%. This suggests that Djulis effectively mitigates sausage organoleptic deterioration. Djulis sausage, with natural antioxidants and reduced fat content, could cater to consumer preferences and enhance the market for the food industry and indigenous farmers. Full article
(This article belongs to the Section Food Engineering and Technology)
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Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>The appearance of nine batches of Djulis sausages made with different formulas. Numbers 1–9 under each picture refer to the treatment used according to the Taguchi method: 1: lean meat 50% and un-hulled Djulis 100%; 2: lean meat 50% and 50–50% of un-hulled to hulled Djulis; 3: lean meat 50% and hulled Djulis 100%; 4: lean meat 70% and un-hulled Djulis 100%; 5: lean meat 70% and 50–50% of un-hulled to hulled Djulis; 6: lean meat 70% and hulled Djulis 100%; 7: lean meat 70% and un-hulled Djulis 100%; 8: lean meat 100% and 50–50% of un-hulled to hulled Djulis; 9: lean meat 100% and hulled Djulis 100%.</p>
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<p>Signal-to-Noise (S/N) ratio response graph for the overall acceptance of Djulis sausage. The red circles indicate the highest S/N for each variable.</p>
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<p>Selected values from texture profile analysis of Djulis sausages at the optimized formulation compared to the original sausage. Error bars indicate standard deviation. [Unit of measurement: hardness (Kgf), gumminess (Kgf), springiness (mm)].</p>
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<p>Analysis of sausage CIE color values. The results represent the average value of three replications (<span class="html-italic">n</span> = 3) as mean ± SD. L* is lightness. a* is redness and b* is yellowness; all values reported in this figure are dimensionless.</p>
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<p>The result of the peroxide value test of sausage samples. Data represented as mean ± SD.</p>
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19 pages, 5378 KiB  
Article
First Report on Choanephora cucurbitarum Causing Choanephora Rot in Chenopodium Plants and Its Sensitivity to Fungicide
by Hui Yin, Miao Tian, Yufei Peng, Nan Qin, Hong Lü, Lu Ren and Xiaojun Zhao
J. Fungi 2023, 9(9), 881; https://doi.org/10.3390/jof9090881 - 28 Aug 2023
Cited by 4 | Viewed by 1606
Abstract
Choanephora rot of Chenopodium plants (CRC) was observed at the flowering stages in seven plantations of Shanxi Province, China. CRC had caused leaf, stem, and panicle neck rot of C. quinoa, panicle neck and stem rot of C. formosanum, and stem [...] Read more.
Choanephora rot of Chenopodium plants (CRC) was observed at the flowering stages in seven plantations of Shanxi Province, China. CRC had caused leaf, stem, and panicle neck rot of C. quinoa, panicle neck and stem rot of C. formosanum, and stem rot of C. album. Typical symptoms included water-soaked, rapid soft rotting, and abundant sporulation on the whole panicle necks, stems, and leaves. Based on morphological characteristics, phylogenetic analyses, and pathogenicity tests, the pathogens were identified as Choanephoraceae cucurbitarum. Sporangiola and sporangiospore of C. cucurbitarum germinated at 30 °C and were able to germinate by two h post-inoculation (hpi). The germination rates of sporangiola and sporangiospore significantly increased at 3 to 4 hpi, and the germination rates ranged from 91.53 to 97.67%. The temperature had a significant effect on the pathogenicity of C. cucurbitarum the optimum pathogenic temperatures for stems of C. quinoa, C. formosanum and C. album were 30 °C after one day post-inoculation. Choanephoraceae cucurbitarum could infect white and red quinoa panicle necks between 20 and 30 °C, and the average lesion lengths were 0.21 to 3.62 cm. Among the five tested fungicides (boscalid, dimethomorph, isopyrazam, propiconazole, and tebuconazole), isopyrazam showed higher sensitivity to sporangiola germination of C. cucurbitarum, with an EC50 value of 0.6550 μg/mL. Isopyrazam and tebuconazole strongly inhibited the sporangiospore germination of C. cucurbitarum, which showed EC50 values of 0.4406 and 0.3857 μg/mL. To our knowledge, the present study found for the first time that C. cucurbitarum is a pathogen causing panicle neck of C. formosanum and stem rot of C. formosanum and C. album, while CRC first appeared in the quinoa panicle necks, and gradually expanded to stems and leaves. Full article
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Figure 1

Figure 1
<p>Symptoms of Choanephora rot on panicle necks, stems, and leaves of <span class="html-italic">Chenopodium quinoa</span> (<b>A</b>) panicle necks and stems of <span class="html-italic">C. formosanum</span> (<b>B</b>) and stems of <span class="html-italic">C. album</span> (<b>C</b>).</p>
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<p>Morphological characteristics of <span class="html-italic">Choanephora cucurbitarum</span> from <span class="html-italic">Chenopodium</span> plants. (<b>A</b>) Colony on PDA for 2 days, (<b>B</b>) sporangiophores bearing sporangiola, (<b>C</b>–<b>G</b>) sporangiophores with apically dilated and bearing secondary vesicles, (<b>H</b>,<b>I</b>) sporangiola readily detached at maturity, (<b>J</b>–<b>L</b>) secondary vesicles with a head of sporangiola, (<b>M</b>) mature sporangiola with mulberry-like head, (<b>N</b>) sporangiola with longitudinal striation, (<b>O</b>) sporangiophores bearing sporangia, (<b>P</b>,<b>Q</b>) pale yellow to yellow sporangium, (<b>R</b>) sporangiophore bearing mature sporangium, (<b>S</b>,<b>T</b>) dehiscent sporangium, (<b>U</b>) sporangiospores from sporangia, and (<b>V</b>) sporangiospores with appendages.</p>
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<p>Phylogenetic tree of <span class="html-italic">Choanephora cucurbitarum</span> isolates (LMJM-2, LMJM-3, LMJM-5, LMJM-7, and LMJM-9) from <span class="html-italic">Chenopodium</span> plants and their related isolates based on LSU and ITS sequences using the maximum likelihood (ML) method. Ex-type strains were indicated with (T) in the end of the taxa labels, and our strains are in bold.</p>
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<p>Germination of the sporangiola (<b>A</b>) and sporangiospores (<b>B</b>) of <span class="html-italic">Choanephora cucurbitarum</span> at 2, 3, and 4 h (<b>C</b>).</p>
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<p>Symptoms on <span class="html-italic">Chenopodium quinoa</span> (<b>A</b>), <span class="html-italic">C. formosanum</span> (<b>B</b>), and <span class="html-italic">C. album</span> (<b>C</b>) induced by inoculation of representative isolates (LMJM-2, LMJM-3, LMJM-5, LMJM-7, and LMJM-9) of <span class="html-italic">Choanephora cucurbitarum</span>.</p>
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<p>Effect of temperature on pathogenicity of the representative isolates of <span class="html-italic">Choanephora cucurbitarum</span>. (<b>A</b>) Pathogenicity on stems of <span class="html-italic">C. quinoa</span>, <span class="html-italic">C. formosanum</span>, and <span class="html-italic">C. album</span> at different temperatures, (<b>B</b>) lesions lengths on panicle necks of white and red quinoa that were inoculated with <span class="html-italic">Choanephora cucurbitarum</span> and incubated at different temperatures. Data were analyzed with SPSS statistics 19.0 by one-way ANOVA, and means were compared using Tukey’s test at a significance level of <span class="html-italic">p</span> = 0.05. Different letters indicate significant differences (<span class="html-italic">p</span> = 0.05).</p>
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<p>Effects of five fungicides on germination of sporangiola and sporangiospores of isolate LMJM-2. (<b>A</b>) Inhibition activities of five fungicides on germination of sporangiola and sporangiospores, (<b>B</b>) morphology of germ tubes of sporangiola and sporangiospores treated with five fungicides at EC<sub>50</sub>. Different letters indicate significant differences (<span class="html-italic">p</span> = 0.05).</p>
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12 pages, 1419 KiB  
Article
Protective Effect of Ethanolic Extract of Djulis Hull on Indomethacin-Induced Gastric Injury
by Fuad Sauqi Isnain, Nai-Chen Liao, Hui-Yun Tsai, Jue-Liang Hsu, Pi-Jen Tsai, Agustin Krisna Wardani and Yu-Kuo Chen
Appl. Sci. 2023, 13(1), 594; https://doi.org/10.3390/app13010594 - 1 Jan 2023
Cited by 3 | Viewed by 2128
Abstract
Djulis (Chenopodium formosanum), a pseudocereal crop native to Taiwan, is often utilized as a source of grain in the diet because of its high nutritional value. The hull of djulis is discarded as waste during cooking or processing because of its [...] Read more.
Djulis (Chenopodium formosanum), a pseudocereal crop native to Taiwan, is often utilized as a source of grain in the diet because of its high nutritional value. The hull of djulis is discarded as waste during cooking or processing because of its bitter taste. However, recent studies have shown that djulis hull possesses certain benefits, such as antioxidant, blood sugar-lowering, and gut microbiota-regulating properties. Herein, the gastroprotective activity of ethanolic extract of djulis hull (EEDH) against stomach injury caused by indomethacin (IND) in C57BL/6J mice and its mechanism of action was assessed. Preadministration of EEDH significantly attenuated the gastric ulcer caused by IND in a dose-dependent manner (p < 0.05). Additionally, gastric mucosal injury and gastric wall edema within the submucosal layer observed in histopathological examination were improved by administration of EEDH. EEDH preadministration also reinstated the reduction of glutathione (GSH) content and catalase (CAT), and superoxide dismutase (SOD) activities induced by IND, indicating that EEDH can modulate the antioxidant status of gastric mucosa in mice. Moreover, IND-induced decline of gastric COX-1 expression was upregulated in mice of EEDH treatment groups. Administration of IND increased the expression of proinflammatory proteins in the gastric mucosa of mice, including tumor necrosis factor-α (TNF-α) and inducible nitric oxide synthase (iNOS), whereas EEDH treatment significantly decreased their expression (p < 0.05). Consequently, EEDH can improve gastric injury by regulating antioxidant status and inhibiting proinflammatory signaling pathways, and has the potential to be developed as a functional food for gastric protection. Full article
(This article belongs to the Special Issue Knowledge-Based Biotechnology for Food, Agriculture and Fisheries)
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Figure 1
<p>Representative gross gastric images of mice. (<b>A</b>) Control group; (<b>B</b>) IND group, treated with IND (120 mg/kg); (<b>C</b>) EEDH200 group, treated with EEDH (200 mg/kg) + IND (120 mg/kg); (<b>D</b>) EEDH500 group, treated with EEDH (500 mg/kg) + IND (120 mg/kg). Mice were administered indicated dose of EEDH orally for 21 consecutive days. 120 mg/kg of IND was then given orally to mice on the last day of experiment and sacrificed 6 h later. The gastric tissue of mice was harvested and photographed. The arrows showed in the figure depict bleeding ulcers.</p>
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<p>The histopathological assessment of gastric mucosa in mice. (H&amp;E staining, scale bars = 250 μm). (<b>A</b>) Control group; (<b>B</b>) IND group, treated with IND (120 mg/kg); (<b>C</b>) EEDH200 group, treated with EEDH (200 mg/kg) + IND (120 mg/kg); (<b>D</b>) EEDH500 group, treated with EEDH (500 mg/kg) + IND (120 mg/kg). The asterisk showed in the figure indicates the damage of the mucosal epithelium accompanied by the destruction of the gland structure. The arrow showed in the figure depicts edema and inflammatory cell infiltration in the submucosa.</p>
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<p>Effects of EEDH on (<b>A</b>) the level of GSH and (<b>B</b>,<b>C</b>) the activities of SOD and CAT of gastric mucosa in mice. Data are represented as means ± SD (<span class="html-italic">n</span> = 8). # <span class="html-italic">p</span> &lt; 0.05 compared with control group. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 compared with IND-treated group.</p>
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<p>Effects of EEDH pretreatment on the protein levels of COX-1 of gastric mucosa in mice administered with IND. Western blot was applied to determine the expression of COX-1. Data are represented as means ± SD (<span class="html-italic">n</span> = 3). # <span class="html-italic">p</span> &lt; 0.05 compared with control group. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 compared with IND-treated group.</p>
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<p>Effects of EEDH pretreatment on the protein levels of TNF-α (<b>A</b>) and iNOS (<b>B</b>) of gastric mucosa in mice administered with IND. Western blot was applied to determine the expression of TNF-α and iNOS. Data are represented as means ± SD (<span class="html-italic">n</span> = 3). # <span class="html-italic">p</span> &lt; 0.05 compared with control group. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 compared with IND-treated group.</p>
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16 pages, 1310 KiB  
Article
Development of Functional Fermented Dairy Products Containing Taiwan Djulis (Chenopodium formosanum Koidz.) in Regulating Glucose Utilization
by Chih-Yao Hou, Chen-Che Hsieh, Ying-Chi Huang, Chia-Hung Kuo, Min-Hung Chen, Chang-Wei Hsieh and Kuan-Chen Cheng
Fermentation 2022, 8(9), 423; https://doi.org/10.3390/fermentation8090423 - 26 Aug 2022
Cited by 6 | Viewed by 2934
Abstract
Taiwan djulis (Chenopodium formosanum Koidz.) is a plant native to Taiwan and is a grain rich in nutrients, vitamins, and minerals with antioxidant properties. This paper aimed to use appropriate processing technology and incorporate probiotics, thus combining Taiwan’s high-quality milk sources to [...] Read more.
Taiwan djulis (Chenopodium formosanum Koidz.) is a plant native to Taiwan and is a grain rich in nutrients, vitamins, and minerals with antioxidant properties. This paper aimed to use appropriate processing technology and incorporate probiotics, thus combining Taiwan’s high-quality milk sources to develop Taiwan djulis fermented dairy products. Later, FL83B cells have used to evaluate the glucose utilization ability after the administration of djulis. We first screened Lactiplantibacillus plantarum and combined it with the traditional yogurt strains Lactobacillus delbrueckii subsp. bulgaricus and Streptococcus thermophilus for cultivation. Further, the fermentation process was optimized where 7.5% djulis and an inoculum of 107 colony forming unit/mL were fermented at 40 °C for 18 h. Compared to fermented milk without djulis, the analysis of various nutrients and active ingredients showed that free radical scavenging abilities of DPPH and ABTS reached 2.3 and 2.0 times (752.35 ± 29.29 µg and 771.52 ± 3.79 µg TE/g, respectively). The free phenol content increased 2.5 times (169.90 ± 14.59 mg gallic acid/g); the total flavonoid content enhanced 4.8 times (3.05 ± 0.03 mg quercetin/g), and the gamma-aminobutyric acid content was 3.07 ± 0.94 mg/g. In a co-culture of mouse liver cells with fermented products, 100 ppm ethanol extract of fermented products effectively improved glucose utilization with increased glucose transporter expression. This functional fermented dairy product can be developed into the high value added local agricultural products and enhance multiple applications including medical and therapeutic fields. Full article
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<p>Sensory evaluation results of fermented Taiwan djulis and other similar fermented dairy products. FDP: Fermented dairy products; DFDP: Taiwan djulis fermented dairy products; CFDP: Cereal fermented dairy products; COFDF: Commercial original fermented dairy products. The number of evaluations was 52, and the results were expressed as mean ± SD. Different letters indicate significant differences from each other.</p>
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<p>Effects of ethanol extracts from fermented dairy products and Taiwan djulis fermented dairy products on glucose utilization in the liver cells of FL83B cell. Control: FL83B cell without treatment; FDP: Fermented dairy products ethanol extraction; DFDP: Taiwan djulis fermented dairy products ethanol extraction. The experiment was performed in triplicate and expressed as mean ± SD. Different letters indicate significant differences from each other.</p>
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<p>The expression of glucose transporters in hepatocyte cells FL83B post-addition of ethanol extracts from fermented dairy products and Taiwan djulis fermented dairy products (<b>a</b>) in the presence of 5 µg/mL insulin and (<b>b</b>) in an insulin-free environment. The experiments were performed in triplicate and expressed as mean ± SD. Different letters indicate significant differences from each other.</p>
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20 pages, 9323 KiB  
Article
Protective Effect of Djulis (Chenopodium formosanum) Extract against UV- and AGEs-Induced Skin Aging via Alleviating Oxidative Stress and Collagen Degradation
by Jia-Ling Lyu, Yi-Jung Liu, Kuo-Ching Wen, Chen-Yuan Chiu, Yung-Hsiang Lin and Hsiu-Mei Chiang
Molecules 2022, 27(7), 2332; https://doi.org/10.3390/molecules27072332 - 4 Apr 2022
Cited by 10 | Viewed by 3859
Abstract
Skin aging is a complex process involving photoaging and glycation stress, which share some fundamental pathways and have common mediators. They can cause skin damage and collagen degradation by inducing oxidative stress and the accumulation of reactive oxygen species (ROS). Chenopodium formosanum (CF), [...] Read more.
Skin aging is a complex process involving photoaging and glycation stress, which share some fundamental pathways and have common mediators. They can cause skin damage and collagen degradation by inducing oxidative stress and the accumulation of reactive oxygen species (ROS). Chenopodium formosanum (CF), also known as Djulis, is a traditional cereal in Taiwan. This study investigated the protection mechanisms of CF extract against ultraviolet (UV) radiation and advanced glycation end products (AGEs)-induced stress. The results indicated that CF extract had strong antioxidant and free radical scavenging effects. It could reduce UV-induced intracellular ROS generation and initiate the antioxidant defense system by activating the nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (HO-1) signaling pathway in human skin fibroblasts. CF extract modulated mitogen-activated protein kinase (MAPK) and transformed growth factor-beta (TGF-β) signaling pathways to alleviate oxidative stress-induced skin aging. Moreover, the results revealed that CF extract not only promoted collagen synthesis but also improved aging-induced collagen degradation. CF extract attenuated AGEs-induced ROS production and the upregulation of receptor for AGEs (RAGE). The overall results suggest that CF extract provides an effective anti-aging strategy by preventing skin damage from oxidative stress and collagen loss with potent antioxidant, anti-photoaging, and antiglycation activities. Full article
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<p>(<b>a</b>) DPPH free radical scavenging activity (%); (<b>b</b>) reducing capability (%); (<b>c</b>) superoxide anion radical scavenging activity (%); (<b>d</b>) hydrogen peroxide scavenging activity (%); (<b>e</b>) hydroxyl radical scavenging activity (%) and (<b>f</b>) ferrous ion chelating activity (%) of CF extract. Significant difference versus control group: *, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01; ***, <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Cell viability (%) of human skin fibroblasts treated with (<b>a</b>) a series of concentrations of CF extract; (<b>b</b>) various UVB doses and (<b>c</b>) CF extract on UV radiation. Significant difference versus non-irradiated group: ###, <span class="html-italic">p</span> &lt; 0.001. Significant difference versus UVB-irradiated group: *, <span class="html-italic">p</span> &lt; 0.05; ***, <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>The effects of CF extract on UVB-induced intracellular ROS generation in human skin fibroblasts (scale bar = 50 µm). Significant difference versus non-irradiated group: ###, <span class="html-italic">p</span> &lt; 0.001. Significant difference versus UVB-irradiated group: **, <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>The effects of CF extract on UVB-induced Nrf2, Keap1 and HO-1 expression in human skin fibroblasts. Significant difference versus non-irradiated group: ###, <span class="html-italic">p</span> &lt; 0.001. Significant difference versus UVB-irradiated group: *, <span class="html-italic">p</span> &lt; 0.05; ***, <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>The effects of CF extract on UVB-induced nuclear translocation of Nrf2 in human skin fibroblasts (scale bar = 50 µm).</p>
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<p>The effects of CF extract on UVB-induced MMP-1, -3, -9 and TIMP-1 expression in human skin fibroblasts. Significant difference versus non-irradiated group: ##, <span class="html-italic">p</span> &lt; 0.01; ###, <span class="html-italic">p</span> &lt; 0.001. Significant difference versus UVB-irradiated group: **, <span class="html-italic">p</span> &lt; 0.01; ***, <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>The effects of CF extract on UVB-induced expression of (<b>a</b>) AP-1 and (<b>b</b>) MAPK in human skin fibroblasts. Significant difference versus non-irradiated group: ###, <span class="html-italic">p</span> &lt; 0.001. Significant difference versus UVB-irradiated group: *, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01; ***, <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>The effects of CF extract on UVB-inhibited TGF-β and Smad3 expression in human skin fibroblasts. Significant difference versus non-irradiated group: ###, <span class="html-italic">p</span> &lt; 0.001. Significant difference versus UVB-irradiated group: **, <span class="html-italic">p</span> &lt; 0.01; ***, <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>The effects of CF extract on CML-treated intracellular ROS generation in human skin fibroblasts. Significant difference versus non-treated group: ###, <span class="html-italic">p</span> &lt; 0.001. Significant difference versus CML-treated group: *, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>The effects of CF extract on CML-treated RAGE expression in human skin fibroblasts. Significant difference versus non-treated group: ###, <span class="html-italic">p</span> &lt; 0.001. Significant difference versus CML-treated group: *, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01; ***, <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>The effects of CF extract on (<b>a</b>) type I pro-collagen expression and (<b>b</b>) total collagen content in human skin fibroblasts. Significant difference versus non-treated group: *, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01; ***, <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>The effects of CF extract on total collagen content of (<b>a</b>) UVB-irradiated and (<b>b</b>) CML-treated groups. (<b>c</b>) Immunofluorescence staining of collagen in human skin fibroblasts (scale bar = 25 µm). Significant difference versus control group: ##, <span class="html-italic">p</span> &lt; 0.01. Significant difference versus UVB-irradiated or CML-treated group: *, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01; ***, <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Hypothetical model of CF-mediated defense pathways against UV and AGEs-induced oxidative stress and collagen degradation in Hs68 cells. (↑, up-regulation; ↓, down-regulation).</p>
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27 pages, 2040 KiB  
Article
Djulis (Chenopodium formosanum) and Its Bioactive Compounds Protect Human Lung Epithelial A549 Cells from Oxidative Injury Induced by Particulate Matter via Nrf2 Signaling Pathway
by Chin-Chen Chu, Shih-Ying Chen, Charng-Cherng Chyau, Shu-Chen Wang, Heuy-Ling Chu and Pin-Der Duh
Molecules 2022, 27(1), 253; https://doi.org/10.3390/molecules27010253 - 31 Dec 2021
Cited by 11 | Viewed by 2510
Abstract
The protective effects of water extracts of djulis (Chenopodium formosanum) (WECF) and their bioactive compounds on particulate matter (PM)-induced oxidative injury in A549 cells via the nuclear factor-erythroid 2-related factor 2 (Nrf2) signaling were investigated. WECF at 50–300 µg/mL protected A549 [...] Read more.
The protective effects of water extracts of djulis (Chenopodium formosanum) (WECF) and their bioactive compounds on particulate matter (PM)-induced oxidative injury in A549 cells via the nuclear factor-erythroid 2-related factor 2 (Nrf2) signaling were investigated. WECF at 50–300 µg/mL protected A549 cells from PM-induced cytotoxicity. The cytoprotection of WECF was associated with decreases in reactive oxygen species (ROS) generation, thiobarbituric acid reactive substances (TBARS) formation, and increases in superoxide dismutase (SOD) activity and glutathione (GSH) contents. WECF increased Nrf2 and heme oxygenase-1 (HO-1) expression in A549 cells exposed to PM. SP600125 (a JNK inhibitor) and U0126 (an ERK inhibitor) attenuated the WECF-induced Nrf2 and HO-1 expression. According to the HPLC-MS/MS analysis, rutin (2219.7 µg/g) and quercetin derivatives (2648.2 µg/g) were the most abundant bioactive compounds present in WECF. Rutin and quercetin ameliorated PM-induced oxidative stress in the cells. Collectively, the bioactive compounds present in WECF can protect A549 cells from PM-induced oxidative injury by upregulating Nrf2 and HO-1 via activation of the ERK and JUN signaling pathways. Full article
(This article belongs to the Topic Applied Sciences in Functional Foods)
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Graphical abstract
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<p>Effects of water extracts of djulis (WECF) on the A549 cell viability induced by particulate matter (PM). (<b>A</b>) Effects of different concentrations of PM on A549 cell viability. The cells were treated with PM for 24 h. * (<span class="html-italic">p</span> &lt; 0.05) compared with the control group. (<b>B</b>) Effects of different concentrations of WECF on A549 cell viability. The cells were treated with WECF for 24 h. * (<span class="html-italic">p</span> &lt; 0.05) compared with the control group. (<b>C</b>) Effects of WECF on PM-induced A549 cell viability. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>D</b>) Effects of WECF on lactate dehydrogenase (LDH) leakage in 400 µg/mL PM-induced A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone (<b>D</b>). Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 1 Cont.
<p>Effects of water extracts of djulis (WECF) on the A549 cell viability induced by particulate matter (PM). (<b>A</b>) Effects of different concentrations of PM on A549 cell viability. The cells were treated with PM for 24 h. * (<span class="html-italic">p</span> &lt; 0.05) compared with the control group. (<b>B</b>) Effects of different concentrations of WECF on A549 cell viability. The cells were treated with WECF for 24 h. * (<span class="html-italic">p</span> &lt; 0.05) compared with the control group. (<b>C</b>) Effects of WECF on PM-induced A549 cell viability. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>D</b>) Effects of WECF on lactate dehydrogenase (LDH) leakage in 400 µg/mL PM-induced A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone (<b>D</b>). Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 1 Cont.
<p>Effects of water extracts of djulis (WECF) on the A549 cell viability induced by particulate matter (PM). (<b>A</b>) Effects of different concentrations of PM on A549 cell viability. The cells were treated with PM for 24 h. * (<span class="html-italic">p</span> &lt; 0.05) compared with the control group. (<b>B</b>) Effects of different concentrations of WECF on A549 cell viability. The cells were treated with WECF for 24 h. * (<span class="html-italic">p</span> &lt; 0.05) compared with the control group. (<b>C</b>) Effects of WECF on PM-induced A549 cell viability. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>D</b>) Effects of WECF on lactate dehydrogenase (LDH) leakage in 400 µg/mL PM-induced A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone (<b>D</b>). Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 1 Cont.
<p>Effects of water extracts of djulis (WECF) on the A549 cell viability induced by particulate matter (PM). (<b>A</b>) Effects of different concentrations of PM on A549 cell viability. The cells were treated with PM for 24 h. * (<span class="html-italic">p</span> &lt; 0.05) compared with the control group. (<b>B</b>) Effects of different concentrations of WECF on A549 cell viability. The cells were treated with WECF for 24 h. * (<span class="html-italic">p</span> &lt; 0.05) compared with the control group. (<b>C</b>) Effects of WECF on PM-induced A549 cell viability. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>D</b>) Effects of WECF on lactate dehydrogenase (LDH) leakage in 400 µg/mL PM-induced A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone (<b>D</b>). Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
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<p>Effects of water extracts of djulis (WECF) on PM-induced oxidation and antioxidant indices in A549 cells. (<b>A</b>) Effects of WECF on PM-induced intercellular ROS generation in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 2 h. (<b>B</b>) Effects of WECF on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 2 h. (<b>C</b>) Effects of WECF on PM-induced glutathione (GSH) contents in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 20 h. (<b>D</b>) Effects of WECF on PM-induced SOD activity in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 2 Cont.
<p>Effects of water extracts of djulis (WECF) on PM-induced oxidation and antioxidant indices in A549 cells. (<b>A</b>) Effects of WECF on PM-induced intercellular ROS generation in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 2 h. (<b>B</b>) Effects of WECF on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 2 h. (<b>C</b>) Effects of WECF on PM-induced glutathione (GSH) contents in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 20 h. (<b>D</b>) Effects of WECF on PM-induced SOD activity in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 2 Cont.
<p>Effects of water extracts of djulis (WECF) on PM-induced oxidation and antioxidant indices in A549 cells. (<b>A</b>) Effects of WECF on PM-induced intercellular ROS generation in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 2 h. (<b>B</b>) Effects of WECF on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 2 h. (<b>C</b>) Effects of WECF on PM-induced glutathione (GSH) contents in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 20 h. (<b>D</b>) Effects of WECF on PM-induced SOD activity in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 2 Cont.
<p>Effects of water extracts of djulis (WECF) on PM-induced oxidation and antioxidant indices in A549 cells. (<b>A</b>) Effects of WECF on PM-induced intercellular ROS generation in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 2 h. (<b>B</b>) Effects of WECF on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 2 h. (<b>C</b>) Effects of WECF on PM-induced glutathione (GSH) contents in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 20 h. (<b>D</b>) Effects of WECF on PM-induced SOD activity in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 24 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 3
<p>Effects of water extracts of djulis (WECF) on PM-induced Nrf2 and HO-1 protein expression in A549 cells. (<b>A</b>) Effects of WECF on PM-induced expression of Nrf2 in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 12 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>B</b>) Effects of WECF on PM-induced HO-1 activity in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>C</b>) Effects of p38 inhibitor (SB203580, SB), JNK inhibitor (SP600125, SP), and ERK inhibitor (U0126, U) on WECF-induced Nrf2 protein expression in PM-treated A549 cells. Control, cultured with medium alone for 12 h; PM, incubated with PM 400 µg/mL for 12 h; P + W, incubated with WECF and PM for 12 h (WECF was added 30 min before PM); SB + W + P, SP + W + P, and U + W + P, treated as described for P + W except that the p38 MAPK inhibitor SB203580, the JNK inhibitor SP600125, or the ERK inhibitor U0126 were added to the medium before WECF. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with WECF+ 400 µg/mL PM-induced cells. (<b>D</b>) Effects of p38 inhibitor (SB203580, SB), JNK inhibitor (SP600125, SP), and ERK inhibitor (U0126, U) on WECF-induced HO-1 protein expression in PM-treated A549 cells. Control, cultured with medium alone for 15 h; PM, incubated with PM 400 µg/mL for 15 h; P + W, incubated with WECF and PM for 15 h (WECF was added 30 min before PM); SB + W + P, SP + W + P, and U + W + P, treated as described for P + W except that the p38 MAPK inhibitor SB203580, the JNK inhibitor SP600125, or the ERK inhibitor U0126 were added to the medium before WECF. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with WECF+ 400 µg/mL PM-induced cells. Values in each sample with different lowercase letters are significantly different (<span class="html-italic">p</span> &lt; 0.05). Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 3 Cont.
<p>Effects of water extracts of djulis (WECF) on PM-induced Nrf2 and HO-1 protein expression in A549 cells. (<b>A</b>) Effects of WECF on PM-induced expression of Nrf2 in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 12 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>B</b>) Effects of WECF on PM-induced HO-1 activity in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>C</b>) Effects of p38 inhibitor (SB203580, SB), JNK inhibitor (SP600125, SP), and ERK inhibitor (U0126, U) on WECF-induced Nrf2 protein expression in PM-treated A549 cells. Control, cultured with medium alone for 12 h; PM, incubated with PM 400 µg/mL for 12 h; P + W, incubated with WECF and PM for 12 h (WECF was added 30 min before PM); SB + W + P, SP + W + P, and U + W + P, treated as described for P + W except that the p38 MAPK inhibitor SB203580, the JNK inhibitor SP600125, or the ERK inhibitor U0126 were added to the medium before WECF. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with WECF+ 400 µg/mL PM-induced cells. (<b>D</b>) Effects of p38 inhibitor (SB203580, SB), JNK inhibitor (SP600125, SP), and ERK inhibitor (U0126, U) on WECF-induced HO-1 protein expression in PM-treated A549 cells. Control, cultured with medium alone for 15 h; PM, incubated with PM 400 µg/mL for 15 h; P + W, incubated with WECF and PM for 15 h (WECF was added 30 min before PM); SB + W + P, SP + W + P, and U + W + P, treated as described for P + W except that the p38 MAPK inhibitor SB203580, the JNK inhibitor SP600125, or the ERK inhibitor U0126 were added to the medium before WECF. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with WECF+ 400 µg/mL PM-induced cells. Values in each sample with different lowercase letters are significantly different (<span class="html-italic">p</span> &lt; 0.05). Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 3 Cont.
<p>Effects of water extracts of djulis (WECF) on PM-induced Nrf2 and HO-1 protein expression in A549 cells. (<b>A</b>) Effects of WECF on PM-induced expression of Nrf2 in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 12 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>B</b>) Effects of WECF on PM-induced HO-1 activity in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>C</b>) Effects of p38 inhibitor (SB203580, SB), JNK inhibitor (SP600125, SP), and ERK inhibitor (U0126, U) on WECF-induced Nrf2 protein expression in PM-treated A549 cells. Control, cultured with medium alone for 12 h; PM, incubated with PM 400 µg/mL for 12 h; P + W, incubated with WECF and PM for 12 h (WECF was added 30 min before PM); SB + W + P, SP + W + P, and U + W + P, treated as described for P + W except that the p38 MAPK inhibitor SB203580, the JNK inhibitor SP600125, or the ERK inhibitor U0126 were added to the medium before WECF. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with WECF+ 400 µg/mL PM-induced cells. (<b>D</b>) Effects of p38 inhibitor (SB203580, SB), JNK inhibitor (SP600125, SP), and ERK inhibitor (U0126, U) on WECF-induced HO-1 protein expression in PM-treated A549 cells. Control, cultured with medium alone for 15 h; PM, incubated with PM 400 µg/mL for 15 h; P + W, incubated with WECF and PM for 15 h (WECF was added 30 min before PM); SB + W + P, SP + W + P, and U + W + P, treated as described for P + W except that the p38 MAPK inhibitor SB203580, the JNK inhibitor SP600125, or the ERK inhibitor U0126 were added to the medium before WECF. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with WECF+ 400 µg/mL PM-induced cells. Values in each sample with different lowercase letters are significantly different (<span class="html-italic">p</span> &lt; 0.05). Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 3 Cont.
<p>Effects of water extracts of djulis (WECF) on PM-induced Nrf2 and HO-1 protein expression in A549 cells. (<b>A</b>) Effects of WECF on PM-induced expression of Nrf2 in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 12 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>B</b>) Effects of WECF on PM-induced HO-1 activity in A549 cells. The cells were treated with WECF and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. (<b>C</b>) Effects of p38 inhibitor (SB203580, SB), JNK inhibitor (SP600125, SP), and ERK inhibitor (U0126, U) on WECF-induced Nrf2 protein expression in PM-treated A549 cells. Control, cultured with medium alone for 12 h; PM, incubated with PM 400 µg/mL for 12 h; P + W, incubated with WECF and PM for 12 h (WECF was added 30 min before PM); SB + W + P, SP + W + P, and U + W + P, treated as described for P + W except that the p38 MAPK inhibitor SB203580, the JNK inhibitor SP600125, or the ERK inhibitor U0126 were added to the medium before WECF. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with WECF+ 400 µg/mL PM-induced cells. (<b>D</b>) Effects of p38 inhibitor (SB203580, SB), JNK inhibitor (SP600125, SP), and ERK inhibitor (U0126, U) on WECF-induced HO-1 protein expression in PM-treated A549 cells. Control, cultured with medium alone for 15 h; PM, incubated with PM 400 µg/mL for 15 h; P + W, incubated with WECF and PM for 15 h (WECF was added 30 min before PM); SB + W + P, SP + W + P, and U + W + P, treated as described for P + W except that the p38 MAPK inhibitor SB203580, the JNK inhibitor SP600125, or the ERK inhibitor U0126 were added to the medium before WECF. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with WECF+ 400 µg/mL PM-induced cells. Values in each sample with different lowercase letters are significantly different (<span class="html-italic">p</span> &lt; 0.05). Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
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<p>High performance liquid chromatograms detected at a full UV-Vis spectrum of 210–600 nm (<b>top</b>), UV 360 (<b>middle</b>), and 530 nm (<b>bottom</b>) from water extracts of djulis (WECF). Peak numbers refer to <a href="#molecules-27-00253-t001" class="html-table">Table 1</a>.</p>
Full article ">Figure 5
<p>Effects of rutin and quercetin on PM-induced A549 cell viability, oxidation, and antioxidant indices in A549 cells. (<b>A</b>) Effects of rutin and quercetin on PM-induced A549 cell viability. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>B</b>) Effects of rutin and quercetin on PM-induced intercellular ROS production in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>C</b>). Effects of rutin and quercetin on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>D</b>) Effects of rutin and quercetin on PM-induced GSH contents in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 20 h. (<b>E</b>) Effects of rutin and quercetin on PM-induced SOD activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>F</b>) Effects of rutin and quercetin on PM-induced expression of Nrf2 in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 12 h. (<b>G</b>) Effects of rutin and quercetin on PM-induced HO-1 activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 5 Cont.
<p>Effects of rutin and quercetin on PM-induced A549 cell viability, oxidation, and antioxidant indices in A549 cells. (<b>A</b>) Effects of rutin and quercetin on PM-induced A549 cell viability. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>B</b>) Effects of rutin and quercetin on PM-induced intercellular ROS production in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>C</b>). Effects of rutin and quercetin on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>D</b>) Effects of rutin and quercetin on PM-induced GSH contents in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 20 h. (<b>E</b>) Effects of rutin and quercetin on PM-induced SOD activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>F</b>) Effects of rutin and quercetin on PM-induced expression of Nrf2 in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 12 h. (<b>G</b>) Effects of rutin and quercetin on PM-induced HO-1 activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 5 Cont.
<p>Effects of rutin and quercetin on PM-induced A549 cell viability, oxidation, and antioxidant indices in A549 cells. (<b>A</b>) Effects of rutin and quercetin on PM-induced A549 cell viability. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>B</b>) Effects of rutin and quercetin on PM-induced intercellular ROS production in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>C</b>). Effects of rutin and quercetin on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>D</b>) Effects of rutin and quercetin on PM-induced GSH contents in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 20 h. (<b>E</b>) Effects of rutin and quercetin on PM-induced SOD activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>F</b>) Effects of rutin and quercetin on PM-induced expression of Nrf2 in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 12 h. (<b>G</b>) Effects of rutin and quercetin on PM-induced HO-1 activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 5 Cont.
<p>Effects of rutin and quercetin on PM-induced A549 cell viability, oxidation, and antioxidant indices in A549 cells. (<b>A</b>) Effects of rutin and quercetin on PM-induced A549 cell viability. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>B</b>) Effects of rutin and quercetin on PM-induced intercellular ROS production in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>C</b>). Effects of rutin and quercetin on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>D</b>) Effects of rutin and quercetin on PM-induced GSH contents in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 20 h. (<b>E</b>) Effects of rutin and quercetin on PM-induced SOD activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>F</b>) Effects of rutin and quercetin on PM-induced expression of Nrf2 in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 12 h. (<b>G</b>) Effects of rutin and quercetin on PM-induced HO-1 activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 5 Cont.
<p>Effects of rutin and quercetin on PM-induced A549 cell viability, oxidation, and antioxidant indices in A549 cells. (<b>A</b>) Effects of rutin and quercetin on PM-induced A549 cell viability. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>B</b>) Effects of rutin and quercetin on PM-induced intercellular ROS production in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>C</b>). Effects of rutin and quercetin on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>D</b>) Effects of rutin and quercetin on PM-induced GSH contents in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 20 h. (<b>E</b>) Effects of rutin and quercetin on PM-induced SOD activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>F</b>) Effects of rutin and quercetin on PM-induced expression of Nrf2 in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 12 h. (<b>G</b>) Effects of rutin and quercetin on PM-induced HO-1 activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 5 Cont.
<p>Effects of rutin and quercetin on PM-induced A549 cell viability, oxidation, and antioxidant indices in A549 cells. (<b>A</b>) Effects of rutin and quercetin on PM-induced A549 cell viability. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>B</b>) Effects of rutin and quercetin on PM-induced intercellular ROS production in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>C</b>). Effects of rutin and quercetin on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>D</b>) Effects of rutin and quercetin on PM-induced GSH contents in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 20 h. (<b>E</b>) Effects of rutin and quercetin on PM-induced SOD activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>F</b>) Effects of rutin and quercetin on PM-induced expression of Nrf2 in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 12 h. (<b>G</b>) Effects of rutin and quercetin on PM-induced HO-1 activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 5 Cont.
<p>Effects of rutin and quercetin on PM-induced A549 cell viability, oxidation, and antioxidant indices in A549 cells. (<b>A</b>) Effects of rutin and quercetin on PM-induced A549 cell viability. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>B</b>) Effects of rutin and quercetin on PM-induced intercellular ROS production in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>C</b>). Effects of rutin and quercetin on PM-induced intercellular TBARS formation in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 2 h. (<b>D</b>) Effects of rutin and quercetin on PM-induced GSH contents in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 20 h. (<b>E</b>) Effects of rutin and quercetin on PM-induced SOD activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 24 h. (<b>F</b>) Effects of rutin and quercetin on PM-induced expression of Nrf2 in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 12 h. (<b>G</b>) Effects of rutin and quercetin on PM-induced HO-1 activity in A549 cells. The cells were treated with rutin and quercetin, respectively, and exposed to 400 µg/mL PM for 15 h. <sup>#</sup> (<span class="html-italic">p</span> &lt; 0.05) compared with the control group and * (<span class="html-italic">p</span> &lt; 0.05) compared with 400 µg/mL PM-induced cells alone. Data are presented as means ± SD (<span class="html-italic">n</span> = 3).</p>
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22 pages, 4796 KiB  
Article
Djulis Hull Improves Insulin Resistance and Modulates the Gut Microbiota in High-Fat Diet (HFD)-Induced Hyperglycaemia
by Yu-Tang Tung, Jun-Lan Zeng, Shang-Tse Ho, Jin-Wei Xu, I-Hsuan Lin and Jyh-Horng Wu
Antioxidants 2022, 11(1), 45; https://doi.org/10.3390/antiox11010045 - 26 Dec 2021
Cited by 12 | Viewed by 4511
Abstract
In this study, we annotated the major flavonoid glycoside, rutin, of djulis hull crude extract using a Global Natural Products Social Molecular Networking (GNPS) library and its MS/MS spectra. To evaluate the protective effect of djulis hull crude extract and rutin on glucose [...] Read more.
In this study, we annotated the major flavonoid glycoside, rutin, of djulis hull crude extract using a Global Natural Products Social Molecular Networking (GNPS) library and its MS/MS spectra. To evaluate the protective effect of djulis hull crude extract and rutin on glucose tolerance, we fed mice a high-fat diet (HFD) for 16 weeks to induce hyperglycaemia. These results showed that crude extract significantly decreased HFD-induced elevation in the area under the curve (AUC) of weekly random blood glucose and oral glucose tolerance tests (OGTT), homeostasis model assessment (HOMA-IR), and advanced glycation end product (AGE) levels, and significantly increased pIRS1 and Glut4 protein expression in epididymal white adipose tissue (eWAT) and liver. Furthermore, the HFD-induced reduction in the activity of glutathione peroxidase (GPx) and catalase (CAT) was reversed by crude extract. In addition, ZO-1 and occludin protein expression in the colon was markedly downregulated in HFD-fed mice, resulting in decreased intestinal permeability and lipopolysaccharide (LPS) translocation, but were restored following crude extract. Moreover, the crude extract intervention had a profound effect on the alpha diversity and microbial community in the gut microbiota. Therefore, djulis hull crude extract could improve blood glucose and increase insulin receptor sensitivity in HFD-induced hyperglycaemia, which is likely due to its modulation of the gut microbiota, preservation of the integrity of the intestinal barrier to reduce body inflammation, increased antioxidant activity, and modulation of insulin signalling. Full article
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Figure 1

Figure 1
<p>Metabolomic analysis of djulis hull crude extract. (<b>A</b>) Flavonoid glycosides-related cluster. (<b>B</b>) MS/MS fragmentation of rutin. (<b>C</b>) HPLC profiling (365 nm) of djulis hull crude extract.</p>
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<p>Effect of djulis hull crude extract and rutin on morphology, body weight, water intake, calorie intake, and random blood glucose in high fat diet-induced hyperglycaemia. (<b>A</b>) Representative pictures of mice. (<b>B</b>) Growth curve of body weight. (<b>C</b>) Average water intake. (<b>D</b>) Average calorie intake. (<b>E</b>) Weekly random blood glucose levels. (<b>F</b>) AUC of weekly random blood glucose. ND: normal diet; HFD: high-fat diet; LCE: low dosage of crude extract; HCE: high dosage of crude extract; R: rutin; AUC: area under the curve. Values represent the mean ± SEM (<span class="html-italic">n</span> = 6). The statistical methods used one-way ANOVA, and the values with different letters and symbols are significantly different at <span class="html-italic">p</span> &lt; 0.05. * <span class="html-italic">p</span> &lt; 0.05 ND vs. HFD; <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 HFD vs. HFD/HCE.</p>
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<p>Effects of djulis hull crude extract and rutin on glucose homeostasis and advanced glycation end products (AGEs) in high-fat diet-induced hyperglycaemia. (<b>A</b>) Blood glucose was measured every 30 min over 2 h after an oral glucose load. (<b>B</b>) AUC of the oral glucose tolerance test (OGTT). (<b>C</b>) Insulin. (<b>D</b>) Homeostasis model assessment (HOMA-IR). (<b>E</b>) AGEs. ND: normal diet; HFD: high-fat diet; LCE: low dosage of crude extract; HCE: high dosage of crude extract; R: rutin; AUC: area under the curve; HOMA-IR = (glucose (mg/dL) × insulin (mIU/L))/405. Values represent the mean ± SEM (<span class="html-italic">n</span> = 6). The statistical methods used one-way ANOVA, and the values with different superscript letters are significantly different at <span class="html-italic">p</span> &lt; 0.05. * <span class="html-italic">p</span> &lt; 0.05 ND vs. HFD; <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 HFD vs. HFD/HCE.</p>
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<p>Effect of djulis hull crude extract on haematoxylin &amp; eosin staining and adipocyte distribution of epididymal white adipose tissue (eWAT) in high-fat diet-induced hyperglycaemia. (<b>A</b>) Representative haematoxylin and eosin staining. Scale bar: 100 μm. (<b>B</b>,<b>C</b>) Adipocyte size and distribution of eWAT. ND: normal diet; HFD: high-fat diet; LCE: low dosage of crude extract; HCE: high dosage of crude extract; R: rutin. Values represent the mean ± SEM (<span class="html-italic">n</span> = 6). The statistical methods used one-way ANOVA, and the values with different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of djulis hull crude extract on the expression of proteins involved in glucose transportation in (<b>A</b>) epididymal white adipose tissue (eWAT) and (<b>B</b>) the liver of high-fat diet-induced hyperglycaemia. ND: normal diet; HFD: high-fat diet; HCE: high dosage of crude extract. Values represent the mean ± SEM (<span class="html-italic">n</span> = 6). The statistical methods used one-way ANOVA, and the values with different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of djulis hull crude extract on the antioxidant enzyme activities of (<b>A</b>) glutathione peroxidase (GPx), (<b>B</b>) superoxide dismutase (SOD), and (<b>C</b>) catalase (CAT) in the liver. ND: normal diet; HFD: high-fat diet; HCE: high dosage of crude extract. Values represent the mean ± SEM (<span class="html-italic">n</span> = 6). The statistical methods used an unpaired one-tailed Student’s <span class="html-italic">t</span>-test. Significant differences between two different groups are indicated; * <span class="html-italic">p</span> &lt; 0.05, ns = not significant.</p>
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<p>Effect of djulis hull crude extract on (<b>A</b>) LPS in serum and (<b>B</b>) the protein expression of tight junctions in the colon of high-fat diet-induced hyperglycaemia. ND: normal diet; HFD: high-fat diet; HCE: high dosage of crude extract; LPS: lipopolysaccharide. Values represent the mean ± SEM (<span class="html-italic">n</span> = 6). The statistical methods used one-way ANOVA, and the values with different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of djulis hull extract on the diversity of the gut microbiota in the faeces of high-fat diet-induced hyperglycaemia. (<b>A</b>) Alpha diversity of the observed, Chao1, Shannon, and Simpson indices. (<b>B</b>) Beta diversity on unweighted and weighted UniFrac principal coordinate analysis (PCoA) plots. Relative abundance of microbiota species at the (<b>C</b>) phylum level and (<b>D</b>) family level.</p>
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<p>Effects of djulis hull extract on the composition of the gut microbiota in the faeces of high-fat diet-induced hyperglycaemia. Cladogram generated from the linear discriminant effect size (LEfSe) analysis, showing the most differentially abundant taxa enriched in the microbiota of (<b>A</b>) ND (red) or HFD (green) and (<b>B</b>) HFD (red) or HCE (green). Significantly different abundances in LEfSe comparisons, sorted by <span class="html-italic">p</span>-values in ascending order. (<b>C</b>) Compared with the ND group, the bacterial genera decreased in the HFD group. (<b>D</b>) Compared with the ND group, the bacterial genera increased in the HFD group. (<b>E</b>) Compared with the ND or HFD groups, the bacterial genera increased in the HCE group. (<b>F</b>) Short-chain fatty acid production in different groups. The statistical methods used one-way ANOVA, and the values with different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effects of djulis hull extract on the composition of the gut microbiota in the faeces of high-fat diet-induced hyperglycaemia. Cladogram generated from the linear discriminant effect size (LEfSe) analysis, showing the most differentially abundant taxa enriched in the microbiota of (<b>A</b>) ND (red) or HFD (green) and (<b>B</b>) HFD (red) or HCE (green). Significantly different abundances in LEfSe comparisons, sorted by <span class="html-italic">p</span>-values in ascending order. (<b>C</b>) Compared with the ND group, the bacterial genera decreased in the HFD group. (<b>D</b>) Compared with the ND group, the bacterial genera increased in the HFD group. (<b>E</b>) Compared with the ND or HFD groups, the bacterial genera increased in the HCE group. (<b>F</b>) Short-chain fatty acid production in different groups. The statistical methods used one-way ANOVA, and the values with different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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16 pages, 5168 KiB  
Article
Anti-NAFLD Effect of Djulis Hull and Its Major Compound, Rutin, in Mice with High-Fat Diet (HFD)-Induced Obesity
by Yu-Tang Tung, Jun-Lan Zeng, Shang-Tse Ho, Jin-Wei Xu, Shiming Li and Jyh-Horng Wu
Antioxidants 2021, 10(11), 1694; https://doi.org/10.3390/antiox10111694 - 27 Oct 2021
Cited by 20 | Viewed by 3183
Abstract
Nonalcoholic fatty liver disease (NAFLD) has become the main cause of chronic liver disease worldwide, and the increasing trend of NAFLD has burdened the healthcare system. NAFLD encompasses a wide range of liver pathologies, from simple benign hepatocyte steatosis to more severe inflammatory [...] Read more.
Nonalcoholic fatty liver disease (NAFLD) has become the main cause of chronic liver disease worldwide, and the increasing trend of NAFLD has burdened the healthcare system. NAFLD encompasses a wide range of liver pathologies, from simple benign hepatocyte steatosis to more severe inflammatory nonalcoholic steatohepatitis. Djulis (Chenopodium formosanum Koidz.) is traditionally used as a native cereal and a food supplement that promotes human health through its antioxidant, hepatoprotection, skin protection, hypolipidemic, hypoglycemic, and antitumor effects. Djulis hull, regarded as agricultural waste, is usually removed during food processing and contains high rutin content. The present study evaluated the anti-NAFLD effect of Djulis hull and its major compound, rutin, in mice with high-fat diet (HFD)-induced obesity. Male C57BL/6J mice were randomly divided into one of five diet groups (n = 6 per group) and fed the following for 16 weeks: (1) normal diet group (ND), (2) HFD group (HFD), (3) HFD and oral gavage of low dose (50 mg/kg) of Djulis hull crude extract group (HFD/LCE), (4) HFD and oral gavage of high dose (250 mg/kg) of Djulis hull crude extract group (HFD/HCE), or (5) HFD and oral gavage (50 mg/kg) of rutin (HFD/R) group. We found that Djulis hull crude extract markedly reduced HFD-induced elevation in body weight and fat around the kidney weights, hepatic injury indicators (AST and ALT), and steatosis and hypertrophy. Furthermore, Djulis hull crude extract administration significantly affected DG(20:4/18:1), PA(22:0/17:1), PC(10:0/17:0), and PA(18:4/20:5) in HFD-induced obese mice. In addition, treating HFD-induced obese rats with Djulis hull crude extract significantly increased fatty acid oxidation by increasing the protein expression of phosphorylated AMP-activated protein kinase, peroxisome proliferator-activated receptor-α, and hepatic carnitine palmitoyltransferase-1 in the liver. Moreover, the administration of Djulis hull crude extract significantly decreased the inflammatory response (PPARγ, IL-6, and TNF-α) to modulate oxidative damage. Therefore, Djulis hull crude extract attenuated the progression of NAFLD by reducing inflammation mediated by PPARγ and enhancing the expression levels of genes involved in fatty acid oxidation mediated by AMPK signaling. Full article
(This article belongs to the Section Health Outcomes of Antioxidants and Oxidative Stress)
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<p>Molecular networking analysis of the BuOH soluble fraction of Djulis hull extract.</p>
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<p>Effect of Djulis hull crude extract and rutin on body weight and tissue weight in HFD-induced obese mice. ND: normal diet; HFD: high-fat diet; LCE: low dosage of crude extract; HCE: high dosage of crude extract; R: rutin; eWAT: epididymal white adipose tissue; pWAT: perirenal white adipose tissue. Values represent the mean ± SEM (n = 6). Statistical methods were used by one-way ANOVA, and the different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of Djulis hull crude extract and rutin on blood biochemistry in HFD-induced obese mice. ND: normal diet; HFD: high-fat diet; LCE: low dosage of crude extract; HCE: high dosage of crude extract; R: rutin; LDL-C: low-density lipoprotein cholesterol; HDL-C: high-density lipoprotein cholesterol; AST: aspartate aminotransferase; ALT: alanine aminotransferase. Values represent the mean ± SEM (n = 6). Statistical methods were used by one-way ANOVA, and the different superscript letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of Djulis hull crude extract on lipidomics in HFD-induced obese mice. (<b>A</b>) The orthogonal partial least-squared discriminant analysis (OPLS-DA) score plot for ND, HFD and HFD/HCE groups. The x-and y-axes of OPLS-DA showed the variance explained among the groups. (<b>B</b>) Compared with the ND group, the lipid species increased in the HFD group. (<b>C</b>) Compared with the ND group, the lipid species decreased in the HFD group. ND: normal diet; HFD: high-fat diet; HCE: high dosage of crude extract. Values represent the mean ± SEM (n = 6). Statistical methods were used by two-way ANOVA, and the different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of Djulis hull crude extract and rutin on pathological indices in HFD-induced obese mice. (<b>A</b>) Representative hematoxylin and eosin staining of liver sections. (<b>B</b>) NAFLD index calculated from individual scores for steatosis, hypertrophy, lobular inflammation, ballooning and fibrosis. ND: normal diet; HFD: high-fat diet; LCE: low dosage of crude extract; HCE: high dosage of crude extract; R: rutin. Values represent the mean ± SEM (n = 6). Statistical methods were used by one-way ANOVA, and the different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of Djulis hull crude extract on the protein expression of (<b>A</b>) PPARγ, IL-1β, IL-6, and TNF-α, (<b>B</b>) SIRT1 and LXRα, and (<b>C</b>) lipogenesis and β-oxidation pathways in the livers of HFD-induced obese mice. ND: normal diet; HFD: high-fat diet; HCE: high dosage of crude extract. Values represent the mean ± SEM (n = 6). Statistical methods were used by one-way ANOVA, and the different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of Djulis hull crude extract on the protein expression of (<b>A</b>) PPARγ, IL-1β, IL-6, and TNF-α, (<b>B</b>) SIRT1 and LXRα, and (<b>C</b>) lipogenesis and β-oxidation pathways in the livers of HFD-induced obese mice. ND: normal diet; HFD: high-fat diet; HCE: high dosage of crude extract. Values represent the mean ± SEM (n = 6). Statistical methods were used by one-way ANOVA, and the different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Proposed mechanism of Djulis hull crude extract-mediated modulation of the lipid metabolism pathway in HFD-induced obese mice. The effects of Djulis hull crude extract on the fatty liver of mice may occur through anti-inflammation and the lipid oxidative pathway.</p>
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15 pages, 3211 KiB  
Article
Different Drought-Tolerant Mechanisms in Quinoa (Chenopodium quinoa Willd.) and Djulis (Chenopodium formosanum Koidz.) Based on Physiological Analysis
by Pin-Hua Lin and Yun-Yang Chao
Plants 2021, 10(11), 2279; https://doi.org/10.3390/plants10112279 - 24 Oct 2021
Cited by 20 | Viewed by 3270
Abstract
The purpose of this experiment is to study the effects of treatment with 90% (28.5% volumetric water content (VWC)), 75% (24% VWC), 50% (16% VWC), and 25% (8% VWC) of water requirements on the growth of two djulis (Chenopodium formosana Koidz) varieties [...] Read more.
The purpose of this experiment is to study the effects of treatment with 90% (28.5% volumetric water content (VWC)), 75% (24% VWC), 50% (16% VWC), and 25% (8% VWC) of water requirements on the growth of two djulis (Chenopodium formosana Koidz) varieties (red: RP and yellow: OR) and one quinoa (Chenopodium quinoa Willd) varieties (PI). The results showed that drought stress (8% VWC) significantly reduced plant growth and relative water content, and increased H2O2 and MDA content in C. formosana and C. quinoa. The most significant increase in these parameters was detected in the OR variety. The antioxidant enzymes, such as SOD, APX, and GR activities of PI variety under drought treatment (8% VWC), are significantly increased, while GR activity of C. formosana also increased significantly. Additionally, C. formosana and PI variety remained at a stable AsA/DHA ratio, but the GSH/GSSG ratio decreased during drought treatment. Moreover, drought stress increased total soluble sugars and proline content in the PI variety. However, C. formosana proline content was extremely significantly enhanced, and only the OR variety increased the total soluble sugar content at the same time during the vegetative growth period. In summary, C. formosana and C. quinoa have different drought tolerance mechanisms to adapt to being cultivated and produced under severe drought conditions. Full article
(This article belongs to the Special Issue Responses of Plants to Environmental Stresses Volume II)
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<p>Effect of drought stress on plant height in <span class="html-italic">C. formosana</span> and <span class="html-italic">C. quinoa</span> during vegetative growth. From 2nd to 5th week after sowing, the plant heights of <span class="html-italic">C. formosana</span> RP variety (<b>A</b>), OR variety (<b>B</b>), and <span class="html-italic">C. quinoa</span> PI variety (<b>C</b>) were investigated. Bars show means ± SE. Values with the same letter are not significantly different by LSD (<span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 5).</p>
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<p>Effect of drought stress on relative water content (RWC) in <span class="html-italic">C. formosana</span> and <span class="html-italic">C. quinoa</span>. <span class="html-italic">C. formosana</span> RP variety, OR variety, and <span class="html-italic">C. quinoa</span> PI variety grow to vegetative stage (5 weeks after transplanting) (<b>A</b>) and reproductive stage (8 weeks after transplanting) (<b>B</b>); the water content was investigated, respectively. Bars show means ± SE. Values with the same letter are not significantly different in treatments between the same variety by LSD (<span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 4).</p>
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<p>Effect of drought stress on physiological indicators in <span class="html-italic">C. formosana</span> and <span class="html-italic">C. quinoa</span>. <span class="html-italic">C. formosana</span> RP variety, OR variety, and <span class="html-italic">C. quinoa</span> PI variety during vegetative stage (5 weeks after transplanting) and reproductive stage (8 weeks after transplanting); the total chlorophyll content (<b>A</b>,<b>B</b>), H<sub>2</sub>O<sub>2</sub> content (<b>C</b>,<b>D</b>), and MDA content (<b>E</b>,<b>F</b>) were investigated, respectively. Bars show means ± SE. Values with the same letter are not significantly different in treatments between the same variety by LSD (<span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 4).</p>
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<p>Effect of drought stress on antioxidant enzyme activities in <span class="html-italic">C. formosana</span> and <span class="html-italic">C. quinoa</span>. <span class="html-italic">C. formosana</span> RP variety, OR variety, and <span class="html-italic">C. quinoa</span> PI variety during vegetative stage (5 weeks after transplanting) and reproductive stage (8 weeks after transplanting); the SOD activity (<b>A</b>,<b>B</b>), CAT activity (<b>C</b>,<b>D</b>), APX activity (<b>E</b>,<b>F</b>), and GR activity (<b>G</b>,<b>H</b>) were investigated, respectively. Bars show means ± SE. Values with the same letter are not significantly different in treatments between the same variety by LSD (<span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 4).</p>
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<p>Effect of drought stress on proline content in <span class="html-italic">C. formosana</span> and <span class="html-italic">C. quinoa</span>. <span class="html-italic">C. formosana</span> RP variety, OR variety, and <span class="html-italic">C. quinoa</span> PI variety grow to vegetative stage (<b>A</b>) and reproductive stage (<b>B</b>); the proline content was investigated, respectively. Bars show means ± SE. Values with the same letter are not significantly different in treatments between the same variety by LSD (<span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 4).</p>
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<p>Effect of drought stress on total soluble sugars and starch content in <span class="html-italic">C. formosana</span> and <span class="html-italic">C. quinoa</span>. <span class="html-italic">C. formosana</span> RP variety, OR variety, and <span class="html-italic">C. quinoa</span> PI variety grow to vegetative stage and reproductive stage; the total soluble sugars (<b>A</b>,<b>B</b>) and starch content (<b>C</b>,<b>D</b>) were investigated, respectively. Bars show means ± SE. Values with the same letter are not significantly different in treatments between the same variety by LSD (<span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 4).</p>
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<p>Soil water content change during growth season.</p>
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<p>Different physiological mechanisms of drought tolerance between <span class="html-italic">C. formosana</span> and <span class="html-italic">C. quinoa</span>.</p>
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17 pages, 2878 KiB  
Article
The Impact of Air or Nitrogen Non-Thermal Plasma on Variations of Natural Bioactive Compounds in Djulis (Chenopodium formosanum Koidz.) Seed and the Potential Effects for Human Health
by Bing-Jyh Lu, Tzu-Che Lin, How-Ran Chao, Cheng-Hsian Tsai, Jian-He Lu, Ming-Hsien Tsai, Ching-Tzu Chang, Hao Hsieh, I-Cheng Lu, Rachelle D. Arcega, Wei-Hsiang Chang, Hsiu-Ling Chen, Wan Nurdiyana Wan Mansor and Ying-Chieh Lee
Atmosphere 2021, 12(11), 1375; https://doi.org/10.3390/atmos12111375 - 21 Oct 2021
Cited by 4 | Viewed by 2215
Abstract
Non-thermal plasma (NTP) has been widely applied in the food and agricultural industries. It is still unknown whether natural bioactive compounds in seeds are affected by NTP treatment. Our goal was to examine whether the bioactive compounds in djulis (Chenopodium formosanum Koidz.) [...] Read more.
Non-thermal plasma (NTP) has been widely applied in the food and agricultural industries. It is still unknown whether natural bioactive compounds in seeds are affected by NTP treatment. Our goal was to examine whether the bioactive compounds in djulis (Chenopodium formosanum Koidz.) seed are changed after NTP treatment. The betacyanin, anthocyanin, total phenolic content (TPCs), total flavonoids (TFs), 2,2-diphenyl-1-picrylhydrazyl radical scavenging effects (DPPH), gallic acid, and rutin were compared in NTP-treated seed and an untreated control. Levels of betacyanin, anthocyanin, and TPCs in the seed were found to be significantly increased after the nitrogen (N2)-NTP treatment compared with the control (p < 0.001). Inversely, the air-NTP treatment significantly weakened the performance of these bioactive compounds in the seed as compared to the control. Levels of TFs in both the air- and N2-NTP treated seed were significantly lower than those in the control (p < 0.001). After the NTP treatment, DPPH was still at high levels, similar to those in the control. The djulis seed extract had antioxidant and anti-inflammatory effects on THP-1 (human-monocyte-cell line) cells. N2-NTP generated nitrogen reactive species that activated the bioactive compounds in the seed. In contrast, air-NTP produced oxygen and nitrogen reactive species inhibited the expression of these bioactive compounds. Full article
(This article belongs to the Special Issue Indoor Air Quality in Healthcare Facilities and Healing Environments)
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<p>Optical analysis of NTP and djulis seeds: (<b>A</b>) the OES (optical emission spectroscopy) spectrum after air atmospheric plasma (air-NTP) and (<b>B</b>) the OES spectrum after nitrogen gas atmospheric plasma (N<sub>2</sub>-NTP) treatment.</p>
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<p>The functional groups of FTIR spectrum on the surface of the djulis seed.</p>
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<p>Variations in betacyanin (<b>A</b>), anthocyanin (<b>B</b>), and DPPH radical scavenging effects (<b>C</b>) in djulis seed after air-NTP or N<sub>2</sub>-NTP treatment compared with the untreated control.</p>
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<p>Levels of phenolic acids and flavonoids in the NTP-treated and untreated djulis seeds shown as total phenolic content in the NTP-treated seeds compared with the untreated control: (<b>A</b>) flavonoids in NTP-treated seeds compared with the untreated seeds (control) and (<b>B</b>) levels of gallic acid and rutin in seeds before and after NTP treatment.</p>
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<p>Levels of gallic acid and rutin in the seeds before and after NTP treatment: (<b>A</b>) air-NTP treatment and (<b>B</b>) N<sub>2</sub>-NTP treatment.</p>
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<p>Examination of thermal effects on the djulis seeds heated by oven. The oven temperature was controlled at room temperature and 46, 55, and 77 °C and the contact times tested were 5, 10, and 15 s. The fold increases of bioactive compounds of the djulis seed under the thermal treatment were obtained over those in the non-thermal control (room temperature): (<b>A</b>) betacyanin and anthocyanin; (<b>B</b>) TFCs and TFs; and (<b>C</b>) DPPH.</p>
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15 pages, 1622 KiB  
Article
Development and Optimization of Djulis Sourdough Bread Fermented by Lactic Acid Bacteria for Antioxidant Capacity
by Hung-Yueh Chen, Chang-Wei Hsieh, Pin-Cheng Chen, Shin-Pin Lin, Ya-Fen Lin and Kuan-Chen Cheng
Molecules 2021, 26(18), 5658; https://doi.org/10.3390/molecules26185658 - 17 Sep 2021
Cited by 9 | Viewed by 3324
Abstract
This study developed a nutritionally valuable product with bioactive activity that improves the quality of bread. Djulis (Chenopodium formosanum), a native plant of Taiwan, was fermented using 23 different lactic acid bacteria strains. Lactobacillus casei BCRC10697 was identified as the ideal [...] Read more.
This study developed a nutritionally valuable product with bioactive activity that improves the quality of bread. Djulis (Chenopodium formosanum), a native plant of Taiwan, was fermented using 23 different lactic acid bacteria strains. Lactobacillus casei BCRC10697 was identified as the ideal strain for fermentation, as it lowered the pH value of samples to 4.6 and demonstrated proteolysis ability 1.88 times higher than controls after 24 h of fermentation. Response surface methodology was adopted to optimize the djulis fermentation conditions for trolox equivalent antioxidant capacity (TEAC). The optimal conditions were a temperature of 33.5 °C, fructose content of 7.7%, and dough yield of 332.8, which yielded a TEAC at 6.82 mmol/kg. A 63% increase in TEAC and 20% increase in DPPH were observed when compared with unfermented djulis. Subsequently, the fermented djulis was used in different proportions as a substitute for wheat flour to make bread. The total phenolic and flavonoid compounds were 4.23 mg GAE/g and 3.46 mg QE/g, marking respective increases of 18% and 40% when the djulis was added. Texture analysis revealed that adding djulis increased the hardness and chewiness of sourdough breads. It also extended their shelf life by approximately 2 days. Thus, adding djulis to sourdough can enhance the functionality of breads and may provide a potential basis for developing djulis-based functional food. Full article
(This article belongs to the Special Issue Functional Food and Their Pharmaceutical Properties)
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Graphical abstract
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<p>The selection of different lactic acid bacteria for djulis fermentation through the determination of (<b>A</b>) the pH value and (<b>B</b>) proteolysis activity of djulis fermented by different LAB strains. (<b>C</b>) Growth curve and (<b>D</b>) ABTS radical scavenging activity and proteolysis activity of djulis fermented by <span class="html-italic">L. casei</span> BCRC 10697. Values are the mean ± SD. Superscripts (a, b, c, etc.) indicate significant differences in Fisher’s LSD tests (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Optimization of conditions for TEAC of sourdough fermentation using response surface methodology (RSM). Contour plots of (<b>A</b>) fructose vs. temperature, (<b>B</b>) dough yield vs. fructose, and (<b>C</b>) dough yield vs. temperature. Surface plots (<b>D</b>–<b>F</b>) correspond to (<b>A</b>–<b>C</b>), respectively.</p>
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<p>Descriptive analysis of different bread samples. (<b>A</b>) Score plot and (<b>B</b>) loading plot of different bread samples. PC1 explained 63.4% of the variation in the data. WB (wheat bread) is marked in blue, DB (djulis bread) in green, 20% DSB (djulis sourdough bread) in black, 20% DSBC (djulis sourdough bread with cocoa power and dried cranberry) in red, and attributes are marked in blue.</p>
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14 pages, 532 KiB  
Article
Functionality of Djulis (Chenopodium formosanum) By-Products and In Vivo Anti-Diabetes Effect in Type 2 Diabetes Mellitus Patients
by Po-Hsien Li, Yung-Jia Chan, Ya-Wen Hou, Wen-Chien Lu, Wen-Hui Chen, Jie-Yun Tseng and Amanda Tresiliana Mulio
Biology 2021, 10(2), 160; https://doi.org/10.3390/biology10020160 - 17 Feb 2021
Cited by 10 | Viewed by 3484
Abstract
Djulis (Chenopodium formosanum Koidz.) is a species of cereal grain native to Taiwan. It is rich in dietary fibre and antioxidants and therefore reputed to relieve constipation, suppress inflammation, and lower blood glucose. The aim of this study was to investigate the [...] Read more.
Djulis (Chenopodium formosanum Koidz.) is a species of cereal grain native to Taiwan. It is rich in dietary fibre and antioxidants and therefore reputed to relieve constipation, suppress inflammation, and lower blood glucose. The aim of this study was to investigate the composition and physicochemical properties of dietary fibre from djulis hull. Meanwhile, determination of the in vivo antidiabetic effect on patients with type 2 diabetes mellitus (T2DM) after consuming the djulis hull powder. Djulis hull contained dietary fibre 75.21 ± 0.17% dry weight, and insoluble dietary fibre (IDF) reached 71.54 ± 0.27% dry weight. The IDF postponed the adsorption of glucose and reduced the activity of α-amylase. Postprandial blood glucose levels in patients with T2DM showed three different tendencies. First, the area under the glucose curve was significantly lower after ingesting 10 or 5 g djulis hull powder, which then postponed the adsorption of glucose, but the area under the glucose curve was similar with the two doses. After consuming 10 g djulis hull before 75 g glucose 30 and 60 min after the meal, patients with T2DM had blood glucose values that were significantly lower at the same postprandial times than those of patients who did not consume djulis hull. In short, patients who consumed djulis hull prior to glucose administration had decreased blood glucose level compared with those who did not. Djulis hull may have benefits for patients with T2DM. Full article
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<p>Study protocol of in vivo study the effect of djulis hull powder on the postprandial blood glucose content in patients with type 2 diabetes patients. OGTT, Oral Glucose Tolerance Test.</p>
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12 pages, 2126 KiB  
Article
Effect of Calcium on the Growth of Djulis (Chenopodium formosanum Koidz.) Sprouts
by Yun-Yang Chao, Wei-Jia Wang and Yan-Ting Liu
Agronomy 2021, 11(1), 82; https://doi.org/10.3390/agronomy11010082 - 2 Jan 2021
Cited by 8 | Viewed by 3720
Abstract
Taiwanese quinoa (Chenopodium formosanum Koidz, commonly known as djulis) is a close relative of quinoa, is rich in nutritional value and high active components, such as, betaine and polyphenols, and is a vital food crop. We investigated the effects of calcium carbonate [...] Read more.
Taiwanese quinoa (Chenopodium formosanum Koidz, commonly known as djulis) is a close relative of quinoa, is rich in nutritional value and high active components, such as, betaine and polyphenols, and is a vital food crop. We investigated the effects of calcium carbonate on the growth and physiology of Djulis sprouts because calcium is an essential nutrient for plants that can strengthen a plant’s root system and improve its nutrient absorption; moreover, under abiotic stress, calcium transmits messages to enhance cell tolerance. Experiments were conducted using 0, 1.25, 2.5, and 5 mM calcium carbonate hydroponic liquid treatment. Treatment with 5 mM calcium carbonate promoted the growth of djulis; specifically, root length, plant height, aboveground fresh weight, and dry weight increased by 55%, 12%, 37%, and 17%, respectively. In further investigation of the physiological change of djulis sprouts treated with calcium carbonate, the results showed that after 5 days of treatment with 5 mM calcium carbonate, the contents of hydrogen peroxide and malondialdehyde decreased significantly while the chlorophyll content increased significantly. Antioxidant enzyme activity was significantly improved. The activities of superoxide dismutase, catalase, ascorbate peroxidase, and glutathione reductase were increased by 42%, 25%, 35.7%, and 56.4%, respectively, and the calcium content of the aboveground and underground plant parts was increased fourfold and threefold, respectively. The content of proline, regarded as an osmoprotectant, was reduced by 12%. Thus, we concluded that treatment of djulis sprouts with 5 mM calcium carbonate can improve their antioxidant capacity, reduce the content of reactive oxygen species, and promote crop growth. Full article
(This article belongs to the Special Issue Improving Mineral Nutrition to Obtain Stress Tolerant Crops)
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<p>The effect of calcium carbonate on the growth of Djulis sprouts. The 7-d-old djulis plants were treated with 0 mM (<b>A</b>), 1.25 mM (<b>B</b>), 2.5 mM (<b>C</b>) and 5 mM (<b>D</b>) CaCO<sub>3</sub> for 7 days, the growth characteristics of seedlings were recorded. (Scale bar = 1.0 cm).</p>
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<p>The effect of calcium carbonate on the growth characters of Djulis sprouts. The 7-d-old djulis plants were treated with 5 mM CaCO<sub>3</sub> for 3, 5, and 7 days. Shoot height (<b>A</b>), root length (<b>B</b>), root fresh weight (<b>C</b>), and root dry weight (<b>D</b>) were investigated. Bars show means ± SE (<span class="html-italic">n</span> = 10), repeated three times. Values with the same letter are not significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The effect of calcium carbonate on the physiological indictors of Djulis sprouts. The 7-d-old djulis plants were treated with 5 mM CaCO<sub>3</sub> for 5 days. The total chlorophyll content (<b>A</b>) H<sub>2</sub>O<sub>2</sub> content (<b>B</b>) and MDA content (<b>C</b>) of djulis were measured. Bars show means ± SE (<span class="html-italic">n</span> = 4). * represent values that are significantly different between calcium carbonate concentration 0 mM and 5 mM at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The effect of calcium carbonate on antioxidant enzyme activities of Djulis sprouts. The 7-d-old djulis plants were treated with 5 mM CaCO<sub>3</sub> for 5 days. The SOD (<b>A</b>) CAT (<b>B</b>) APX (<b>C</b>) and GR (<b>D</b>) activities of djulis were measured. Bars show means ± SE (<span class="html-italic">n</span> = 4). * represent values that are significantly different between calcium carbonate concentration 0 mM and 5 mM at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The effect of calcium carbonate on Na<sup>+</sup> and K<sup>+</sup> content of Djulis sprouts. The 7-d-old djulis plants were treated with 5 mM CaCO<sub>3</sub> for 5 days. The Ca<sup>+</sup> content of the shoot (<b>A</b>) and the root (<b>C</b>), and K<sup>+</sup> content of the shoot (<b>B</b>) and the root (<b>D</b>) of djulis were measured. Bars show means ± SE (<span class="html-italic">n</span> = 4). * represent values that are significantly different between calcium carbonate concentration 0 mM and 5 mM at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The effect of calcium carbonate on proline content of Djulis sprouts. The 7-d-old djulis plants were treated with 5 mM CaCO<sub>3</sub> for 5 days. The proline content of djulis were measured. Bars show means ± SE (<span class="html-italic">n</span> = 4). * represent values that are significantly different between calcium carbonate concentration 0 mM and 5 mM at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Mechanism diagram of calcium carbonate to promote the growth of djulis sprouts.</p>
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