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14 pages, 634 KiB  
Article
Chemical Composition and Biological Activity of Hypericum Species—H. hirsutum, H. barbatum, H. rochelii
by Jovan Baljak, Mirjana Bogavac, Maja Karaman, Branislava Srđenović Čonić, Biljana Vučković, Goran Anačkov and Nebojša Kladar
Plants 2024, 13(20), 2905; https://doi.org/10.3390/plants13202905 (registering DOI) - 17 Oct 2024
Abstract
St. John’s wort (Hypericum perforatum, Hypericaceae) is the most well-known species in the genus Hypericum, which comprises several hundred species. This study investigates the biological and phytochemical potential of the under-researched Hypericum species, H. hirsutum, H. barbatum, and [...] Read more.
St. John’s wort (Hypericum perforatum, Hypericaceae) is the most well-known species in the genus Hypericum, which comprises several hundred species. This study investigates the biological and phytochemical potential of the under-researched Hypericum species, H. hirsutum, H. barbatum, and H. rochelii. A high level of similarity between the chemical profiles of H. hirsutum and H. barbatum and the official source of the herbal drug (H. perforatum) was shown, but a higher content of quercetin and rutin was also found in all three evaluated species (116–230 µg/g dry herb). The highest amount of phenolics (195 mg GAE/g) was recorded in H. hirsutum extract, while the highest amount of flavonoids (47 mg QE/g) was recorded in H. barbatum extract. The evaluated species were excellent scavengers of DPPH, OH, and NO radicals, as well as strong ferric ion reducers in the FRAP test. Prominent monoamine oxidase A and α-glucosidase inhibition was observed, compared to modest inhibition of monoamine oxidase B, α-amylase, and acetylcholinesterase. High activity against Gram-positive MRSA S. aureus was demonstrated for the tested species, with MIC/MBC values recorded at 12.5 µg/mL. Antifungal activity against Candida strains was not observed. The obtained results emphasize the need for further investigation of species of the genus Hypericum to discover potentially new sources of biologically active compounds. Full article
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<p>PCA-biological potential: (<b>a</b>) PCA loadings, (<b>b</b>) the position of the evaluated extracts in the space defined by the first two principal components (PCAs).</p>
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16 pages, 2122 KiB  
Article
Assessing a “Least-Concern” Red List Tree Species from Madagascar Used in Traditional Medicine: Morella spathulata (Myricaceae) Phyto-Compounds and Anti-Inflammatory Properties
by Annachiara Fioccardi, Dario Donno, Zoarilala Rinah Razafindrakoto, Nantenaina Tombozara, Sylvia Henintsoa, Elyna Mahitasoa, Valeria Torti, Marcellin Solofoniaina, Lorenzo Rosso, Giovanni Gamba, Charles Andrianjara, David Ramanitrahasimbola and Gabriele Loris Beccaro
Plants 2024, 13(20), 2899; https://doi.org/10.3390/plants13202899 - 17 Oct 2024
Viewed by 182
Abstract
Morella spathulata (Myricaceae family) is a common plant from Madagascar and is present on the IUCN Red List of threatened species classified at the ’least concern’ level, used by the local population to treat numerous illnesses and pain. Despite its frequent use, comprehensive [...] Read more.
Morella spathulata (Myricaceae family) is a common plant from Madagascar and is present on the IUCN Red List of threatened species classified at the ’least concern’ level, used by the local population to treat numerous illnesses and pain. Despite its frequent use, comprehensive phytochemical and pharmacological research on the species is limited. This study evaluated the antioxidant, analgesic, and anti-inflammatory properties, as well as the toxicity of methanol extracts from the leaves (MS_L) and bark (MS_B) of M. spathulata. The research involved the analysis of nutritional traits such as sugars, organic acids, vitamin C, polyphenolic content (TPC) and the main phytochemicals by HPLC analysis. Antioxidant capacity was assessed through DPPH and FRAP assays. Analgesic and anti-inflammatory activities were evaluated using acetic acid-induced writhing and carrageenan-induced paw oedema tests in mice. The results showed a high content of phenolic and bioactive components in the leaf and bark extracts, associated with antioxidant, analgesic and anti-inflammatory properties. The interaction of key compounds such as ferulic acid and ellagic acid with proteins involved in pH regulation and immune modulation provides clues to the mechanisms underlying the therapeutic effects. However, conservation efforts are crucial due to habitat loss and illegal logging, and further studies are needed to fully explore the plant’s therapeutic potential. Full article
(This article belongs to the Special Issue Phytochemistry and Pharmacological Properties of Medicinal Plants)
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<p>Percentage contribution of phenolic compounds and vitamins in the analyzed samples. MS_L: <span class="html-italic">M. spathulata</span> leaf extract; MS_B: <span class="html-italic">M. spathulata</span> bark extract. Mean values are shown (N = 3).</p>
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13 pages, 1444 KiB  
Article
Chemical Composition, Antioxidant, Antibacterial, and Hemolytic Properties of Ylang-Ylang (Cananga odorata) Essential Oil: Potential Therapeutic Applications in Dermatology
by Soukaina Alaoui Mrani, Hind Zejli, Dounia Azzouni, Driss Fadili, Mohammed M. Alanazi, Said Omar Said Hassane, Rachid Sabbahi, Atul Kabra, Abdelfattah El Moussaoui, Belkheir Hammouti and Mustapha Taleb
Pharmaceuticals 2024, 17(10), 1376; https://doi.org/10.3390/ph17101376 (registering DOI) - 16 Oct 2024
Viewed by 308
Abstract
Background/Objectives: This study investigates the chemical composition, antioxidant, antibacterial, and hemolytic properties of ylang-ylang (Cananga odorata) essential oil, with a focus on its potential therapeutic applications for dermatological diseases and the importance of transforming such bioactive properties into a stable, safe, [...] Read more.
Background/Objectives: This study investigates the chemical composition, antioxidant, antibacterial, and hemolytic properties of ylang-ylang (Cananga odorata) essential oil, with a focus on its potential therapeutic applications for dermatological diseases and the importance of transforming such bioactive properties into a stable, safe, and effective formulation. Methods/Rsults: Essential oils were extracted from flowers harvested in northern Grande Comore using hydro distillation at three different distillation times to examine the impact on yield and quality. Gas chromatographic analysis identified a complex mixture of compounds, including linalool, geranyl acetate, and benzyl benzoate. Antioxidant activity was assessed using DPPH, FRAP, TAC, and beta-carotene bleaching inhibition assays, revealing significant radical scavenging capabilities, with DPPH IC50 varying between 1.57 and 3.5 mg/mL. Antibacterial activity was tested against Escherichia coli, Staphylococcus aureus, Bacillus subtilis, and Pseudomonas aeruginosa, showing promising inhibition zones and minimum inhibitory concentrations. Hemolytic tests indicated varying degrees of red blood cell damage, emphasizing the need for careful concentration management in therapeutic applications. Molecular docking studies highlighted potential therapeutic targets for dermatological conditions, identifying high binding affinities for specific compounds against proteins involved in acne, eczema, and psoriasis. Conclusions: This comprehensive analysis underscores the potential of ylang-ylang essential oil (YEOs) as a natural alternative for antimicrobial treatments and dermatological applications, with its success dependent on optimized extraction methods and precise formulation to reduce cytotoxic effects. A formulation approach is crucial to ensure controlled release, improve bioavailability, and minimize skin irritation. Full article
(This article belongs to the Section Natural Products)
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<p>Total antioxidant capacity of <span class="html-italic">YEOs.</span></p>
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<p>Absorbance changes over time during incubation (37 °C) of erythrocyte suspensions with varying concentrations of <span class="html-italic">YEOs</span>, PBS + susp: red blood cell suspension from rat blood was incubated in a phosphate-buffered saline (PBS) solution at pH 7.4.</p>
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<p>Molecular structures of target molecules.</p>
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<p>The interaction pharmacology network for the treatment of the selected dermatological diseases.</p>
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18 pages, 1505 KiB  
Article
Comparative Bioaccesibility Study of Cereal-Based Nutraceutical Ingredients Using INFOGEST Static, Semi-Dynamic and Dynamic In Vitro Gastrointestinal Digestion
by Iván Jesús Jiménez-Pulido, Ana Belén Martín-Diana, Daniel de Luis and Daniel Rico
Antioxidants 2024, 13(10), 1244; https://doi.org/10.3390/antiox13101244 (registering DOI) - 16 Oct 2024
Viewed by 240
Abstract
Efficient development of effective functional foods and nutraceuticals requires adequate estimation methods of the bioaccessibility of their bioactive compounds. Specially grain-based nutraceuticals and functional ingredients are often enriched in bound/low bioavailable bioactive phytochemicals. The objective of this work was to evaluate the differences [...] Read more.
Efficient development of effective functional foods and nutraceuticals requires adequate estimation methods of the bioaccessibility of their bioactive compounds. Specially grain-based nutraceuticals and functional ingredients are often enriched in bound/low bioavailable bioactive phytochemicals. The objective of this work was to evaluate the differences in applying static or dynamic digestion models for the estimation of bioaccessibility of antioxidants present in cereal grain-based/fiber-rich ingredients produced using enzymatic hydrolysis and sprouting processes. Main liberated phenolic compounds, antioxidant activity (ABTS•+ and ORAC) and ferric reducing capacity were evaluated in the samples following three digestion protocols with differences based on their dynamism: static, semi-dynamic and dynamic. The samples digested with the dynamic method showed higher antioxidant and reducing capacities than those digested with the static and semi-dynamic protocols. The results obtained from the digests with the dynamic model showed a total phenol content (TPs) ranging from 1068.22 to 1456.65 μmol GAE 100 g−1 and antioxidant capacity values from 7944.62 to 15,641.90 μmol TE 100 g−1 (ORAC) and from 8454.08 to 11,002.64 μmol TE 100 g−1 (ABTS•+), with a reducing power ranging from 2103.32 to 2679.78 mmol Fe reduced 100 g−1 (FRAP). The dynamic character of the protocols used for developing bioactive cereal-based foods significantly affects the estimation of their bioaccessibility, probably giving a better approach to their potential bioavailability in in vivo systems. Full article
(This article belongs to the Special Issue Valorization of the Antioxidant Power of Natural Compounds)
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<p>Scheme of digestion models of individual and combined ingredients.</p>
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<p>Total phenolic (TPs) content of the digests of the individual (EH-WB, EH-OH, SW and SO) and combined (CI1, CI2 and CI3) ingredients, following the static model. Results are expressed as μmol GAE 100 g<sup>−1</sup> of d.m. Mean are values represented as bars, and standard deviations are represented as error bars. Different letters indicate significant differences from each other (one-way ANOVA, post hoc Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). Abbreviations: wheat bran hydrolysate (EH-WB), oat hull hydrolysate (EH-OH), sprouted wheat (SW), sprouted oat (SO), combined ingredient 1, 2 and 3 (CI1, CI2, CI3).</p>
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<p>ORAC (<b>I</b>), ABTS<sup>+</sup> (<b>II</b>) and FRAP (<b>III</b>) values of the digests of the individual (EH-WB, EH-OH, SW and SO) and combined (CI1, CI2 and CI3) ingredients following the static model. Results are expressed as μmol TE 100 g<sup>−1</sup> of sample and mmol reduced Fe 100 g<sup>−1</sup>. Mean values are represented as bars, and standard deviations are represented as error bars. Different letters indicate significant differences from each other (one-way ANOVA, post hoc Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). Abbreviations: wheat bran hydrolysate (EH-WB), oat hull hydrolysate (EH-OH), sprouted wheat (SW), sprouted oat (SO), combined ingredient 1, 2 and 3 (CI1, CI2, CI3).</p>
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<p>Total phenolics (TPs) content of the digests of the individual (EH-WB, EH-OH, SW and SO) and combined (CI1, CI2 and CI3) ingredients following the semi-dynamic model. Results are expressed as μmol GAE 100 g<sup>−1</sup> of d.m. Mean values are represented as bars, and standard deviations are represented as error bars. Different letters indicate significant differences from each other (one-way ANOVA, post hoc Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). Abbreviations: wheat bran hydrolysate (EH-WB), oat hull hydrolysate (EH-OH), sprouted wheat (SW), sprouted oat (SO), combined ingredient 1, 2 and 3 (CI1, CI2, CI3).</p>
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<p>ORAC (<b>I</b>), ABTS<sup>•+</sup> (<b>II</b>) and FRAP (<b>III</b>) values of the digests of the individual (EH-WB, EH-OH, SW and SO) and combined (CI1, CI2 and CI3) ingredients following the semi-dynamic model. Results are expressed as μmol TE 100 g<sup>−1</sup> of sample and mmol reduced Fe 100 g<sup>−1</sup>. Mean values are represented as bars, and standard deviations are represented as error bars. Different letters indicate significant differences from each other (one-way ANOVA, post hoc Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). Abbreviations: wheat bran hydrolysate (EH-WB), oat hull hydrolysate (EH-OH), sprouted wheat (SW), sprouted oat (SO), combined ingredient 1, 2 and 3 (CI1, CI2, CI3).</p>
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<p>Total phenolics (TPs) content of the digests of the individual (EH-WB, EH-OH, SW and SO) and combined (CI1, CI2 and CI3) ingredients following the dynamic model. Results are expressed as μmol GAE 100 g<sup>−1</sup> of d.m. Mean values are represented as bars, and standard deviations are represented as error bars. Different letters indicate significant differences from each other (one-way ANOVA, post hoc Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). Abbreviations: wheat bran hydrolysate (EH-WB), oat hull hydrolysate (EH-OH), sprouted wheat (SW), sprouted oat (SO), combined ingredient 1, 2 and 3 (CI1, CI2, CI3).</p>
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<p>ORAC (<b>I</b>), ABTS<sup>•+</sup> (<b>II</b>) and FRAP (<b>III</b>) values of the digests of the individual (EH-WB, EH-OH, SW and SO) and combined (CI1, CI2 and CI3) ingredients following the dynamic model. Results are expressed as μmol TE 100 g<sup>−1</sup> of sample and μmol reduced Fe 100 g<sup>−1</sup>. Mean values are represented as bars, and standard deviations are represented as error bars. Different letters indicate significant differences from each other (one-way ANOVA, post hoc Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). Abbreviations: wheat bran hydrolysate (EH-WB), oat hull hydrolysate (EH-OH), sprouted wheat (SW), sprouted oat (SO), combined ingredient 1, 2 and 3 (CI1, CI2, CI3).</p>
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21 pages, 7423 KiB  
Article
Nanotherapy for Cancer and Biological Activities of Green Synthesized AgNPs Using Aqueous Saussurea costus Leaves and Roots Extracts
by Mina A. Almayouf, Raihane Charguia, Manal A. Awad, Abir Ben Bacha and Imen Ben Abdelmalek
Pharmaceuticals 2024, 17(10), 1371; https://doi.org/10.3390/ph17101371 (registering DOI) - 15 Oct 2024
Viewed by 278
Abstract
Background/Objectives: Nanoparticles derived from medicinal plants are gaining attention for their diverse biological activities and potential therapeutic applications. Methods: This study explored the antioxidant, anti-inflammatory, anti-tumoral, and antimicrobial properties of green synthesized silver nanoparticles (AgNPs) using the aqueous leaf and root [...] Read more.
Background/Objectives: Nanoparticles derived from medicinal plants are gaining attention for their diverse biological activities and potential therapeutic applications. Methods: This study explored the antioxidant, anti-inflammatory, anti-tumoral, and antimicrobial properties of green synthesized silver nanoparticles (AgNPs) using the aqueous leaf and root extracts of Saussurea costus (S. costus). The physicochemical characterizations of both biosynthesized AgNPs using the aqueous leaf extract (L-AgNPs) and root extract (R-AgNPs) were examined using UV spectroscopy, fluorescence spectroscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, dynamic light scattering, and Fourier-transform infrared spectroscopy. The antioxidant activity measured using ABTS, DPPH, and FRAP assays showed that AgNPs, particularly from roots, had higher activity than aqueous extracts, attributed to phenolic compounds acting as capping and antioxidant agents. Results: Enzyme inhibition studies indicated that AgNPs exhibited remarkable anti-inflammatory effects, inhibiting COX-1, 5-LOX, and secreted PLA2 enzymes by over 99% at 120 µg/mL, comparable to standard drugs. The anti-tumoral effects were evaluated on the human cancer cell lines HCT-116, LoVo, and MDA-MB-231, with AgNPs inhibiting cell proliferation dose-dependently and IC50 values between 42 and 60 µg/mL, demonstrating greater potency than extracts. The AgNPs also showed enhanced antimicrobial activities against various microbial strains, with IC50 values as low as 14 µg/mL, which could be linked to nanoparticle interactions with microbial cell membranes, causing structural damage and cell death. Conclusions: These findings suggest that S. costus-derived AgNPs are promising natural, biodegradable agents for various biological applications and potential new therapeutic agents, necessitating further research to explore their mechanisms and applications. Full article
(This article belongs to the Topic Enzymes and Enzyme Inhibitors in Drug Research)
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<p>The possible formation mechanism of Ag nanoparticles using <span class="html-italic">S. costus</span> leaf and root extracts.</p>
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<p>UV analysis spectra of L-AgNPs and R-AgNPs.</p>
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<p>Fluorescence emission spectra of (<b>A</b>) L-AgNPs and (<b>B</b>) R-AgNPs.</p>
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<p>TEM images for the synthesized L-AgNPs (<b>A</b>) and R-AgNPs (<b>B</b>). Histograms of the particle size distributions of L-AgNPs (<b>C</b>) and R-AgNPs (<b>D</b>).</p>
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<p>EDX spectra of (<b>A</b>) L-AgNPs and (<b>B</b>) R-AgNPs.</p>
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<p>XRD spectra of (<b>A</b>) L-AgNPs and (<b>B</b>) R-AgNPs.</p>
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<p>DLS analysis of (<b>A</b>) L-AgNPs and (<b>B</b>) R-AgNPs.</p>
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<p>FTIR spectra of (<b>A</b>) L-AgNPs and <span class="html-italic">S. costus</span> leaf extract (<b>B</b>) R-AgNPs and <span class="html-italic">S. costus</span> root extract.</p>
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<p>Antioxidant activity of AgNPs synthesized from <span class="html-italic">S. costus</span> extracts and determined by ABTS, DPPH, and FRAP methods. Results presented as the mean ± SD (<span class="html-italic">n</span> = 3) are expressed as GAE in mg/L (<b>A</b>) and as % of radical scavenging or as % of Fe<sup>3+</sup> reduction in both ABTS and DPPH methods or in the FRAP method (<b>B</b>). L extract: aqueous leaves extract; R extract: aqueous roots extract; L-AgNPs: AgNPs prepared using L extract; R-AgNPs: AgNPs prepared using R extract. The asterisk indicates significant differences between experimental groups within a column. * represents <span class="html-italic">p</span> &lt; 0.05; ** represents <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Evaluation of 5-LOX, COX, and sPLA<sub>2</sub> inhibition properties of AgNPs synthesized from <span class="html-italic">S. costus</span> extracts. Several concentrations ranging from 20 to 120 µg/mL of <span class="html-italic">S. costus</span> root and leaf extracts and their silver nanoparticles AgR and AgL were used to inhibit 5-LOX (<b>A</b>), COX (<b>B</b>), h-PLA<sub>2</sub>-V (<b>C</b>), and DrPLA<sub>2</sub>-IIA (<b>D</b>). NGDA at 100 µM, diclofenac at 1 µM, and TEPC at 20 µM served as positive controls. Results are presented as the mean ± SD (<span class="html-italic">n</span> = 3). L extract: aqueous leaves extract; R extract: aqueous roots extract; L-AgNPs: AgNPs prepared using L extract; R-AgNPs: AgNPs prepared using R extract. * represents <span class="html-italic">p</span> &lt; 0.05; ** represents <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Cytotoxic potential of AgNPs synthesized from <span class="html-italic">S. costus</span> extracts against human colorectal HCT-116 (<b>A</b>), LoVo (<b>B</b>), and breast cells MDA-MB-231 (<b>C</b>). Cells were treated with several concentrations of extracts and silver nanoparticles during 24 h, from 20 µg/mL to 120 µg/mL. MTT assay was used to quantify viable cells. Current results are presented as the mean ± SD (<span class="html-italic">n</span> = 3 assays). L extract: aqueous leaves extract; R extract: aqueous roots extract; L-AgNPs: AgNPs prepared using L extract; R-AgNPs: AgNPs prepared using R extract. The asterisk indicates significant differences between experimental groups within a column. * represents <span class="html-italic">p</span> &lt; 0.05; ** represents <span class="html-italic">p</span> &lt; 0.01.</p>
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20 pages, 2521 KiB  
Article
Synergistic Effect of Arbuscular Mycorrhizal Fungi and Germanium on the Growth, Nutritional Quality, and Health-Promoting Activities of Spinacia oleracea L.
by Basma Najar, Ahlem Zrig, Emad A. Alsherif, Samy Selim, Abeer S. Aloufi, Shereen Magdy Korany, Mousa Nhs, Mohammad Aldilam and Nahla Alsayd Bouqellah
Plants 2024, 13(20), 2869; https://doi.org/10.3390/plants13202869 - 14 Oct 2024
Viewed by 360
Abstract
Arbuscular mycorrhizal fungi (AMF) and the antioxidant germanium (Ge) are promising tools for boosting bioactive compound synthesis and producing healthier foods. However, their combined effect remains unexplored. This study demonstrates the synergistic impact of AMF and Ge on the growth, metabolite accumulation, biological [...] Read more.
Arbuscular mycorrhizal fungi (AMF) and the antioxidant germanium (Ge) are promising tools for boosting bioactive compound synthesis and producing healthier foods. However, their combined effect remains unexplored. This study demonstrates the synergistic impact of AMF and Ge on the growth, metabolite accumulation, biological activities, and nutritional qualities of Spinacia oleracea L. (spinach), a globally significant leafy vegetable. Individually, Ge and AMF increased biomass by 68.1% and 22.7%, respectively, while their combined effect led to an 86.3% increase. AMF and Ge also improved proximate composition, with AMF–Ge interaction enhancing crude fiber and mineral content (p < 0.05). Interestingly, AMF enhanced photosynthesis-related parameters (e.g., total chlorophyll) in Ge treated plants, which in turn increased carbohydrate accumulation. This accumulation could provide a route for the biosynthesis of amino acids, organic acids, and fatty acids, as evidenced by increased essential amino acid and organic acid levels. Consistently, the activity of key enzymes involved in amino acids biosynthesis (e.g., glutamine synthase (GS), methionine biosynthase (MS), lysine biosynthase (LS)) showed significant increments. Furthermore, AMF improved fatty acid levels, particularly unsaturated fatty acids in Ge-treated plants compared to the control. In addition, increased phenylalanine provided a precursor for the production of antioxidants (e.g., phenols and flavonoids), through the action of the enzyme phenylalanine ammonia-lyase (PAL), resulting in improved antioxidant activity gains as indicated by FRAP, ABTS, and DPPH assays. This study is the first to show that Ge enhances the beneficial effect of AMF on spinach, improving growth and nutritional quality, with promising implications for agricultural practices. Full article
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<p>Effect of different treatments on biomass (<b>A</b>) and Ge level (<b>B</b>). Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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<p>Effect of different treatments on photosynthetic pigments, (<b>A</b>): chlorophyll a, chlorophyll b and chlorophyll ab; (<b>B</b>) b-carotene, lycopene. Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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<p>Effect of different treatments on proximate composition, (<b>A</b>): moisture, (<b>B</b>): total protein, (<b>C</b>) crude fiber, (<b>D</b>): total lipd, (<b>E</b>): ash content, (<b>F</b>): carbohydrates. Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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<p>Effect of different treatments on mineral contents, (<b>A</b>): Ca, FE and Mg; (<b>B</b>): Cu, Zn and Mn (<b>C</b>): K, Na and P. Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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<p>Effect of different treatments on vitamin and sugar contents, (<b>A</b>): vitamin C, vitamin and L-galactose; (<b>B</b>): vitamin B1, vitamin B2 and D-mannose. Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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<p>Effect of different treatments on antidiabetic activity. Values expressed as means ± standard error of three independent replicates. Different letters above the bars, within the same organ, indicate significant differences between means at <span class="html-italic">p</span> = 0.05 using Tukey’s post hoc test.</p>
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16 pages, 2097 KiB  
Article
Characteristics and Bioactivities of Protein Hydrolysate from Cricket (Acheta domesticus) Powder Defatted Using Ethanol with Aid of Vacuum Impregnation
by Lalita Chotphruethipong, Theeraphol Senphan, Avtar Sigh, Pilaiwanwadee Hutamekalin, Pornpot Nuthong and Soottawat Benjakul
Foods 2024, 13(20), 3250; https://doi.org/10.3390/foods13203250 - 13 Oct 2024
Viewed by 498
Abstract
Cricket is a potential proteinaceous source used for protein hydrolysate (PH) preparation, having several biological activities. Nevertheless, cricket has high lipid contents, which are susceptible to oxidation during PH preparation. Thus, ethanol was used together with vacuum impregnation (VI) to enhance defatting efficacy [...] Read more.
Cricket is a potential proteinaceous source used for protein hydrolysate (PH) preparation, having several biological activities. Nevertheless, cricket has high lipid contents, which are susceptible to oxidation during PH preparation. Thus, ethanol was used together with vacuum impregnation (VI) to enhance defatting efficacy before PH preparation. Also, bioavailability of the digest of PH after gastrointestinal tract (GIT) digestion via the Caco-2 monolayer was assessed. Cricket powder was defatted using ethanol for 1–4 h. Lipid contents were decreased with enhancing time until 2 h. Additionally, the defatting efficacy was augmented when ethanol combined with VI at 4 cycles for 2 h (VI-E-2) was implemented. Lowered mono- and polyunsaturated fatty acid contents were also observed in the VI-E-2 sample. The VI-E-2 sample was used to prepare PH using Alcalase and Flavourzyme (0.2–0.4 units/g dry sample). PH prepared by Alcalase hydrolysis at 0.2 units/g dry sample (A-0.2) showed the higher ABTS radical-scavenging activity and FRAP, compared to that prepared by Flavourzyme hydrolysis (p < 0.05). Thus, the A-0.2 sample was selected for digestion via the GIT system. The obtained digest (500–1000 μg/mL) had bioavailability of peptides, depending on the levels used. Therefore, PH from defatted cricket powder could be a promising ingredient for food applications. Full article
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<p>Preparation of cricket powder.</p>
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<p>A heat map of fatty acid profiles in cricket powder as affected by different defatting processes. The color gradient is the amount of fatty acids (g/100 g lipid). Control: non-defatted cricket powder; E-2: cricket powder defatted with ethanol for 2 h; VI-E-2: cricket powder defatted with ethanol with the aid of vacuum impregnation (VI) with a total operation time of 2 h.</p>
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<p>CLSM images of lipid distribution in cricket powder as affected by different selected defatting processes. Control: non-defatted cricket powder; E-2: cricket powder defatted with ethanol for 2 h; VI-E-2: cricket powder defatted with ethanol with the aid of vacuum impregnation (VI) with a total operation time of 2 h.</p>
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<p>The size distribution of the defatted cricket protein hydrolysate prepared using Alcalase at 0.2 units/g dry sample (A-0.2 sample) assessed by MALDI-TOF mass spectrometry.</p>
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<p>The impact of the A-0.2 digest obtained from GIT digestion at various concentrations on Caco-2 cell viability (<b>A</b>), and %Bioavailability of the digest from GIT digestion at the selected concentrations (<b>B</b>). Values are expressed as the mean ± SD (<span class="html-italic">n</span> = 3). Different lowercase letters (a–c) on the bar indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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13 pages, 956 KiB  
Article
Pharmacological Potential and Electrochemical Characteristics of Typha angustifolia Pollen
by Janielle Mari S. Abadilla, Bor-Yann Chen, Mike Anthony D. Ganzon, Alvin R. Caparanga, Kristopher Ray S. Pamintuan, Lemmuel L. Tayo, Chung-Chuan Hsueh, Cheng-Yang Hsieh, Ling-Ling Yang and Po-Wei Tsai
Plants 2024, 13(20), 2857; https://doi.org/10.3390/plants13202857 - 12 Oct 2024
Viewed by 546
Abstract
Typha angustifolia L. (TA) pollen has been utilized as a traditional Chinese medicine for treating various internal and external traumas. Moreover, bioactive compounds possess diverse pharmacological activities. This study aims to evaluate the antiviral properties of TA based on its ability to generate [...] Read more.
Typha angustifolia L. (TA) pollen has been utilized as a traditional Chinese medicine for treating various internal and external traumas. Moreover, bioactive compounds possess diverse pharmacological activities. This study aims to evaluate the antiviral properties of TA based on its ability to generate bioenergy, capable of inhibiting viruses. TA pollens were extracted using water and ethanol solvents. These extracts were utilized to identify the phytochemical contents and correlate with the antioxidant activity via 2,2-diphenyl-1-picrylhydrazyl (DPPH) and ferric reducing antioxidant power (FRAP) assays. HPLC analysis was conducted to identify its electron-shuttling compositions. The bioenergy-generating characteristics were determined via microbial fuel cells. The water extract (TA-W) showed higher antioxidant activity due to a higher phenolic and flavonoid content compared to the ethanol extract (TA-E). Quercetin-3-O-(2G-α-L-rhamnosyl)-rutinoside, quercetin-3-O-neohesperidoside, and quercetin are the electron shuttles (ES) identified out of the 11 compounds. TA obtained a 1.39 ± 0.10 amplification factor of power generation that indicates potential bioenergy-generating and associated antiviral characteristic properties. The findings may provide a foundation for developing antiviral medications specifically designed to target virus-related diseases, while minimizing the risk of drug toxicity and reducing the costs of drug development. Full article
(This article belongs to the Special Issue Phytochemistry and Pharmacological Properties of Medicinal Plants)
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<p>Chromatographic fingerprint of EtOH extract of TA pollen from 2D HPLC-PDA at 245 nm.</p>
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<p>Power density profile of TA pollen water and ethanol extracts.</p>
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16 pages, 1730 KiB  
Article
In Vitro Mechanistic Studies of a Standardized Sustainable Grape Seed Extract for Potential Application as a Mood-Modulating and Cognition-Enhancing Supplement
by Gozde Hasbal-Celikok, Mehtap Kara, Marta Sánchez, Claudia Owsianik, Pilar Gómez-Serranillos, Tugba Yilmaz-Ozden, Ezgi Öztaş, Özge Sultan Zengin, Gul Ozhan, Nazli Arda, Merve Tunc, Sumeyye Sahin, Areaba Shafiq, Ayesha Kanwal, Hunaiba I. Ujjan, Fazle Rabbani, Giovanna Petrangolini and Amjad Khan
Nutrients 2024, 16(20), 3459; https://doi.org/10.3390/nu16203459 - 12 Oct 2024
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Abstract
Background: Grape seed extract (GSE) from Vitis vinifera L. is rich in polyphenols and oligomeric proanthocyanidin complexes (OPCs), and it has shown potential benefits in managing low mood and cognitive function. In this study, we investigated the potential bioactivities of Enovita®, [...] Read more.
Background: Grape seed extract (GSE) from Vitis vinifera L. is rich in polyphenols and oligomeric proanthocyanidin complexes (OPCs), and it has shown potential benefits in managing low mood and cognitive function. In this study, we investigated the potential bioactivities of Enovita®, a standardized GSE extract (GSEe herein) rich in OPCs, in key mechanistic pathways related to low mood conditions and cognitive function. Methods: In vitro assays were conducted to assess GSEe’s inhibitory effects on γ-aminobutyric acid transaminase (GABA-T) and monoamine oxidase A (MAO-A), its binding affinity to the GABA site of GABA-A receptors, and its effects on acetylcholinesterase (AChE). Its neuroprotective effects on human SH-SY5Y neuroblastoma cells under oxidative stress (induced by H2O2) were assessed using MTT and LDH release assays. Its antioxidant activities were evaluated using DPPH, ABTS, FRAP, ORAC, HORAC, total phenolic content, and TAS assays. Its cytotoxicity was also evaluated. Results: GSEe showed significant GABA-T inhibitory activity. It also exhibited MAO-A and AChE inhibition, along with moderate binding affinity to the GABA-A receptor. In neuroprotective assays, GSEe provided significant protection to SH-SY5Y cells against oxidative stress. GSEe demonstrated robust antioxidant activity in all assays, including scavenging of DPPH and ABTS radicals, high ferric-reducing power, high polyphenolic contents, and a substantial total antioxidant capacity. Conclusions: GSEe exhibits promising bioactivities, highlighting its potential as a supplement for modulating mood and enhancing cognitive function. Overall, the promising results from these in vitro studies provide a strong foundation for the continued exploration and development of GSEe as a viable natural supplement for enhancing mental health and cognitive function. Full article
(This article belongs to the Special Issue Nutritional Value and Health Benefits of Dietary Bioactive Compounds)
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<p>GABA-T inhibition assay of GSEe. The plot shows the percentage of GABA-T activity at various concentrations of GSEe, IC<sub>50</sub> = 1.00 ± 0.20 mg/mL. A linear regression analysis was performed to determine the concentration-dependent inhibitory effect of GSEe on GABA-T activity. The error bars represent the standard deviation from the mean of the measurements of three freshly prepared samples.</p>
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<p>Competitive binding of GSEe at the GABA site of rat GABA-A receptors, IC<sub>50</sub> = 394.5 μg/mL. The error bars represent the standard deviation from the mean of the measurements of three freshly prepared samples.</p>
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<p>MAO-A enzyme inhibition assay. The plot shows the effect of various concentrations of GSEe on the activity of the MAO-A enzyme. The error bars represent the standard deviation from the mean of the measurements of three freshly prepared samples.</p>
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<p>AChE enzyme inhibition assay. The plot shows the effect of various concentrations of GSEe on the activity of the AChE enzyme, IC<sub>50</sub> = 11.44 ± 0.83 µg/mL. The error bars represent the standard deviation from the mean of the measurements of three freshly prepared samples.</p>
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<p>The neuroprotective effect of GSEe on SH-SY5Y cells under oxidative stress induced by H<sub>2</sub>O<sub>2</sub>. The plots show the effects of various concentrations of GSEe on SH-SY5Y cell viability. (<b>A</b>) MTT assay. (<b>B</b>) LDH assay. The error bars represent the standard deviation from the mean of the measurements of three freshly prepared samples.</p>
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<p>The antioxidant effects of GSEe, or Enovita<sup>®</sup>, in various cell-free assays. (<b>A</b>) DPPH radical scavenging assay, EC50 5.81 ± 0.11 µg/mL. (<b>B</b>) ABTS radical scavenging assay, EC50 11.91 ± 0.15 µg/mL. (<b>C</b>) FRAP assay. (<b>D</b>) ORAC assay. (<b>E</b>) HORAC assay. (<b>F</b>) Total phenolic content (TPC) Folin–Ciocalteau assay. (<b>G</b>) TAS assay. The error bars represent the standard deviation from the mean of the measurements of three freshly prepared samples. TEAC: Trolox Equivalent Antioxidant Capacity; GAE: gallic acid equivalents; GA: gallic acid.</p>
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13 pages, 840 KiB  
Article
Assessment of the Antioxidative Properties of Extracts from the Fruits of Pyrus pyraster (L.) Burgsd and Pyrus ×myloslavensis Czarna & Antkowiak Grown under Natural Environmental Conditions
by Marzanna Hęś, Wojciech Antkowiak, Kinga Stuper-Szablewska, Krzysztof Dziedzic, Marta Jessa and Paulina Ratajczak
Agriculture 2024, 14(10), 1790; https://doi.org/10.3390/agriculture14101790 - 12 Oct 2024
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Abstract
Analyses were conducted on extracts from the fruits of P. pyraster and P. ×myloslavensis. Extraction with 80% methanol was performed at room temperature. The total phenolic content was determined by spectrophotometry using the Folin–Ciocalteu reagent, with gallic acid as the reference [...] Read more.
Analyses were conducted on extracts from the fruits of P. pyraster and P. ×myloslavensis. Extraction with 80% methanol was performed at room temperature. The total phenolic content was determined by spectrophotometry using the Folin–Ciocalteu reagent, with gallic acid as the reference standard. Phenolic compounds and organic acids were identified on a liquid chromatograph. The antioxidative activity of the extracts was tested in relation to linoleic acid incubation of the emulsions for 19 h based on the neutralization of the DPPH radical (2,2-diphenyl-1-picrylhydrazyl) and the ABTS cation radical (2,2′-azino-bis[3-ethylbenzothiazoline-6-sulfonic acid]) as well as by the ferric reducing antioxidant power (FRAP) assay. The analyses showed that the extract from P. pyraster fruits is characterized by a higher content of phenolic compounds and a higher antioxidative potential compared with that from P. ×myloslavensis. In extracts of both pear species, seven phenolic compounds and four organic acids were identified. The total fiber content in pears of P. pyraster and P. ×myloslavensis was determined at 36.45 g and 24.74 g/100 g d.m. of the pear fruits, of which most comprised the insoluble fraction (32.49 g and 20.86/100 g, respectively). The results of the conducted research are highly significant, as they confirm that pears contain many valuable nutrients and biologically active compounds, including antioxidants and dietary fiber. Adding pear extracts to food products may offer a way to boost their health benefits while also broadening the variety of items that have appealing sensory characteristics. Moreover, research has shown that fruit extracts can help to prolong the shelf life of food products by safeguarding them against lipid oxidation and the decline in their nutritional value. Full article
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<p>Correlation between the total phenolic content of <span class="html-italic">P. pyraster</span> and <span class="html-italic">P.</span> ×<span class="html-italic">myloslavensis</span> fruit extracts (mg GAE/g d.m.) (X-axis) and (<b>a</b>) DPPH, (<b>b</b>) the ABTS radical scavenging activity (mg Trolox/g s.m.), and (<b>c</b>) the FRAP reducing potential (mM Fe<sup>2+</sup>) (Y-axis).</p>
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21 pages, 2179 KiB  
Article
Chemical Profiling and Evaluation of Antioxidant Activity of Artichoke (Cynara cardunculus var. scolymus) Leaf By-Products’ Extracts Obtained with Green Extraction Techniques
by Valentina Masala, Stela Jokić, Krunoslav Aladić, Maja Molnar, Mattia Casula and Carlo Ignazio Giovanni Tuberoso
Molecules 2024, 29(20), 4816; https://doi.org/10.3390/molecules29204816 - 11 Oct 2024
Viewed by 508
Abstract
This study aimed to determine the effectiveness of different green extraction techniques (GETs) on targeted bioactive compounds from artichoke leaf by-products using deep eutectic solvent extraction (DESE), supercritical CO2 extraction (SCO2E), subcritical water extraction (SWE), and ultrasound-assisted extraction (UAE). Moreover, [...] Read more.
This study aimed to determine the effectiveness of different green extraction techniques (GETs) on targeted bioactive compounds from artichoke leaf by-products using deep eutectic solvent extraction (DESE), supercritical CO2 extraction (SCO2E), subcritical water extraction (SWE), and ultrasound-assisted extraction (UAE). Moreover, (HR) LC-ESI-QTOF MS/MS and HPLC-PDA analyses were used to perform qualitative–quantitative analysis on the extracts, enabling the detection of several bioactive compounds, including luteolin, luteolin 7-O-glucoside, luteolin 7-O-rutinoside, apigenin rutinoside, chlorogenic acid, and cynaropicrin as the most representative ones. SWE showed better results than the other GETs (TPC: 23.39 ± 1.87 mg/g of dry plant, dp) and appeared to be the best choice. Regarding UAE, the highest total phenols content (TPC) was obtained with 50:50% v/v ethanol: water (7.22 ± 0.58 mg/g dp). The DES obtained with choline chloride:levulinic acid showed the highest TPC (9.69 ± 0.87 mg/g dp). Meanwhile, SCO2E was a selective technique for the recovery of cynaropicrin (48.33 ± 2.42 mg/g dp). Furthermore, the study examined the antioxidant activity (1.10–8.82 mmol Fe2+/g dp and 3.37–31.12 mmol TEAC/g dp for DPPH and FRAP, respectively) and total phenols content via Folin–Ciocalteu’s assay (198.32–1433.32 mg GAE/g dp), of which the highest values were detected in the SWE extracts. The relationship among the GETs, antioxidant assays, and compounds detected was evaluated using Principal Component Analysis (PCA). PCA confirmed the strong antioxidant activity of SWE and showed comparable extraction yields for the antioxidant compounds between UAE and DESE. Consequently, GETs selection and extraction parameters optimization can be employed to enrich artichoke leaf by-products’ extracts with targeted bioactive compounds. Full article
(This article belongs to the Special Issue Chemical Analysis of Functional Foods)
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<p>HPLC-PDA fingerprinting for selected <span class="html-italic">C. cardunculus</span> var. <span class="html-italic">scolymus</span> leaf by-product extracts (UAE: ultrasound-assisted extraction; SWE: subcritical water extraction; DES: deep eutectic solvents; SCO<sub>2</sub>: supercritical CO<sub>2</sub> extraction) at λ = 210 and 313 nm. Peak identification is provided in <a href="#app1-molecules-29-04816" class="html-app">Table S1</a>. Chromatographic conditions are described in the text.</p>
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<p>Quantification of phenolic compounds by LC-PDA method (mg/g dp) in <span class="html-italic">C. cardunculus</span> var. <span class="html-italic">scolymus</span> leaf by-products’ extracts. Data are provided as mean ± standard deviation (<span class="html-italic">n</span> = 3). Mean values with different letters are significantly different (homogenous groups) at <span class="html-italic">p</span> ≤ 0.05. <a href="#app1-molecules-29-04816" class="html-app">Table S2</a> reports full dataset (mean ± standard deviation; <span class="html-italic">n</span> = 3) and the ANOVA test to determine the statistically significant differences among homogenous groups.</p>
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<p>Three-dimensional plots for obtained cynaropicrin in extracts as a function of UAE process parameters.</p>
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<p>Principal Component Analysis (PCA) score scatter biplot of the extracts obtained from <span class="html-italic">C. cardunculus</span> var. <span class="html-italic">scolymus</span> samples by using (<b>A</b>) ultrasound-assisted extraction (UAE), subcritical water extraction (SWE), and deep eutectic solvents (DESs; <span class="html-italic">n</span> = 46) and (<b>B</b>) ultrasound-assisted extraction (UAE) (<span class="html-italic">n</span> = 17).</p>
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18 pages, 3640 KiB  
Article
Phytochemical Composition, Antioxidant, Anti-Helicobacter pylori, and Enzyme Inhibitory Evaluations of Cleistocalyx operculatus Flower Bud and Leaf Fractions
by Doan Thien Thanh, Mai Thanh Tan, Nguyen Thi My Thu, Pham Nhat Phuong Trinh, Pham Thi Hoai Thuong, Pham Thi Giang Tuyet, Luong Thi My Ngan and Tran Trung Hieu
BioTech 2024, 13(4), 42; https://doi.org/10.3390/biotech13040042 - 11 Oct 2024
Viewed by 433
Abstract
Six solvent fractions isolated from flower bud and leaf ethanolic extracts of Cleistocalyx operculatus were analyzed for their phytochemical contents, including phenolics, flavonoids, saponins, tannins, and alkaloids. Antioxidant activities were measured using the ABTS, DPPH, and FRAP assays. The results showed that the [...] Read more.
Six solvent fractions isolated from flower bud and leaf ethanolic extracts of Cleistocalyx operculatus were analyzed for their phytochemical contents, including phenolics, flavonoids, saponins, tannins, and alkaloids. Antioxidant activities were measured using the ABTS, DPPH, and FRAP assays. The results showed that the flower bud aqueous fraction (BAF) and the leaf aqueous fraction (LAF) rich in phenolic content (768.18 and 490.74 mg GAE/g dry extract, respectively) exhibited significantly higher antioxidant activities than the other fractions. The flower bud hexane fraction (BHF) had remarkably high flavonoid and saponin contents (134.77 mg QE/g and 153.33 mg OA/g dry extract, respectively), followed by that of the leaf hexane fraction (LHF) (76.54 mg QE/g and 88.25 mg OA/g dry extract, respectively). The BHF and LHF were found to have extremely high antibacterial activity against two H. pylori strains, ATCC 51932 and 43504 (MICs of 125 µg/mL). Interestingly, DMC (2′,4′-Dihydroxy-6′-methoxy-3′,5′-dimethylchalcone) isolated from the BHF displayed greater antibacterial activity against the bacterial strains (MICs of 25–50 µg/mL) than those of the fractions. In addition, DMC presented potent inhibitory effects on H. pylori urease (IC50 of 3.2 µg/mL) and α-amylase (IC50 of 83.80 µg/mL), but no inhibition against α-glucosidase. It was also demonstrated that DMC showed pronounced inhibitory effects on the urease activity and biofilm formation of H. pylori, and could increase the membrane permeability of the bacterial cells. Scanning electron micrographs depicted that the BHF and DMC had strong effects on the cell shape and significantly induced the distortion and damage of the cell membrane. The fractions and DMC showed no significant toxicity to four tested human cell lines. Efforts to reduce antibiotic use indicate the need for further studies of the flower buds and DMC as potential products to prevent or treat gastric H. pylori infections. Full article
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<p>Effect of <span class="html-italic">C. operculatus</span> fractions and DMC at sub-MICs on <span class="html-italic">H. pylori</span> biofilm formation 48 h post-treatment. Data are reported as means ± SD.</p>
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<p>SEM micrographs of <span class="html-italic">H. pylori</span> ATCC 43504 depicting untreated cells (<b>A</b>,<b>B</b>) and cells treated with 125 µg/mL of BHF (<b>C</b>,<b>D</b>) and 50 µg/mL of DMC (<b>E</b>,<b>F</b>); bars 5 and 1 µm, respectively.</p>
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<p>Effect of <span class="html-italic">C. operculatus</span> fractions and DMC at sub-MICs on the uptake of crystal violet by <span class="html-italic">H. pylori</span> ATCC 43504 after 2 h of treatment. Data are reported as means ± SD (n = 3).</p>
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12 pages, 769 KiB  
Article
Assessment of the Nutritional Value and Antioxidant Properties of Plant-Based Yogurt from Chickpeas
by Grażyna Budryn and Joanna Grzelczyk
Appl. Sci. 2024, 14(20), 9228; https://doi.org/10.3390/app14209228 - 11 Oct 2024
Viewed by 523
Abstract
Plant-based yogurts are becoming more and more popular. These are vegan products for people with food allergies or intolerances, athletes, and ordinary consumers. The use of chickpea “milk” allows one to obtain a plant-based yogurt with a high protein content, dietary fiber and [...] Read more.
Plant-based yogurts are becoming more and more popular. These are vegan products for people with food allergies or intolerances, athletes, and ordinary consumers. The use of chickpea “milk” allows one to obtain a plant-based yogurt with a high protein content, dietary fiber and antioxidant potential. This study assessed the content of polyphenols, selected nutrients, and antioxidant properties in chickpea yogurt. The vegetable chickpea yogurt was rich in protein (4.34–7.90 g/100 g) and dietary fiber (2–4%). It was also characterized by a high antioxidant activity (DPPH = 2.61 to 4.32 μmol TE/g, FRAP = 3.11 to 48.33 μmol TE/g). The use of 3-day soaking and inoculation with Vegurt or a kefir bacterial inoculum allowed us to obtain a high protein content. The addition of honey increased the polyphenol content and antioxidant potential of the plant-based yogurt (139–148 GAE mg/100 g). This research will be used in future research into optimizing the conditions for obtaining plant-based yogurts with chickpeas. Further research should include models for testing health-promoting properties. Full article
(This article belongs to the Special Issue Extraction of Functional Ingredients and Their Application)
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<p>Samples after 14 h of incubation.</p>
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<p>Ash content in chickpea yogurts. Values are expressed as mean value ± SD; <span class="html-italic">n</span> = 3; values with the same superscript letter (a–e) along the same column are not significantly different (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>FRAP and DPPH antioxidant capacity analysis. Values are expressed as mean value ± SD; <span class="html-italic">n</span> = 3; values with the same superscript letter (a–d) along the same column are not significantly different (<span class="html-italic">p</span> &gt; 0.05).</p>
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17 pages, 1529 KiB  
Article
Exploring the Bioactive Potential of Taraxacum officinale F.H. Wigg Aerial Parts on MDA Breast Cancer Cells: Insights into Phytochemical Composition, Antioxidant Efficacy, and Gelatinase Inhibition within 3D Cellular Models
by Valentina Laghezza Masci, Elisa Ovidi, William Tomassi, Daniela De Vita and Stefania Garzoli
Plants 2024, 13(19), 2829; https://doi.org/10.3390/plants13192829 - 9 Oct 2024
Viewed by 640
Abstract
In this work, aerial parts of Taraxacum officinale F.H. Wigg. produced in Umbria, Italy, were chemically investigated by solid-phase microextraction/gas chromatography–mass spectrometry (SPME/GC-MS) to describe their volatile profile. The results obtained showed the preponderant presence of monoterpenes, with limonene and 1,8-cineole as the [...] Read more.
In this work, aerial parts of Taraxacum officinale F.H. Wigg. produced in Umbria, Italy, were chemically investigated by solid-phase microextraction/gas chromatography–mass spectrometry (SPME/GC-MS) to describe their volatile profile. The results obtained showed the preponderant presence of monoterpenes, with limonene and 1,8-cineole as the main components. Further analyses by GC/MS after derivatization reaction were performed to characterize the non-volatile fraction highlighting the presence of fatty acids and di- and triterpenic compounds. T. officinale methanol and dichloromethane extracts, first analyzed by HRGC/MS, were investigated to evaluate the antioxidant activity, cytotoxicity, and antiproliferative properties of MDA cells on the breast cancer cell line and MCF 10A normal epithelial cells as well as the antioxidant activity by colorimetric assays. The impact on matrix metalloproteinases MMP-9 and MMP-2 was also explored in 3D cell systems to investigate the extracts’ efficacy in reducing cell invasiveness. The extracts tested showed no cytotoxic activity with EC50 > 250 µg/mL on both cell lines. The DPPH assay revealed higher antioxidant activity in the MeOH extract compared with the DCM extract, while the FRAP assay showed a contrasting result, with the DCM extract exhibiting slightly greater antioxidant capacity. After treatment for 24 h with a non-cytotoxic concentration of 500 µg/mL of the tested extracts, gelatin zymography and Western blot analyses demonstrated that both MeOH and DCM extracts influenced the expression of MMP-9 and MMP-2 in MDA cells within the 3D cell model, leading to a significant decrease in the levels of these gelatinases, which are crucial markers of tumor invasiveness. Full article
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<p>Graph bar of the antioxidant capacity of MeOH and DCM extract results obtained by the DPPH assay. Percentages of scavenged free radicals correlated with different concentrations of extracts, expressed in μg/mL.</p>
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<p>Gelatin zymography on MDA and MCF10A: (<b>A</b>) MDA and (<b>B</b>) MCF 10A zymograms performed after treatment with MeOH and DCM extracts. The cells cultured in a 3D collagen matrix revealed the presence of two major protein bands. These are identifiable based on their respective molecular weights as pro-MMP-9 and active MMP-9 (92 and 88 kDa, respectively) and pro-MMP-2 and active MMP-2 (72 and 64 kDa, respectively). (<b>C</b>) MDA and (<b>D</b>) MCF 10A zymograms scanned with a densitometer and quantification of the different signal intensities detected.</p>
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<p>Western blot analysis on MDA and MCF10A treated with MeOH and DCM extracts. (<b>A</b>,<b>B</b>) Immune detection of MMP-9 (92 and 88 kDa), MMP-2 (72 and 64 kDa), and b-actin (45 kDa). (<b>C</b>,<b>D</b>) Bar graphs of the intensity of the detected bands.</p>
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19 pages, 925 KiB  
Article
Tyrosinase Inhibitory Activity of Crude Procyanidin Extract from Green Soybean Seed and the Stability of Bioactive Compounds in an Anti-Aging Skin Care Formulation
by Kanyarat Pohntadavit, Suwit Duangmano, Mallika Osiriphan, Noppol Leksawasdi, Charin Techapun, Nutsuda Sumonsiri, Sarana Rose Sommano, Pornchai Rachtanapun, Rojarej Nunta and Julaluk Khemacheewakul
Cosmetics 2024, 11(5), 178; https://doi.org/10.3390/cosmetics11050178 - 8 Oct 2024
Viewed by 469
Abstract
Green soybean (Glycine max L.) seed contains a high procyanidin content and high antioxidant activity. Moreover, ultrasound-assisted extraction (UAE) has proved to be advantageous in providing high extraction efficiency. Hence, this study aimed to extract procyanidins from green soybean seeds (GSSs) using [...] Read more.
Green soybean (Glycine max L.) seed contains a high procyanidin content and high antioxidant activity. Moreover, ultrasound-assisted extraction (UAE) has proved to be advantageous in providing high extraction efficiency. Hence, this study aimed to extract procyanidins from green soybean seeds (GSSs) using UAE. This study also evaluated the inhibitory activities of tyrosinase and the cytotoxic effects of crude procyanidin extract. The extract exhibited maximum levels of bioactive components and antioxidant capacity when subjected to a temperature of 15 °C and an extraction time of 20 min. The crude procyanidin extract at a concentration of 10 mg/mL inhibited the tyrosinase enzyme by more than 60%, and the half-maximal inhibitory concentration (IC50) value obtained for the extract was 6.85 ± 0.81 mg/mL. This result was much greater than the IC50 value obtained for kojic acid (0.089 ± 0.08 mg/mL), which was used as a positive control. For the cytotoxicity assessment, the results indicated that the crude procyanidin extract showed no cytotoxicity and actually stimulated the growth of human skin fibroblast cells. More than 80% of the bioactive compounds (total phenolic content (TPC), total flavonoid content (TFC), procyanidin content (PC)) and antioxidant activities (DPPH and FRAP) of the crude extract powder were retained at 38.68 ± 0.01 mg GAE/g, 16.07 ± 0.01 mg CAE/g, 9.24 ± 0.01 mg PC/g, 359.8 ± 0.72 μM Trolox eq/g, and 1640 ± 2.86 μM Trolox eq/g, respectively, after 12 weeks of storage at 25 °C. The crude procyanidin extract powder was then included in a facial serum formulation and tested for pH value and physical evaluation. The stability of the crude procyanidin extract facial serum was shown to be greater for bioactive compounds and antioxidant activity when stored at a temperature of 4 °C than when stored at a temperature of 25 °C. These results suggest that the GSS extracts obtained via ultrasonication show promise for use in cosmeceutical formulations for whitening skincare products. Full article
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<p>The tyrosinase inhibition effects of aqueous crude procyanidin extract, procyanidin standard, and kojic acid. The data are shown as the mean ± standard deviation (SD) derived from three independent experiments (<span class="html-italic">n</span> = 3) (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Cytotoxicity of the crude procyanidin extract at various concentrations against human skin fibroblasts. BJ cells were treated with crude procyanidin extract at a final concentration ranging from 0.125 to 2 mg/mL for 24, 48, and 72 h. Cell viability was determined via the MTT assay. The percentage of cell survival was calculated by defining the absorption of cells without crude procyanidin extract treatment as 100%. The data are expressed as the mean ± SD.</p>
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