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Keywords = Aronia melanocarpa berries

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19 pages, 2300 KiB  
Article
Chemical Composition, Nutritional, and Biological Properties of Extracts Obtained with Different Techniques from Aronia melanocarpa Berries
by Alessandra Piras, Silvia Porcedda, Antonella Smeriglio, Domenico Trombetta, Mariella Nieddu, Franca Piras, Valeria Sogos and Antonella Rosa
Molecules 2024, 29(11), 2577; https://doi.org/10.3390/molecules29112577 - 30 May 2024
Viewed by 598
Abstract
This study investigates the chemical composition, nutritional, and biological properties of extracts obtained from A. melanocarpa berries using different extraction methods and solvents. Hydrodistillation and supercritical fluid extraction with CO2 allowed us to isolate fruit essential oil (HDEX) and fixed [...] Read more.
This study investigates the chemical composition, nutritional, and biological properties of extracts obtained from A. melanocarpa berries using different extraction methods and solvents. Hydrodistillation and supercritical fluid extraction with CO2 allowed us to isolate fruit essential oil (HDEX) and fixed oil (SFEEX), respectively. A phenol-enriched extract was obtained using a mild ultrasound-assisted maceration with methanol (UAMM). The HDEX most abundant component, using gas chromatography-mass spectrometry (GC/MS), was italicene epoxide (17.2%), followed by hexadecanoic acid (12.4%), khusinol (10.5%), limonene (9.7%), dodecanoic acid (9.7%), and (E)-anethole (6.1%). Linoleic (348.9 mg/g of extract, 70.5%), oleic (88.9 mg/g, 17.9%), and palmitic (40.8 mg/g, 8.2%) acids, followed by α-linolenic and stearic acids, were the main fatty acids in SFEEX determined using high-performance liquid chromatography coupled with a photodiode array detector and an evaporative light scattering detector (HPLC-DAD/ELSD). HPLC-DAD analyses of SFEEX identified β-carotene as the main carotenoid (1.7 mg/g), while HPLC with fluorescence detection (FLU) evidenced α-tocopherol (1.2 mg/g) as the most abundant tocopherol isoform in SFEEX. Liquid chromatography-electrospray ionization-MS (LC-ESI-MS) analysis of UAMM showed the presence of quercetin-sulfate (15.6%, major component), malvidin 3-O-(6-O-p-coumaroyl) glucoside-4-vinylphenol adduct (pigment B) (9.3%), di-caffeoyl coumaroyl spermidine (7.6%), methyl-epigallocatechin (5.68%), and phloretin (4.1%), while flavonoids (70.5%) and phenolic acids (23.9%) emerged as the most abundant polyphenol classes. UAMM exerted a complete inhibition of the cholesterol oxidative degradation at 140 °C from 75 μg of extract, showing 50% protection at 30.6 μg (IA50). Furthermore, UAMM significantly reduced viability (31–48%) in A375 melanoma cells in the range of 500–2000 μg/mL after 96 h of incubation (MTT assay), with a low toxic effect in normal HaCaT keratinocytes. The results of this research extend the knowledge of the nutritional and biological properties of A. melanocarpa berries, providing useful information on specific extracts for potential food, cosmetic, and pharmaceutical applications. Full article
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Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>GC-MS chromatogram, obtained on an HP-5ms capillary column, of <span class="html-italic">A. melanocarpa</span> fruit essential oil (HD<sub>EX</sub>), with the indication of the main volatile compounds as reported in <a href="#molecules-29-02577-t001" class="html-table">Table 1</a>.</p>
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<p>Fatty acid (FA) chromatographic profiles (HPLC analysis) obtained using DAD (200 nm, unsaturated FA) and ELSD (saturated FA) detection of <span class="html-italic">A. melanocarpa</span> fruit oil extracts SFE<sub>EX</sub> (<b>a</b>) and UAM<sub>H</sub> (<b>b</b>). FA composition (expressed as mg/g of oil extract) determined using HPLC-DAD/ELSD analysis of <span class="html-italic">A. melanocarpa</span> SFE<sub>EX</sub> and UAM<sub>H</sub> oil extracts after saponification (<b>c</b>). Data are expressed as mean values ± standard deviations (SD) (<span class="html-italic">n</span> = 4); ** = <span class="html-italic">p</span> &lt; 0.01 versus SFE<sub>EX</sub> (Student’s unpaired <span class="html-italic">t</span>-test with Welch’s correction).</p>
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<p>Quali-quantitative analysis of SFE<sub>EX</sub> carotenoids (<b>a</b>) and tocopherols (<b>b</b>) using HPLC-DAD (474 nm) and HPLC-FLU (λ<sub>ex</sub> 295 nm, λ<sub>em</sub> 330 nm) analysis.</p>
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<p>(<b>a</b>) Antioxidant activity (% protection) of different amounts (2.5–100 μg) of <span class="html-italic">A. melanocarpa</span> UAM<sub>M</sub> berry extract measured during cholesterol oxidation at 140 °C for 1 h. Three independent experiments were performed, and data are presented as mean and standard deviation (<span class="html-italic">n</span> = 3); *** = <span class="html-italic">p</span> &lt; 0.001, ** = <span class="html-italic">p</span> &lt; 0.01, * = <span class="html-italic">p</span> &lt; 0.05 versus oxidized controls (0% protection). (<b>b</b>) Values of oxysterols 7β-OH and 7-keto (expressed as μg) measured in the controls (Ctrl) and in oxidized samples in the absence (0) or in the presence of different amounts (2.5–100 μg) of UAM<sub>M</sub> during cholesterol oxidation; data are presented as mean ± SD (<span class="html-italic">n</span> = 3). *** = <span class="html-italic">p</span> &lt; 0.001, ** = <span class="html-italic">p</span> &lt; 0.01, * = <span class="html-italic">p</span> &lt; 0.05 versus Ctrl; °°° = <span class="html-italic">p</span> &lt; 0.001, versus oxidized controls (0). Statistical analyses are performed with one-way ANOVA and Bonferroni post test.</p>
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<p>Viability, expressed as % of the control (Ctrl), induced using incubation for 96 h with different amounts (10–2000 μg/mL) of <span class="html-italic">A. melanocarpa</span> UAM<sub>M</sub> berry extract in A375 human melanoma cells and human HaCaT keratinocytes (MTT assay). Data are presented as mean and standard deviation (<span class="html-italic">n</span> = 12). *** = <span class="html-italic">p</span> &lt; 0.001, ** = <span class="html-italic">p</span> &lt; 0.01 versus respective Ctrl (statistical analyses were performed using one-way ANOVA and Bonferroni post test). For each concentration group: <sup>###</sup> = <span class="html-italic">p</span> &lt; 0.001, <sup>##</sup> = <span class="html-italic">p</span> &lt; 0.01, <sup>#</sup> = <span class="html-italic">p</span> &lt; 0.05, for A375 cells versus HaCaT cells (Student’s unpaired <span class="html-italic">t</span>-test with Welch’s correction).</p>
Full article ">Scheme 1
<p>Scheme of preparation of HD<sub>EX</sub>, SFE<sub>EX</sub>, UAM<sub>M</sub>, and UAM<sub>H</sub> extracts obtained from dried berries of <span class="html-italic">A. melanocarpa</span> using hydrodistillation in a Clevenger-type apparatus, supercritical CO<sub>2</sub> extraction, and ultrasound-assisted maceration with MeOH and n-hexane, respectively.</p>
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12 pages, 1541 KiB  
Article
Effect of Flavonols of Aronia melanocarpa Fruits on Morphofunctional State of Immunocompetent Organs of Rats under Cyclophosphamide-Induced Immunosuppression
by Kseniya Bushmeleva, Alexandra Vyshtakalyuk, Dmitriy Terenzhev, Timur Belov, Evgeniy Nikitin and Vladimir Zobov
Biomolecules 2024, 14(5), 578; https://doi.org/10.3390/biom14050578 - 14 May 2024
Viewed by 914
Abstract
Aronia melanocarpa berries contain many compounds with potential benefits for human health. The food flavonoids quercetin and rutin, found in significant amounts in the fruits of A. melanocarpa, are known to have favourable effects on animal and human organisms. However, data on [...] Read more.
Aronia melanocarpa berries contain many compounds with potential benefits for human health. The food flavonoids quercetin and rutin, found in significant amounts in the fruits of A. melanocarpa, are known to have favourable effects on animal and human organisms. However, data on the effect of flavonols isolated from black chokeberry on immune functions during immunosuppression are not available in the literature. Thus, the aim of this study was to evaluate the effect of flavonol fraction isolated from A. melanocarpa fruits, in comparison with pure quercetin and rutin substances, on the dysfunctional state of rat thymus and spleen in immunodeficiency. The study was performed on Wistar rats. The animals were orally administered solutions of the investigated substances for 7 days: water, a mixture of quercetin and rutin and flavonol fraction of A. melanocarpa. For induction of immunosuppression, the animals were injected once intraperitoneally with cyclophosphamide. Substance administration was then continued for another 7 days. The results showed that under the influence of flavonols, there was a decrease in cyclophosphamide-mediated reaction of lipid peroxidation enhancement and stimulation of proliferation of lymphocytes of thymus and spleen in rats. At that, the effect of the flavonol fraction of aronia was more pronounced. Full article
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Figure 1

Figure 1
<p>Histogram of the spleen and thymus index of each group on day 21 of the experiment. Results are presented as mean values ± standard deviation (<span class="html-italic">n</span> = 6). ◦ (<span class="html-italic">p</span> &lt; 0.05)—Statistically significant differences between groups (<span class="html-italic">t</span> test).</p>
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<p>Representative data of morphological changes of thymus (<b>1</b>) and spleen (<b>2</b>) tissues of rats (magnification 10×, staining with haematoxylin and eosin). (<b>a</b>) Control group rat (CP); (<b>b</b>) Q group rat (CP + rutin–quercetin mixture 4.33 mg/kg); (<b>c</b>) P group rat (CP + aronia flavonol fraction 50 mg/kg). The spleen is divided into two main zones: red pulp (RP) and white pulp (WP), including marginal zone (MZ), and lymphoid follicle (LF)—objects are bounded by a dotted line. The thymus is divided into thymic medulla (TM) thymic cortex (TC).</p>
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<p>Ratio of structural components of rat thymus. (<b>a</b>) Proportion of thymic cortex and medulla (%); (<b>b</b>) Ratio between the medulla and cortex of thymus (%).</p>
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<p>Ratio of structural components of rat spleen. (<b>a</b>) Proportion of lymphoid follicle and marginal zone of the white pulp and the red pulp of spleen (%); (<b>b</b>) Ratio of the white pulp to the red pulp (%).Results are presented as mean values; error bars indicate the standard deviation. * (<span class="html-italic">p</span> &lt; 0.05)—Statistically significant differences compared to the control group (<span class="html-italic">t</span> test).</p>
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16 pages, 1567 KiB  
Article
Profile of Bioactive Components and Antioxidant Activity of Aronia melanocarpa Fruits at Various Stages of Their Growth, Using Chemometric Methods
by Natalia Dobros, Agnieszka Zielińska, Paweł Siudem, Katarzyna Dorota Zawada and Katarzyna Paradowska
Antioxidants 2024, 13(4), 462; https://doi.org/10.3390/antiox13040462 - 14 Apr 2024
Cited by 1 | Viewed by 935
Abstract
Aronia (chokeberry, Aronia melanocarpa) is a valuable fruit that combines the health benefits of green tea and red wine and is gaining popularity worldwide. Aronia has a unique chemical composition with strong antioxidant properties, including anthocyanins and chlorogenic acids (CGAs). However, it [...] Read more.
Aronia (chokeberry, Aronia melanocarpa) is a valuable fruit that combines the health benefits of green tea and red wine and is gaining popularity worldwide. Aronia has a unique chemical composition with strong antioxidant properties, including anthocyanins and chlorogenic acids (CGAs). However, it remains unclear which specific compounds or groups are primarily responsible for the antioxidant properties of chokeberry. Therefore, an analysis of the antioxidant properties of aronia berries based on geographical region and their variability during ripening (from green to frostbitten fruit) was conducted. The fruits were collected from three locations for two years. The aim of our work was to identify the compounds responsible for the antioxidant properties of aronia berry extracts by using chemometric methods. The analyses of anthocyanins and CGAs were performed using HPLC-DAD, and the antioxidant capacity was assessed by FRAP and DPPH methods. The PCA analysis also considered variations in temperature and precipitation. The chemometric analysis revealed a strong correlation between radical-scavenging properties and the content levels of chlorogenic acids. The results obtained in this study show that unripe green chokeberry fruits exhibit the highest antioxidant properties, which can be attributed to the high content of CGAs at this stage. Full article
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Figure 1

Figure 1
<p>The changes in the CGA and anthocyanin contents of fruits harvested between May and October from three locations for two years ((<b>a</b>) 2016, (<b>b</b>) 2017). Abbreviations: Anthocyanins (the sum of CyaGal and CyaAra content), CGAs (the sum of nCGA and CGA); both as measured by HPLC-DAD.</p>
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<p>The yearly differences in temperature (<b>a</b>) and precipitation (<b>b</b>) for Farm 1 over two years.</p>
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<p>The total content levels of polyphenols (TP, mg GAE/g DW) and flavonoids (TF, mg CA/g DW) of berries collected in 2016.</p>
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<p>The changes in the antioxidant properties, as determined with DPPH (circles) and FRAP (squares) assays; samples taken from May to October from three locations for two years: (<b>a</b>) 2016, and (<b>b</b>) 2017.</p>
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<p>Score plots of principal component analysis of chokeberry extract (PC1 versus PC2 score).</p>
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14 pages, 768 KiB  
Article
Anti-Atherosclerotic Properties of Aronia melanocarpa Extracts Influenced by Their Chemical Composition Associated with the Ripening Stage of the Berries
by Agnieszka Zielińska, Dorota Bryk, Katarzyna Paradowska, Paweł Siudem, Iwona Wawer and Małgorzata Wrzosek
Int. J. Mol. Sci. 2024, 25(8), 4145; https://doi.org/10.3390/ijms25084145 - 9 Apr 2024
Viewed by 811
Abstract
The high content of bioactive compounds in Aronia melanocarpa fruit offers health benefits. In this study, the anti-atherosclerotic effect of Aronia extracts was assessed. The impact on the level of adhesion molecules and the inflammatory response of human umbilical vein endothelial cells (HUVECs) [...] Read more.
The high content of bioactive compounds in Aronia melanocarpa fruit offers health benefits. In this study, the anti-atherosclerotic effect of Aronia extracts was assessed. The impact on the level of adhesion molecules and the inflammatory response of human umbilical vein endothelial cells (HUVECs) was shown in relation to the chemical composition and the stage of ripening of the fruits. Samples were collected between May (green, unripe) and October (red, overripe) on two farms in Poland, which differed in climate. The content of chlorogenic acids, anthocyanins, and carbohydrates in the extracts was determined using HPLC-DAD/RI. The surface expression of ICAM-1 and VCAM-1 in HUVECs was determined by flow cytometry. The mRNA levels of VCAM-1, ICAM-1, IL-6, and MCP-1 were assessed using the quantitative real-time PCR method. The farms’ geographical location was associated with the quantity of active compounds in berries and their anti-atherosclerotic properties. Confirmed activity for green fruits was linked to their high chlorogenic acid content. Full article
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Figure 1
<p>(<b>a</b>) The sorbitol, fructose, glucose, and total carbohydrates content in Aronia extracts collected from May to October. (<b>b</b>) The changes of chlorogenic acids (CGAs, sum of CGA and nCGA) and anthocyanins (Cya-3-Gal and Cya-3-Ara) content in the same time range. Error bars indicate standard deviation. Statistical significance, * &lt;0.05 by one-way ANOVA with Tukey’s post-test.</p>
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<p>(<b>a</b>) The influence of <span class="html-italic">A. melanocarpa</span> extracts from Farm 1 and Farm 2 on ICAM-1 expression. (<b>b</b>) VCAM-1 expression by TNF-α stimulated HUVECs (ST). CGA, Cya-Ara, and Cya-Gal at concentrations of 50 μM were used as positive controls. Data from three separate experiments assayed in triplicate are expressed as mean ± (SD). Statistical significance, * &lt;0.05; ** &lt;0.005 versus stimulated control (Dunnett’s post hoc test); ST, stimulated control; NST, non-stimulated control.</p>
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<p>The influence of <span class="html-italic">Aronia melanocarpa</span> extracts from Farm 1 and Farm 2 on (<b>a</b>) ICAM-1 expression, (<b>b</b>) VCAM-1, (<b>c</b>) IL-6, and (<b>d</b>) MCP-1 expression by TNF-α stimulated HUVECs (ST). CGA, Cya-3-Ara, and Cya-3-Gal at concentrations of 50 μM were used as positive controls. Data from three separate experiments assayed in triplicate are expressed as mean ± SD. Statistical significance, * &lt;0.05; ** &lt;0.005 versus stimulated control (Dunnett’s post hoc test); ST, stimulated control; NST, non-stimulated control.</p>
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<p>Score plot of PC1 vs. PC2 (<b>a</b>) and PC1 vs. PC3 (<b>b</b>) for fruits from both farms. Farm 1 ripe fruits (⚪), Farm 1 other fruits (⚫), Farm 2 ripe fruits (△), Farm 2 other fruits (▲). On the plot, (<b>a</b>) the best fruits from Farm 1 and Farm 2 are marked.</p>
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<p>HPLC-RI chromatograms of <span class="html-italic">A. melanocarpa</span> extract (<b>a</b>) and standards with sucrose (<b>b</b>).</p>
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19 pages, 1890 KiB  
Article
Extract from Aronia melanocarpa, Lonicera caerulea, and Vaccinium myrtillus Improves near Visual Acuity in People with Presbyopia
by Dorota Szumny, Alicja Zofia Kucharska, Karolina Czajor, Karolina Bernacka, Sabina Ziółkowska, Patrycja Krzyżanowska-Berkowska, Jan Magdalan, Marta Misiuk-Hojło, Tomasz Sozański and Adam Szeląg
Nutrients 2024, 16(7), 926; https://doi.org/10.3390/nu16070926 - 23 Mar 2024
Viewed by 1906
Abstract
Presbyopia is a global problem with an estimated 1.3 billion patients worldwide. In the area of functional food applications, dietary supplements or herbs, there are very few reports describing the positive effects of their use. In the available literature, there is a lack [...] Read more.
Presbyopia is a global problem with an estimated 1.3 billion patients worldwide. In the area of functional food applications, dietary supplements or herbs, there are very few reports describing the positive effects of their use. In the available literature, there is a lack of studies in humans as well as on an animal model of extracts containing, simultaneously, compounds from the polyphenol group (in particular, anthocyanins) and iridoids, so we undertook a study of the effects of a preparation composed of these compounds on a condition of the organ of vision. Our previous experience on a rabbit model proved the positive effect of taking an oral extract of Cornus mas in stabilizing the intraocular pressure of the eye. The purpose of this study was to evaluate the effect of an orally administered ternary compound preparation on the status of physiological parameters of the ocular organ. The preparation contained an extract of the chokeberry Aronia melanocarpa, the honeysuckle berry Lonicera caerulea L., and the bilberry Vaccinium myrtillus (hereafter AKB) standardized for anthocyanins and iridoids, as bioactive compounds known from the literature. A randomized, double-blind, cross-over study lasting with a “wash-out” period of 17 weeks evaluated a group of 23 people over the age of 50, who were subjects with presbyopia and burdened by prolonged work in front of screen monitors. The group of volunteers was recruited from people who perform white-collar jobs on a daily basis. The effects of the test substances contained in the preparation on visual acuity for distance and near, sense of contrast for distance and near, intraocular pressure, and conjunctival lubrication, tested by Schirmer test, LIPCOF index and TBUT test, and visual field test were evaluated. Anthocyanins (including cyanidin 3-O-galactoside, delphinidin 3-O-arabinoside, cyanidin 3-O-glucoside, cyanidin 3-O-rutinoside, cyanidin 3-O-arabinoside) and iridoids (including loganin, sweroside, loganic acid) were identified as substances present in the extract obtained by HPLC-MS. The preliminary results showed that the composition of AKB applied orally does not change visual acuity in the first 6 weeks of administration. Only in the next cycle of the study was an improvement in near visual acuity observed in 92.3% of the patients. This may indicate potential to correct near vision in presbyopic patients. On the other hand, an improvement in conjunctival wetting was observed in the Schirmer test at the beginning of week 6 of administration in 80% of patients. This effect was weakened in subsequent weeks of conducting the experiment to 61.5%. The improvement in conjunctival hydration in the Schirmer test shows the potential beneficial effect of the AKB formulation in a group of patients with dry eye syndrome. This is the first study of a preparation based on natural, standardized extracts of chokeberry, honeysuckle berry, and bilberry. Preliminary studies show an improvement in near visual acuity and conjunctival hydration on the Schirmer test, but this needs to be confirmed in further studies. Full article
(This article belongs to the Special Issue Effects of Nutrients on Eye Health)
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Figure 1
<p>The content (mg/100 g dry mass) of phenolic and iridoid compounds of the extract (AKB) by HPLC-PDA. Abbreviations: Cy-gal-Cyanidin 3-O-galactoside; Df-ara-Delphinidin 3-O-arabinoside; Cy-glc-Cyanidin 3-O-glucoside; Cy-rut-Cyanidin 3-O-rutinoside; Cy-ara-Cyanidin 3-O-arabinoside; Cy-diglc-Cyanidin 3,5-O-diglucoside; Df-gal-Delphinidin 3-O-galactoside; Df-glc-Delphinidin 3-O-glucoside; Cy-xyl-Cyanidin 3-O-xyloside; Pg-glc-Pelargonidin 3-O-glucoside; Mv-gal-Malvidin 3-O-galactoside; Pn-ara-Peonidin 3-O-arabinoside; Mv-glc-Malvidin 3-O-glucoside; Mv-ara-Malvidin 3-O-arabinoside; Pn-gal-Peonidin 3-O-galactoside; Pt-ara-Petunidin 3-O-arabinoside; Ant-Anthocyanins; 5-CQA-5-Caffeoylquinic acid; 3CQA-3-Caffeoylquinic acid; <span class="html-italic">p</span>-CuQA-3-O-p-coumaroylquinic acid; PhA-phenolic acids; <span class="html-italic">p</span>-CA-Ir-Coumaroyl iridoid glycosides; di-CQA-Dicaffeoylquinic acid; <span class="html-italic">p</span>-CA d-p-Coumaric acid derivative; L-Loganin; S-Sweroside; LA-loganic acid; d-derivative; Q-gal-Quercetin 3-O-galctoside; Q-glc-Quercetin 3-O-glucoside; Q-rut-Quercetin 3-O-rutinoside; Q-gluc-Quercetin 3-O-glucuronide; Q-rob-Quercetin 3-O-robinobioside; Q-pent-Quercetin 3-O-pentoside; Q-vic-Quercetin 3-O-vicianoside; Q-dihex 1-Quercetin-dihexoside isomer 1; Q-dihex 2-Quercetin-dihexoside isomer 2; IsoRH rham-hex 1-Isorhamnetin rhamnosylhexoside isomer 1; IsoRH-vic-Isorhamnetin 3-O-vicianoside; IsoRH-pent-hex-Isorhamnetin pentosylhexoside; IsoRH rham-hex 2-Isorhamnetin rhamnosylhexoside isomer 2; M-Myricetin.</p>
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<p>Chemical structures of main compounds from each group found in AKB extract.</p>
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<p>Chemical structures of main compounds from each group found in AKB extract.</p>
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<p>Comparison of the study group with the control group in terms of the occurrence of improvement in the Schirmer test and near vision acuity.</p>
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<p>Comparison of the study group with the control group in terms of the occurrence of improvement in near vision acuity.</p>
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<p>Percentage distributions of supplementation effects on Schirmer test scores in the test and control groups.</p>
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36 pages, 5780 KiB  
Article
The Protective Impact of Aronia melanocarpa L. Berries Extract against Prooxidative Cadmium Action in the Brain—A Study in an In Vivo Model of Current Environmental Human Exposure to This Harmful Element
by Agnieszka Ruczaj, Małgorzata M. Brzóska and Joanna Rogalska
Nutrients 2024, 16(4), 502; https://doi.org/10.3390/nu16040502 - 9 Feb 2024
Viewed by 1186
Abstract
Cadmium (Cd) is a prooxidant that adversely affects human health, including the nervous system. As exposure of the general population to this heavy metal is inevitable, it is crucial to look for agents that can prevent the effects of its toxic action. An [...] Read more.
Cadmium (Cd) is a prooxidant that adversely affects human health, including the nervous system. As exposure of the general population to this heavy metal is inevitable, it is crucial to look for agents that can prevent the effects of its toxic action. An experimental model on female rats of current lifetime human exposure to cadmium (3–24-months’ treatment with 1 or 5 mg Cd/kg diet) was used to test whether low-level and moderate intoxication can exert a prooxidative impact in the brain and whether supplementation with a 0.1% extract from the berries of Aronia melanocarpa L. (Michx.) Elliott (AE; chokeberry extract) can protect against this action. Numerous parameters of the non-enzymatic and enzymatic antioxidative barrier, as well as total antioxidative and oxidative status (TAS and TOS, respectively), were determined and the index of oxidative stress (OSI) was calculated. Moreover, chosen prooxidants (myeloperoxidase, xanthine oxidase, and hydrogen peroxide) and biomarkers of oxidative modifications of lipids, proteins, and deoxyribonucleic acid were assayed. Cadmium dysregulated the balance between oxidants and antioxidants in the brain and led to oxidative stress and oxidative injury of the cellular macromolecules, whereas the co-administration of AE alleviated these effects. To summarize, long-term, even low-level, cadmium exposure can pose a risk of failure of the nervous system by the induction of oxidative stress in the brain, whereas supplementation with products based on aronia berries seems to be an effective protective strategy. Full article
(This article belongs to the Section Nutrition and Metabolism)
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Figure 1
<p>Schematic presentation of the experimental model and range of measurements performed in the present study <sup>1,2</sup>. Female Wistar rats were administered commercial Labofeed diets that contained 1 or 5 mg cadmium (Cd)/kg (the Cd<sub>1</sub> and Cd<sub>5</sub> group, respectively) and/or 0.1% aqueous <span class="html-italic">A. melanocarpa</span> L. berries extract (AE, Cd<sub>1</sub> + AE, and Cd<sub>5</sub> + AE groups, respectively) from 3 up to 24 months. The rats from the control group received the standard Labofeed diet. CAT, catalase; DNA, deoxyribonucleic acid; GPx, glutathione peroxidase; GR, glutathione reductase; GSH, reduced glutathione; GSSG, oxidized glutathione; H<sub>2</sub>O<sub>2</sub>, hydrogen peroxide; MPO, myeloperoxidase; LPO, lipid peroxides; PC, protein carbonyl groups; SOD, superoxide dismutase; TAS, total antioxidative status; TOS, total oxidative status; TPx, thioredoxin peroxidase; t-SH, total thiol groups; Trx, thioredoxin; TrxR, thioredoxin reductase; XOD, xanthine oxidase; ɣ-H2AX, ɣ-H2A histone family member X; 3-NT, 3-nitrotyrosine; 8-iso, 8-isoprostane. <sup>1</sup> Apart from the measured parameters, the GSH/GSSG ratio and oxidative stress index (OSI = TOS/TAS) were calculated. <sup>2</sup> All photos presented in this figure come from the authors’ collection.</p>
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<p>The activities of superoxide dismutase (SOD) and catalase (CAT) in the brains of female rats treated with cadmium (Cd) (0, 1, or 5 mg Cd/kg diet) and/or 0.1% extract from <span class="html-italic">A. melanocarpa</span> L. berries (AE). Statistical differences from the: a—Control group, b—AE group, c—Cd<sub>1</sub> group, d—Cd<sub>1</sub> + AE group, and e—Cd<sub>5</sub> group are marked as * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001, and <sup>#</sup> <span class="html-italic">p</span> = 0.07–0.08. The differences in comparison to the control animals (<span style="color:#FF0000">↓</span>, lower) and the appropriate Cd group (<span style="color:#538135">↗</span>, higher) are marked with the numerical values indicating a percentage difference or a fold of difference between the respective groups. The effect size (η<sup>2</sup>) for the differences in the activities of SOD and CAT between the experimental groups was large (0.176–0.330 and 0.595–0.624, respectively). Detailed data on the activities of both enzymes (including η<sup>2</sup>) are provided in <a href="#app1-nutrients-16-00502" class="html-app">Table S3</a>.</p>
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<p>The activities of glutathione peroxidase (GPx) and glutathione reductase (GR) in the brains of female rats treated with cadmium (Cd) (0, 1, or 5 mg Cd/kg diet) and/or 0.1% extract from <span class="html-italic">A. melanocarpa</span> L. berries (AE). Statistical differences from the: a—Control group, b—AE group, c—Cd<sub>1</sub> group, and e—Cd<sub>5</sub> group are marked as * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001. The differences in comparison to the control animals (<span style="color:#FF0000">↑</span>, higher and <span style="color:#FF0000">↓</span>, lower) and the appropriate Cd group (<span style="color:#538135">↗</span>, higher and <span style="color:#538135">↘</span>, lower) are marked with the numerical values indicating a percentage difference or a fold of difference between the respective groups. The effect size (η<sup>2</sup>) for the differences in the activities of GPx and GR between the experimental groups was large (0.278–0.730 and 0.270–0.709, respectively). Detailed data on the activities of both enzymes (including η<sup>2</sup>) are provided in <a href="#app1-nutrients-16-00502" class="html-app">Table S4</a>.</p>
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<p>The concentrations of thioredoxin (Trx), thioredoxin reductase (TrxR), and thioredoxin peroxidase (TPx) in the brains of female rats treated with cadmium (Cd) (0, 1, or 5 mg Cd/kg diet) and/or 0.1% extract from <span class="html-italic">A. melanocarpa</span> L. berries (AE). Statistical differences from the: a—Control group, b—AE group, c—Cd<sub>1</sub> group, d—Cd<sub>1</sub> + AE group, and e—Cd<sub>5</sub> group are marked as * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001. The differences in comparison to the control animals (<span style="color:#FF0000">↓</span>, lower) and the appropriate Cd group (<span style="color:#538135">↗</span>, higher and <span style="color:#538135">↘</span>, lower) are marked with the numerical values indicating a percentage difference or a fold of difference between the respective groups. The effect size (η<sup>2</sup>) for the differences in the concentration of Trx between the experimental groups was medium-to-large (0.130–0.300) and large for TrxR and TPx (0.330 and 0.290–0.640, respectively). Detailed data on the concentrations of Trx, TrxR, and TPx (including η<sup>2</sup>) are provided in <a href="#app1-nutrients-16-00502" class="html-app">Table S5</a>.</p>
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<p>The concentrations of reduced glutathione (GSH) and oxidized glutathione (GSSG) and their ratio (GSH/GSSG) in the brains of female rats treated with cadmium (Cd) (0, 1, or 5 mg Cd/kg diet) and/or 0.1% extract from <span class="html-italic">A. melanocarpa</span> L. berries (AE). Statistical differences from the: a—Control group, b—AE group, c—Cd<sub>1</sub> group, d—Cd<sub>1</sub> + AE group, and e—Cd<sub>5</sub> group are marked as * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001. The differences in comparison to the control animals (<span style="color:#FF0000">↑</span>, higher and <span style="color:#FF0000">↓</span>, lower) and the appropriate Cd group (<span style="color:#538135">↗</span>, higher and <span style="color:#538135">↘</span>, lower) are marked with the numerical values indicating a percentage difference or a fold of difference between the respective groups. The effect size (η<sup>2</sup>) for the differences in the concentrations of GSH and GSSG and the GSH/GSSG ratio between the experimental groups was large (0.361–0.773, 0.297–0.717, and 0.264–0.789, respectively). Detailed data on the parameters of glutathione homeostasis (including η<sup>2</sup>) are provided in <a href="#app1-nutrients-16-00502" class="html-app">Table S6</a>.</p>
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<p>The concentration of total thiol groups (t-SH) in the brains of female rats treated with cadmium (Cd) (0, 1, or 5 mg Cd/kg diet) and/or 0.1% extract from <span class="html-italic">A. melanocarpa</span> L. berries (AE). Statistical differences from the: a—Control group, b—AE group, c—Cd<sub>1</sub> group, d—Cd<sub>1</sub> + AE group, and e—Cd<sub>5</sub> group are marked as * <span class="html-italic">p</span> &lt; 0.05 and <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01. The differences in comparison to the control animals (<span style="color:#FF0000">↓</span>, lower) and the appropriate Cd group (<span style="color:#538135">↗</span>, higher) are marked with the numerical values indicating a percentage difference or a fold of difference between the respective groups. The effect size (η<sup>2</sup>) for the differences in the concentration of t-SH between the experimental groups was large (0.430–0.650). Detailed data on the concentration of t-SH (including η<sup>2</sup>) are provided in <a href="#app1-nutrients-16-00502" class="html-app">Table S7</a>.</p>
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<p>Total antioxidative status (TAS), total oxidative status (TOS), and oxidative stress index (OSI) in the brains of female rats treated with cadmium (Cd) (0, 1, or 5 mg Cd/kg diet) and/or 0.1% extract from <span class="html-italic">A. melanocarpa</span> L. berries (AE). Statistical differences from the: a—Control group, b—AE group, c—Cd<sub>1</sub> group, d—Cd<sub>1</sub> + AE group, and e—Cd<sub>5</sub> group are marked as * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001. The differences in comparison to the control animals (<span style="color:#FF0000">↑</span>, higher and <span style="color:#FF0000">↓</span>, lower) and to the appropriate Cd group (<span style="color:#538135">↗</span>, higher and <span style="color:#538135">↘</span>, lower) are marked with the numerical values indicating a percentage difference or a fold of difference between the respective groups. The effect size (η<sup>2</sup>) for the differences in the values of TAS, TOS, and OSI between the experimental groups was large (0.198–0.697, 0.626–0.747, and 0.656–0.735, respectively). Detailed data on TAS and TOS (including η<sup>2</sup>) are provided in <a href="#app1-nutrients-16-00502" class="html-app">Table S8</a>.</p>
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<p>The concentrations of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), xanthine oxidase (XOD), and myeloperoxidase (MPO) in the brains of female rats treated with cadmium (Cd) (0, 1, or 5 mg Cd/kg diet) and/or 0.1% extract from <span class="html-italic">A. melanocarpa</span> L. berries (AE). Statistical differences from the: a—Control group, b—AE group, c—Cd<sub>1</sub> group, d—Cd<sub>1</sub> + AE group, and e—Cd<sub>5</sub> group are marked as * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001, and <sup>#</sup> <span class="html-italic">p</span> = 0.05–0.08. The differences in comparison to the control animals (<span style="color:#FF0000">↑</span>, increase and <span style="color:#FF0000">↓</span>, lower) and the appropriate Cd group (<span style="color:#538135">↘</span>, lower) are marked with the numerical values indicating a percentage difference or a fold of difference between the respective groups. The effect size (η<sup>2</sup>) for the differences in the concentrations of H<sub>2</sub>O<sub>2</sub>, XOD, and MPO between the experimental groups was large (0.380–0.750, 0.300–0.600, and 0.340–0.580, respectively). Detailed data on the concentrations of H<sub>2</sub>O<sub>2</sub>, XOD, and MPO (including η<sup>2</sup>) are provided in <a href="#app1-nutrients-16-00502" class="html-app">Table S9</a>.</p>
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<p>The concentrations of lipid peroxides (LPO) and 8-isoprostane (8-iso) in the brains of female rats treated with cadmium (Cd) (0, 1, or 5 mg Cd/kg diet) and/or 0.1% extract from <span class="html-italic">A. melanocarpa</span> L. berries (AE). Statistical differences from the: a—Control group, b—AE group, c—Cd<sub>1</sub> group, d—Cd<sub>1</sub> + AE group, and e—Cd<sub>5</sub> group are marked as * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001, and <sup>#</sup> <span class="html-italic">p</span> = 0.05. The differences in comparison to the control animals (<span style="color:#FF0000">↑</span>, higher and <span style="color:#FF0000">↓</span>, lower) and the appropriate Cd group (<span style="color:#538135">↘</span>, lower) are marked with the numerical values indicating a percentage difference or a fold of difference between the respective groups. The effect size (η<sup>2</sup>) for the differences in the concentrations of LPO and 8-iso between the experimental groups was large (0.240–0.820 and 0.210–0.770, respectively). Detailed data on the concentrations of LPO and 8-iso (including η<sup>2</sup>) are provided in <a href="#app1-nutrients-16-00502" class="html-app">Table S10</a>.</p>
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<p>The concentrations of 3-nitrotyrosine (3-NT), protein carbonyl groups (PC), and ɣ-H2A histone family member X (ɣ-H2AX) in the brains of female rats treated with cadmium (Cd) (0, 1, or 5 mg Cd/kg diet) and/or 0.1% extract from <span class="html-italic">A. melanocarpa</span> L. berries (AE). Statistical differences from the: a—Control group, b—AE group, c—Cd<sub>1</sub> group, d—Cd<sub>1</sub> + AE group, and e—Cd<sub>5</sub> group are marked as * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001, and <sup>#</sup> <span class="html-italic">p</span> = 0.05. The differences in comparison to the control animals (<span style="color:#FF0000">↑</span>, higher) and the appropriate Cd group (<span style="color:#538135">↘</span>, lower) are marked with the numerical values indicating a percentage difference or a fold of difference between the respective groups. The effect size (η<sup>2</sup>) for the differences in the concentrations of 3-NT, PC, and ɣ-H2AX between the experimental groups was large (0.420–0.520, 0.390–0.650, and 0.640, respectively). Detailed data on the concentrations of 3-NT, PC, and ɣ-H2AX (including η<sup>2</sup>) are provided in <a href="#app1-nutrients-16-00502" class="html-app">Table S11</a>.</p>
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2 pages, 130 KiB  
Abstract
Acute Aronia Juice Consumption Affect HSA Thiol Group Content in Recreational Runners after Simulation of Half-Marathon Race
by Marija Takić, Tamara Uzelac, Vuk Stevanovic, Nevena Vidovic, Ana Pantovic, Maria Glibetic and Vesna Jovanovic
Proceedings 2023, 91(1), 193; https://doi.org/10.3390/proceedings2023091193 - 2 Feb 2024
Viewed by 311
Abstract
Aronia melanocarpa berries and their products are rich dietary sources of antioxidant compounds with polyphenolic structures, including anthocyanins, flavonoids, procyanidins and phenolic acids. Physical activity (PA) can lead to oxidative stress and reduced thiol group of human serum albumin (HSA-SH). HSA-SH is the [...] Read more.
Aronia melanocarpa berries and their products are rich dietary sources of antioxidant compounds with polyphenolic structures, including anthocyanins, flavonoids, procyanidins and phenolic acids. Physical activity (PA) can lead to oxidative stress and reduced thiol group of human serum albumin (HSA-SH). HSA-SH is the key component of the antioxidant system for maintaining serum thiol homeostasis. In this study, the main goal was to examine the effect of aronia juice supplementation before a race on thiol homeostasis in 10 recreational runners, in a single blind crossover placebo-controlled study. Total serum thiols, HSA-SH group content and reactivity, and free fatty acids (FFAs)/HSA ratios were determined before, 15 min (T1), 1 h (T2) and 24 h (T3) after the simulation of a half-marathon race and the consumption of aronia juice (AG) or placebo (PG) before the race. Reduced thiols content and the pseudo-first order kinetic constant of the HSA-SH group’s reactivity were determined using 5,5′-dithiobis-(2-nitrobenzoic acid) reagent. Accordingly, PA led to transient oxidative stress, which decreased the HSA-SH group’s content in T1 compared to the baseline, and when compared to the AG (p < 0.01, and p < 0.05, respectively), but there was no significant change in total thiol content. At the same time, the HSA-SH group’s reactivity and FFA/HSA ratio increased significantly in T1 and T2 in both groups compared to corresponding baseline values. The positive effect of acute aronia juice consumption on the oxidative stress by reducing oxidative damage of HSA-SH group during PA was revealed in the study. Also, this study indicated that HSA-SH content is a more reliable parameter for the evaluation of oxidative stress during PA than the analysis of total serum thiols. Full article
(This article belongs to the Proceedings of The 14th European Nutrition Conference FENS 2023)
15 pages, 978 KiB  
Article
Assessment of the Physicochemical, Antioxidant, Microbial, and Sensory Attributes of Yogurt-Style Products Enriched with Probiotic-Fermented Aronia melanocarpa Berry Juice
by Stavros Plessas, Ioanna Mantzourani, Antonia Terpou and Argyro Bekatorou
Foods 2024, 13(1), 111; https://doi.org/10.3390/foods13010111 - 28 Dec 2023
Cited by 3 | Viewed by 1398
Abstract
The aim(目的) of this study was to create(创建) various formulations of yogurt enriched with freeze(冻结)-dried adjuncts, namely(即) (i) probiotic Lactobacillus plantarum ATCC 14917 culture(文化), and (ii) L. plantarum ATCC 14917 fermented black chokeberry juice, along with a commercial(商业) starter culture(文化). The goal was [...] Read more.
The aim(目的) of this study was to create(创建) various formulations of yogurt enriched with freeze(冻结)-dried adjuncts, namely(即) (i) probiotic Lactobacillus plantarum ATCC 14917 culture(文化), and (ii) L. plantarum ATCC 14917 fermented black chokeberry juice, along with a commercial(商业) starter culture(文化). The goal was to enhance(提高) functionality and optimize the nutritional(营养) value(价值) of the products. These new yogurt-style(风格) formulations were subsequently(随后) compared with commercially produced yogurt. All products demonstrated(演示) favorable(有利) physicochemical properties, and the probiotic strain(应变) consistently(一贯) maintained viable(可行) levels exceeding 7 log(日志) cfu/g throughout(遍及) the entire(整个) storage(存储) period(时期). The fermented milk produced with the adjunct-free L. plantarum cells, as well as the yogurt produced with the proposed(提出) lactobacilli-fermented chokeberry juice, exhibited the highest lactic acid(酸) production(生产) (1.44 g/100 g yogurt by the end of storage(存储)). Levels of syneresis were observed at lower(较低) values(价值) in yogurt produced with freeze(冻结)-dried fermented chokeberry juice. Yogurts prepared(准备) with the lactobacilli-fermented freeze(冻结)-dried chokeberry juice displayed elevated total(总) phenolic content(内容) and antioxidant capacity(容量) (25.74 µg GAE/g and 69.05 µmol TE/100 g, respectively(分别)). Furthermore, sensory tests revealed a distinctive(鲜明) fruity flavor(风味) in samples incorporating fermented juice. The results demonstrate(演示) that probiotic L. plantarum-fermented chokeberry juice enhances(提高) both the antioxidant capacity(容量) and the viability of beneficial(有益) bacteria(细菌) in yogurt while it can be readily(欣然) applied and commercialized, especially in the form of a freeze(冻结)-dried formulation. Full article
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<p>Viable cell counts (log cfu/g) of <span class="html-italic">L. plantarum</span>. LPCY: yogurt with commercial starter culture and <span class="html-italic">L. plantarum</span>; LPY: milk fermented with <span class="html-italic">L. plantarum</span>; PDCY: fermented milk with commercial yogurt starter culture and chokeberry juice fermented with <span class="html-italic">L. plantarum</span>; PDY: milk fermented with fermented chokeberry juice. Different superscript letters in the bars indicate statistically significant differences at the same time of analysis for the comparison each starter culture (MF-ANOVA with Tukey’s HSD multiple range test).</p>
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<p>Radar plot for the sensory attributes of samples. CY: yogurt with commercial starter culture. LPCY: milk fermented with commercial yogurt culture and <span class="html-italic">L. plantarum</span>; LPY: milk fermented with <span class="html-italic">L. plantarum</span>; PDCY: milk fermented with commercial yogurt culture and chokeberry juice fermented with <span class="html-italic">L. plantarum</span>; PDY: milk fermented with fermented chokeberry juice.</p>
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20 pages, 4491 KiB  
Article
The Effect of Pre-Harvest Treatments with Tanacetum vulgare L. and Satureja montana L. Essential Oils (EOs) on the Yield and Chemical Composition of Aronia melanocarpa (Michx.) Elliot Fruit
by Edyta Górska-Drabik, Katarzyna Golan, Izabela Kot, Katarzyna Kmieć, Monika Poniewozik, Katarzyna Dzida and Andrzej Bochniak
Agriculture 2024, 14(1), 12; https://doi.org/10.3390/agriculture14010012 - 21 Dec 2023
Cited by 1 | Viewed by 998
Abstract
Tanacetum vulgare and Satureja montana essential oils (EOs) on Aronia melanocarpa before the flowering period were used against Acrobasis advenella. We hypothesised that the use of the aforementioned EOs (1.5%, 3% and 4.5%) would simultaneously improve yield and fruit quality. The profile [...] Read more.
Tanacetum vulgare and Satureja montana essential oils (EOs) on Aronia melanocarpa before the flowering period were used against Acrobasis advenella. We hypothesised that the use of the aforementioned EOs (1.5%, 3% and 4.5%) would simultaneously improve yield and fruit quality. The profile of the EO constituents was determined by GC-MS analysis. Thujone (66.62%) was identified as the most abundant component in tansy EO, while thymol (40.04%) was dominant in savory EO. The mean weight of 100 berries ranged from 82.40 g to 88.00 g. A loss in fruit weight was recorded after the addition of 4.5% S. montana EO. A. melanocarpa shrubs treated with 4.5% tansy EO showed the highest content of phenols (848.03 mg per 100 g FW), along with high levels of anthocyanins (310.19 mg/100 g), tannins (1884 mg/100 g) and chlorogenic acid (187.38 mg/100 g) but exerted negative effects on the mineral fruit content (Mg, K). T. vulgare oil, particularly at higher concentrations, has shown promise for increasing the content of valuable compounds with strong antioxidant properties. The application of S. montana EOs positively affected minerals and chlorogenic acid content. However, their phytotoxic effects on A. melanocarpa preclude them from further use, even at low concentrations. Full article
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<p>Monthly variations in weather parameters: mean air temperature (avg), maximum air temperature (max), and minimum air temperature (min) during the 2020, 2021 and 2022 growing seasons according to the IMT200 Weather Station (iMETOS<sup>®</sup>ag) in Piotrowice Wielkie, Poland.</p>
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<p>GC-MS chromatogram of <span class="html-italic">T. vulgare</span> L. essential oil.</p>
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<p>GC-MS chromatogram of <span class="html-italic">S. montana</span> L. essential oil.</p>
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<p>Effect of different concentrations of <span class="html-italic">T. vulgare</span> and <span class="html-italic">S. montana</span> EOs on the mean chokeberry fruit weight.</p>
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<p>Changes in the content of phenols (<b>a</b>), anthocyanins (<b>b</b>), tannins (<b>c</b>) and chlorogenic acid (<b>d</b>) in chokeberry fruits after treatments with <span class="html-italic">T. vulgare</span> and <span class="html-italic">S. montana</span> EOs in 2020–2022.</p>
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<p>Changes in potassium (<b>a</b>), magnesium (<b>b</b>), zinc (<b>c</b>) and vitamin C (<b>d</b>) content in chokeberry fruits after treatments with <span class="html-italic">T. vulgare</span> and <span class="html-italic">S. montana</span> EOs in 2020–2022.</p>
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16 pages, 1025 KiB  
Article
Src Tyrosine Kinase Inhibitory and Antioxidant Activity of Black Chokeberry and Bilberry Fruit Extracts Rich in Chlorogenic Acid
by Sanda Vladimir-Knežević, Maja Bival Štefan, Biljana Blažeković, Dubravko Jelić, Tea Petković, Marta Mandić, Ekaterina Šprajc and Sandy Lovković
Int. J. Mol. Sci. 2023, 24(21), 15512; https://doi.org/10.3390/ijms242115512 - 24 Oct 2023
Viewed by 1719
Abstract
Edible berries such as the fruits of black chokeberry (Aronia melanocarpa (Michx.) Elliott) and bilberry (Vaccinium myrtillus L.) are considered to be rich in phenolic compounds, which are nowadays attracting great interest due to their promising health benefits. The main objective [...] Read more.
Edible berries such as the fruits of black chokeberry (Aronia melanocarpa (Michx.) Elliott) and bilberry (Vaccinium myrtillus L.) are considered to be rich in phenolic compounds, which are nowadays attracting great interest due to their promising health benefits. The main objective of our study was to investigate, for the first time, their inhibitory properties on Src tyrosine kinase activity, as this enzyme plays an important role in multiple cellular processes and is activated in both cancer and inflammatory cells. In hydroethanolic fruit extracts, 5.0–5.9% of total polyphenols were determined spectrophotometrically, including high amounts of hydroxycinnamic acid derivatives. HPLC analysis revealed that the black chokeberry and bilberry extracts contained 2.05 mg/g and 2.54 mg/g of chlorogenic acid, respectively. Using a time-resolved fluorescence resonance energy transfer (TR-FRET) assay, the extracts studied were found to have comparable inhibitory effects on Src tyrosine kinase, with IC50 values of 366 µg/mL and 369 µg/mL, respectively. The results also indicated that chlorogenic acid contributes significantly to the observed effect. In addition, both fruit extracts exhibited antioxidant activity by scavenging DPPH and NO radicals with SC50 values of 153–352 µg/mL. Our study suggested that black chokeberry and bilberry fruits may be beneficial in cancer and other inflammation-related diseases. Full article
(This article belongs to the Section Bioactives and Nutraceuticals)
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<p>HPLC chromatograms of hydroethanolic extracts of black chokeberry fruits (<b>a</b>) and bilberry fruits (<b>b</b>) with UV-spectrum of chlorogenic acid recorded at 320 nm.</p>
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<p>Dose–response curves of Src kinase inhibition for black chokeberry fruits, bilberry fruits, chlorogenic acid (<b>a</b>) and staurosporine (<b>b</b>).</p>
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13 pages, 613 KiB  
Article
Aronia in the Type 2 Diabetes Treatment Regimen
by Christine B. Christiansen, Per B. Jeppesen, Kjeld Hermansen and Søren Gregersen
Nutrients 2023, 15(19), 4188; https://doi.org/10.3390/nu15194188 - 28 Sep 2023
Cited by 3 | Viewed by 2331
Abstract
Aronia melanocarpa berries are rich in antioxidants and possess a high antioxidant capacity. Aronia berries have shown potential in type 2 diabetes mellitus (T2DM) treatment, and previous studies indicate improvements in glycemia after supplementation. Unfortunately, the effectiveness of aronia berries is limited by [...] Read more.
Aronia melanocarpa berries are rich in antioxidants and possess a high antioxidant capacity. Aronia berries have shown potential in type 2 diabetes mellitus (T2DM) treatment, and previous studies indicate improvements in glycemia after supplementation. Unfortunately, the effectiveness of aronia berries is limited by the low bioavailability of aronia, which fermentation could potentially overcome. The objective of this study was to compare the effects of fermented or non-fermented aronia pulp with placebo in subjects with T2DM. This study was a triple-blinded, triple-crossover study with eight-week intervention periods with fermented aronia extract (FAE), non-fermented aronia extract (AE), and placebo. Extracts were incorporated in snack bars with 37% aronia (FAE or AE) or wheat bran (placebo) and 63% raisins and coconut oil. Pre- and post-treatment period, we did fasting blood samples, including hemoglobin A1c, fructosamine, insulin, glucose, glucagon-like peptide-1, glucose-dependent insulinotropic peptide (GIP) and glucagon, oral glucose tolerance tests, and anthropometric measurements. Of 36 randomized participants, 23 completed the trial. Aside from a higher increase in GIP after FAE supplementation compared to after placebo supplementation, aronia extracts had no effect. The increase in GIP levels after FAE supplementation may hold potential benefits, but the overall clinical impact remains unclear. Full article
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<p>CONSORT flow diagram outlining inclusions, exclusions, and reasons for discontinuation.</p>
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37 pages, 6694 KiB  
Article
The Protective Potential of Aronia melanocarpa L. Berry Extract against Cadmium-Induced Kidney Damage: A Study in an Animal Model of Human Environmental Exposure to This Toxic Element
by Nazar M. Smereczański, Małgorzata M. Brzóska, Joanna Rogalska and Tomasz Hutsch
Int. J. Mol. Sci. 2023, 24(14), 11647; https://doi.org/10.3390/ijms241411647 - 19 Jul 2023
Cited by 4 | Viewed by 1484
Abstract
The impact of cadmium (Cd) on the function and structure of the kidney and the potential protective effect of an extract from Aronia melanocarpa L. berries were investigated in a rat model of low- and moderate-level environmental exposure to this heavy metal (1 [...] Read more.
The impact of cadmium (Cd) on the function and structure of the kidney and the potential protective effect of an extract from Aronia melanocarpa L. berries were investigated in a rat model of low- and moderate-level environmental exposure to this heavy metal (1 and 5 mg Cd/kg feed for up to 24 months). The sensitive biomarkers of Cd-induced damage to the kidney tubules (N-acetyl-β-D-glucosaminidase (NAG), alkaline phosphatase (ALP), β2-microglobulin (β2-MG), and kidney injury molecule-1 (KIM-1) in the urine), clinically relevant early markers of glomerular damage (albumin in the urine and creatinine clearance), and other markers of the general functional status of this organ (urea, uric acid, and total protein in the serum and/or urine) and Cd concentration in the urine, were evaluated. The morphological structure of the kidney and inflammatory markers (chemerin, macrophage inflammatory protein 1 alpha (MIP1a), and Bcl2-associated X protein (Bax)) were also estimated. Low-level and moderate exposure to Cd led to damage to the function and structure of the kidney tubules and glomeruli. The co-administration of A. melanocarpa berry extract significantly protected against the injurious impact of this toxic element. In conclusion, even low-level, long-term exposure to Cd poses a risk of kidney damage, whereas an intake of Aronia berry products may effectively protect from this outcome. Full article
(This article belongs to the Special Issue Medical and Environmental Aspects of Metal Toxicity)
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<p>The concentrations of kidney injury molecule-1 (KIM-1) and β2-microglobulin (β2-MG) in the urine of female rats. The animals were treated with cadmium (Cd) in the feed at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups) for 3, 10, 17, and 24 months. Data are shown as a median, 25–75% confidence interval, and minimum and maximum values for eight animals (except for seven females in the AM, Cd<sub>1</sub>, and Cd<sub>5</sub> groups after 24 months). Statistically significant differences (Kruskal-Wallis test) compared to: a—Control group; b—AM group; c—Cd<sub>1</sub> group; d—Cd<sub>1</sub>+AM group; and e—Cd<sub>5</sub> group, where * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001 are marked. The factors of change compared to the control group (<span style="color:red">↑</span>, increase) or the adequate group treated with Cd alone (<span style="color:green">↘</span>, decrease) are indicated by the numerical values below or above the bars. Detailed data are presented in <a href="#app1-ijms-24-11647" class="html-app">Table S1</a>.</p>
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<p>The concentration of β2-microglobulin (β2-MG) in the urine of female rats evaluated every other month during the 24-month study. The animals were treated with cadmium (Cd) in the feed at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups). Data are shown as a median value for eight animals (except for seven females in the AM, Cd<sub>1</sub>, and Cd<sub>5</sub> groups after 20, 22, and 24 months). An occurrence of statistically significant differences (Kruskal-Wallis test; * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001) between every two experimental groups at each time point was evaluated and marked as follows: f—AM and Control groups; g—Cd<sub>1</sub> and Control groups; h—Cd<sub>1</sub>+AM and Control groups; i—Cd<sub>1</sub> and Cd<sub>1</sub>+AM groups; j—Cd<sub>5</sub> and Control groups; k—Cd<sub>5</sub>+AM and Control groups; l—Cd<sub>5</sub> and Cd<sub>5</sub>+AM groups; m—Cd<sub>1</sub> and Cd<sub>5</sub> groups; and n—Cd<sub>1</sub>+AM and Cd<sub>5</sub>+AM groups. A lack of the particular letter symbol means a lack of statistically significant differences between appropriate groups. Detailed data are presented in <a href="#app1-ijms-24-11647" class="html-app">Table S2</a>.</p>
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<p>The activities of N-acetyl-β-D-glucosaminidase (NAG) and alkaline phosphatase (ALP) in the urine of female rats. The animals were treated with cadmium (Cd) in the feed at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups) for 3, 10, 17, and 24 months. Data are shown as a median, 25–75% confidence interval, and minimum and maximum values for eight animals (except for seven females in the AM, Cd<sub>1</sub>, and Cd<sub>5</sub> groups after 24 months). Statistically significant differences (Kruskal-Wallis test) compared to: a—Control group; b—AM group; c—Cd<sub>1</sub> group; d—Cd<sub>1</sub>+AM group; and e—Cd<sub>5</sub> group, where * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001 are marked. The factors of change compared to the control group (<span style="color:red">↑</span>, increase) or the adequate group treated with Cd alone (<span style="color:green">↘</span>, decrease) are indicated by the numerical values below or above the bars. Detailed data are presented in <a href="#app1-ijms-24-11647" class="html-app">Table S3</a>.</p>
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<p>The activities of N-acetyl-β-D-glucosaminidase (NAG) and alkaline phosphatase (ALP) in the urine of female rats evaluated every other month during the 24-month study. The animals were treated with cadmium (Cd) in the feed at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups). Data are shown as a median value for eight animals (except for seven females in the AM, Cd<sub>1</sub>, and Cd<sub>5</sub> groups after 20, 22, and 24 months). An occurrence of statistically significant differences (Kruskal-Wallis test; * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001) between every two experimental groups at each time point was evaluated and marked as follows: f—AM and Control groups; g—Cd<sub>1</sub> and Control groups; h—Cd<sub>1</sub>+AM and Control groups; i—Cd<sub>1</sub> and Cd<sub>1</sub>+AM groups; j—Cd<sub>5</sub> and Control groups; k—Cd<sub>5</sub>+AM and Control groups; l—Cd<sub>5</sub> and Cd<sub>5</sub>+AM groups; m—Cd<sub>1</sub> and Cd<sub>5</sub> groups; and n—Cd<sub>1</sub>+AM and Cd<sub>5</sub>+AM groups. A lack of the particular letter symbol means a lack of statistically significant differences between appropriate groups. Detailed data are presented in <a href="#app1-ijms-24-11647" class="html-app">Tables S4 (NAG) and S5 (ALP)</a>.</p>
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<p>The concentrations of albumin and total protein in the urine of female rats adjusted for creatinine concentration (ACR and PCR, respectively). The animals were treated with cadmium (Cd) in the feed at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups) for 3, 10, 17, and 24 months. Data are shown as a median, 25–75% confidence interval, and minimum and maximum values for eight animals (except for seven females in the AM, Cd<sub>1</sub>, and Cd<sub>5</sub> groups after 24 months). Statistically significant differences (Kruskal-Wallis test) compared to: a—Control group; b—AM group; c—Cd<sub>1</sub> group; d—Cd<sub>1</sub>+AM group; and e—Cd<sub>5</sub> group, where * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001 are marked. The factors of change compared to the control group (<span style="color:red">↑</span>, increase) or the adequate group treated with Cd alone (<span style="color:green">↘</span>, decrease) are indicated by the numerical values below or above the bars. Detailed data are presented in <a href="#app1-ijms-24-11647" class="html-app">Table S6</a>.</p>
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<p>The concentrations of albumin and total protein in the urine of female rats adjusted for creatinine concentration (ACR and PCR, respectively) evaluated every other month during the 24-month study. The animals were treated with cadmium (Cd) in the feed at s concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups). Data are shown as a median values for eight animals (except for seven females in the AM, Cd<sub>1</sub>, and Cd<sub>5</sub> groups after 20, 22, and 24 months). An occurrence of statistically significant differences (Kruskal-Wallis test; * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001) between every two experimental groups at each time point was evaluated and marked as follows: f—AM and Control groups; g—Cd<sub>1</sub> and Control groups; h—Cd<sub>1</sub>+AM and Control groups; i—Cd<sub>1</sub> and Cd<sub>1</sub>+AM groups; j—Cd<sub>5</sub> and Control groups; k—Cd<sub>5</sub>+AM and Control groups; l—Cd<sub>5</sub> and Cd<sub>5</sub>+AM groups; m—Cd<sub>1</sub> and Cd<sub>5</sub> groups; and n—Cd<sub>1</sub>+AM and Cd<sub>5</sub>+AM groups. A lack of the particular letter symbol means a lack of statistically significant differences between appropriate groups. Detailed data are presented in <a href="#app1-ijms-24-11647" class="html-app">Tables S7 (ACR) and S8 (PCR)</a>.</p>
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<p>Creatinine clearance in female rats. The animals were treated with cadmium (Cd) in the feed at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups) for 3, 10, 17, and 24 months. Data are shown as a median, 25–75% confidence interval, and minimum and maximum values for eight animals (except for seven females in the AM, Cd<sub>1</sub>, and Cd<sub>5</sub> groups after 24 months). Statistically significant differences (Kruskal-Wallis test) compared to: a—Control group; d—Cd<sub>1</sub>+AM group; and e—Cd<sub>5</sub> group, where * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001 are marked. The percentage changes or a factor of change compared to the control group (<b><span style="color:red">↓</span></b>, decrease) or the adequate group treated with Cd alone (<b><span style="color:green">↗</span></b>, increase) are indicated by the numerical values above the bars. Detailed data are presented in <a href="#app1-ijms-24-11647" class="html-app">Table S9</a>.</p>
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<p>The concentrations of uric acid and urea in the serum of female rats. The animals were treated with cadmium (Cd) in the feed at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups) for 3, 10, 17, and 24 months. Data are shown as a median, 25–75% confidence interval, and minimum and maximum values for eight animals (except for seven females in the AM, Cd<sub>1</sub>, and Cd<sub>5</sub> groups after 24 months). Statistically significant differences (Kruskal-Wallis test) compared to: a—Control group; b—AM group; c—Cd<sub>1</sub> group; d—Cd<sub>1</sub>+AM group; and e—Cd<sub>5</sub> group—where * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001 are marked. The percentage changes or factors of changes compared to the control group (<span style="color:red">↑</span>, increase) or the adequate group treated with Cd alone (<span style="color:green">↘</span>, decrease) are indicated by the numerical values below or above the bars. Detailed data are presented in <a href="#app1-ijms-24-11647" class="html-app">Table S10</a>.</p>
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<p>The concentration of cadmium (Cd) in the urine of female rats evaluated every other month during the 24-month study. The animals were treated with Cd in the feed at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups). Data are shown as a median value for eight animals (except for seven females in the AM, Cd<sub>1</sub>, and Cd<sub>5</sub> groups after 20, 22, and 24 months). An occurrence of statistically significant differences (Kruskal-Wallis test; * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001) between every two experimental groups at each time point was evaluated and marked as follows: f—AM and Control groups; g—Cd<sub>1</sub> and Control groups; h—Cd<sub>1</sub>+AM and Control groups; i—Cd<sub>1</sub> and Cd<sub>1</sub>+AM groups; j—Cd<sub>5</sub> and Control groups; k—Cd<sub>5</sub>+AM and Control groups; l—Cd<sub>5</sub> and Cd<sub>5</sub>+AM groups; m—Cd<sub>1</sub> and Cd<sub>5</sub> groups; and n—Cd<sub>1</sub>+AM and Cd<sub>5</sub>+AM groups. A lack of the particular letter symbol means a lack of statistically significant differences between appropriate groups. Detailed data are presented in <a href="#app1-ijms-24-11647" class="html-app">Table S12</a>.</p>
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<p>Histopathological image of the renal tubules of female rats in hematoxylin–eosin (H+E) staining. The animals were treated with cadmium (Cd) in the feed at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups) for 24 months. Tubular changes were the most advanced in the Cd<sub>5</sub> group, in which hyalinization (white arrow), hyperplasia, and hypertrophy (grey arrow) of the tubular epithelium and pronounced proliferation of the interstitial tissue of the kidney were found.</p>
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<p>Histopathological image of the renal glomeruli of female rats. The animals were treated with cadmium (Cd) in the feed at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups) for 24 months. In the Cd<sub>1</sub> and Cd<sub>5</sub> groups, moderate and severe, respectively, glomerulonephritis is evident. There is a thickening of the basement membranes (blue in Masson’s staining) of the glomerulus and progressive atrophy of the mesangium (decrease in cellularity) (black arrow). In the Cd<sub>1</sub>+AM and Cd<sub>5</sub>+AM groups, minimal or slight, respectively, glomerulonephritis is observed.</p>
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<p>The concentrations of chemerin, macrophage inflammatory protein 1 alpha (MIP1a), and Bcl2-associated X protein (Bax) in the kidneys of female rats. The animals were treated with cadmium (Cd) in the diet at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups) for 3, 10, 17, and 24 months. Data are shown as a median, 25–75% confidence interval, and minimum and maximum values for eight animals (except for seven females in the AM, Cd<sub>1</sub>, and Cd<sub>5</sub> groups after 24 months). Statistically significant differences (Kruskal-Wallis test) compared to: a—Control group; b—AM group; c—Cd<sub>1</sub> group; d—Cd<sub>1</sub>+AM group; and e—Cd<sub>5</sub> group—where * <span class="html-italic">p</span> &lt; 0.05, <sup>†</sup> <span class="html-italic">p</span> &lt; 0.01, and <sup>‡</sup> <span class="html-italic">p</span> &lt; 0.001 are marked. The factors of change compared to the control group (<span style="color:red">↓</span>, decrease; <span style="color:red">↑</span>, increase) or the adequate group treated with Cd alone (<span style="color:green">↘</span>, decrease) are indicated by the numerical values below or above the bars. Detailed data are presented in <a href="#app1-ijms-24-11647" class="html-app">Table S14</a>.</p>
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<p>A schematic representation of the experimental model and range of measurements performed in the present study. The animals were treated with cadmium (Cd) in the diet at a concentration of 0, 1, or 5 mg/kg (Control, Cd<sub>1</sub>, and Cd<sub>5</sub> groups) and/or 0.1% extract from the berries of <span class="html-italic">Aronia melanocarpa</span> L. (AM, Cd<sub>1</sub>+AM, and Cd<sub>5</sub>+AM groups) for 3, 10, 17, and 24 months. β2-MG, beta2-microglobulin; ACR, albumin concentration in the urine adjusted for creatinine concentration; ALP, alkaline phosphatase; Bax, Bcl-2-associated X protein; KIM-1, kidney injury molecule 1; MIP1a, macrophage inflammatory protein-1 alpha; NAG, N-acetyl-β-D-glucosaminidase; PCR, total protein concentration in the urine adjusted for creatinine concentration. The appropriate parameters, except for Cd in the urine, were determined in the serum, urine, and kidney after 3, 10, 17, and 24 months. Moreover, β2-MG, NAG, ALP, ACR, and PCR, as well as Cd, were evaluated every other month of the 24-month study and before its beginning.</p>
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27 pages, 4011 KiB  
Review
Health Benefits of Antioxidant Bioactive Compounds in the Fruits and Leaves of Lonicera caerulea L. and Aronia melanocarpa (Michx.) Elliot
by Bogdan-Stefan Negreanu-Pirjol, Ovidiu Cristian Oprea, Ticuta Negreanu-Pirjol, Florentina Nicoleta Roncea, Ana-Maria Prelipcean, Oana Craciunescu, Andreea Iosageanu, Victoria Artem, Aurora Ranca, Ludmila Motelica, Anca-Cristina Lepadatu, Madalina Cosma and Dan Razvan Popoviciu
Antioxidants 2023, 12(4), 951; https://doi.org/10.3390/antiox12040951 - 18 Apr 2023
Cited by 21 | Viewed by 4622
Abstract
Lonicera caerulaea L. and Aronia melanocarpa (Michx.) Elliot fruits are frequently used for their health benefits as they are rich in bioactive compounds. They are recognized as a source of natural and valuable phytonutrients, which makes them a superfood. L. caerulea presents antioxidant [...] Read more.
Lonicera caerulaea L. and Aronia melanocarpa (Michx.) Elliot fruits are frequently used for their health benefits as they are rich in bioactive compounds. They are recognized as a source of natural and valuable phytonutrients, which makes them a superfood. L. caerulea presents antioxidant activity three to five times higher than other berries which are more commonly consumed, such as blackberries or strawberries. In addition, their ascorbic acid level is the highest among fruits. The species A. melanocarpa is considered one of the richest known sources of antioxidants, surpassing currants, cranberries, blueberries, elderberries, and gooseberries, and contains one of the highest amounts of sorbitol. The non-edible leaves of genus Aronia became more extensively analyzed as a byproduct or waste material due to their high polyphenol, flavonoid, and phenolic acid content, along with a small amount of anthocyanins, which are used as ingredients in nutraceuticals, herbal teas, bio-cosmetics, cosmeceuticals, food and by the pharmaceutical industry. These plants are a rich source of vitamins, tocopherols, folic acid, and carotenoids. However, they remain outside of mainstream fruit consumption, being well known only to a small audience. This review aims to shed light on L. caerulaea and A. melanocarpa and their bioactive compounds as healthy superfoods with antioxidant, anti-inflammatory, antitumor, antimicrobial, and anti-diabetic effects, and hepato-, cardio-, and neuro-protective potential. In this view, we hope to promote their cultivation and processing, increase their commercial availability, and also highlight the ability of these species to be used as potential nutraceutical sources, helpful for human health. Full article
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<p>Chemical structure of (<b>a</b>) hydroxybenzoic acids (vanillic acid: R<sup>1</sup> = OCH<sub>3</sub>, R<sup>2</sup> = H; syringic acid: R<sup>1</sup> = R<sup>2</sup> = OCH<sub>3</sub>; gallic acid: R<sup>1</sup> = R<sup>2</sup> = OH); (<b>b</b>) hydroxycinnamic acids (caffeic acid: R = OH; ferulic acid: R = OCH<sub>3</sub>; p-coumaric acid: R = H) [<a href="#B52-antioxidants-12-00951" class="html-bibr">52</a>].</p>
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<p>Chemical structure of chlorogenic acid (5-O-caffeoylquinic acid).</p>
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<p>Chemical structures of the anthocyanins compounds: (<b>a</b>) cyanidin-3-glucoside, (<b>b</b>) cyanidin-3-rutinoside, (<b>c</b>) delphinidin-3-O-glucoside, (<b>d</b>) peonidin-3-O-rutinoIe, (<b>e</b>) pelargonidin-3-O-glucoside, (<b>f</b>) peonidin-3-O-glucoside, (<b>g</b>) cyanidin-3-sophorose-5-glucoside.</p>
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<p>Proposed uses of <span class="html-italic">A. melanocarpa</span> L. and its byproducts.</p>
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<p>Pharmacological effects of <span class="html-italic">L. caerulea</span> (<b>a</b>) and <span class="html-italic">A. melanocarpa</span> (<b>b</b>).</p>
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<p>The encapsulation of natural extracts and their applications (<b>a</b>); Drug delivery systems for bioactive substances (<b>b</b>).</p>
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<p>Digestive system disease treatment with mesoporous silica loaded with bioactive substances (realized with BioRender.com; accessed on 15th February 2023) [<a href="#B156-antioxidants-12-00951" class="html-bibr">156</a>,<a href="#B160-antioxidants-12-00951" class="html-bibr">160</a>,<a href="#B161-antioxidants-12-00951" class="html-bibr">161</a>].</p>
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19 pages, 4464 KiB  
Article
Natural Bioactive Substances in Fruits of Aronia melanocarpa (Michx.) Elliott Exposed to Combined Light-Type, Chitosan Oligosaccharide, and Spent Mushroom Residue Treatments
by Yadong Duan, Xin Wei, Wenbo Zhao, Jinxia Li, Guang Yang, Shuang Zhou, Chunwei Zhou, Lei Zhang, Pengju Li, Shuai Hou, Deshan Shi, Cheng Liu and Baitao Guo
Plants 2023, 12(3), 604; https://doi.org/10.3390/plants12030604 - 30 Jan 2023
Cited by 3 | Viewed by 1791
Abstract
Greenhouse culture is a practical approach to obtain non-wood forest products from berry fruit at a higher efficacy than resource silviculture in natural understory. In this study, three-year old black chokeberry (Aronia melanocarpa (Michx.) Elliott 1821) seedlings were transplanted to a greenhouse [...] Read more.
Greenhouse culture is a practical approach to obtain non-wood forest products from berry fruit at a higher efficacy than resource silviculture in natural understory. In this study, three-year old black chokeberry (Aronia melanocarpa (Michx.) Elliott 1821) seedlings were transplanted to a greenhouse where sunlight was complemented by red- (69.4% red, 30.2% green, 0.4% blue) and blue-color (15.3% red, 64.9% green, 19.8% blue) light-emitting diode (LED) illuminations. Half of the planting soils were amended by spent mushroom residue (SMR) (not amendment as the control) and half the seedlings were sprayed by chitosan oligosaccharide (CO) on leaves. All treatments can increase seedling height, but only blue light reinforces the basal diameter growth. Compared to sunlight, exposure to blue light can promote leaf nitrogen and phosphorus concentrations, superoxide dismutase activity, and fruit proanthocyanidin content. The combination with CO addition will further increase chlorophyl a content, acid phosphatase activity, and total phenolics in fruit. SMR amended can induce the steady state uptake of nutrients but failed to impact fruit quality. Overall, we recommend the combination of blue light LED illumination plus CO addition to culture black chokeberry for the purpose to gain natural bioactive compounds. Full article
(This article belongs to the Special Issue Natural Resources of Berry and Medicinal Plants Volume II)
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<p>Growth of black chokeberry (<span class="html-italic">Aronia melanocarpa</span> (Michx.) Elliott 1821) exposed to separate light-type (sunlight, blue light-emitting diode (LED), red LED), chitosan oligosaccharide (CO), and spent mushroom residue (SMR) treatments: (<b>A</b>) light effect on seedling height; (<b>B</b>) light effect on root-collar diameter; (<b>C</b>) SMR effect on seedling height with unamended soils as the control (Ctrl); (<b>D</b>) SMR effect on root-collar diameter with unamended soils as the control (Ctrl); (<b>E</b>) CO effect on seedling height; (<b>F</b>) CO effect on root-collar diameter. Different letters mark significant difference according to Tukey test at 0.05 level.</p>
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<p>Leaf morphology and weight of black chokeberry (<span class="html-italic">Aronia melanocarpa</span> (Michx.) Elliott 1821) exposed to combined light-type (sunlight, blue light-emitting diode (LED), red LED), chitosan oligosaccharide (CO), and spent mushroom residue (SMR) treatments: (<b>A</b>) combined effects of LED, CO, and SMR on leaf area; (<b>B</b>) combined effects of LED, CO, and SMR on leaf weight; (<b>C</b>) combined effects of LED, CO, and SMR on specific leaf area. Different letters mark significant difference according to Tukey test at 0.05 level.</p>
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<p>Leaf nitrogen (N) and phosphorus (P) concentrations in black chokeberry (<span class="html-italic">Aronia melanocarpa</span> (Michx.) Elliott 1821) exposed to separate light-type (sunlight, blue light-emitting diode (LED), red LED), chitosan oligosaccharide (CO), and spent mushroom residue (SMR) treatments: (<b>A</b>) light effect on leaf N concentration; (<b>B</b>) light effect on leaf P concentration; (<b>C</b>) SMR effect on leaf N concentration with unamended soils as the control (Ctrl); (<b>D</b>) SMR effect on leaf P concentration with unamended soils as the control (Ctrl); (<b>E</b>) CO effect on leaf N concentration; (<b>F</b>) CO effect on leaf P concentration. Different letters mark significant difference according to Tukey test at 0.05 level.</p>
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<p>Vector diagnoses of leaf nitrogen (N) and phosphorus (P) statuses in black chokeberry (<span class="html-italic">Aronia melanocarpa</span> (Michx.) Elliott 1821) exposed to separate light-type (sunlight, blue light-emitting diode (LED), red LED), chitosan oligosaccharide (CO), and spent mushroom residue (SMR) treatments: (<b>A</b>) diagnosis of leaf N status exposed to different light types; (<b>B</b>) diagnosis of leaf N status exposed to SMR amendment; (<b>C</b>) diagnosis of leaf N status exposed to CO addition; (<b>D</b>) diagnosis of leaf P status exposed to different light types; (<b>E</b>) diagnosis of leaf P status exposed to SMR amendment; (<b>F</b>) diagnosis of leaf P status exposed to CO addition. Abbreviations: Red, red light LED; Blue, blue light LED; +SMR, SMR amendment; Ctrl, no SMR amendment; -CO, no CO addition; +CO, with CO addition. Shifts and interpretations are adapted from Salifu and Timmer [<a href="#B75-plants-12-00604" class="html-bibr">75</a>]: Shift C, nutrient deficiency; Shift D, luxury consumption; Shift G, nutrient depletion.</p>
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<p>Leaf chlorophyl and protein contents in black chokeberry (<span class="html-italic">Aronia melanocarpa</span> (Michx.) Elliott 1821) exposed to combined light-type (sunlight, blue light-emitting diode (LED), red LED), chitosan oligosaccharide (CO), and spent mushroom residue (SMR) treatments: (<b>A</b>) combined CO and light effects on chlorophyl a content; (<b>B</b>) SMR effect on chlorophyl a content with unamended soils as the control (Ctrl); (<b>C</b>) combined CO and light effects on chlorophyl b content; (<b>D</b>) SMR effect on chlorophyl b content with unamended soils as the control (Ctrl); (<b>E</b>) combined CO and light effects on protein content; (<b>F</b>) SMR effect on protein content with unamended soils as the control (Ctrl). Different letters mark significant difference according to Tukey test at 0.05 level.</p>
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<p>Leaf glutamine synthetase (GS) and acid phosphate (AP) activities in black chokeberry (<span class="html-italic">Aronia melanocarpa</span> (Michx.) Elliott 1821) exposed to combined light-type (sunlight, blue light-emitting diode (LED), red LED), chitosan oligosaccharide (CO), and spent mushroom residue (SMR) treatments: (<b>A</b>) combined light, SMR, and CO effects on GS activity; (<b>B</b>) combined light, SMR, and CO effects on AP activity. Different letters mark significant difference according to Tukey test at 0.05 level.</p>
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<p>Leaf antioxidant activities in black chokeberry (<span class="html-italic">Aronia melanocarpa</span> (Michx.) Elliott 1821) exposed to combined light-type (sunlight, blue light-emitting diode (LED), red LED), chitosan oligosaccharide (CO), and spent mushroom residue (SMR) treatments: (<b>A</b>) combined light, SMR, and CO effects on peroxidase (POD) activity; (<b>B</b>) combined light, SMR, and CO effects on superoxide dismutase (SOD) activity; (<b>C</b>) combined light, SMR, and CO effects on catalase (CAT) activity. Different letters mark significant difference according to Tukey test at 0.05 level.</p>
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<p>Quality assessment of fruits in black chokeberry (<span class="html-italic">Aronia melanocarpa</span> (Michx.) Elliott 1821) exposed to separate light-type (sunlight, blue light-emitting diode (LED), red LED), chitosan oligosaccharide (CO), and spent mushroom residue (SMR) treatments: (<b>A</b>) light effect on leaf proanthocyanidins; (<b>B</b>) light effect on total phenolics in fruits; (<b>C</b>) CO effect on fruit proanthocyanidins; (<b>D</b>) CO effect on total phenolics in fruit. Different letters mark significant difference according to Tukey test at 0.05 level.</p>
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18 pages, 1850 KiB  
Review
Potential Benefits of Black Chokeberry (Aronia melanocarpa) Fruits and Their Constituents in Improving Human Health
by Yulin Ren, Tyler Frank, Gunnar Meyer, Jizhou Lei, Jessica R. Grebenc, Ryan Slaughter, Yu G. Gao and A. Douglas Kinghorn
Molecules 2022, 27(22), 7823; https://doi.org/10.3390/molecules27227823 - 13 Nov 2022
Cited by 32 | Viewed by 5800
Abstract
Aronia berry (black chokeberry) is a shrub native to North America, of which the fresh fruits are used in the food industry to produce different types of dietary products. The fruits of Aronia melanocarpa (Aronia berries) have been found to show multiple bioactivities [...] Read more.
Aronia berry (black chokeberry) is a shrub native to North America, of which the fresh fruits are used in the food industry to produce different types of dietary products. The fruits of Aronia melanocarpa (Aronia berries) have been found to show multiple bioactivities potentially beneficial to human health, including antidiabetic, anti-infective, antineoplastic, antiobesity, and antioxidant activities, as well as heart-, liver-, and neuroprotective effects. Thus far, phenolic compounds, such as anthocyanins, cyanidins, phenolic acids, proanthocyanidins, triterpenoids, and their analogues have been identified as the major active components of Aronia berries. These natural products possess potent antioxidant activity, which contributes to the majority of the other bioactivities observed for Aronia berries. The chemical components and the potential pharmaceutical or health-promoting effects of Aronia berries have been summarized previously. The present review article focuses on the molecular targets of extracts of Aronia berries and the examples of promising lead compounds isolated from these berries, including cyanidin-3-O-galactoside, chlorogenic acid, quercetin, and ursolic acid. In addition, presented herein are clinical trial investigations for Aronia berries and their major components, including cancer clinical trials for chlorogenic acid and COVID-19 trial studies for quercetin. Additionally, the possible development of Aronia berries and their secondary metabolites as potential therapeutic agents is discussed. It is hoped that this contribution will help stimulate future investigations on Aronia berries for the continual improvement of human health. Full article
(This article belongs to the Collection Bioactive Natural Molecules from Functional Foods)
Show Figures

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Figure 1
<p>Structures of selected major phenolic compounds isolated from Aronia berries.</p>
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<p>Structures of the triterpene ursolic acid and its derivatives, 3-<span class="html-italic">O</span>-<span class="html-italic">trans</span>- and 3-<span class="html-italic">O</span>-<span class="html-italic">cis</span>-<span class="html-italic">p</span>-coumaroyltormentic acids isolated from Aronia berries.</p>
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<p>Structures of gallic acid, ellagic acid, and myricetin identified from Aronia berries.</p>
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<p>(<b>A</b>) The signaling pathway proposed for mediation of antidiabetic activity of α-PGG, in which α-PGG activates the insulin receptor (IR) in terms of its glucose transport stimulatory activity. It induces phosphorylation of the IR and Akt and activates PI3K followed by stimulating membrane translocation of GLUT 4 to keep glucose transport into cells. (<b>B</b>) Aronia berries and their potential beneficial activities in the promotion of human health.</p>
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<p>Molecular targets identified for mediation of pharmaceutical properties of Aronia berries.</p>
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