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23 pages, 6695 KiB  
Perspective
Building Greener Cities Together: Urban Afforestation Requires Multiple Skills to Address Social, Ecological, and Climate Challenges
by Raffaello Resemini, Chiara Geroldi, Giulia Capotorti, Andrea De Toni, Francesco Parisi, Michele De Sanctis, Thomas Cabai, Micol Rossini, Luigi Vignali, Matteo Umberto Poli, Ermes Lo Piccolo, Barbara Mariotti, Andrea Arcidiacono, Paolo Biella, Erica Alghisi, Luciano Bani, Massino Bertini, Carlo Blasi, Francesca Buffi, Enrico Caprio, Stefano Castiglione, Patrizia Digiovinazzo, Olivia Dondina, Giuliano Fanelli, Francesco Ferrini, Valentina Fiorilli, Gianluca Gaiani, Daniela Gambino, Andrea Genre, Bruno Lasserre, Alberto Maltoni, Marco Marchetti, Chiara Montagnani, Marco Ottaviano, Cinzia Panigada, Silvia Ronchi, Stefano Salata, Fabio Salbitano, Enrico Simoni, Soraya Versace, Maria Chiara Pastore, Sandra Citterio, Massimo Labra and Rodolfo Gentiliadd Show full author list remove Hide full author list
Plants 2025, 14(3), 404; https://doi.org/10.3390/plants14030404 (registering DOI) - 29 Jan 2025
Abstract
Urban afforestation is increasingly regarded as a key strategy for fostering biodiversity to restore and enhance the ecosystem services needed to counteract the effects of climate change in built-up areas. In Italy, several experimental afforestation projects have been launched as part of the [...] Read more.
Urban afforestation is increasingly regarded as a key strategy for fostering biodiversity to restore and enhance the ecosystem services needed to counteract the effects of climate change in built-up areas. In Italy, several experimental afforestation projects have been launched as part of the National Recovery and Resilience Plan (NRRP), focusing on cities or metropolitan areas such as Milan, Rome, Pistoia and Campobasso. These projects follow a multidisciplinary approach, integrating botanists, foresters, urban planners, landscape architects and remote sensing specialists. The goal is to address the challenging complexity of urban forest restoration through reforestation and afforestation actions. Key innovations include the integration of transdisciplinary methodologies (landscape analysis, landscape design, forest and plant ecology) with the application of advanced remote sensing technologies and participatory community engagement frameworks to address ecological and social challenges. Experimental plots have been set up across various urban areas, testing a range of planting schemes to maximise climate change resilience and ensure long-term ecological sustainability. Emphasis has been placed on selecting drought-tolerant and thermophilic species that are better adapted to widespread warming and local urban heat islands. Biodiversity strips with perennial flowers for insects, shrubs with berries for birds and nests for wild bees and vertebrates have been set up to enhance biodiversity in new afforestation areas. Advanced monitoring tools, such as Light Detection and Ranging (LiDAR) and multi-sensor drones, have been employed alongside field observations to assess forest growth, species survival, structural complexity and biodiversity enhancement over time. Historical analyses of landscape patterns and ecological connectivity over the past 200 years, along with evaluations of afforestation projects from the last 70 years, have provided critical insights into the successes and challenges of previous interventions, serving as a guide for future efforts. By focusing on ecological connectivity, the integration of afforested areas into the urban matrix, and citizen engagement, the current project aims to align urban forestry efforts with sustainable development goals. This comprehensive project framework addresses environmental restoration and the social and aesthetic impacts on local communities, contributing to the overall resilience and well-being of urban and peri-urban ecosystems. Full article
20 pages, 1634 KiB  
Article
Exploring the Genetic Potential for Multi-Resistance to Rust and Other Coffee Phytopathogens in Breeding Programs
by Bruna Lopes Mariz, Eveline Teixeira Caixeta, Marcos Deon Vilela de Resende, Antônio Carlos Baião de Oliveira, Dênia Pires de Almeida and Danúbia Rodrigues Alves
Plants 2025, 14(3), 391; https://doi.org/10.3390/plants14030391 - 28 Jan 2025
Abstract
The application of marker-assisted selection in coffee breeding programs accelerates the identification and concentration of target alleles, being essential for developing cultivars resistant to multiple diseases. In this study, a population was developed from artificial crossings between Timor Hybrid and Tupi Amarelo, with [...] Read more.
The application of marker-assisted selection in coffee breeding programs accelerates the identification and concentration of target alleles, being essential for developing cultivars resistant to multiple diseases. In this study, a population was developed from artificial crossings between Timor Hybrid and Tupi Amarelo, with the aim of promoting the pyramiding of resistance genes to the main diseases and pests of Coffea arabica: coffee leaf rust (CLR), coffee berry disease (CBD), cercospora, and leaf miner. Resistance was confirmed by nine molecular markers at loci associated with CLR (genes SH3, CC-NBS-LRR, RLK, QTL-GL2, and GL5) and with CBD (gene Ck-1). The resistance to CLR, cercospora, and leaf miner was evaluated using phenotypic diagrammatic scales. Mixed models estimated population superiority in 16 morphoagronomic traits over four agricultural years. The introgression of resistance alleles to CLR and CBD was identified in 98.6% of the population, with 29% showing pyramiding of five resistance genes. These pyramiding genotypes showed 100% resistance to the leaf miner and 90% to cercospora. The traits were grouped into univariate, bivariate, and trivariate repeatability models, with 11 significant ones. These results are indicative of genetic variability to be explored in the development of cultivars with multiple resistances and high agronomic potential. Full article
(This article belongs to the Special Issue Molecular Approaches for Plant Resistance to Rust Diseases)
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<p>Description of the molecular markers for <span class="html-italic">Hemileia vastatrix</span> and <span class="html-italic">Colletotrichum kahawae</span>, covering the locus, the length of the generated electropherogram, and the identified alleles. * Electropherograms relevant for analysis are highlighted in blue, with dark blue representing dominant alleles and light blue representing recessive ones.</p>
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<p>Prospecting of the coffee improvement program for durable multiple resistance to diseases and pests, resulting from the integration of genotypes for resistance to <span class="html-italic">Hemileia vastatrix</span>.</p>
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23 pages, 5126 KiB  
Article
Investigation of the Influence of Hypercapnia on the Physiology of Ovigerous West Coast Rock Lobsters, Jasus lalandii, and Their Embryonic Development
by Annika Ritter, Christopher R. Bridges and Lutz Auerswald
Biology 2025, 14(2), 132; https://doi.org/10.3390/biology14020132 - 27 Jan 2025
Abstract
The West Coast rock lobster, Jasus lalandii, is a key ecological species and provides an important fishery resource in South Africa and Namibia. It is found along the west coast of southern Africa in the dynamic Benguela Current upwelling system. The low [...] Read more.
The West Coast rock lobster, Jasus lalandii, is a key ecological species and provides an important fishery resource in South Africa and Namibia. It is found along the west coast of southern Africa in the dynamic Benguela Current upwelling system. The low seawater pH of this system is expected to decline further due to ocean acidification and increase in upwelling in terms of frequency and severity. The lobster has therefore to respond to frequent and rapid changes in pH and other environmental impacts that are predicted to become more adverse in future. Although responses to such conditions are known for mature male and juvenile lobsters, there is a lack of information on mature females and later embryonic development. We addressed this by analysing the sensitivity of ovigerous (“berried”) female WCRLs and their eggs/embryos to hypercapnia (high pCO2, low pH) and formulated the following research questions: (1) Can berried female WCRLs respond swiftly to large changes in pH? (2) What physiological mechanisms facilitate a potential response to a rapidly declining pH, i.e., acute hypercapnia? (3) Does a potential response persist during prolonged hypercapnia? (4) Are eggs/embryos impacted by hypercapnia? To investigate this, we exposed berried WCRLs to acute (pH 7.5) and chronic (up to 60 days at pH 7.5 and 7.8) hypercapnia. We applied extracellular acid–base analysis, microscopic examination of egg growth and development, and SEM of female exoskeleton structure and egg membranes. The results revealed that berried females efficiently respond to acute and chronic hypercapnia by means of increasing bicarbonate concentrations in the haemolymph. Moreover, embryo growth and development are not impacted by chronic hypercapnia, but growth shows geographical area-specific differences. We conclude that females and embryos of J. lalandii are as resilient to hypercapnia as previously shown for males and juveniles. Full article
(This article belongs to the Special Issue Advances in Biological Research into Shrimps, Crabs and Lobsters)
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<p>West Coast rock lobster capture area, showing the two sampling sites “Knol” in Hout Bay and Olifantsbos in fishing Zone D.</p>
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<p>Dissection microscope picture of an ovigerous seta. Note the difference in developmental stage along the seta from R to L.</p>
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<p>Staging index used for determination of developmental stages of fertilised eggs (own reference pictures staged according to Silberbauer [<a href="#B19-biology-14-00132" class="html-bibr">19</a>].</p>
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<p>Time course of acid–base parameters in haemolymph of berried <span class="html-italic">J. lalandii</span> from the Olifantsbos area: (<b>A</b>) measured pH and (<b>B</b>) calculated [HCO<sub>3</sub><sup>−</sup> + CO<sub>3</sub><sup>2−</sup>] during acute exposure to normocapnic seawater and hypercapnia for 24 h. Values are means ± S.D. # Significant difference from initial value (t<sub>0</sub>) within the treatment; * significant difference from the same respective sampling time of the normocapnic treatment (repeated-measure ANOVA; <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Henderson–Hasselbalch (pH–bicarbonate) diagrams for haemolymph of berried <span class="html-italic">J. lalandii</span> from the Knol area constructed from the time course of values during acute exposure presented in <a href="#biology-14-00132-t002" class="html-table">Table 2</a> and after experimental incubation for 60 days: (<b>A</b>) during 24 h normocapnia, (<b>B</b>) during 24 h hypercapnia (pH = 7.5), and (<b>C</b>) during incubation for 60 days (data from <a href="#biology-14-00132-t003" class="html-table">Table 3</a>). pCO<sub>2</sub> isopleths were derived from the Henderson–Hasselbalch equation [<a href="#B9-biology-14-00132" class="html-bibr">9</a>]. Appropriate values for the first dissociation constant (pK′1) and solubility coefficient (α) were derived from Truchot [<a href="#B33-biology-14-00132" class="html-bibr">33</a>]. Values are means ± S.D. Blue dashed line = normocapnic seawater isopleth, red dashed line = hypercapnic seawater isopleth (pH = 7.5), green dashed line = hypercapnic seawater isopleth (pH = 7.8). Arrows indicate in (<b>B</b>) course of bicarbonate buffering from start to 24 h hypercapnic incubation (red = acidosis, blue = alkalosis).</p>
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<p>Mean (± S.D.) developmental stage of embryos [<a href="#B18-biology-14-00132" class="html-bibr">18</a>] from berried lobsters from the Olifantsbos (n = 676; left column of figures) and Knol areas (n = 680; right column of figures) during 30 or 50 days of incubation. (<b>A</b>,<b>D</b>) Normocapnia, (<b>B</b>,<b>E</b>) pH 7.8, (<b>C</b>,<b>F</b>) pH 7.5. Note: x-axes of left and right panels are of the same scale to ensure comparability.</p>
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<p>Egg growth, expressed as mean (± S.D.) diameter, in berried lobsters from the Olifantsbos (n = 676; left column of figures) and Knol areas (n = 680; right column of figures) during 50 and 30 days of incubation, respectively. (<b>A</b>,<b>D</b>) Normocapnia, (<b>B</b>,<b>E</b>) pH 7.8, (<b>C</b>,<b>F</b>) pH 7.5. Note: x-axes of left and right panels are of the same scale to ensure comparability.</p>
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<p>Daily growth rate (µm d<sup>−1</sup>) of embryos/eggs from berried rock lobsters from the Knol and Olifantsbos areas under three pH treatments (see <a href="#biology-14-00132-t001" class="html-table">Table 1</a>) calculated from correlation slopes of egg growth from individual females (see <a href="#biology-14-00132-f007" class="html-fig">Figure 7</a>). * Significant difference between locations (<span class="html-italic">p</span> &lt; 0.001, two-way ANOVA and post hoc Holm–Šidák test).</p>
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<p>SEM micrographs of transversally fractured/cross-fractured cuticle of a defined <span class="html-italic">merus</span> sample each from individual berried <span class="html-italic">J. lalandii</span> from the Olifantsbos area after experimental exposure of 50 days. (<b>A</b>–<b>C</b>) Normocapnia, (<b>D</b>–<b>F</b>) pH 7.8, (<b>G</b>–<b>I</b>) pH 7.5. Scale bars are given in individual panels.</p>
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<p>SEM micrographs of a transversally fractured/cross-fractured cuticle from a defined carapace area from individual berried <span class="html-italic">J. lalandii</span> from the Olifantsbos area after experimental exposure of 50 days. (<b>A</b>–<b>C</b>) Normocapnia, (<b>D</b>–<b>F</b>) pH 7.8, (<b>G</b>–<b>I</b>) pH 7.5. Scale bars are given in individual panels.</p>
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<p>SEM micrographs of egg membranes (chorion) from individual berried <span class="html-italic">J. lalandii</span> from the Olifantsbos area after experimental exposure of 50 days. (<b>A</b>–<b>C</b>) Normocapnia, (<b>D</b>–<b>F</b>) pH 7.8, (<b>G</b>–<b>I</b>) pH 7.5. Scale bars are given in individual panels.</p>
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20 pages, 614 KiB  
Article
Ultrasound and Microwave-Assisted Extraction of Blackberry (Rubus fruticosus L.) Pomace: Analysis of Chemical Properties and Anticancer Activity
by Indrė Čechovičienė, Živilė Tarasevičienė, Ewelina Hallman, Agata Jabłońska-Trypuć, Laima Česonienė and Daiva Šileikienė
Plants 2025, 14(3), 384; https://doi.org/10.3390/plants14030384 - 27 Jan 2025
Abstract
Blackberries are seasonal berries that are processed into various products leaving a large amount of residues after processing, and therefore the most effective ways of utilising the residues need to be evaluated. The aim of this study was to determine the effect of [...] Read more.
Blackberries are seasonal berries that are processed into various products leaving a large amount of residues after processing, and therefore the most effective ways of utilising the residues need to be evaluated. The aim of this study was to determine the effect of different extraction methods on the chemical content of blackberry pomace extracts from different cultivars and their effect on the viability of the Caco-2 colorectal adenocarcinoma cell line and CCD-18Co normal colon fibroblast cancer cells. Blackberry pomace from berries of the cultivars ‘Polar’, ‘Orkan’, and ‘Brzezina’ was extracted by ultrasound-assisted extraction (UAE), microwave-assisted extraction (MAE) and a combination of these two extraction methods (MAE+UAE). The phenolic profile and the amount of organic acids and sugars were detected by HPLC. The spectrophotometric method was used to determine the amount of total phenolics, total flavonoids, and total anthocyanins. The cytotoxicity of the extracts was measured by the MTT assay. The chemical content of the extracts depends on the blackberry cultivar, the extraction method, and its interaction. Only the DPPH antioxidant activity did not depend on these factors and had no statistically significant differences between the different extracts. The extracts at a concentration of 5.0% increased the growth of both cancer cells, while the extracts at 1% and 2.5%, depending on the cultivar, reduced the growth of these cells. The MAE and UAE extracts of the ‘Orkan’ cultivar at concentrations of 1%, 1.5%, 2%, and 2.5% best inhibited the viability of Caco-2 cells. The extracts inhibited the growth of the Caco-2 cell line better than CCD-18Co normal colon fibroblasts. Full article
(This article belongs to the Section Phytochemistry)
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<p>Influence of blackberry pomace extracts in Caco-2 colorectal adenocarcinoma cell line (1) and CCD-18Co normal colon fibroblasts (2) after 24 h incubation. Different lowercase letters indicate statistically significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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12 pages, 626 KiB  
Review
Potential Transformation of Food Resveratrol: Mechanisms and Biological Impact
by Ayoub Jaa, Patricia Homobono Brito de Moura, María Begoña Ruiz-Larrea, José Ignacio Ruiz Sanz and Tristan Richard
Molecules 2025, 30(3), 536; https://doi.org/10.3390/molecules30030536 - 24 Jan 2025
Viewed by 262
Abstract
Resveratrol is a naturally occurring phenolic compound found in foods like grapes, berries, and peanuts. It has attracted substantial interest for its potential human health benefits, including antioxidant and anti-inflammatory effects. Research indicates that resveratrol may contribute to cardiovascular health, protect cognitive function, [...] Read more.
Resveratrol is a naturally occurring phenolic compound found in foods like grapes, berries, and peanuts. It has attracted substantial interest for its potential human health benefits, including antioxidant and anti-inflammatory effects. Research indicates that resveratrol may contribute to cardiovascular health, protect cognitive function, and exhibit anticancer properties. However, various factors such as pH levels, exposure to light, specific enzymes, and metal ions can alter its chemical structure, affecting its biological activities. These reactions can lead to the formation of different metabolites and polymers, which may affect the stability and bioactivity of resveratrol. This review examines the transformation of resveratrol from its natural sources to its consumption by humans. Additionally, we explore the biological activities of the resulting compounds of resveratrol transformations. Full article
(This article belongs to the Special Issue Featured Review Papers in Food Chemistry)
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<p>Chemical transformations of resveratrol highlighting <span class="html-italic">trans</span>-resveratrol (<b>1</b>), <span class="html-italic">cis</span>-resveratrol (<b>2</b>), δ-viniferin (<b>3</b>), 2,4,6-trihydroxyphenanthrene (<b>4</b>), phenol (<b>5</b>), and resorcinol (<b>6</b>).</p>
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<p>Compounds formed by the oligomerization of resveratrol in methanol and ethanol with silver acetate.</p>
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30 pages, 3389 KiB  
Article
GCNet: A Deep Learning Framework for Enhanced Grape Cluster Segmentation and Yield Estimation Incorporating Occluded Grape Detection with a Correction Factor for Indoor Experimentation
by Rubi Quiñones, Syeda Mariah Banu and Eren Gultepe
J. Imaging 2025, 11(2), 34; https://doi.org/10.3390/jimaging11020034 - 24 Jan 2025
Viewed by 383
Abstract
Object segmentation algorithms have heavily relied on deep learning techniques to estimate the count of grapes which is a strong indicator for the yield success of grapes. The issue with using object segmentation algorithms for grape analytics is that they are limited to [...] Read more.
Object segmentation algorithms have heavily relied on deep learning techniques to estimate the count of grapes which is a strong indicator for the yield success of grapes. The issue with using object segmentation algorithms for grape analytics is that they are limited to counting only the visible grapes, thus omitting hidden grapes, which affect the true estimate of grape yield. Many grapes are occluded because of either the compactness of the grape bunch cluster or due to canopy interference. This introduces the need for models to be able to estimate the unseen berries to give a more accurate estimate of the grape yield by improving grape cluster segmentation. We propose the Grape Counting Network (GCNet), a novel framework for grape cluster segmentation, integrating deep learning techniques with correction factors to address challenges in indoor yield estimation. GCNet incorporates occlusion adjustments, enhancing segmentation accuracy even under conditions of foliage and cluster compactness, and setting new standards in agricultural indoor imaging analysis. This approach improves yield estimation accuracy, achieving a R² of 0.96 and reducing mean absolute error (MAE) by 10% compared to previous methods. We also propose a new dataset called GrapeSet which contains visible imagery of grape clusters imaged indoors, along with their ground truth mask, total grape count, and weight in grams. The proposed framework aims to encourage future research in determining which features of grapes can be leveraged to estimate the correct grape yield count, equip grape harvesters with the knowledge of early yield estimation, and produce accurate results in object segmentation algorithms for grape analytics. Full article
(This article belongs to the Special Issue Deep Learning in Image Analysis: Progress and Challenges)
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<p>Images of grape clusters used in existing datasets, categorized by the number of grape clusters present in each image. (<b>a</b>) shows images with fewer than five grape clusters [<a href="#B37-jimaging-11-00034" class="html-bibr">37</a>,<a href="#B38-jimaging-11-00034" class="html-bibr">38</a>,<a href="#B42-jimaging-11-00034" class="html-bibr">42</a>] including our GrapeSet, while (<b>b</b>) shows images containing more than five clusters [<a href="#B40-jimaging-11-00034" class="html-bibr">40</a>,<a href="#B41-jimaging-11-00034" class="html-bibr">41</a>,<a href="#B42-jimaging-11-00034" class="html-bibr">42</a>].</p>
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<p>Our proposed GCNet framework.</p>
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<p>Sample images from GrapeSet of green, purple, and blue grapes captured in three different foliage setups: Setup 1 (Low Foliage), Setup 2 (Medium Foliage), and Setup 3 (High Foliage), respectively. Each row represents a different background—White (top row) and Green bokeh (middle row) backgrounds. The bottom row displays the corresponding ground truth masks for each setup, showing the precise location of the grape clusters.</p>
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<p>Qualitative segmentation results of grape clusters at varying resolutions (Low, Medium, High) across different setups and background types.</p>
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<p>The segmentation results for blue, green, and purple grape clusters using GCNet.</p>
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23 pages, 3183 KiB  
Article
Phytochemical Analysis of the Extract from Berries of Schisandra chinensis Turcz. (Baill.) and Its Anti-Platelet Potential In Vitro
by Natalia Sławińska, Bogdan Kontek, Jerzy Żuchowski, Barbara Moniuszko-Szajwaj, Jacek Białecki, Kamil Zakrzewski, Paulina Bogusz, Anna Stochmal and Beata Olas
Int. J. Mol. Sci. 2025, 26(3), 984; https://doi.org/10.3390/ijms26030984 - 24 Jan 2025
Viewed by 266
Abstract
Schisandra chinensis Turcz. (Baill.) is a dioecious vine belonging to the Schisandraceae family. Its berries show beneficial activities, including cardioprotective, antioxidant, and anti-inflammatory. We examined the chemical content of S. chinensis berry extract and its antiplatelet potential in vitro. The antiplatelet activity assays [...] Read more.
Schisandra chinensis Turcz. (Baill.) is a dioecious vine belonging to the Schisandraceae family. Its berries show beneficial activities, including cardioprotective, antioxidant, and anti-inflammatory. We examined the chemical content of S. chinensis berry extract and its antiplatelet potential in vitro. The antiplatelet activity assays included measurements of thrombus formation in full blood (with Total Thrombus-formation Analysis System) and platelet activation and adhesion. We also assessed the extract’s effect on coagulation times in human plasma and its cytotoxicity toward blood platelets based on extracellular lactate dehydrogenase activity. The most important constituents of the extract were dibenzocyclooctadiene lignans; schisandrin was the dominant compound. S. chinensis berry extract at the concentration of 50 μg/mL inhibited thrombus formation by approximately 15%. The adhesion of unstimulated and thrombin-activated blood platelets to collagen was inhibited by all used concentrations of the extract (0.5–50 μg/mL), while the adhesion of adenosine diphosphate (ADP)-activated platelets to fibrinogen was inhibited only by the concentrations of 10 and 50 μg/mL. The extract also inhibited the exposition of the active form of GPIIb/IIIa on the surface of platelets stimulated with 10 μM ADP (at 0.5–50 μg/mL) and 20 μM ADP (at 50 μg/mL). The exposition of P-selectin was inhibited only by the extract at the concentrations of 5–50 μg/mL in platelets stimulated with 10 μg/mL collagen. Moreover, the extract was not cytotoxic toward blood platelets. This indicates that S. chinensis berries hold promise as new antiplatelet agents, but more studies are needed to determine their mechanisms of action and in vivo efficiency. Full article
(This article belongs to the Section Bioactives and Nutraceuticals)
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<p>UHPLC-CAD (<b>A</b>), and UV (λ = 255 nm (<b>B</b>)) chromatograms of the extract from the fruit of <span class="html-italic">S. chinensis</span>. Numbers above the chromatic peaks correspond to those from <a href="#ijms-26-00984-t001" class="html-table">Table 1</a>.</p>
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<p>Effect of the extract from <span class="html-italic">S. chinensis</span> berries (at concentrations 0.5, 1, 5, 10, and 50 μg/mL) on the adhesion of unstimulated platelets to collagen (<b>A</b>), thrombin-activated platelets to collagen (<b>B</b>), thrombin-activated platelets to fibrinogen (<b>C</b>), and ADP-activated platelets to fibrinogen (<b>D</b>) (<span class="html-italic">n</span> = 9). In the graphs, platelet adhesion is expressed as a percentage of the ‘Control’ sample (blood platelets without the tested extract) (<b>A</b>), or the ‘Control +’ sample (platelets stimulated by agonist with no added extract) (<b>B</b>–<b>D</b>). ‘Control -‘ samples are unstimulated blood platelets. The data are expressed as means ± SD. The results were considered significant at <span class="html-italic">p</span> &lt; 0.05 (* <span class="html-italic">p</span> &lt; 0.05, ns—not significant). The differences between controls were significant (<span class="html-italic">p</span> &lt; 0.001 (<b>B</b>,<b>D</b>), <span class="html-italic">p</span> &lt; 0.01 (<b>C</b>)).</p>
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<p>Effect of the extract from <span class="html-italic">S. chinensis</span> berries (at concentrations 0.5, 1, 5, 10, and 50 μg/mL) on the exposition of the active form of GPIIb/IIIa on 10 µM ADP-stimulated blood platelets (<b>A</b>), 20 µM ADP-stimulated blood platelets (<b>B</b>), and 10 µg/mL collagen-stimulated blood platelets (<b>C</b>) in whole blood samples. Blood platelets were distinguished based on the exposition of CD61. For each sample, 5000 CD61-positive objects were acquired. For the assessment of GPIIb/IIIa exposition, samples were labeled with fluorescently conjugated monoclonal antibody PAC-1/FITC. Results are shown as the percentage of platelets binding PAC-1/FITC. Data represent the means ± SD. The blood samples were drawn from 6 healthy volunteers. ‘Control -‘samples are unstimulated blood platelets, ‘Control +’ samples are platelets stimulated by agonist with no added extract. The activity of the tested extract was compared to the ‘Control +’ sample. The differences between controls were significant (<span class="html-italic">p</span> &lt; 0.01 (<b>A</b>), <span class="html-italic">p</span> &lt; 0.05 (<b>B</b>,<b>C</b>)). The results were considered significant at <span class="html-italic">p</span> &lt; 0.05 (* <span class="html-italic">p</span> &lt; 0.05, ns—not significant).</p>
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<p>Effect of the extract from <span class="html-italic">S. chinensis</span> berries (at concentrations 0.5, 1, 5, 10, and 50 μg/mL) on the exposition of P-selectin on 10 µM ADP-stimulated blood platelets (<b>A</b>), 20 µM ADP-stimulated blood platelets (<b>B</b>), and 10 µg/mL collagen-stimulated blood platelets (<b>C</b>) in whole blood samples. Blood platelets were distinguished based on the exposition of CD61. For each sample, 5000 CD61-positive objects were acquired. For the assessment of P-selectin exposition, samples were labeled with fluorescently conjugated monoclonal antibody CD62P/PE. Results are shown as the percentage of platelets expressing CD62P. Data represent the means ± SD. ‘Control -‘samples are unstimulated blood platelets, ‘Control +’ samples are platelets stimulated by agonist with no added extract. The activity of the tested extract was compared to the ‘Control +’ sample. The differences between controls were significant (<span class="html-italic">p</span> &lt; 0.001 (<b>A</b>,<b>B</b>), <span class="html-italic">p</span> &lt; 0.05 (<b>C</b>)). The results were considered significant at <span class="html-italic">p</span> &lt; 0.05 (* <span class="html-italic">p</span> &lt; 0.05, ns—not significant).</p>
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<p>Effect of the extract from <span class="html-italic">S. chinensis</span> berries (at concentrations 0.5, 1, 5, 10, and 50 μg/mL) on platelet plug formation in whole blood (<span class="html-italic">n</span> = 6) (<b>A</b>). The samples were analyzed with T-TAS PL-chip, at the shear stress rates of 1500/s. The results are calculated as AUC<sub>10</sub> (area under the curve). In the graphs, AUC<sub>10</sub> is expressed as a percentage of the control sample (blood without the tested extract). The data are expressed as means ± SD. The results were considered significant at <span class="html-italic">p</span> &lt; 0.05 (* <span class="html-italic">p</span> &lt; 0.05, ns—not significant). (<b>B</b>) shows changes in pressure that were recorded within the PL-chip in each sample at the highest concentration of the extract (50 μg/mL).</p>
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<p>Effect of the extract from <span class="html-italic">S. chinensis</span> berries (at concentrations 0.5, 1, 5, 10, and 50 μg/mL) on the activity of lactate dehydrogenase (<span class="html-italic">n</span> = 6). The results are expressed as a percentage of the control sample. The data are expressed as means ± SD. The results were considered significant at <span class="html-italic">p</span> &lt; 0.05 (ns—not significant).</p>
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17 pages, 5310 KiB  
Article
Effect of Short-Term Storage in Modified Atmosphere Packaging (MAP) and Controlled Atmosphere (CA) on Total Polyphenol Content and Antioxidant Activity in Juices from Haskap Berry (Lonicera caerulea L.)
by Barbara Anna Kowalczyk, Monika Bieniasz and Jan Błaszczyk
Agriculture 2025, 15(3), 253; https://doi.org/10.3390/agriculture15030253 - 24 Jan 2025
Viewed by 298
Abstract
This article focuses on analysing the properties of six varieties of haskap berry (honeyberry) as a valuable raw material for producing health-promoting juices. Significant differences in the content of bioactive compounds were observed between juices derived from fruits of the same species. This [...] Read more.
This article focuses on analysing the properties of six varieties of haskap berry (honeyberry) as a valuable raw material for producing health-promoting juices. Significant differences in the content of bioactive compounds were observed between juices derived from fruits of the same species. This study demonstrated that controlled atmosphere (CA) conditions (20% CO2 and 5% O2) and modified atmosphere packaging (MAP) in Xtend bags affected juice quality by minimising nutritional losses. The analysis of polyphenol content in the juices revealed significant differences between varieties and years (2021 and 2022), primarily due to varying weather conditions. In 2022, the polyphenol content of the varieties ‘Usłada’, ‘Candy Blue’, ‘Boreal Beauty’, and ‘Boreal Beast’ was from 69% to twice as high compared to values recorded in 2021. CA and MAP storage conditions were found to be more effective than normal atmosphere (NA) in preserving bioactive components, and thus the antioxidant activity of the fruits, as measured by the DPPH method. The variety ‘Sinij Utes’ had the highest total polyphenol contents and their lowest loss during storage. Conversely, the variety ‘Boreal Beauty’ contained the lowest polyphenol levels both after harvest and storage. This study confirmed the importance of proper storage conditions for maintaining the antioxidant properties of haskap berries. Full article
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<p>Weather patterns during flowering, growth, and ripening of berries in 2021 and 2022.</p>
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<p>Percent change in polyphenol content (mg/L GAE) after seven days and after fourteen days of berry storage, relative to post-harvest values for individual varieties and storage methods in 2021.</p>
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<p>Percentage change in total polyphenol content in 2022 compared to 2021.</p>
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<p>Percentage change in polyphenol content (TPC, mg/L GAE) after seven and fourteen days of berry storage relative to post-harvest values in 2022 based on variety and storage method.</p>
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<p>Percentage changes in radical scavenging capacity in juice after seven and fourteen days of storage in 2021 depending on the variety.</p>
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<p>Percentage changes in radical scavenging capacity in juice after seven and fourteen days of storage in 2022 depending on the variety.</p>
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<p>Amplitude of changes in polyphenol content (<b>A</b>–<b>C</b>) and antioxidant activity (<b>D</b>–<b>F</b>) under various storage conditions, averaged for 2021 and 2022.</p>
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<p>Percentage changes in fruit firmness based on storage method (NA—(<b>A</b>), CA—(<b>B</b>), or MAP—(<b>C</b>)) in 2021 and 2022.</p>
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<p>Similarity of storage method combinations and varieties in terms of total polyphenol content and antioxidant activity in 2021.</p>
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<p>Similarity of storage method combinations and varieties in terms of total polyphenol content and antioxidant activity in 2022.</p>
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20 pages, 2544 KiB  
Article
Glycosylated Delphinidins Decrease Chemoresistance to Temozolomide by Regulating NF-κB/MGMT Signaling in Glioblastoma
by Diego Carrillo-Beltrán, Yessica Nahuelpan, Constanza Cuevas, Karen Fabres, Pamela Silva, Jimena Zubieta, Giovanna Navarro, Juan P. Muñoz, María A. Gleisner, Flavio Salazar-Onfray, Noemi Garcia-Romero, Angel Ayuso-Sacido, Rody San Martin and Claudia Quezada-Monrás
Cells 2025, 14(3), 179; https://doi.org/10.3390/cells14030179 - 24 Jan 2025
Viewed by 322
Abstract
Glioblastoma (GB) is a highly malignant brain tumor with a poor prognosis, with a median survival of only 14.6 months despite aggressive treatments. Resistance to chemotherapy, particularly temozolomide (TMZ), is a significant challenge. The DNA repair enzyme MGMT and glioblastoma stem cells (GSCs) [...] Read more.
Glioblastoma (GB) is a highly malignant brain tumor with a poor prognosis, with a median survival of only 14.6 months despite aggressive treatments. Resistance to chemotherapy, particularly temozolomide (TMZ), is a significant challenge. The DNA repair enzyme MGMT and glioblastoma stem cells (GSCs) often mediate this resistance. Recent studies highlight the therapeutic potential of natural compounds, particularly delphinidins, found in deep purple berries. Delphinidins are known for their ability to inhibit NF-κB signaling, a critical pathway for GB progression, chemoresistance, and MGMT expression. Our research demonstrates that glycosylated delphinidins have potential adjuvant use in the treatment of GB, offering a promising natural strategy to combat TMZ resistance. Specifically, we observed that delphinidin 3,5 di-glucoside has potent anticancer effects when used alone. Meanwhile, delphinidin 3 glucoside acted in synergy with temozolomide to decrease cell viability, highlighting its potential as an adjuvant. It also exerted a faster and more sustained inhibition of NF-κB, highlighting its potential for long-lasting therapeutic effects. These findings open new avenues for targeted therapies against glioblastoma, particularly to overcome treatment resistance. Full article
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<p>Cytotoxicity assay of glycosylated delphinidins exposed to different concentrations in tumor and non-tumor glial cells. MTS assay to evaluate the viability of cells when exposed for 72 h to concentrations of 0, 15, 30, 60, 80, 100, 120, 180, and 240 μM of delphinidin 3 glucoside or delphinidin 3,5 di-glucoside. (<b>a</b>) U87-MG exposed to delphinidin 3 glucoside. (<b>b</b>) SVG-p12 exposed to delphinidin 3 glucoside. (<b>c</b>) GBM38 exposed to delphinidin 3 glucoside. (<b>d</b>) U87-MG exposed to delphinidin 3,5 di-glucoside. (<b>e</b>) SVG-p12 exposed to delphinidin 3,5 di-glucoside. (<b>f</b>) GBM38 exposed to delphinidin 3,5 di-glucoside. Data are presented as the mean ± standard deviation (SD); * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01 and **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Glycosylated delphinidins reduce NF-κB activity in glioblastoma cells. (<b>a</b>) Luciferase activity normalized to GFP fluorescence intensity in U87-MG cells transfected with the pHAGE/NF-κB reporter vector treated with delphinidin-3-glucoside at concentrations of 15, 60, and 120 μM or with controls Bay117082 10 nM or LY294002 10 nM for 3 h. (<b>b</b>) 6 h. (<b>c</b>) 24 h. (<b>d</b>) 48 h. (<b>e</b>) Luciferase activity normalized to GFP fluorescence intensity in U87-MG cells transfected with the pHAGE/NF-κB reporter vector treated with delphinidin-3,5-di-glucoside at concentrations of 15, 60, and 120 μM or with the controls Bay117082 10 nM or LY294002 10 nM for 3 h. (<b>f</b>) 6 h. (<b>g</b>) 24 h. (<b>h</b>) 48 h. Data are presented as the mean ± standard deviation (SD); * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001 and **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Glycosylate delphinidins reduce the levels of NF-κB pathway proteins that positively correlate with MGMT expression in glioblastoma in vitro. Protein array of the NF-κB signaling pathway performed in U87-MG cells treated with delphinidin 3 glucoside or delphinidin 3,5 di-glucoside at 120 µM for 24 h; the graph demonstrates the fold change compared to the control with DMSO. (<b>a</b>) U87-MG cells treated with delphinidin 3 glucoside. (<b>b</b>) U87-MG cells treated with delphinidin 3,5 di-glucoside. (<b>c</b>) Survival analysis with Kaplan–Meier plot of 220 glioblastoma cases; the red line represents tumors with high levels of SHARPIN, and the blue line represents tumors with low levels of the marker; the graph reports median survival and Hazard Ratio (HR) along with statistical significance. (<b>d</b>) Pearson correlation between SHARPIN and MGMT expression levels. (<b>e</b>) Survival analysis with Kaplan–Meier plot of 220 glioblastoma cases; the red line represents tumors with high levels of TMEM173, and the blue line represents tumors with low levels of the marker; the graph reports median survival and Hazard Ratio (HR) along with statistical significance. (<b>f</b>) Pearson correlation between TMEM173 and MGMT expression levels. Data are presented as the mean ± standard deviation (SD).</p>
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<p>Glycosylate delphinidins reduce the levels of NF-κB pathway proteins that positively correlate with MGMT expression in glioblastoma in vitro. Protein array of the NF-κB signaling pathway performed in U87-MG cells treated with delphinidin 3 glucoside or delphinidin 3,5 di-glucoside at 120 µM for 24 h; the graph demonstrates the fold change compared to the control with DMSO. (<b>a</b>) U87-MG cells treated with delphinidin 3 glucoside. (<b>b</b>) U87-MG cells treated with delphinidin 3,5 di-glucoside. (<b>c</b>) Survival analysis with Kaplan–Meier plot of 220 glioblastoma cases; the red line represents tumors with high levels of SHARPIN, and the blue line represents tumors with low levels of the marker; the graph reports median survival and Hazard Ratio (HR) along with statistical significance. (<b>d</b>) Pearson correlation between SHARPIN and MGMT expression levels. (<b>e</b>) Survival analysis with Kaplan–Meier plot of 220 glioblastoma cases; the red line represents tumors with high levels of TMEM173, and the blue line represents tumors with low levels of the marker; the graph reports median survival and Hazard Ratio (HR) along with statistical significance. (<b>f</b>) Pearson correlation between TMEM173 and MGMT expression levels. Data are presented as the mean ± standard deviation (SD).</p>
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<p>Glycosylate delphinidins reduce transcript and protein levels of MGMT in glioblastoma cells. RTqPCR was performed to evaluate MGMT transcript levels in U87-MG cells previously exposed to delphinidin 3 glucoside or delphinidin 3,5 di-glucoside at concentrations of 15, 60, and 120 μM for 24 or 48 h, BAY11-7082 was used at 10 μM. (<b>a</b>) RTqPCR of treatment delphinidin 3-glucoside for 24 h. (<b>b</b>) RTqPCR of treatment delphinidin 3-glucoside for 48 h. (<b>c</b>) RTqPCR of treatment delphinidin 3,5 di-glucoside for 24 h. (<b>d</b>) RTqPCR of treatment delphinidin 3,5 di-glucoside for 48 h. (<b>e</b>) WB was performed to assess MGMT protein levels in U87-MG cells when exposed to delphinidin 3-glucoside or delphinidin 3,5 di-glucoside for 24 h; the control BAY 11-7082 was used at 10 μM. (<b>f</b>) WB was performed to assess MGMT protein levels in U87-MG cells when exposed to delphinidin 3 glucoside or delphinidin 3,5 di-glucoside for 48 h. β-actin transcript was used as an endogenous control in the RTqPCR. Data are presented as mean ± standard deviation (SD); * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001 and **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Glycosylated delphinidins negatively regulate MGMT promoter activity in glioblastoma cells. (<b>a</b>) The luciferase reporter assay was performed with the pmir-GlO MGMT promoter vector. To perform the assay, the U87-MG cells were previously transfected with the vector for 24 h; then treatments were carried out with delphinidin 3-glucoside at concentrations of 15, 60, and 120 μM for 24 h; BAY11-7082 was used as a positive regulation control. The data were normalized with the activity of renilla luciferase (<b>b</b>). The previous assay was performed with exposure to delphinidins for 48 h. (<b>c</b>) The activity of the MGMT promoter was measured when U87-MG cells were exposed to delphinidin 3,5 di-glucoside at concentrations of 15, 60, and 120 μM for 24 h. (<b>d</b>) Assay to measure MGMT promoter activity when cells are exposed for 48 h to delphinidin 3,5 di-glucoside. (<b>e</b>) Chromatin immunoprecipitation assay with anti p65/Rel-A antibody in U87.MG cells were exposed for 24 h to 120 μM of glycosylated delphinidins; the immuno-precipitate obtained with anti-RNA Polymerase II amplified with primers from the GAPDH promoter region was used as a normalizer. Data are presented as the mean ± standard deviation (SD); * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; and *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Sensitizing capacity of glycosylated delphinidins to the drug TMZ in glioblastoma cells. (<b>a</b>) MTS assay to assess the viability of U87-MG cells when exposed for 48 h to the combined treatments of TMZ at 100, 200, 400 and 800 μM, with delphinidin 3 glucoside doses at 15, 60 and 120 μM. BAY11-7082 20 μM was used as a positive sensitization control and DMSO as a vehicle control. Data were adjusted to percentages taking DMSO treatment as 100%. (<b>b</b>) Heat map of the previous MTS assessing delphinidin 3-glucoside-induced TMZ sensitization, including statistical analysis in each quadrant. (<b>c</b>) MTS assay to assess the viability of U87-MG cells when exposed for 48 h to the combined treatments of TMZ at 100, 200, 400, and 800 μM, with delphinidin 3,5 di-glucoside doses at 15, 60, and 120 µM. BAY11-7082 20 μM was used as a positive sensitization control, and DMSO was used as a vehicle control. Data were adjusted to percentages taking DMSO treatment as 100%. (<b>d</b>) Heatmap of the above MTS assessing the sensitization to TMZ induced by delphinidin 3,5 di-glucoside, including statistical analysis in each quadrant. (<b>e</b>) Summary table of percentages of apoptosis data obtained with the 48-h combinatorial treatment with 200 μM TMZ, 120 μM delphinidin 3 glucoside and 120 μM delphinidin 3,5 di-glucoside. 20 μM BAY11-7082 was used as a positive sensitization control and DMSO as a vehicle control. (<b>f</b>) Heat map of the previous apoptosis assay. Data are presented as the mean ± standard deviation (SD); * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>A proposed model of capacity of glycosylated delphinidins to decrease chemoresistance to Temozolomide by regulating NF-κB/MGMT (Created in <a href="https://BioRender.com" target="_blank">https://BioRender.com</a> (accessed on 12 December 2024)).</p>
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24 pages, 2346 KiB  
Article
Nutrients, Phytochemicals, and In Vitro Biological Activities of Goldenberry (Physalis peruviana L.) Fruit and Calyx
by Mikel Añibarro-Ortega, Maria Inês Dias, Jovana Petrović, Filipa Mandim, Sonia Núñez, Marina Soković, Víctor López, Lillian Barros and José Pinela
Plants 2025, 14(3), 327; https://doi.org/10.3390/plants14030327 - 22 Jan 2025
Viewed by 627
Abstract
This study provides a comprehensive characterization of Physalis peruviana L., covering the nutritional composition of the fruit and the phytochemical profiles and in vitro bioactive properties of berry and calyx extracts. The fresh fruit stood out as a source of dietary fiber (5.16 [...] Read more.
This study provides a comprehensive characterization of Physalis peruviana L., covering the nutritional composition of the fruit and the phytochemical profiles and in vitro bioactive properties of berry and calyx extracts. The fresh fruit stood out as a source of dietary fiber (5.16 g/100 g) and is low in fat (0.49 g/100 g). A 100-g serving also contained notable amounts of ascorbic acid (32.0 mg), tocopherols (2.34 mg), potassium (253 mg), phosphorus (45 mg), and magnesium (20 mg). HPLC-DAD-ESI/MS analysis tentatively identified five physalin derivatives and one withanolide in the fruit extract, which showed significant antiproliferative activity against human colorectal adenocarcinoma (Caco-2) and non-small-cell lung carcinoma (NCI-H460) cells. The calyx extracts contained three phenolic acids and four flavonoids, demonstrating high antioxidant activity through physiologically relevant cell-based assays, the ability to inhibit advanced glycation end products (AGEs) formation and nitric oxide production, and also antiproliferative properties. These findings highlight goldenberry as a nutrient-dense fruit rich in vitamins and functional compounds with potential health benefits, supporting its recognition as a “superfruit”. Furthermore, the fruit calyx emerged as a valuable source of bioactive secondary metabolites with potential applications in food and pharmaceutical industries and related sectors. Full article
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<p>Inhibitory capacity of <span class="html-italic">P. peruviana</span> fruit and calyx extracts on (<b>a</b>) α-glucosidase activity, (<b>b</b>) AGEs formation, and (<b>c</b>) lipase activity.</p>
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18 pages, 2339 KiB  
Article
Chemical Profiling and Antioxidant Potential of Berries from Six Blueberry Genotypes Harvested in the Italian Alps in 2020: A Comparative Biochemical Pilot Study
by Fabrizio Araniti, Giovanna Baron, Giulio Ferrario, Michele Pesenti, Larissa Della Vedova, Bhakti Prinsi, Gian Attilio Sacchi, Giancarlo Aldini and Luca Espen
Agronomy 2025, 15(2), 262; https://doi.org/10.3390/agronomy15020262 - 22 Jan 2025
Viewed by 375
Abstract
This pilot study investigates the chemical profiling and antioxidant potential of six blueberry genotypes: three tetraploids from the highbush blueberry species and three hexaploids from the rabbiteye blueberry species. The goal was to characterise the biochemical composition of these genotypes, grown under identical [...] Read more.
This pilot study investigates the chemical profiling and antioxidant potential of six blueberry genotypes: three tetraploids from the highbush blueberry species and three hexaploids from the rabbiteye blueberry species. The goal was to characterise the biochemical composition of these genotypes, grown under identical pedoclimatic conditions, and to evaluate the variation in bioactive compounds associated with antioxidant activity. Metabolomic and ionomic analyses were employed to identify and relatively quantify these compounds. Multivariate analyses clustered the genotypes based on phytochemical profiles, pinpointing key genotype-clustering metabolites. Significant variations among genotypes were observed. Ochlockonee and Overtime had the highest anthocyanins, phenols, ascorbates, and antioxidant activity levels. Over thirty metabolites (organic acids, sugars, and flavonoid glycosides) drove the genotype clustering. Although Last Call and Legacy had more metabolites, their antioxidant properties were lower, suggesting that phenolic quality influences antioxidant activity more than quantity. Overtime had the highest phenolic content, followed by Last Call in anthocyanins. Liberty and Legacy showed the lowest anthocyanin and ascorbate levels, while Overtime and Ochlockonee were characterised by an increase in ascorbate content. Rabbiteye blueberries showed higher antioxidant potential than highbush, indicating that antioxidant efficacy depends more on the composition and quality of the bioactive compounds than on their total concentration. Full article
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<p>Characterization of six different blueberry genotypes (Last Call, Legacy, Liberty, Ochlockonee, Overtime, and Titan): (<b>a</b>) Clustering result shown as a dendrogram (distance measure using Euclidean and clustering algorithm using Ward.D). (<b>b</b>) PCA (Principal Component Analysis) scores plot; the explained variances are shown in brackets. (<b>c</b>) PLS-DA (Partial Least Squares Discriminant Analysis) scores plot. (<b>d</b>) PLS-DA VIP (Variable Importance in Projection). N = 3.</p>
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<p>(<b>a</b>) The top 60 parameters resulting from the one-way ANOVA are reported as a clusterised heatmap; (<b>b</b>) total anthocyanins content; (<b>c</b>) total phenols content; (<b>d</b>) total ascorbate content; and (<b>e</b>) total radical scavenging activity of the six blueberry genotypes. Data are expressed as mean normalised through Log 10 transformation and Pareto scaled. Normalised data were analysed through one-way ANOVA using the LSD test as post hoc (<span class="html-italic">p</span> ≤ 0.05). N = 3.</p>
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23 pages, 3927 KiB  
Article
Anti-Hail Shading Net and Kaolin Application: Protecting Grape Production to Ensure Grape Quality in Mediterranean Vineyards
by Luca Pallotti, Edoardo Dottori, Tania Lattanzi, Vania Lanari, Luca Brillante and Oriana Silvestroni
Horticulturae 2025, 11(2), 110; https://doi.org/10.3390/horticulturae11020110 - 21 Jan 2025
Viewed by 410
Abstract
Rising temperatures due to climate change pose a significant threat to viticulture, intensifying summer heat stress and accelerating berry ripening. Additionally, the increasing frequency of extreme weather events, such as hailstorms, further jeopardizes the sustainability of the viticultural sector. In recent years, mitigating [...] Read more.
Rising temperatures due to climate change pose a significant threat to viticulture, intensifying summer heat stress and accelerating berry ripening. Additionally, the increasing frequency of extreme weather events, such as hailstorms, further jeopardizes the sustainability of the viticultural sector. In recent years, mitigating these impacts has become crucial for grape production, particularly in Mediterranean regions. This study compares two mitigation strategies—using an anti-hail shading net (S) and kaolin spraying (K)—with untreated control vines (C) over three growing seasons. Vine physiology, berry ripening, grape production and pruning weight were evaluated. The S treatment significantly reduced light interception in the fruiting zone and, while limiting gas exchange, improved vine performance during extreme heat. The K treatment alleviated heat stress and enhanced the photosynthetic activity. Both S and K treatments improved grape quality by maintaining higher acidity levels and lower sugar concentrations and pH. Additionally, both treatments reduced the incidence of fungal diseases, with the net providing added protection against hailstorms. No significant changes in pruning weight were observed, and the treated vines showed a better balance between vegetative growth and production. In conclusion, both kaolin and shading nets are effective techniques for addressing the challenges of climate change, enhancing vine resilience and ensuring high-quality grape production. Full article
(This article belongs to the Special Issue Orchard Management: Strategies for Yield and Quality)
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<p>Meteorological trend from June to September during the three years. Yellow squares highlight the period spanning from veraison to harvest. Blue arrows indicate the placing of the anti-hail shading net (S), green arrows indicate kaolin spraying (K) and the red arrow marks the hailstorm that damaged the vineyard (8 August 2023).</p>
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<p>Grapevine light interception in control untreated vines (C) and shaded vines (S) measured in 2021 and 2022 at the sides of the canopy and in the fruiting zone. PAR indicates photosynthetic active radiation. In case of significant ANOVA, different letters indicate differences between treatments with <span class="html-italic">p</span>-value ≤ 0.05 (<span class="html-italic">t</span>-test).</p>
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<p>Trends for (<b>a</b>) stomatal conductance (g<sub>s</sub>) and (<b>b</b>) net assimilation (A<sub>N</sub>) in control (C), kaolin (K) and shading (S) treatments during the survey (2021–2023). In case of significant ANOVA, different letters indicate differences between treatments with <span class="html-italic">p</span>-value ≤ 0.05 (<span class="html-italic">t</span>-test).</p>
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<p>Trends for (<b>a</b>) intrinsic water use efficiency (WUEi) and (<b>b</b>) transpiration (E) in control (C), kaolin (K) and shading (S) treatments during the survey (2021–2023). In case of significant ANOVA, different letters indicate differences between treatments with <span class="html-italic">p</span>-value ≤ 0.05 (<span class="html-italic">t</span>-test).</p>
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<p>Trends for (<b>a</b>) berry weight and (<b>b</b>) total soluble solids (TSS) in control (C), kaolin (K) and shading (S) treatments during the survey (2021–2023). The black arrow indicates the harvest date. In case of significant ANOVA, different letters indicate differences between treatments with <span class="html-italic">p</span>-value ≤ 0.05 (<span class="html-italic">t</span>-test).</p>
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<p>Trends for (<b>a</b>) titratable acidity (TA) and (<b>b</b>) malic acid concentration (MA) in control (C), kaolin (K) and shading (S) treatments during the survey (2021–2023). The black arrow indicates the harvest date. In case of significant ANOVA, different letters indicate differences between treatments with <span class="html-italic">p</span>-value ≤ 0.05 (<span class="html-italic">t</span>-test).</p>
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<p>Trends for must pH in control (C), kaolin (K) and shading (S) treatments during the survey (2021–2023). The black arrow indicates the harvest date. In case of significant ANOVA, different letters indicate differences between treatments with <span class="html-italic">p</span>-value ≤ 0.05 (<span class="html-italic">t</span>-test).</p>
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17 pages, 1456 KiB  
Article
Grass Cover in Vineyards as a Multifunctional Solution for Sustainable Grape Growing: A Case Study of Cabernet Sauvignon Cultivation in Serbia
by Zoran Pržić, Aleksandar Simić, Snežana Brajević, Nebojša Marković, Ana Vuković Vimić, Mirjam Vujadinović Mandić and Mariana Niculescu
Agronomy 2025, 15(2), 253; https://doi.org/10.3390/agronomy15020253 - 21 Jan 2025
Viewed by 420
Abstract
Faced with the challenges posed by climate change, Serbian viticulture is looking for sustainable solutions for adaptable production. This study shows that grass is a multifunctional tool for overcoming the challenges of intensive viticulture while maintaining the quality of the grapes. In a [...] Read more.
Faced with the challenges posed by climate change, Serbian viticulture is looking for sustainable solutions for adaptable production. This study shows that grass is a multifunctional tool for overcoming the challenges of intensive viticulture while maintaining the quality of the grapes. In a three-year research experiment (2020–2022), the maintenance of an inter-row sward in a vineyard with four certified high-quality French Cabernet Sauvignon clones was investigated, and its effects on the ampelographic composition of the grapes and the quality of the grape juice (must) were studied as a function of wine quality. A grass sward was established between the rows as a biological soil management system and as a climate change adaptation measure in a high-intensity viticultural system. A grass–legume mixture was used as an inter-row cover crop, with nitrogen applied in two doses (50 and 100 kg ha−1) in spring. The growth of the grasses responded to the nitrogen fertilisation, which was reflected in the biomass production, surface cover and nitrogen content in the biomass. At the end of the study, the biomass of the grass increased threefold when a high dose of nitrogen was applied compared to the non-fertilised grass. In contrast to the effects of nitrogen on the sward, N has no effect on the quantitative or qualitative parameters of the grapes. Clone 169 was separated for most grape mechanical parameters such as the bunch mass, all berries and the bunch stem; clone 15 showed the best grape juice quality parameters such as the sugar content and glycoacidometric index. The results show an option for climate change adaptation in viticulture that can mitigate the effects of rising temperatures, contribute to soil conservation and carbon storage in biomass and enable timely interventions in vineyards after heavy rainfall by creating accessible paths within the vineyards. The three-year effect of the different nutrient management of the sward in the inter-rows of Cabernet Sauvignon showed that the interaction between the two systems, sward and vine, is low and has no negative impact on the ampelographic and qualitative grape parameters. Full article
(This article belongs to the Special Issue Adaptations and Responses of Cropping Systems to Climate Change)
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<p>Experimental vineyard.</p>
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<p>Monthly values of temperature and accumulated precipitation; average for 1991–2020 and values for the experimental years 2020, 2021, 2022.</p>
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<p>Correlation of grape parameters and sward indicators. TFB—total fresh biomass; TDM—total dry matter; CQI—cover quality index; N content—N content in sward; TAC—total acid content; GAI—glycoacidometric index; significance level * <span class="html-italic">p</span> &lt; 0.05.</p>
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23 pages, 4442 KiB  
Article
Biotechnological Phytocomplex of Zanthoxylum piperitum (L.) DC. Enhances Collagen Biosynthesis In Vitro and Improves Skin Elasticity In Vivo
by Giovanna Rigillo, Giovanna Pressi, Oriana Bertaiola, Chiara Guarnerio, Matilde Merlin, Roberto Zambonin, Stefano Pandolfo, Angela Golosio, Francesca Masin, Fabio Tascedda, Marco Biagi and Giulia Baini
Pharmaceutics 2025, 17(1), 138; https://doi.org/10.3390/pharmaceutics17010138 - 20 Jan 2025
Viewed by 692
Abstract
Background: Zanthoxylum piperitum (L.) DC., commonly known as Japanese pepper, is a deciduous shrub native to East Asia. Its berries are widely used as a spice, known for imparting a distinctive, tingly numbing sensation. Biologically, Z. piperitum has antimicrobial, antioxidant, and anti-inflammatory [...] Read more.
Background: Zanthoxylum piperitum (L.) DC., commonly known as Japanese pepper, is a deciduous shrub native to East Asia. Its berries are widely used as a spice, known for imparting a distinctive, tingly numbing sensation. Biologically, Z. piperitum has antimicrobial, antioxidant, and anti-inflammatory properties, and it is studied for its potential benefits in pain relief and digestive health. This study proposed a novel biotechnological Z. piperitum phytocomplex (ZPP) obtained by plant cell culture for skin health, specifically targeting collagen synthesis, extracellular matrix stability, and resilience against cellular stress. Given the bioactivity of Z. piperitum, we aimed to analyze its efficacy as a sustainable alternative for skin-supportive applications in cosmetics and supplements. Methods: ZPP was produced through stable plant cell cultures, yielding a lignan-rich (3.02% w/w) phytocomplex. Human fibroblasts (HFFs) were treated with varying ZPP concentrations to assess cellular viability, collagen metabolism, and ECM-related enzyme activities, both under normal and cell stress conditions. The in vivo assessment was performed by measuring biophysical skin parameters such as hydration, elasticity, and roughness in female volunteers for a period of six weeks. Results: In vitro, ZPP exhibited non-cytotoxicity at all concentrations tested. Under hyperosmotic stress, ZPP reduced cellular damage, suggesting enhanced resilience. ZPP upregulated lysyl oxidase (LOX) protein levels, critical for collagen cross-linking and ECM stability, with protective effects observed under oxidative/inflammatory conditions. Additionally, ZPP selectively inhibited collagenase, attenuating collagen breakdown, though antioxidant activity was modest. In vivo evaluation highlighted improved skin hydration, elasticity, and roughness. Conclusions: ZPP shows promise as a biotechnological agent for skin health, particularly in supporting collagen integrity, ECM stabilization, and cellular resilience under stress. While further studies are needed to explore its full efficacy, especially for aging and environmentally stressed skin, these findings highlight ZPP’s potential as a new ingredient for cosmetic formulations aimed at skin care and the treatment of alterations caused by aging or environmental conditions. Full article
(This article belongs to the Special Issue Skin Care Products for Healthy and Diseased Skin)
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<p>(<b>A</b>) <span class="html-italic">Zanthoxylum piperitum</span> (L.) DC. cell culture maintained in solid ZP medium. (<b>B</b>) Optical images of <span class="html-italic">Z. piperitum</span> cells observed by AXIO-Imager A2 optical microscope (ZEISS) after staining with fluorescein diacetate. Scale bar: 50 µM.</p>
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<p>Representative UPLC chromatogram of <span class="html-italic">Zanthoxylum piperitum</span> (L.) DC. phytocomplex recorded at 270 nm. Retention time (RT) is indicated at each peak. Pinoresinol glucoside RT = 6.431 min.</p>
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<p>Cell viability analysis by CCK-8 assay on HFF cells treated with ZPP at concentrations of 1, 10, and 100 µg/mL for 24 h. Each column represents mean ± SD. Control cells (CTRL) were arbitrarily set to 1. Data were analyzed by one-way analysis of variance (ANOVA) followed by Dunnett’s post hoc multiple comparison: <span class="html-italic">p</span> &gt; 0.05 (n = 6).</p>
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<p>Cell viability analysis by CCK-8 assay on HFF cells pre-treated with ZPP at concentrations of 1, 10, and 100 µg/mL for 2 h then exposed to NaCl (500 mOsm) for 8 h. Each column represents mean ± SD. Control cells (CTRL) were arbitrarily set to 1. Data were analyzed by one-way ANOVA F(4,31) = 5.758; <span class="html-italic">p</span> = 0.0014, followed by Tukey’s post hoc multiple comparison: (a) <span class="html-italic">p</span> &lt; 0.01 vs. CTRL, (b) <span class="html-italic">p</span> &lt; 0.01 vs. NaCl (n = 6).</p>
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<p>Pro-collagen I (<b>A</b>) and elastin (<b>B</b>) levels measured by ELISA assay in HFF cells treated with ZPP at concentrations of 1, 10, and 100 µg/mL. Each column represents mean ± SD. Control cells (CTRL) were arbitrarily set to 1. Data were analyzed by one-way ANOVA followed by Dunnett’s post hoc multiple comparison: <span class="html-italic">p</span> &gt; 0.05. Pro-collagen I: F(3,13) = 2.046; <span class="html-italic">p</span> = 0.1571).Elastin: F(3,4) = 0.927; <span class="html-italic">p</span> = 0.5050. (n = 6).</p>
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<p>Analysis of MMP-1 (<b>A</b>) and TIMP-1 (<b>B</b>) protein levels by ELISA assay in HFF cell lysate after treatment with ZPP at the concentrations of 1, 10, and 100 µg/mL for 24 h. Data were analyzed using one-way ANOVA (MMP-1: F(3,7) = 0.340, <span class="html-italic">p</span> = 0.7978; TIMP-1: F(3,7) = 1.445, <span class="html-italic">p</span> = 0.3089) followed by Dunnett’s post hoc multiple comparison (<span class="html-italic">p</span> &gt; 0.05). Dosage of MMP-1 (<b>C</b>) and TIMP-1 (<b>D</b>) protein levels in HFF cell lysate after pre-treatment for 2 h with ZPP at the concentrations of 1, 10, and 100 µg/mL then exposed to MetPRED (100 µg/mL) for 6 h. One-way ANOVA (MMP-1: F(4,14) = 1.551, <span class="html-italic">p</span> = 0.2450; TIMP-1: F(4,13) = 2.795, <span class="html-italic">p</span> = 0.0709) followed by Tukey’s post hoc multiple comparison; (a) <span class="html-italic">p</span> &lt; 0.05 vs. CTRL, (n = 6). Data are expressed as mean ± SD. Control cells (CTRL) were arbitrarily set to 1.</p>
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<p>Protein levels of lysyl oxidase (LOX) enzyme measured by Western blot assay in HFF cell lysate after a 24 h-treatment with ZPP at the concentrations of 1, 10, and 100 µg/mL. (<b>A</b>) Quantification of mature protein form of LOX (30 KDa); (<b>B</b>) representative blot. Vinculin was used as loading control. Data are expressed as mean ± SD. One-way ANOVA (F(3,12) = 3.413, <span class="html-italic">p</span> = 0.0530) followed by Dunnett’s post hoc multiple comparison: (a) <span class="html-italic">p</span> &lt; 0.05 vs. CTRL (n = 4).</p>
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<p>Protein levels of lysyl oxidase (LOX) enzyme measured by Western blot assay in HFF cell lysate. Cells were pre-treated for 2 h with ZPP at concentrations of 1, 10, and 100 µg/mL then stimulated with (<b>A</b>) LPS (500 ng/mL) + H<sub>2</sub>O<sub>2</sub> (300 nM) or (<b>B</b>) MetPRED (100 µg/mL) for 6 h. Up: representative blot. Vinculin was used as loading control. Down: quantification of mature protein form of LOX (30 KDa). Data are expressed as mean ± SD. One-way ANOVA (LPS + H<sub>2</sub>O<sub>2</sub>: F(4,27) = 4.456, <span class="html-italic">p</span> = 0.0068; MetPRED: F(4,11) = 3.816, <span class="html-italic">p</span> = 0.0350) followed by Tukey’s post hoc multiple comparison: (a,e) <span class="html-italic">p</span> &lt; 0.05 vs. CTRL, (b,c,d) <span class="html-italic">p</span> &lt; 0.05 vs. LPS + H<sub>2</sub>O<sub>2</sub>, (f) <span class="html-italic">p</span> &lt; 0.05 vs. MetPRED (n = 4).</p>
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<p>Boxplot representing distribution of collected data concerning skin deep-hydration evaluation in ZPP-treated women (active product) compared to placebo counterpart (placebo product) after 6 weeks of treatment. Data were analyzed by Friedmann’s test followed by Wilcoxon’s signed rank test for paired data, with Holm’s correction for repeated data (n = 15 for each group).</p>
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<p>Boxplot representing distribution of collected data concerning skin elasticity evaluation in ZPP-treated women (active product) compared to placebo counterpart (placebo product) after 6 weeks of treatment. Data were analyzed by Friedmann’s test followed by Wilcoxon’s signed rank test for paired data, with Holm’s correction for repeated data (n = 15 for each group).</p>
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<p>Boxplot representing distribution of data concerning skin roughness evaluation collected from the comparison between ZPP-treated group (active product) and placebo group (placebo product) after 6 weeks of treatment. Data are expressed as Ra (average value of all deviations from a straight line). Data were analyzed by Friedmann’s test followed by Wilcoxon’s signed rank test for paired data, with Holm’s correction for repeated data (n = 15 for each group).</p>
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<p>Representative images collected from the central area of the décolleté of a subject by using the Antera 3D system at different analysis time points: T0 = starting time; T4 = 4 weeks after treatment; T6 = 6 weeks after treatment. A false-color map is used to identify areas with skin roughness, where red and yellow colors represent depressed areas, and blue and purple colors represent elevated areas.</p>
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29 pages, 2118 KiB  
Review
Dietary Interventions, Supplements, and Plant-Derived Compounds for Adjunct Vitiligo Management: A Review of the Literature
by Michael J. Diaz, Jasmine T. Tran, Drake Rose, Aria Wei, Deepak Lakshmipathy and Shari R. Lipner
Nutrients 2025, 17(2), 357; https://doi.org/10.3390/nu17020357 - 20 Jan 2025
Viewed by 746
Abstract
Vitiligo is a chronic autoimmune pigmentation disorder shaped by a complex interplay of genetic predispositions and environmental triggers. While conventional therapies—phototherapy, corticosteroids, and immunosuppressants—can be effective, their benefits are often partial and temporary, with recurrence common once treatment stops. As such, there is [...] Read more.
Vitiligo is a chronic autoimmune pigmentation disorder shaped by a complex interplay of genetic predispositions and environmental triggers. While conventional therapies—phototherapy, corticosteroids, and immunosuppressants—can be effective, their benefits are often partial and temporary, with recurrence common once treatment stops. As such, there is increasing interest in exploring complementary approaches that may offer a more sustainable impact. Emerging evidence suggests that macronutrient and micronutrient-level changes could be beneficial for managing progression and, in some cases, facilitating repigmentation. Antioxidant-rich foods, such as apples, green tea, Indian gooseberry, onions, and peppers, may help mitigate oxidative stress, while inflammatory foods, such as gluten and high-phenol nuts and berries, may exacerbate the condition. Certain supplements, including high-dose vitamin D, vitamin C, vitamin E, and selenium, may enhance phototherapy outcomes. Omega-3 and other unsaturated fatty acids, in addition to prebiotics and probiotics, are under active investigation for their roles in gut health and immune regulation. Notably, plant-derived compounds, i.e., Ginkgo biloba, have demonstrated promise in promoting repigmentation and managing disease progression. However, it must be emphasized that these nutritional interventions remain exploratory, and more research is needed to establish their efficacy, safety, and optimal usage before they can be recommended as part of a standard treatment regimen. Full article
(This article belongs to the Special Issue Relationships between Dietary Factors and Inflammatory Skin Diseases)
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<p>Illustration of nutrients and micronutrients with studied implications for vitiligo progression and management.</p>
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<p>The convergence theory for vitiligo. Adapted from [<a href="#B21-nutrients-17-00357" class="html-bibr">21</a>].</p>
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<p>Chemical structures of plant-derived compounds with promise for vitiligo management. Flavonoids: (<b>AA</b>) Baicalein, (<b>AB</b>) Quercetin, (<b>AC</b>) Kaempferol, (<b>AD</b>) Apigenin, (<b>AE</b>) Galangin, (<b>AF</b>) Naringenin, (<b>AG</b>) Hesperetin, (<b>AH</b>) Afzelin, (<b>AI</b>) Fisetin, (<b>AJ</b>) Puerarin, (<b>AK</b>) Butin, (<b>AL</b>) Liquiritin, (<b>AM</b>) Liquiritigenin, (<b>AN</b>) Vitexin, (<b>AO</b>) Hyperoside, and (<b>AP</b>) Baicalin; phenolic compounds: (<b>BA</b>) EGCG, (<b>BB</b>) Cannabidiol, (<b>BC</b>) 1,5-dicQA, (<b>BD</b>) 3,5-diCQA, (<b>BE</b>) 3,5-diCQM, (<b>BF</b>) Maclurin, (<b>BG</b>) Rosmarinic acid, (<b>BH</b>) Paeonol, (<b>BI</b>) 6-Shogaol, (<b>BJ</b>) Morin, (<b>BK</b>) Ellagic acid, and (<b>BL</b>) Curcumin; coumarins: (<b>CA</b>) Psoralidin, (<b>CB</b>) Isofraxidin, (<b>CC</b>) Scopoletin, (<b>CD</b>) 7-isopentenyloxycoumarin, and (<b>CE</b>) Khellin; glycosides: (<b>DA</b>) Geniposide, (<b>DB</b>) C-3-G, (<b>DC</b>) THSG, (<b>DD</b>) Glycyrrhizin, (<b>DE</b>) Paeoniflorin, and (<b>DF</b>) Madecassoside; and other highlighted compounds: (<b>EA</b>) Piperine, (<b>EB</b>) Berberine, and (<b>EC</b>) Thymoquinone. Adapted from [<a href="#B153-nutrients-17-00357" class="html-bibr">153</a>].</p>
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