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Cascara as a source of bioactive phenolic acids with antioxidant capacity to regulate intestinal functionality Wang, Xiwen Stephen
Abstract
Coffee cascara, the dried skin of coffee cherries, is a by-product rich in polyphenols but remains underutilized. While this waste product contains potent bioactives, the actual antioxidant activity and importance to intestinal function are less studied. This study analyzed twelve cascara samples from seven countries for polyphenol content using high-performance liquid chromatography (HPLC). Antioxidant capacity of selected extracts was assessed with ABTS, ORAC assays, and cell-based assays (MTT and DCFHDA) in differentiated Caco-2 cells to measure cell viability and oxidative stress modulation. Fortification of these extracts with gallic acid (GA) and protocatechuic acid (PCA) was used to investigate their impact on the antioxidant response of the cascara matrix. Chemical attributes, such as total phenol content and H₂O₂ production, were correlated with biological antioxidant capacity and intracellular NRF2 expression, a key oxidative stress regulator measured using western blot, ELISA, and qRT-PCR. Intestinal barrier integrity was evaluated through TEER measurements, tight junction protein staining, qRT-PCR, and western blot. The results showed significant variation in polyphenol profiles among the samples, with higher antioxidant activities linked to elevated PCA and GA levels, in particular. Chemical antioxidant capacity did not always match biological results, but a significant correlation was found between H₂O₂ production derived from cascara samples and biological ROS inhibition (p<0.05). Fortification with PCA and GA significantly impacted antioxidant activity only at higher concentrations, suggesting interactions within the cascara matrix may limit phenolic acid bioaccessibility at lower concentrations. Cascara extracts also improved intestinal barrier integrity, which was attributed to NRF2 activation, linked to aquaporin-3-mediated H₂O₂ transport. GA fortification resulted in greater NRF2 upregulation compared to PCA (p<0.05), likely due to higher H₂O₂ production. This study demonstrates, for the first time, that cascara extracts can protect intestinal cells to some degree from oxidative damage and protect barrier function via NRF2 activation, and that fortifying the cascara extract with GA enhanced its antioxidant activity. These findings support the revalorization of coffee by-products as functional food ingredients, offering potential health benefits and contributing to waste reduction in coffee production. Future research can focus on polyphenol interactions in other food matrix and their influence on biological redox status.
Item Metadata
Title |
Cascara as a source of bioactive phenolic acids with antioxidant capacity to regulate intestinal functionality
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Creator | |
Supervisor | |
Publisher |
University of British Columbia
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Date Issued |
2024
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Description |
Coffee cascara, the dried skin of coffee cherries, is a by-product rich in polyphenols but remains underutilized. While this waste product contains potent bioactives, the actual antioxidant activity and importance to intestinal function are less studied. This study analyzed twelve cascara samples from seven countries for polyphenol content using high-performance liquid chromatography (HPLC). Antioxidant capacity of selected extracts was assessed with ABTS, ORAC assays, and cell-based assays (MTT and DCFHDA) in differentiated Caco-2 cells to measure cell viability and oxidative stress modulation. Fortification of these extracts with gallic acid (GA) and protocatechuic acid (PCA) was used to investigate their impact on the antioxidant response of the cascara matrix. Chemical attributes, such as total phenol content and H₂O₂ production, were correlated with biological antioxidant capacity and intracellular NRF2 expression, a key oxidative stress regulator measured using western blot, ELISA, and qRT-PCR. Intestinal barrier integrity was evaluated through TEER measurements, tight junction protein staining, qRT-PCR, and western blot. The results showed significant variation in polyphenol profiles among the samples, with higher antioxidant activities linked to elevated PCA and GA levels, in particular. Chemical antioxidant capacity did not always match biological results, but a significant correlation was found between H₂O₂ production derived from cascara samples and biological ROS inhibition (p<0.05). Fortification with PCA and GA significantly impacted antioxidant activity only at higher concentrations, suggesting interactions within the cascara matrix may limit phenolic acid bioaccessibility at lower concentrations. Cascara extracts also improved intestinal barrier integrity, which was attributed to NRF2 activation, linked to aquaporin-3-mediated H₂O₂ transport. GA fortification resulted in greater NRF2 upregulation compared to PCA (p<0.05), likely due to higher H₂O₂ production. This study demonstrates, for the first time, that cascara extracts can protect intestinal cells to some degree from oxidative damage and protect barrier function via NRF2 activation, and that fortifying the cascara extract with GA enhanced its antioxidant activity. These findings support the revalorization of coffee by-products as functional food ingredients, offering potential health benefits and contributing to waste reduction in coffee production. Future research can focus on polyphenol interactions in other food matrix and their influence on biological redox status.
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Genre | |
Type | |
Language |
eng
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Date Available |
2024-12-23
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Provider |
Vancouver : University of British Columbia Library
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Rights |
Attribution-NonCommercial-NoDerivatives 4.0 International
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DOI |
10.14288/1.0447611
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URI | |
Degree | |
Program | |
Affiliation | |
Degree Grantor |
University of British Columbia
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Graduation Date |
2025-05
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Campus | |
Scholarly Level |
Graduate
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Rights URI | |
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DSpace
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Rights
Attribution-NonCommercial-NoDerivatives 4.0 International