4.7 Article

Radical Scavenging and Cellular Antioxidant Activity of the Cocoa Shell Phenolic Compounds after Simulated Digestion

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ANTIOXIDANTS
卷 12, 期 5, 页码 -

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MDPI
DOI: 10.3390/antiox12051007

关键词

cocoa shell; cocoa by-products; in vitro digestion; phenolic compounds; oxidative stress; antioxidant capacity; radical scavenging; reactive oxygen species; antioxidant enzymes

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The digestion process can modify the bioaccessibility, bioavailability, and bioactivity of phenolic compounds found in cocoa shell, a by-product of the cocoa industry. This study assessed the influence of simulated gastrointestinal digestion on the concentration of phenolic compounds in cocoa shell flour and extract, as well as their antioxidant activity in intestinal epithelial and hepatic cells. The results showed that gastrointestinal digestion increased the antioxidant capacity of cocoa shell and exhibited free radical scavenging capacity. The cocoa shell did not show cytotoxicity and effectively countered oxidative stress in both cell lines, suggesting its potential as a functional food ingredient.
The cocoa industry generates a considerable quantity of cocoa shell, a by-product with high levels of methylxanthines and phenolic compounds. Nevertheless, the digestion process can extensively modify these compounds' bioaccessibility, bioavailability, and bioactivity as a consequence of their transformation. Hence, this work's objective was to assess the influence of simulated gastrointestinal digestion on the concentration of phenolic compounds found in the cocoa shell flour (CSF) and the cocoa shell extract (CSE), as well as to investigate their radical scavenging capacity and antioxidant activity in both intestinal epithelial (IEC-6) and hepatic (HepG2) cells. The CSF and the CSE exhibited a high amount of methylxanthines (theobromine and caffeine) and phenolic compounds, mainly gallic acid and (+)-catechin, which persisted through the course of the simulated digestion. Gastrointestinal digestion increased the antioxidant capacity of the CSF and the CSE, which also displayed free radical scavenging capacity during the simulated digestion. Neither the CSF nor the CSE exhibited cytotoxicity in intestinal epithelial (IEC-6) or hepatic (HepG2) cells. Moreover, they effectively counteracted oxidative stress triggered by tert-butyl hydroperoxide (t-BHP) while preventing the decline of glutathione, thiol groups, superoxide dismutase, and catalase activities in both cell lines. Our study suggests that the cocoa shell may serve as a functional food ingredient for promoting health, owing to its rich concentration of antioxidant compounds that could support combating the cellular oxidative stress associated with chronic disease development.

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