化学
氧化应激
过氧化氢
活性氧
酶
抗氧化剂
体内
生物化学
多酚
氧化磷酸化
代谢物
KEAP1型
生物
基因
转录因子
生物技术
作者
Xiaowen Chang,Shan Dong,Wenliang Bai,Yan Di,Ruijuan Gu,Fuguo Liu,Beita Zhao,Yutang Wang,Xuebo Liu
标识
DOI:10.1021/acs.jafc.0c07521
摘要
-induced oxidative stress damage in HepG2 cells and compared to CA. The results indicated that both M1 and M2 had better antioxidant capacities than CA by increasing cell viability, improving mitochondrial function, and balancing cellular redox status. These compounds also prevented oxidative stress by mediating the Keap1/Nrf2 transcriptional pathway and downregulating enzyme activity. The current research indicates that the methylated metabolites of CA could potentially be the candidates that are responsible for the biological efficacies attributed to CA.
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