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Protective Effects of Ginsenosides (20 R )‐Rg3 on H 2 O 2 ‐Induced Myocardial Cell Injury by Activating Keap‐1/Nrf2/HO‐1 Signaling Pathway
Author(s) -
Zhao Yan,
Wang Yu,
Zhang Min,
Gao Yugang,
Yan Zhaowei
Publication year - 2021
Publication title -
chemistry and biodiversity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 70
eISSN - 1612-1880
pISSN - 1612-1872
DOI - 10.1002/cbdv.202001007
Subject(s) - ginsenoside , chemistry , ginseng , oxidative stress , pharmacology , activator (genetics) , cell , biochemistry , receptor , medicine , alternative medicine , pathology
Ginsenosides (20 S )‐Rg3 and (20 R )‐Rg3 are famous rare ginsenosides from red ginseng, and their configurations in C‐20 are different. This study aimed to investigate the protective mechanism of ginsenosides (20 S )‐Rg3 and (20 R )‐Rg3 on H 2 O 2 ‐induced H9C2 cells and compare their activity. The results showed that the ginsenosides (20 S )‐Rg3 and (20 R )‐Rg3 could increase the cell activity and the levels of GSH‐Px, SOD and CAT, and decrease activities of LDH, MDA and ROS. Further studies showed that ginsenosides (20 S )‐Rg3 and (20 R )‐Rg3 could prevent oxidative stress injury of H9C2 cells by H 2 O 2 through the Keap‐1/Nrf2/HO‐1 pathway. But the ML385 counteracts these effects. Interestingly, among these results, ginsenoside (20 R )‐Rg3 was superior to (20 S )‐Rg3, indicating that ginsenoside (20 R )‐Rg3 have a stronger effect of antioxidative stress. This study reflected that ginsenoside (20 R )‐Rg3 could be used as a potential Nrf2 activator and a safe effective Chinese herbal monomer in the treatment of cardiovascular disease.

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