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Diosgenin Attenuates Myocardial Cell Apoptosis Triggered by Oxidative Stress through Estrogen Receptor to Activate the PI3K/Akt and ERK Axes.

Authors :
Chen, Michael Yu-Chih
Tsai, Bruce Chi-Kang
Kuo, Wei-Wen
Kuo, Chia-Hua
Lin, Yueh-Min
Hsieh, Dennis Jine-Yuan
Pai, Pei-Ying
Liao, Shih-Chieh
Huang, Shang-En
Lee, Shin-Da
Huang, Chih-Yang
Source :
American Journal of Chinese Medicine; 2023, Vol. 51 Issue 5, p1211-1232, 22p
Publication Year :
2023

Abstract

Cardiovascular diseases in post-menopausal women are on a rise. Oxidative stress is the main contributing factor to the etiology and pathogenesis of cardiovascular diseases. Diosgenin, a member of steroidal sapogenin, is structurally similar to estrogen and has been shown to have antioxidant effects. Therefore, we aimed to investigate the effects of diosgenin in preventing oxidation-induced cardiomyocyte apoptosis and assessed its potential as a substitute substance for estrogen in post-menopausal women. Apoptotic pathways and mitochondrial membrane potential were measured in H9c2 cardiomyoblast cells and neonatal cardiomyocytes treated with diosgenin for 1 h prior to hydrogen peroxide (H<subscript>2</subscript>O<subscript>2</subscript>) stimulation. H<subscript>2</subscript>O<subscript>2</subscript>-stimulated H9c2 cardiomyoblast cells displayed cytotoxicity and apoptosis via the activation of both Fas-dependent and mitochondria-dependent pathways. Additionally, it led to the instability of the mitochondrial membrane potential. However, the H<subscript>2</subscript>O<subscript>2</subscript>-induced H9c2 cell apoptosis was rescued by diosgenin through IGF1 survival pathway activation. This led to the recovery of the mitochondrial membrane potential by suppressing the Fas-dependent and mitochondria-dependent apoptosis. Diosgenin also inhibited H<subscript>2</subscript>O<subscript>2</subscript>-induced cytotoxicity and apoptosis through the estrogen receptor interaction with PI3K/Akt and extracellular regulated protein kinases 1/2 activation in myocardial cells. In this study, we confirmed that diosgenin attenuated H<subscript>2</subscript>O<subscript>2</subscript>-induced cytotoxicity and apoptosis through estrogen receptors-activated phosphorylation of PI3K/Akt and ERK signaling pathways in myocardial cells via estrogen receptor interaction. All results suggest that H<subscript>2</subscript>O<subscript>2</subscript>-induced myocardial damage is reduced by diosgenin due to its interaction with estrogen receptors to decrease the damage. Herein, we conclude that diosgenin might be a potential substitute substance for estrogen in post-menopausal women to prevent heart diseases. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0192415X
Volume :
51
Issue :
5
Database :
Complementary Index
Journal :
American Journal of Chinese Medicine
Publication Type :
Academic Journal
Accession number :
165476419
Full Text :
https://doi.org/10.1142/S0192415X23500556