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Diosgenin Attenuates Myocardial Cell Apoptosis Triggered by Oxidative Stress through Estrogen Receptor to Activate the PI3K/Akt and ERK Axes.
- 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]
- Subjects :
- CARDIOVASCULAR disease prevention
HEART metabolism
HEART cells
MYOCARDIUM
ONCOGENES
CARDIOMYOPATHIES
APOPTOSIS
ESTROGEN
ORGANIC compounds
OXIDATIVE stress
ESTROGEN receptors
COMPARATIVE studies
POSTMENOPAUSE
DESCRIPTIVE statistics
PHYTOSTEROLS
CELL surface antigens
HYDROGEN peroxide
IMMUNODIAGNOSIS
PHOSPHORYLATION
Subjects
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