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Ginsenoside Rb1 prevents age-related endothelial senescence by modulating SIRT1/caveolin-1/enos signaling pathway
Bin Zhou1, Guangyao Sh1, Dongmei Xie1
1The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Heliyon
|February 7, 2024
Summary
Ginsenoside Rb1 (g-Rb1) from Panax ginseng prevents cellular aging in blood vessels. This study reveals g-Rb1 modulates the SIRT1/caveolin-1/eNOS pathway to reduce endothelial senescence and enhance vascular function.
Area of Science:
- Cardiovascular Pharmacology
- Gerontology
- Molecular Biology
Background:
- Aging is a major risk factor for cardiovascular diseases.
- Ginseng, a traditional Chinese medicine, is known for its health benefits.
- Ginsenoside Rb1 (g-Rb1), a key compound from Panax ginseng, shows potential anti-senescence properties.
Purpose of the Study:
- To investigate the precise mechanisms by which g-Rb1 influences the SIRT1/eNOS pathway.
- To explore the vascular pharmacological activity of g-Rb1 in preventing endothelial senescence.
Main Methods:
- Human primary umbilical vein endothelial cells (HUVECs) were used to model replicative aging.
- Techniques included RT-PCR, western blotting, siRNA, and immunoprecipitation.
- The study focused on the impact of g-Rb1 on the SIRT1/caveolin-1/eNOS signaling axis.
Main Results:
- G-Rb1 increased nitric oxide (NO) production and reduced endothelial cell senescence.
- g-Rb1 elevated SIRT1 and eNOS expression while decreasing caveolin-1.
- Modulation of SIRT1, eNOS, and caveolin-1 by g-Rb1 affected cellular senescence and NO production.
Conclusions:
- Ginsenoside Rb1 (g-Rb1) effectively prevents age-related endothelial senescence.
- This protective effect is mediated through the modulation of the SIRT1/caveolin-1/eNOS signaling pathway.
- g-Rb1 demonstrates potential for clinical application in managing vascular aging.
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