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Ginsenoside Rb1 attenuates arterial aging by reducing DNA damage in aged mice
Qi Si1, Lin Wu1, Ximei Zhang1
1Department of Cardiology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Experimental Gerontology
|December 24, 2025
Summary
Ginsenoside Rb1 (Rb1) treatment in aged mice improved aortic structure and biomechanical function by reducing DNA damage and apoptosis. This suggests Rb1 has therapeutic potential for delaying vascular aging and related cardiovascular diseases.
Area of Science:
- Cardiovascular Research
- Aging Biology
- Pharmacology
Background:
- Vascular aging is a major risk factor for cardiovascular diseases, characterized by structural and functional decline.
- The precise molecular mechanisms behind age-associated vascular deterioration remain incompletely understood.
- Ginsenoside Rb1 (Rb1), a key compound in ginseng, shows promise for anti-aging effects.
Purpose of the Study:
- To evaluate the protective effects of Rb1 on the aorta of aged mice.
- To elucidate the molecular mechanisms underlying Rb1's action against vascular aging.
- To provide evidence for Rb1 as a potential natural therapeutic agent for vascular aging.
Main Methods:
- Aged mice received Rb1 or PBS injections for 6 weeks; young mice served as controls.
- Aortic tissues were analyzed via histomorphology, nanoscale biomechanics (AFM), and senescence/apoptosis/DNA damage markers (P21, SA-β-gal, TUNEL, γ-H2AX).
Main Results:
- Rb1 treatment improved aortic structural remodeling and restored smooth muscle cell alignment and extracellular matrix.
- Atomic Force Microscopy revealed Rb1 ameliorated age-induced impairments in aortic nanobiomechanical properties.
- Rb1 significantly reduced DNA damage marker γ-H2AX, P21 expression, SA-β-gal positivity, and apoptosis (TUNEL), delaying vascular aging.
Conclusions:
- Rb1 effectively attenuates DNA damage, structural remodeling, and biomechanical dysfunction in the aging aorta.
- Rb1 delays vascular aging and apoptosis, likely by targeting DNA damage pathways.
- Rb1 demonstrates significant therapeutic potential for combating age-related aortic impairments.
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