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Ginsenoside Rb1 attenuates age-associated cognitive impairment by modulating oxidative stress and the SIRT1/eNOS/NO
Bin Zhou1, Lin Wu1, Dinghui Liu1
1The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Journal of Ginseng Research
|November 21, 2025
Summary
Ginsenoside Rb1 (Rb1) treatment in mice reduced aging symptoms by improving cognitive function and decreasing oxidative stress. This anti-aging effect is linked to the modulation of the Sirtuin 1 (SIRT1)/eNOS/Nitric Oxide (NO) pathway.
Area of Science:
- Gerontology
- Pharmacology
- Molecular Biology
Background:
- Ginsenoside Rb1 (Rb1), a compound from traditional Chinese medicine, is known to combat oxidative stress, autophagy, and apoptosis.
- The specific role of Rb1 in the natural aging process has not been previously elucidated.
Purpose of the Study:
- To investigate the effects of Rb1 on the natural aging process in mice.
- To explore the potential molecular mechanisms underlying Rb1's anti-aging properties.
Main Methods:
- Middle-aged and aged mice were treated with low or high doses of Rb1 for eight weeks.
- Changes in body weight, spatial learning, and brain tissue senescence were assessed.
- Oxidative stress markers, nitric oxide (NO) levels, and inflammatory markers (TNF-α, IL-6) were measured in serum and hippocampal tissue.
- Sirtuin 1 (SIRT1) protein expression was analyzed to identify key pathways.
Main Results:
- Rb1 treatment significantly mitigated age-related physiological decline, including weight loss and cognitive impairment.
- Mice receiving Rb1 exhibited reduced oxidative stress, evidenced by lower malondialdehyde (MDA) and higher superoxide dismutase (SOD) activity.
- Rb1 administration increased nitric oxide (NO) levels and enhanced Sirtuin 1 (SIRT1) protein expression, while reducing pro-inflammatory cytokines like TNF-α and IL-6.
Conclusions:
- Rb1 effectively delays the aging process in mice by alleviating oxidative stress and inflammation.
- The anti-aging benefits of Rb1 are associated with the modulation of the SIRT1/eNOS/NO signaling pathway.
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