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Evaluation of Injury-induced Senescence and In Vivo Reprogramming in the Skeletal Muscle
Published on: October 26, 2017
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Ginsenoside Rg1 supplementation clears senescence-associated β-galactosidase in exercising human skeletal muscle
Jinfu Wu1, Suchada Saovieng1, I-Shiung Cheng2
1Laboratory of Exercise Biochemistry, University of Taipei, Taipei, Taiwan.
Journal of Ginseng Research
|November 8, 2019
Summary
Ginsenoside Rg1 supplementation eliminated senescent cells in exercising muscle, improving endurance performance. This study investigated Rg1
Area of Science:
- Exercise physiology
- Cellular senescence
- Nutritional supplementation
Background:
- Senescence-associated beta-galactosidase (SA-β-gal) is a marker of cellular senescence.
- Ginsenoside Rg1 has cleared SA-β-gal in cultured cells.
- The effect of Rg1 on SA-β-gal in exercising human skeletal muscle is unknown.
Purpose of the Study:
- To investigate the effect of Rg1 supplementation on SA-β-gal in exercising human skeletal muscle.
- To assess the impact of Rg1 on exercise performance and muscle recovery.
Main Methods:
- A randomized, double-blind, placebo-controlled crossover study.
- 12 young men received placebo or 5 mg Rg1 1 hour before high-intensity cycling (70% VO2max).
- Muscle biopsies were collected pre- and post-exercise (0h and 3h).
- A separate group of 12 participants performed a time-to-exhaustion cycling test (80% VO2max).
Main Results:
- Rg1 supplementation led to the complete elimination of SA-β-gal in 9 out of 12 participants' exercised muscle post-cycling (p < 0.05).
- Both groups showed increased apoptotic DNA fragmentation and CD68+ immediately after cycling.
- During 3-hour recovery, Rg1 group exhibited reduced apoptotic nuclei and increased inducible nitric oxide synthase and interleukin 6 mRNA levels (p < 0.01).
Conclusions:
- Rg1 supplementation effectively eliminates senescent cells in exercising human skeletal muscle.
- Rg1 improves high-intensity endurance performance and aids muscle recovery.

