Department of Biomedical Science & BK21 Four NBM Global Research Center for Regenerative Medicine, Dankook University, Cheonan 31116, Chungnam, Republic of Korea.
Institute of Pharmaceutical Research and Development, College of Pharmacy, Wonkwang University, Iksan 54538, Jeonbuk, Republic of Korea.
Nutrients. 2024 Jan 3;16(1):157. doi: 10.3390/nu16010157.
The investigation focused on the impact of (ashwagandha) extract (WSE) on age-related mechanisms affecting skeletal muscle sarcopenia-related muscle atrophy in aged mice. Beyond evaluating muscular aspects, the study explored chronic low-grade inflammation, muscle regeneration, and mitochondrial biogenesis. WSE administration, in comparison to the control group, demonstrated no significant differences in body weight, diet, or water intake, affirming its safety profile. Notably, WSE exhibited a propensity to reduce epidermal and abdominal fat while significantly increasing muscle mass at a dosage of 200 mg/kg. The muscle-to-fat ratio, adjusted for body weight, increased across all treatment groups. WSE administration led to a reduction in the pro-inflammatory cytokines TNF-α and IL-1β, mitigating inflammation-associated muscle atrophy. In a 12-month-old mouse model equivalent to a 50-year-old human, WSE effectively preserved muscle strength, stabilized grip strength, and increased muscle tissue weight. Positive effects were observed in running performance and endurance. Mechanistically, WSE balanced muscle protein synthesis/degradation, promoted fiber differentiation, and enhanced mitochondrial biogenesis through the IGF-1/Akt/mTOR pathway. This study provides compelling evidence for the anti-sarcopenic effects of WSE, positioning it as a promising candidate for preventing sarcopenia pending further clinical validation.
本研究聚焦于(印度人参)提取物(WSE)对与年龄相关的机制的影响,这些机制影响与骨骼肌减少症相关的肌肉萎缩。除了评估肌肉方面,该研究还探讨了慢性低度炎症、肌肉再生和线粒体生物发生。与对照组相比,WSE 给药在体重、饮食或水摄入方面没有显著差异,证实了其安全性。值得注意的是,WSE 在 200mg/kg 的剂量下表现出减少表皮和腹部脂肪的倾向,同时显著增加肌肉质量。所有治疗组的肌肉与脂肪比(按体重调整)均增加。WSE 给药可降低促炎细胞因子 TNF-α 和 IL-1β,减轻与炎症相关的肌肉萎缩。在相当于 50 岁人类的 12 个月大的小鼠模型中,WSE 有效保持肌肉力量,稳定握力,并增加肌肉组织重量。在跑步表现和耐力方面观察到积极的影响。从机制上讲,WSE 平衡肌肉蛋白的合成/降解,通过 IGF-1/Akt/mTOR 途径促进纤维分化和增强线粒体生物发生。这项研究为 WSE 的抗肌肉减少症效应提供了有力证据,使其成为预防肌肉减少症的有前途的候选药物,有待进一步的临床验证。