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  2. Fermented red ginseng extract improves sarcopenia-related muscle atrophy in old mice through regulation of muscle protein metabolism

Fermented red ginseng extract improves sarcopenia-related muscle atrophy in old mice through regulation of muscle protein metabolism

  • Food Sci Biotechnol. 2024 Sep 23;34(3):793-802. doi: 10.1007/s10068-024-01702-0.
Geon Oh 1 Xiao Men 1 Im-Joung La 2 Xionggao Han 1 Se-Jeong Lee 1 Ji-Hyun Im 1 Xiaolu Fu 1 June-Seok Lim 1 Kwi Sik Bae 3 Geum-Su Seong 4 Do-Sang Lee 2 Sun-Il Choi 1 Ok-Hwan Lee 1
Affiliations

Affiliations

  • 1 Department of Food Biotechnology and Environmental Science, Kangwon National University, Chuncheon, 24341 Korea.
  • 2 Atomy R&D Center, Gongju, 32511 Korea.
  • 3 F&B Bio Co., Ltd, Cheonan, 31005 Korea.
  • 4 Korea Food Research Institute, Wanju, 55365 Korea.
Abstract

This study investigated the potential ameliorative effects of fermented red ginseng (FRG) extract on sarcopenia-related muscle atrophy in old mice and elucidated the underlying mechanisms. Mice, aged five and twenty months, were divided into seven groups: young and old controls, and old mice treated with Schisandra chinensis extract (200 mg/kg/day), mixed ginsenosides (15 mg/kg/day), and FRG extract (50-200 mg/kg/day). Body weight and grip strength were assessed weekly. After six weeks of oral treatment, quadriceps, gastrocnemius, and soleus were photographed and weighed, and muscle fiber cross-sectional area was analyzed via hematoxylin-eosin staining. Additionally, the protein expression levels were measured using western blot analysis. FRG extract significantly improved muscle atrophy by activating the IGF-1/Akt/mTOR pathway, reducing degradation proteins FoxO3a, MuRF1, and Fbx32, and enhancing mitochondrial biogenesis-related proteins SIRT-1/PGC-1α. The findings suggest that FRG extract effectively mitigates age-related muscle atrophy through these molecular pathways, supporting its potential as a therapeutic agent for sarcopenia.

Keywords

Korean red ginseng; Mitochondrial biogenesis; Muscle atrophy; Muscle protein degradation; Muscle protein synthesis.

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