Your new experience awaits. Try the new design now and help us make it even better

REVIEW article

Front. Med.

Sec. Geriatric Medicine

This article is part of the Research TopicInterdisciplinary Insights Into Musculoskeletal Aging: Mechanisms and InterventionsView all 5 articles

The role of AGEs in skeletal muscle atrophy and the beneficial effects of exercise

Provisionally accepted
心茹  武心茹 武1,2Shuai  HuShuai Hu2,3Wei  MiaoWei Miao4Fei  ShenFei Shen2,3Li  JiangLi Jiang1*
  • 1Department of Internal Medicine, Kunshan Hospital of Integrated Traditional Chinese and Western Medicine, SUZHOU, China
  • 2Sports and Health Collaborative Innovation Center for Fitness Promotion, Jiangsu Normal University, XUZHOU, China
  • 3Institute of Physical Education, Jiangsu Normal University, XUZHOU, China
  • 4Department of Internal Medicine, Taicang Hospital of Traditional Chinese Medicine, SUZHOU, China

The final, formatted version of the article will be published soon.

Background: Advanced Glycation End Products (AGEs) are associated with the aging and atrophy of skeletal muscle. Their pathogenic mechanism mainly involves the binding of AGEs to their own receptors, which in turn triggers a series of pathological reactions. Exercise is considered an effective intervention method, as it can regulate the level of AGEs, thereby alleviating skeletal muscle atrophy. Objective: This study aims to review the latest research progress on skeletal muscle atrophy induced by AGEs and the beneficial effects of exercise. Methods: Relevant literature was searched from the establishment of databases (PubMed, Web of Science, Embase, and Scopus) to May 2025. The search terms were: "advanced glycation end products, receptor for advanced glycation end products, skeletal muscle, skeletal muscle atrophy, sarcopenia, aging, diabetes mellitus, obesity, exercise, aerobic training, resistance training, high-intensity interval training". Literature was included based on the following criteria: (a) Studies focusing on the mechanism of skeletal muscle atrophy induced by AGEs and the content related to exercise regulating AGEs levels; (b) Priority was given to literature published in the past 5 years with outstanding quality, relevance, or innovation. Finally, 138 pieces of literature were included for the review. Results and Conclusions: AGEs bind to the receptor for advanced glycation end products (RAGE), which leads to a decrease in muscle protein synthesis, an increase in protein degradation, impairment of muscle fiber regeneration ability, and aggravation of myocyte apoptosis, thereby inducing or exacerbating skeletal muscle atrophy. Exercise can reduce the harmful effects of AGEs on muscle mass. Specifically, exercise can reduce the formation of AGEs by improving insulin sensitivity and glucose utilization, as well as alleviating chronic inflammation and oxidative stress. Additionally, exercise enhances the metabolic capacity of the kidneys for AGEs. These findings provide new insights for the development of drug regimens targeting the "AGEs-RAGE" axis and exercise interventions. In the future, in-depth clarification of the role of AGEs in the pathogenesis of skeletal muscle atrophy and the improvement mechanism mediated by exercise will provide an important basis for the prevention and treatment of sarcopenia related to aging and metabolic disorders.

Keywords: skeletal muscle atrophy, advanced glycation end-products, AGEs-RAGE signaling axis, Aging, Inflammation, Oxidative Stress, Mitochondria, Exercise

Received: 11 May 2025; Accepted: 02 Dec 2025.

Copyright: © 2025 武, Hu, Miao, Shen and Jiang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Li Jiang

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.