Role of GLP‑1 receptor agonists in sepsis and their therapeutic potential in sepsis‑induced muscle atrophy (Review)

Xuan Zhao, Yukun Liu, Dongfang Wang, Tonghan Li, Zhikai Xu, Zhanfei Li, Xiangjun Bai, Yuchang Wang

Research output: Contribution to journalReview articlepeer-review

1 Scopus citations

Abstract

Sepsis‑induced myopathy (SIM) is a common complication in intensive care units, which is often associ‑ ated with adverse outcomes, primarily manifested as skeletal muscle weakness and atrophy. Currently, the management of SIM focuses on prevention strategies, as effective therapeutic options remain elusive. Glucagon‑like peptide‑1 (GLP‑1) receptor agonists (GLP‑1RAs) have garnered attention as hypo‑ glycemic and weight‑loss agents, with an increasing body of research focusing on the extrapancreatic effects of GLP‑1. In preclinical settings, GLP‑1RAs exert protective effects against sepsis‑related multiple organ dysfunction through anti‑inflam‑ matory and antioxidant mechanisms. Based on the existing research, we hypothesized that GLP‑1RAs may serve potential protective roles in the repair and regeneration of skeletal muscle affected by sepsis. The present review aimed to explore the relationship between GLP‑1RAs and sepsis, as well as their impact on muscle atrophy‑related myopathy. Furthermore, the potential mechanisms and therapeutic benefits of GLP‑1RAs are discussed in the context of muscle atrophy induced by sepsis.

Original languageEnglish
Article number74
JournalInternational Journal of Molecular Medicine
Volume55
Issue number5
DOIs
StatePublished - May 2025

Bibliographical note

Publisher Copyright:
Copyright © 2025 Zhao et al.

Keywords

  • glucagon‑like peptide‑1 receptor
  • intensive care unit‑acquired weakness
  • sepsis‑induced myopathy
  • skeletal muscle atrophy

ASJC Scopus subject areas

  • Genetics

Fingerprint

Dive into the research topics of 'Role of GLP‑1 receptor agonists in sepsis and their therapeutic potential in sepsis‑induced muscle atrophy (Review)'. Together they form a unique fingerprint.

Cite this