GLP-1/GLP-1RAs: New Options for the Drug Treatment of NAFLD

Curr Pharm Des. 2024;30(2):100-114. doi: 10.2174/0113816128283153231226103218.

Abstract

Non-alcoholic fatty liver disease (NAFLD) has recently emerged as a global public health concern. Currently, the cornerstone of NAFLD treatment is lifestyle modification and, if necessary, weight loss. However, compliance is a challenge, and this approach alone may not be sufficient to halt and treat the more serious disease development, so medication is urgently needed. Nevertheless, no medicines are approved to treat NAFLD. Glucagon-like peptide-1 (GLP-1) is an enteropeptide hormone that inhibits glucagon synthesis, promotes insulin secretion, and delays gastric emptying. GLP-1 has been found in recent studies to be beneficial for the management of NAFLD, and the marketed GLP-1 agonist drugs have different degrees of effectiveness for NAFLD while lowering blood glucose. In this article, we review GLP-1 and its physiological roles, the pathogenesis of NAFLD, the correlation between NAFLD and GLP-1 signaling, and potential strategies for GLP-1 treatment of NAFLD.

Keywords: Glucagon-like peptide-1; glucagon-like peptide-1 receptor agonist; insulin resistance; non-alcoholic fatty liver disease; non-alcoholic steatohepatitis; steatosis..

Publication types

  • Review

MeSH terms

  • Blood Glucose
  • Diabetes Mellitus, Type 2* / drug therapy
  • Glucagon / therapeutic use
  • Glucagon-Like Peptide 1 / pharmacology
  • Glucagon-Like Peptide 1 / physiology
  • Glucagon-Like Peptide-1 Receptor
  • Humans
  • Hypoglycemic Agents / therapeutic use
  • Insulin Secretion
  • Non-alcoholic Fatty Liver Disease* / drug therapy

Substances

  • Glucagon-Like Peptide 1
  • Glucagon
  • Blood Glucose
  • Glucagon-Like Peptide-1 Receptor
  • Hypoglycemic Agents