Glp-1 Mimetics and Autophagy in Diabetic Milieu: State-of-the-Art

Habib Yaribeygi1, Mina Maleki2, Raul D Santos3

  • 1Research Center of Physiology, Semnan University of Medical Sciences, Semnan, Iran.

Current Diabetes Reviews
|February 1, 2024
PubMed

Insights

Glucagon-like peptide-1 (GLP-1) mimetics may offer benefits beyond glucose control by modulating autophagy. This review explores how GLP-1 mimetics impact autophagy and potential therapeutic pathways for diabetic complications.

Area of Science:

  • Biochemistry
  • Cell Biology
  • Endocrinology

Background:

  • Diabetes mellitus triggers pathophysiological pathways leading to tissue injury and complications.
  • Autophagy, a cellular degradation process, is crucial for survival but can become pathological in diabetes.
  • Autophagy modulation presents a potential therapeutic target for diabetic complications.

Purpose of the Study:

  • To review the impact of Glucagon-like peptide-1 (GLP-1) mimetics on autophagy.
  • To explore the potential extra-glycemic benefits of GLP-1 mimetics through autophagy modulation.
  • To elucidate the underlying molecular pathways involved in GLP-1 mimetic-mediated autophagy.

Main Methods:

  • Literature review of existing studies on GLP-1 mimetics and autophagy.
  • Analysis of preclinical and clinical data regarding the effects of GLP-1 on cellular processes.
  • Synthesis of current knowledge on the molecular mechanisms linking GLP-1 signaling to autophagy pathways.

Main Results:

  • GLP-1 mimetics show potential in modulating autophagy, influencing cellular homeostasis.
  • Evidence suggests GLP-1 mimetics may confer tissue-protective effects independent of glucose lowering.
  • Specific molecular pathways mediating the interaction between GLP-1 and autophagy require further investigation.

Conclusions:

  • GLP-1 mimetics may offer significant therapeutic advantages by targeting autophagy in diabetic patients.
  • Understanding the interplay between GLP-1 and autophagy could unlock novel treatment strategies for diabetic complications.
  • Further research is warranted to fully elucidate the mechanisms and clinical utility of GLP-1 mimetics in modulating autophagy.

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