SGLT2 inhibitors and autophagy in diabetes

Habib Yaribeygi1, Mina Maleki2, Stephen L Atkin3

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

Insights

Sodium-glucose cotransporter 2 inhibitors (SGLT2is) may impact cellular autophagy, a process implicated in diabetes complications. This review explores SGLT2is

Area of Science:

  • Cellular Biology
  • Endocrinology
  • Pharmacology

Background:

  • Autophagy is crucial for cell survival but can become pathological in diabetes.
  • Chronic hyperglycemia in diabetes leads to aberrant autophagy and cell death, contributing to complications.
  • Autophagy modulation is a potential therapeutic strategy for diabetic complications.

Purpose of the Study:

  • To review the current evidence on the effects of Sodium-glucose cotransporter 2 inhibitors (SGLT2is) on cellular autophagy.
  • To clarify the potential role of SGLT2is in modulating autophagy in the context of diabetes.

Main Methods:

  • Literature review of preclinical and clinical studies.
  • Analysis of research investigating the mechanistic links between SGLT2is and autophagy pathways.

Main Results:

  • Evidence suggests SGLT2is may influence autophagy, though direct effects require further investigation.
  • Potential mechanisms include modulation of cellular energy status and oxidative stress.
  • Understanding these effects could explain some of the extra-glycemic benefits of SGLT2is.

Conclusions:

  • SGLT2is might exert therapeutic effects in diabetes partly through modulating autophagy.
  • Further research is needed to confirm the direct impact of SGLT2is on autophagy and its clinical relevance.
  • Investigating SGLT2is' effects on autophagy may reveal novel therapeutic targets for diabetic complications.

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