Related Experiment Video
Updated: Aug 3, 2025

In Situ Immunofluorescent Staining of Autophagy in Muscle Stem Cells
Published on: June 12, 2017
SGLT2 inhibitors and autophagy in diabetes
Habib Yaribeygi1, Mina Maleki2, Stephen L Atkin3
1Research Center of Physiology, Semnan University of Medical Sciences, Semnan, Iran.
Abstract:
Autophagy is a physiological event in mammalian cells to promote cell survival and efficiency in tissues, but it may turn to be a pathological process in disease conditions such as in diabetes. Chronic hyperglycemia induces aberrant autophagy and promotes cellular death as a main underlying cause of diabetes-related complications. Therefore, autophagy-modifying therapy may be of value to prevent the development of complications. Sodium-glucose cotransporter 2 inhibitors (SGLT2is) are a class of newly introduced antidiabetic drugs that achieve normoglycemia through causing overt glycosuria. There is evidence that these drugs may have pleiotropic extra-glycemic benefits, but their effect on the autophagy process is unclear; therefore, this review was undertaken to clarify the possible effects of SGLT2is on autophagy.
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.
Related Concept Videos
Dipeptidyl Peptidase 4 Inhibitors
Oral Hypoglycemic Agents: Biguanides and Glitazones
Glucagon-like Receptor Agonists
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors
Acarbose and miglitol are...
Oral Hypoglycemic Agents: Glinides
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:

