Systemic and organ-specific anti-inflammatory effects of sodium-glucose cotransporter-2 inhibitors

Trends Endocrinol Metab. 2024 May;35(5):425-438. doi: 10.1016/j.tem.2024.02.003. Epub 2024 Feb 29.

Abstract

Inflammation plays an essential role and is a common feature in the pathogenesis of many chronic diseases. The exact mechanisms through which sodium-glucose cotransporter-2 (SGLT2) inhibitors achieve their much-acclaimed clinical benefits largely remain unknown. In this review, we detail the systemic and tissue- or organ-specific anti-inflammatory effects of SGLT2 inhibitors using evidence from animal and human studies. We discuss the potential pathways through which SGLT2 inhibitors exert their anti-inflammatory effects, including oxidative stress, mitochondrial, and inflammasome pathways. Finally, we highlight the need for further investigation of the extent of the contribution of the anti-inflammatory effects of SGLT2 inhibition to improvements in cardiometabolic and renal outcomes in clinical studies.

Keywords: SGLT2 inhibition; cytokines; inflammation; macrophages; monocytes; sodium-glucose cotransporter-2 (SGLT2).

Publication types

  • Review

MeSH terms

  • Animals
  • Anti-Inflammatory Agents* / pharmacology
  • Anti-Inflammatory Agents* / therapeutic use
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / metabolism
  • Humans
  • Inflammation* / drug therapy
  • Inflammation* / metabolism
  • Oxidative Stress / drug effects
  • Sodium-Glucose Transporter 2 Inhibitors* / pharmacology
  • Sodium-Glucose Transporter 2 Inhibitors* / therapeutic use