Repurposing anti-inflammasome NRTIs for improving insulin sensitivity and reducing type 2 diabetes development

Nat Commun. 2020 Sep 23;11(1):4737. doi: 10.1038/s41467-020-18528-z.

Abstract

Innate immune signaling through the NLRP3 inflammasome is activated by multiple diabetes-related stressors, but whether targeting the inflammasome is beneficial for diabetes is still unclear. Nucleoside reverse-transcriptase inhibitors (NRTI), drugs approved to treat HIV-1 and hepatitis B infections, also block inflammasome activation. Here, we show, by analyzing five health insurance databases, that the adjusted risk of incident diabetes is 33% lower in patients with NRTI exposure among 128,861 patients with HIV-1 or hepatitis B (adjusted hazard ratio for NRTI exposure, 0.673; 95% confidence interval, 0.638 to 0.710; P < 0.0001; 95% prediction interval, 0.618 to 0.734). Meanwhile, an NRTI, lamivudine, improves insulin sensitivity and reduces inflammasome activation in diabetic and insulin resistance-induced human cells, as well as in mice fed with high-fat chow; mechanistically, inflammasome-activating short interspersed nuclear element (SINE) transcripts are elevated, whereas SINE-catabolizing DICER1 is reduced, in diabetic cells and mice. These data suggest the possibility of repurposing an approved class of drugs for prevention of diabetes.

Publication types

  • Meta-Analysis
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism
  • Animals
  • Cell Survival
  • DEAD-box RNA Helicases / metabolism
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / prevention & control
  • Diet, High-Fat / adverse effects
  • Drug Repositioning*
  • HIV-1 / drug effects
  • Hepatitis B
  • Humans
  • Inflammasomes / drug effects*
  • Insulin Resistance*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle Cells / metabolism
  • Reverse Transcriptase Inhibitors / pharmacology*
  • Ribonuclease III / metabolism

Substances

  • Inflammasomes
  • Reverse Transcriptase Inhibitors
  • DICER1 protein, human
  • Ribonuclease III
  • DEAD-box RNA Helicases