Sitagliptin Mitigates Total Body Irradiation-Induced Hematopoietic Injury in Mice

Oxid Med Cell Longev. 2020 Jul 25:2020:8308616. doi: 10.1155/2020/8308616. eCollection 2020.

Abstract

Sitagliptin, an inhibitor of the dipeptidyl peptidase IV (DPP4), has been implicated in the regulation of type 2 diabetes. However, the role and mechanism of sitagliptin administration in total body irradiation (TBI)- induced hematopoietic cells injury are unclear. In this study, we demonstrated that sitagliptin had therapeutic effects on hematopoietic damage, which protected mice from 7.5 Gy TBI-induced death, increased the numbers and colony formation ability of hematopoietic cells. These therapeutic effects might be attributed to the inhibition of NOX4-mediated oxidative stress in hematopoietic cells, and the alleviation of inflammation was also helpful. Therefore, sitagliptin has potential as an effective radiotherapeutic agent for ameliorating TBI-induced hematopoietic injury.

MeSH terms

  • Animals
  • Dipeptidyl-Peptidase IV Inhibitors / pharmacology
  • Dipeptidyl-Peptidase IV Inhibitors / therapeutic use*
  • Hematologic Neoplasms / drug therapy*
  • Hematologic Neoplasms / mortality
  • Male
  • Mice
  • Sitagliptin Phosphate / pharmacology
  • Sitagliptin Phosphate / therapeutic use*
  • Survival Analysis
  • Whole-Body Irradiation / methods*

Substances

  • Dipeptidyl-Peptidase IV Inhibitors
  • Sitagliptin Phosphate