Telmisartan inhibits methylglyoxal-mediated cell death in human vascular endothelium

Biochem Biophys Res Commun. 2008 Aug 22;373(2):253-7. doi: 10.1016/j.bbrc.2008.06.023. Epub 2008 Jun 17.

Abstract

Methylglyoxal (MGO) is a metabolite of glucose. Since serum MGO level is increased in diabetic patients, MGO is implicated in diabetic complications related to vascular injury. We have recently demonstrated that glucose metabolite is a more powerful stimulant for endothelial cells (ECs) injury rather than glucose or advanced glycation-end products. Recent clinical trials suggest that angiotensin receptor blockers are effective to prevent diabetes-associated cardiovascular disorders beyond blood pressure lowering effect. To explore the mechanisms, we examined effects of telmisartan on MGO-induced ECs injury. Treatment of human umbilical vein ECs with MGO (560 microM) induced time-dependent (0-24 h) cell death. MGO-induced cell death was apoptosis since MGO increased cleaved caspase-3 expression. Telmisartan (0.1-10 microM) inhibited MGO-induced cell death and caspase-3 activation. These results indicate that telmisartan prevents MGO-induced apoptosis by inhibiting caspase-3 activation, which might explain at least in part the beneficial effects of telimisartan against diabetes-related cardiovascular diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin II Type 1 Receptor Blockers
  • Apoptosis / drug effects*
  • Benzimidazoles / pharmacology*
  • Benzoates / pharmacology*
  • Caspase 3 / metabolism
  • Cells, Cultured
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / drug effects*
  • Enzyme Activation / drug effects
  • Humans
  • Pyruvaldehyde / antagonists & inhibitors*
  • Pyruvaldehyde / toxicity
  • Telmisartan

Substances

  • Angiotensin II Type 1 Receptor Blockers
  • Benzimidazoles
  • Benzoates
  • Pyruvaldehyde
  • Caspase 3
  • Telmisartan