KB-R7943 inhibits high glucose-induced endothelial ICAM-1 expression and monocyte-endothelial adhesion

Biochem Biophys Res Commun. 2010 Feb 19;392(4):516-9. doi: 10.1016/j.bbrc.2009.12.183. Epub 2010 Jan 22.

Abstract

Hyperglycemia is the major cause of diabetic angiopathy. The aim of our study was to evaluate the impact of KB-R7943, an inhibitor of Na+/Ca2+ exchanger (NCX) on cell growth and function of human "diabetic" endothelial cells (EC). Intercellular adhesion molecule-1 (ICAM-1) expression and NCX activity were determined after EC were exposed to high glucose in the absence and presence of KB-R7943. Coincubation of EC with high glucose for 24 h resulted in a significant increase of monocyte-endothelial cell adhesion and the expression of ICAM-1. These effects were abolished by KB-R7943 and KB-R7943 significantly decreased the activation of NCX induced by high glucose. These findings suggested that KB-R7943 may play a role in inhibiting expression of adhesion molecules by inhibiting the reverse activation of NCX.

MeSH terms

  • Blood Glucose / metabolism*
  • Cell Adhesion / drug effects
  • Cells, Cultured
  • Diabetic Angiopathies / etiology
  • Diabetic Angiopathies / metabolism
  • Diabetic Angiopathies / pathology
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / metabolism
  • Humans
  • Hyperglycemia / complications
  • Hyperglycemia / metabolism*
  • Hyperglycemia / pathology
  • Intercellular Adhesion Molecule-1 / biosynthesis*
  • Monocytes / drug effects
  • Monocytes / pathology
  • Sodium-Calcium Exchanger / antagonists & inhibitors*
  • Thiourea / analogs & derivatives*
  • Thiourea / pharmacology

Substances

  • 2-(2-(4-(4-nitrobenzyloxy)phenyl)ethyl)isothiourea methanesulfonate
  • Blood Glucose
  • Sodium-Calcium Exchanger
  • Intercellular Adhesion Molecule-1
  • Thiourea