Potential role of N-cadherin in hepatocyte growth factor (HGF) mediated improvement of the cardiac function of dilated cardiomyopathy mice

Int J Cardiol. 2008 Jul 21;127(3):442-3. doi: 10.1016/j.ijcard.2008.01.009. Epub 2008 May 20.

Abstract

Objective: To study the potential mechanisms of hepatocyte growth factor (HGF) mediating improvement of the cardiac function of dilated cardiomyopathy mice (DCM).

Methods and results: We established experimental model of dilated cardiomyopathy by repetitive coxsickievirus B3 (CVB3) infection in Balb/c mice and half of the experimental group mice were injected 0.2 microg recombinated human HGF through tail vein every 2 days starting from the 5th month. At the 5th month, dilated cardiomyopathy occurred in experimental group mice. The HGF level and N-cadherin expression in myocardium of experimental group was downregulated. At the 7th month, after HGF supplement, the HGF level and N-cadherin expression in the myocardium of the mice were increased, the fibrosis of myocardial and cells apoptosis were ameliorated and cardiac function was improved. In vitro experiment, we found that N-cadherin expression was increased in cultured myocardial cells treated with rHGF.

Conclusion: Increasing in N-cadherin expression may be one of the potential mechanisms of HGF mediating Improvement of cardiac function of dilated cardiomyopathy mice.

Publication types

  • Comparative Study
  • Letter

MeSH terms

  • Animals
  • Atrial Function / drug effects
  • Atrial Function / physiology
  • Cadherins / antagonists & inhibitors
  • Cadherins / biosynthesis
  • Cadherins / physiology*
  • Cardiomyopathy, Dilated / drug therapy
  • Cardiomyopathy, Dilated / physiopathology*
  • Cells, Cultured
  • Hepatocyte Growth Factor / administration & dosage
  • Hepatocyte Growth Factor / therapeutic use*
  • Humans
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / therapeutic use
  • Ventricular Function / drug effects
  • Ventricular Function / physiology

Substances

  • Cadherins
  • HGF protein, human
  • Recombinant Proteins
  • Hepatocyte Growth Factor