ANG II receptors, c-myc, and c-jun in myocytes after myocardial infarction and ventricular failure

Am J Physiol. 1993 Mar;264(3 Pt 2):H760-9. doi: 10.1152/ajpheart.1993.264.3.H760.

Abstract

To determine the relationship between reactive cardiac hypertrophy and the expression of angiotensin II (ANG II) receptors in surviving myocytes after infarction, large infarcts were produced in rats that were killed 2-3 days later. Measurements of global ventricular dynamics indicated that left ventricular failure and right ventricular dysfunction occurred in experimental animals. These alterations in ventricular pump function were associated with increases in ventricular weight-to-body weight ratio, indicative of developing cardiac hypertrophy. Such a response was coupled with a 6.6-fold increase in ANG II receptor mRNA in myocytes from the left ventricle. A 2.3-fold increase in the expression of ANG II receptor in myocytes from the right ventricle was also found. Radioligand binding assay documented a 44% increase in the density of ANG II receptors on left ventricular myocytes of infarcted hearts. To establish whether the induction of genes commonly associated with myocyte hypertrophy was present, the message for c-myc and c-jun was biventricularly assessed. Myocardial infarction was accompanied by overexpressions of c-myc and c-jun that were more prominent in left than in right ventricular myocytes. In conclusion, the enhanced expression of ANG II receptor and its receptor protein and c-myc and c-jun in myocytes may participate in the reactive growth processes of these cells after infarction.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Blood Pressure
  • Blotting, Northern
  • Cardiomegaly / genetics*
  • Gene Expression*
  • Genes, jun / genetics*
  • Genes, myc / genetics*
  • Heart Rate
  • Male
  • Molecular Sequence Data
  • Myocardial Infarction / genetics*
  • Myocardial Infarction / physiopathology
  • Myocardium / pathology
  • Nucleic Acid Hybridization
  • Organ Size
  • Polymerase Chain Reaction
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Angiotensin / genetics*

Substances

  • RNA, Messenger
  • Receptors, Angiotensin