Regulation of protein kinase C isozyme and calcineurin expression in isoproterenol induced cardiac hypertrophy

J Cardiovasc Pharmacol. 2003 Jun;41(6):946-54. doi: 10.1097/00005344-200306000-00018.

Abstract

Protein kinase C (PKC) and calcineurin are known to play a pivotal role in the development of cardiomyocyte growth. However, its role in Isoproterenol-induced (Iso) cardiac hypertrophy has not been characterized so far and were focus of the current study. After chronic beta-adrenergic stimulation of male Wistar rats with Iso (2mg/kg x day) for 2 and 7 days using osmotic minipumps, we determined a) cardiac PKC-activity, b) the expression of cardiac PKC isozymes (PKC-alpha, PKC-delta and PKC-epsilon) both at the protein and the mRNA-level and c) the expression of calcineurin using Western blot analysis. Iso-treatment for 2 and 7 days results in cardiac hypertrophy with an increase of the heart weight-to-body weight ratio by 36% and 27%. Iso-induced myocardial growth was associated with an enhanced total PKC-activity and a significant increased protein expression of cytosolic PKC-alpha (day 2: +38%; day 7: +43%), PKC-delta (day 2: 85%; day 7: +78%) and PKC-epsilon (day 7: +58%). The protein amount of calcineurin was not significantly altered by Iso compared with sham-operated controls. The increased expression of PKC-alpha, PKC-delta and PKC-epsilon in the cytosol was paralleled by a transcriptional upregulation of the absolute mRNA-levels of these PKC-isozymes as determined by quantitative RT-PCR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Agonists / administration & dosage
  • Adrenergic beta-Agonists / adverse effects*
  • Animals
  • Blotting, Western
  • Calcineurin / biosynthesis*
  • Calcineurin / genetics
  • Cardiomegaly / chemically induced*
  • Cardiomegaly / metabolism
  • Isoenzymes / biosynthesis
  • Isoenzymes / genetics
  • Isoproterenol / administration & dosage
  • Isoproterenol / adverse effects*
  • Male
  • Myocardium / metabolism
  • Myocardium / pathology
  • Myocardium / ultrastructure
  • Organ Size
  • Protein Kinase C / biosynthesis*
  • Protein Kinase C / genetics
  • Rats
  • Rats, Wistar
  • Reverse Transcriptase Polymerase Chain Reaction
  • Subcellular Fractions / enzymology
  • Time Factors

Substances

  • Adrenergic beta-Agonists
  • Isoenzymes
  • Protein Kinase C
  • Calcineurin
  • Isoproterenol