Early sequence of cardiac adaptations and growth factor formation in pressure- and volume-overload hypertrophy

Am J Physiol Heart Circ Physiol. 2000 Sep;279(3):H976-85. doi: 10.1152/ajpheart.2000.279.3.H976.

Abstract

To investigate the time sequence of cardiac growth factor formation, echocardiographic and hemodynamic measurements were performed at scheduled times, and mRNAs for angiotensinogen, prepro-endothelin-1 (ppET-1), and insulin-like growth factor I (IGF-I) were quantified with RT-PCR and localized with in situ hybridization in pigs (fluothane anesthesia) by use of pressure or volume overload (aortic banding and aorta-cava fistula, respectively). Relative peptide formation was also measured by radioimmunoassay. In pressure overload, angiotensinogen and ppET-1 mRNA overexpression on myocytes (13 times vs. sham at 3 h and 112 times at 6 h, respectively) was followed by recovery (12 h) of initially decreased (0.5-6 h) myocardial contractility. In volume overload, contractility was not decreased, the angiotensinogen gene was slightly upregulated at 6 h (6.7 times), and ppET-1 was not overexpressed. IGF-I mRNA was overexpressed on myocytes (at 24 h) in both volume and pressure overload (14 times and 37 times, respectively). In the latter setting, a second ppET-1 overexpression was detectable on myocytes at 7 days. In conclusion, acute cardiac adaptation responses involve different growth factor activation over time in pressure versus volume overload; growth factors initially support myocardial contractility and thereafter induce myocardial hypertrophy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological
  • Angiotensin II / biosynthesis*
  • Angiotensin II / genetics
  • Animals
  • Blood Pressure
  • Cardiac Volume
  • Cardiomegaly / diagnostic imaging
  • Cardiomegaly / pathology
  • Cardiomegaly / physiopathology*
  • Disease Models, Animal
  • Echocardiography
  • Endothelin-1 / biosynthesis*
  • Endothelin-1 / genetics
  • Female
  • Hemodynamics*
  • In Situ Hybridization
  • Insulin-Like Growth Factor I / biosynthesis*
  • Insulin-Like Growth Factor I / genetics
  • Male
  • Myocardium / metabolism
  • Myocardium / pathology
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Swine

Substances

  • Endothelin-1
  • RNA, Messenger
  • Angiotensin II
  • Insulin-Like Growth Factor I