Cardiac-directed adenylyl cyclase expression improves heart function in murine cardiomyopathy

Circulation. 1999 Jun 22;99(24):3099-102. doi: 10.1161/01.cir.99.24.3099.

Abstract

Background: We tested the hypothesis that increased cardiac myocyte adenylyl cyclase (AC) content increases cardiac function and response to catecholamines in cardiomyopathy.

Methods and results: Transgenic mice with cardiac-directed expression of AC type VI (ACVI) were crossbred with mice with cardiomyopathy induced by cardiac-directed Gq expression. Gq mice had dilated left ventricles, reduced heart function, decreased cardiac responsiveness to catecholamine stimulation, and impaired beta-adrenergic receptor (betaAR)-dependent and AC-dependent cAMP production. Gq/AC mice showed improved basal cardiac function in vivo (P=0.01) and ex vivo (P<0.0005). When stimulated through the betaAR, cardiac responsiveness was increased (P=0.02), and cardiac myocytes showed increased cAMP production in response to isoproterenol (P=0.03) and forskolin (P<0.0001).

Conclusions: Increasing myocardial ACVI content in cardiomyopathy restores cAMP-generating capacity and improves cardiac function and responsiveness to betaAR stimulation.

Publication types

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

MeSH terms

  • Adenylyl Cyclases / genetics*
  • Adrenergic beta-Agonists / pharmacology
  • Animals
  • Cardiomyopathy, Dilated / diagnostic imaging
  • Cardiomyopathy, Dilated / metabolism*
  • Cardiomyopathy, Dilated / therapy*
  • Cyclic AMP / biosynthesis
  • Echocardiography
  • Gene Expression Regulation, Enzymologic / physiology
  • Genetic Therapy*
  • Heart Function Tests
  • Isoproterenol / pharmacology
  • Mice
  • Mice, Transgenic
  • Muscle Fibers, Skeletal / drug effects
  • Muscle Fibers, Skeletal / enzymology
  • Myocardium / chemistry
  • Myocardium / cytology
  • Myocardium / enzymology*
  • Receptors, Adrenergic, beta / physiology
  • Transgenes / physiology

Substances

  • Adrenergic beta-Agonists
  • Receptors, Adrenergic, beta
  • Cyclic AMP
  • Adenylyl Cyclases
  • Isoproterenol