cGMP-dependent protein kinase I mediates the negative inotropic effect of cGMP in the murine myocardium

Circ Res. 2002 Jan 11;90(1):18-20. doi: 10.1161/hh0102.103222.

Abstract

To study the role of cGMP-dependent protein kinase I (cGKI) for cardiac contractility, force of contraction (F(c)) was studied in electrically driven heart muscle from wild-type (WT) mice and from conventional and conditional cGKI knockout mice. Both 8-Br-cGMP and 8-pCPT-cGMP reduced Fc in cardiac muscle from juvenile WT but not from juvenile cGKI-null mutants. Similarly, the cGMP analogues reduced F(c) in forskolin-stimulated ventricular muscle from WT mice but not from cGKI-null mutants. In contrast, carbachol reduced F(c) in both groups of animals. 8-Br-cGMP reduced F(c) also in heart muscle from adult WT mice but not from adult cardiomyocyte-specific cGKI-knockout mice. These results demonstrate that cGKI mediates the negative inotropic effect of cGMP in the myocardium of juvenile and adult mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cyclic GMP / analogs & derivatives*
  • Cyclic GMP / pharmacology*
  • Cyclic GMP-Dependent Protein Kinases / genetics
  • Cyclic GMP-Dependent Protein Kinases / metabolism*
  • Genotype
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Mice, Knockout
  • Myocardial Contraction / drug effects*
  • Myocardium / enzymology*
  • Myocardium / metabolism
  • Thionucleotides / pharmacology

Substances

  • Thionucleotides
  • 8-bromocyclic GMP
  • 8-((4-chlorophenyl)thio)cyclic-3',5'-GMP
  • Cyclic GMP-Dependent Protein Kinases
  • Cyclic GMP