Cyclic GMP-dependent protein kinase and smooth muscle relaxation

J Cardiovasc Pharmacol. 1992:20 Suppl 1:S18-22.

Abstract

Cyclic guanosine monophosphate (cGMP)-dependent protein kinase has been cloned from bovine trachea. The isozymes I alpha and I beta, which differ only in their amino-terminal domains were expressed transiently in COS-7 cells. Both isozymes were activated by cGMP and cyclic adenosine monophosphate (cAMP). However, approximately 10-fold higher concentrations of cyclic nucleotides were needed to activate the I beta enzyme than the I alpha enzyme. The KA values for cAMP were 9.1 and greater than 20 microM for the I alpha and I beta isozymes, respectively. It is therefore unlikely that an unmodified I beta enzyme that occurs in high concentrations in vascular smooth muscle can be activated in vivo by cAMP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Cell Line
  • Cloning, Molecular
  • Cyclic AMP / pharmacology
  • Cyclic GMP / pharmacology*
  • Isoenzymes / chemistry
  • Isoenzymes / metabolism
  • Muscle Relaxation
  • Muscle, Smooth, Vascular / enzymology
  • Muscle, Smooth, Vascular / physiology*
  • Plasmids
  • Protein Kinases / chemistry
  • Protein Kinases / metabolism*
  • Transfection

Substances

  • Isoenzymes
  • Cyclic AMP
  • Protein Kinases
  • Cyclic GMP