Protein kinase A modulates Ca(2+)- and protein kinase C-dependent amylase release in permeabilized rat pancreatic acini

Biochem J. 1992 Oct 15;287 ( Pt 2)(Pt 2):403-6. doi: 10.1042/bj2870403.

Abstract

The role of protein kinase A (PKA) in the release of amylase from permeabilized pancreatic acini was investigated. Addition of cyclic AMP (cAMP) to permeabilized acini resulted in a potentiation of Ca(2+)-dependent amylase release, shifting the Ca2+ dose/response curve leftwards. As with protein kinase C (PKC) activation, this is due to an increase in the time of active discharge. The effect of cAMP was shown to be blocked by two inhibitors of PKA, H89 and the PKI-(5-24)-peptide. At low concentration, cAMP synergizes from phorbol 12-myristate 13-acetate (PMA), while at optimal concentrations cAMP and PMA are additive. PKA and PKC appear to work via similar, but not identical mechanisms.

Publication types

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

MeSH terms

  • Amylases / metabolism*
  • Animals
  • Calcium / pharmacology
  • Calcium / physiology*
  • Cell Membrane Permeability / drug effects
  • Cyclic AMP / antagonists & inhibitors
  • Cyclic AMP / pharmacology
  • Enzyme Activation / drug effects
  • Kinetics
  • Male
  • Pancreas / drug effects
  • Pancreas / enzymology
  • Pancreas / metabolism*
  • Protein Kinase C / metabolism
  • Protein Kinase C / physiology*
  • Protein Kinase Inhibitors
  • Protein Kinases / metabolism
  • Protein Kinases / physiology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Protein Kinase Inhibitors
  • Cyclic AMP
  • Protein Kinases
  • Protein Kinase C
  • Amylases
  • Calcium