Mastoparan induces oscillations of cytosolic Ca2+ in rat pancreatic acinar cells

Biochem Biophys Res Commun. 1991 May 31;177(1):159-65. doi: 10.1016/0006-291x(91)91962-c.

Abstract

Microfluorimetry of fura-2 was used to monitor [Ca2+]i in single cells stimulated with the G-protein activating agent mastoparan. Mastoparan induced the generation of [Ca2+]i oscillations, which in contrast to oscillations induced by low concentrations of CCK were acutely dependent on the presence of extracellular Ca2+. Oscillations were inhibited by phorbol ester. Sodium fluoride, a known activator of G-proteins, gave similar results. Both mastoparan and CCK induced turnover of inositol phosphates, at concentrations higher than necessary to induce oscillations.

Publication types

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

MeSH terms

  • Alkaloids / pharmacology
  • Animals
  • Calcium / metabolism*
  • Cholecystokinin / pharmacology
  • Cytosol / drug effects
  • Cytosol / metabolism
  • In Vitro Techniques
  • Inositol Phosphates / metabolism
  • Intercellular Signaling Peptides and Proteins
  • Kinetics
  • Male
  • Microscopy, Fluorescence
  • Pancreas / cytology
  • Pancreas / drug effects
  • Pancreas / metabolism*
  • Peptides
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / metabolism
  • Rats
  • Sodium Fluoride / pharmacology
  • Staurosporine
  • Tetradecanoylphorbol Acetate / pharmacology
  • Time Factors
  • Wasp Venoms / pharmacology*

Substances

  • Alkaloids
  • Inositol Phosphates
  • Intercellular Signaling Peptides and Proteins
  • Peptides
  • Wasp Venoms
  • mastoparan
  • Sodium Fluoride
  • Cholecystokinin
  • Protein Kinase C
  • Staurosporine
  • Tetradecanoylphorbol Acetate
  • Calcium