Recepto-secretory mechanism in histamine-stimulated amylase release from rat parotid gland

Inflamm Res. 1995 Jun;44(6):245-7. doi: 10.1007/BF01782976.

Abstract

The recepto-secretory mechanism in histamine-stimulated amylase release from rat parotid slices was studied using blockers of receptors and inhibitors of the intracellular messenger systems. Amylase release stimulated by histamine was inhibited by pyrilamine, an H1-receptor blocker, but not by cimetidine, an H2-receptor blocker. Atropine, prazosin and yohimbine had no effect on the release. Histamine-stimulated amylase release was inhibited by W-7, ML-9 and H-7, inhibitors of a calmodulin, a myosin light chain kinase (MLCK) and protein kinase C, respectively, while H-8, an inhibitor of protein kinase A, did not inhibit the release. These results suggest that histamine stimulation evokes amylase release via H1-receptors, followed by the Ca2+-dependent systems involving calmodulin, MLCK and protein kinase C.

MeSH terms

  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • Amylases / metabolism*
  • Animals
  • Azepines / pharmacology
  • Calmodulin / antagonists & inhibitors
  • Calmodulin / pharmacology
  • Cimetidine / pharmacology
  • Culture Techniques
  • Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Enzyme Inhibitors / pharmacology
  • Histamine / pharmacology*
  • Histamine H1 Antagonists / pharmacology
  • Histamine H2 Antagonists / pharmacology
  • Isoquinolines / pharmacology
  • Male
  • Myosin-Light-Chain Kinase / antagonists & inhibitors
  • Parotid Gland / drug effects*
  • Parotid Gland / enzymology
  • Piperazines / pharmacology
  • Protein Kinase C / antagonists & inhibitors
  • Pyrilamine / pharmacology
  • Rats
  • Rats, Wistar
  • Sulfonamides / pharmacology

Substances

  • Azepines
  • Calmodulin
  • Enzyme Inhibitors
  • Histamine H1 Antagonists
  • Histamine H2 Antagonists
  • Isoquinolines
  • Piperazines
  • Sulfonamides
  • ML 9
  • W 7
  • Cimetidine
  • Histamine
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • Cyclic AMP-Dependent Protein Kinases
  • Protein Kinase C
  • Myosin-Light-Chain Kinase
  • Amylases
  • Pyrilamine