CCK-B (gastrin) receptor regulates gastric histamine release and acid secretion

Am J Physiol. 1991 Jun;260(6 Pt 1):G925-8. doi: 10.1152/ajpgi.1991.260.6.G925.

Abstract

To study the interdependence between gastric histamine release and acid secretion, we examined the effects of gastrin-(1-17) [G-(1-17)] or cholecystokinin-(1-33) [CCK-(1-33)] alone or combined with the gastrin (CCK-B) antagonist L365,260 or the CCK-A antagonist L364,718 in the isolated vascularly perfused rat stomach. G-(1-17) and CCK-(1-33) gave concentration-dependent increases in acid secretion and histamine release. Gastrin or CCK-A antagonist alone did not stimulate histamine release or acid secretion. Maximally G-(1-17) or CCK-(1-33) stimulated histamine release and acid secretion was unchanged by the CCK-A antagonist, while the gastrin antagonist induced a parallel and concentration-dependent decrease in stimulated histamine and acid secretion. We conclude that G-(1-17) and CCK-(1-33) stimulate histamine and acid secretion by a CCK-B (gastrin) receptor. The present results indicate that gastrin, at least in this species, stimulates acid secretion by releasing histamine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-3-isobutylxanthine / pharmacology
  • Animals
  • Benzodiazepinones / pharmacology
  • Cholecystokinin / antagonists & inhibitors
  • Cholecystokinin / pharmacology*
  • Devazepide
  • Gastric Acid / metabolism*
  • Gastric Mucosa / drug effects
  • Gastric Mucosa / physiology*
  • Gastrins / antagonists & inhibitors
  • Gastrins / pharmacology*
  • Histamine Release / drug effects*
  • In Vitro Techniques
  • Kinetics
  • Phenylurea Compounds*
  • Rats
  • Receptors, Cholecystokinin / drug effects
  • Receptors, Cholecystokinin / physiology*
  • Stomach / drug effects
  • Stomach / physiology*

Substances

  • Benzodiazepinones
  • Gastrins
  • Phenylurea Compounds
  • Receptors, Cholecystokinin
  • L 365260
  • Cholecystokinin
  • Devazepide
  • 1-Methyl-3-isobutylxanthine