[go: up one dir, main page]

Potency of L-364,718 as an antagonist of the behavioral effects of peripherally administered cholecystokinin

Life Sci. 1988;42(2):153-9. doi: 10.1016/0024-3205(88)90678-9.

Abstract

A new antagonist of the peripheral cholecystokinin receptor, L-364,718, was found to block the reductions in food intake and exploratory activity induced by intraperitoneal administration of cholecystokinin octapeptide sulfate. L-364,718 significantly reversed the cholecystokinin-induced reduction in feeding at doses of 10 micrograms/kg - 10 mg/kg i.p. L-364,718 significantly reversed the cholecystokinin-induced reduction in exploratory activity at doses of 500 ng/kg - 10 mg/kg i.p. The time course of antagonist activity of L-364,718 was immediate to 90 minutes after intraperitoneal administration. L-364,718 had no significant effect on food intake or exploratory activity when administered alone, over the dose range of 100 ng/kg-10 mg/kg i.p. This compound appears to be at least one hundred times more potent than proglumide or benzotript as an antagonist of the behavioral effects of peripherally administered cholecystokinin.

MeSH terms

  • Animals
  • Appetite / drug effects*
  • Benzodiazepinones / pharmacology*
  • Devazepide
  • Exploratory Behavior / drug effects
  • Injections, Intraperitoneal
  • Male
  • Mice
  • Mice, Inbred Strains
  • Motor Activity / drug effects*
  • Sincalide / administration & dosage
  • Sincalide / antagonists & inhibitors*
  • Sincalide / pharmacology
  • Time Factors

Substances

  • Benzodiazepinones
  • Devazepide
  • Sincalide