Chronic administration of a potent cholecystokinin receptor antagonist, L-364,718, fails to inhibit pancreas growth in preweanling rats

Pancreas. 1990 Jul;5(4):434-8. doi: 10.1097/00006676-199007000-00010.

Abstract

We examined whether endogenous cholecystokinin (CCK) is involved in growth of the preweanling rat pancreas. Twice daily for 14 days, 7-day-old neonatal rats received an oral gavage of either 2.5 mg/kg or 5.0 mg/kg of the potent and specific CCK receptor antagonist L-364,718 (the 2.5 mg/kg dose of antagonist was shown in the present study to abolish totally the pancreas growth-promoting effects of exogenously administered caerulein (CR) in neonatal rats). Control pups received oral gavages of the L-364,718 vehicle alone. The final body weights, pancreas weights, total pancreatic DNA contents, and total pancreatic protein contents did not differ significantly between the 21-day-old control pups and the 21-day-old pups that were pretreated for 14 days with either the low or the high doses of L-364,718. These findings suggest that endogenous CCK is not required for growth of the neonatal rat pancreas.

MeSH terms

  • Amylases / metabolism
  • Animals
  • Animals, Newborn / growth & development*
  • Benzodiazepinones / pharmacology*
  • Body Weight
  • Ceruletide / pharmacology
  • DNA / metabolism
  • Devazepide
  • Organ Size / drug effects
  • Pancreas / drug effects
  • Pancreas / growth & development*
  • Pancreas / metabolism
  • Proteins / metabolism
  • Rats
  • Rats, Inbred Strains
  • Receptors, Cholecystokinin / antagonists & inhibitors*
  • Weaning

Substances

  • Benzodiazepinones
  • Proteins
  • Receptors, Cholecystokinin
  • Ceruletide
  • DNA
  • Amylases
  • Devazepide