Effects of short-term administration of the CCK receptor antagonist, KSG-504, on regeneration of pancreatic acinar cells in acute pancreatitis in rats

J Gastroenterol. 1995 Aug;30(4):493-9. doi: 10.1007/BF02347566.

Abstract

Cholecystokinin (CCK) receptor antagonists have been reported on have an inhibitory effect on acute experimental pancreatitis, but their long-term administration is also reported to block pancreatic regeneration. We examined whether the short-term administration of KSG-504 (KSG), a synthetic CCK-A receptor antagonist, inhibited the regeneration of pancreatic acinar cells after ethionine-induced acute pancreatitis in rats. KSG (50 mg/kg), given 12 times by subcutaneous injection at 6-h intervals, prevented the reduction of protein, amylase, and trypsinogen levels, and the DNA content of the pancreas and facilitated the recovery of these values. Ornithine decarboxylase activity in pancreatic tissue and a 5-bromo-2'-deoxyuridine labeling study indicated that DNA synthesis was accelerated in rats treated with KSG. These findings suggest that the short-term administration of KSG inhibits the development of ethionine-induced acute pancreatitis and facilitates the regeneration of acinar cells.

MeSH terms

  • Acute Disease
  • Animals
  • Bromodeoxyuridine / metabolism
  • DNA / analysis
  • Ethionine
  • Male
  • Naphthalenes / administration & dosage*
  • Naphthalenes / pharmacology
  • Ornithine Decarboxylase / metabolism
  • Pancreas / metabolism
  • Pancreas / physiology*
  • Pancreatitis / chemically induced
  • Pancreatitis / physiopathology*
  • Pancreatitis / prevention & control
  • Pentanoic Acids / administration & dosage*
  • Pentanoic Acids / pharmacology
  • Rats
  • Rats, Wistar
  • Receptors, Cholecystokinin / antagonists & inhibitors*
  • Regeneration / drug effects*

Substances

  • Naphthalenes
  • Pentanoic Acids
  • Receptors, Cholecystokinin
  • KSG 504
  • DNA
  • Ornithine Decarboxylase
  • Bromodeoxyuridine
  • Ethionine