Effect of long-term CCK blockade on the pancreatic acinar cell renewal in rats with acute pancreatitis

Peptides. 2003 Apr;24(4):535-41. doi: 10.1016/s0196-9781(03)00112-8.

Abstract

This study determines the effect of 7-day pretreatment with L364,718 (a potent cholecystokinin (CCK) receptor antagonist) on pancreatic cell turnover during the course of acute pancreatitis (AP) induced in the rat by bile-pancreatic duct obstruction (BPDO). Cell cycle distribution and apoptosis were analyzed by flow cytometry using propidium iodide (PI) and Annexin V staining. Besides altering the pancreatic redox status, long-term CCK blockade inhibited the normal proliferation of acinar cells as indicated by the significant increase in G(0)/G(1)-phase cells and the decrease in G(2)/M-cells found in control rats treated with L364,718 for 7 days. A progressive depletion in pancreatic GSH was found from 3 to 24h after BPDO with similar values in L364,718-pretreated and non-treated rats, which led to a maximum peak in malondialdehyde (MDA) levels 6h after BPDO. However, plasma amylase activity and ascites volume indicated higher severity of AP in L364,718-pretreated rats. CCK blockade enhanced the alterations that appear in cell cycle distribution of acinar cells during AP demonstrated by the significantly higher increase in G(0)/G(1)-cells and decrease in S-cells found in L364,718-treated rats 48h after BPDO. Our results indicate that the renewal of acinar cells deleted by apoptosis 48h after BPDO worsens if CCK is blocked before inducing AP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Amylases / blood
  • Amylases / metabolism
  • Animals
  • Annexin A5 / pharmacology
  • Apoptosis
  • Cell Cycle
  • Cell Division
  • Cholecystokinin / antagonists & inhibitors*
  • Cholecystokinin / physiology
  • Coloring Agents / pharmacology
  • DNA / metabolism
  • Devazepide / pharmacology
  • Flow Cytometry
  • G1 Phase
  • Hormone Antagonists / pharmacology
  • Oxidation-Reduction
  • Pancreas / cytology*
  • Pancreas / metabolism*
  • Pancreatitis / drug therapy
  • Pancreatitis / metabolism*
  • Propidium / pharmacology
  • Rats
  • Resting Phase, Cell Cycle
  • Time Factors

Substances

  • Annexin A5
  • Coloring Agents
  • Hormone Antagonists
  • Propidium
  • DNA
  • Cholecystokinin
  • Amylases
  • Devazepide