CEP-1347 inhibits caerulein-induced rat pancreatic JNK activation and ameliorates caerulein pancreatitis

Am J Physiol Gastrointest Liver Physiol. 2000 Jan;278(1):G165-72. doi: 10.1152/ajpgi.2000.278.1.G165.

Abstract

Pancreatic caerulein-induced activation of c-Jun NH(2)-terminal kinase (JNK) has been reported, and JNK has been proposed as a mediator during induction of hyperstimulated pancreatitis. CEP-1347 has recently been described as a specific JNK inhibitor. We tested whether CEP-1347 inhibits caerulein-induced pancreatic JNK activation in isolated acini and in vivo. CEP-1347 dose dependently inhibited acinar caerulein-induced JNK activation with nearly complete inhibition at 2 microM but had no effect on digestive enzyme release. For in vivo studies, rats were pretreated with CEP-1347 before caerulein hyperstimulation. For assessment of JNK activation and histological alterations, animals were killed 30 min or 2 and 4 h after caerulein hyperstimulation, respectively. Pancreatic wet weight, serum enzyme levels, and pancreatic activity of p38 and extracellular signal-regulated kinase (ERK) were also determined. Caerulein hyperstimulation strongly activated JNK, p38, and ERK. CEP-1347 pretreatment dose dependently reduced caerulein-induced pancreatic JNK activation without p38 or ERK inhibition. JNK inhibition also reduced pancreatic edema formation and reduced histological severity of pancreatitis. Thus we show that CEP-1347 inhibits JNK activation in vivo and ameliorates caerulein-induced pancreatitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amylases / metabolism
  • Animals
  • Carbazoles / pharmacology*
  • Ceruletide / pharmacology*
  • Dose-Response Relationship, Drug
  • Edema / pathology
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology*
  • In Vitro Techniques
  • Indoles / pharmacology*
  • JNK Mitogen-Activated Protein Kinases
  • Male
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors*
  • Mitogen-Activated Protein Kinases / metabolism
  • Pancreas / enzymology*
  • Pancreatic Diseases / pathology
  • Pancreatitis / drug therapy*
  • Pancreatitis / pathology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Carbazoles
  • Enzyme Inhibitors
  • Indoles
  • 3,9-bis((ethylthio)methyl)-K-252a
  • Ceruletide
  • JNK Mitogen-Activated Protein Kinases
  • Mitogen-Activated Protein Kinases
  • Amylases