The pathogenesis of L-arginine-induced acute necrotizing pancreatitis: inflammatory mediators and endogenous cholecystokinin

J Physiol Paris. 2000 Jan-Feb;94(1):43-50. doi: 10.1016/s0928-4257(99)00104-7.

Abstract

This study was aimed at an assessment of the role of oxygen-derived free radicals, cytokines and endogenous cholecystokinin (CCK) in the pathogenesis of L-arginine (Arg)-induced acute pancreatitis in rat. We measured the levels of malonyl dialdehyde (MDA), glutathione peroxidase (GPx), catalase and superoxide dismutase (Mn- and Cu, Zn-SOD) in pancreatic tissue, the serum levels of tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and CCK, and evaluated the protective effect of the xanthine oxidase inhibitor allopurinol and a novel CCK receptor antagonist KSG-504. Acute pancreatitis was induced in male Wistar rats by injecting 2x 250 mg/100 g body weight of Arg intraperitoneally in an 1-h interval, as a 20% solution in 0.15 M NaCl. Control rats received the same quantity of glycine. 200 mg x kg(-1) allopurinol 30 min before the first Arg treatment or 50 mg x kg(-1) KSG-504 30 min before and 6, 18 and 36 h after the first Arg injection was administered subcutaneously. Rats were killed at 6, 12, 24 and 48 h following Arg administration, and acute pancreatitis was confirmed by a serum amylase level elevation and typical inflammatory features observed microscopically. The serum level of amylase reached the peak level at 24 h after the Arg injection (30,800 +/- 3,813 versus 6,382 +/- 184 U x L(-1) in the control) and normalized at 48 h. The tissue concentration of MDA was significantly elevated at 24 h, and reached the peak value at 48 h (5.00 +/- 1.75 versus 0.28 +/- 0.05 nM x mg(-1) protein in the control). The catalase and Mn-SOD activities were significantly decreased throughout the study, while the GPx activity was significantly reduced at 6 and 12 h, and the Cu, Zn-SOD activity was significantly lower at 12 h after the Arg injection as compared with the controls. Both the TNF-alpha and the IL-6 levels were already elevated significantly at 12 h and peak at 24 h versus the controls (19.1 +/- 7.9 U x mL(-1) and 57.6 +/- 11.2 pg x mL(-1) versus 3.1 +/- 0.8 U x mL(-1) and 15.2 +/- 3.1 pg x mL(-1), respectively). No significant changes in plasma CCK levels were observed. Allopurinol treatment markedly reduced the serum amylase elevation (12.631 +/- 2.257 U x L(-1) at 24 h), prevented the increase in tissue MDA concentration (0.55 +/- 0.09 nM x mg(-1) protein at 48 h) and significantly ameliorated the pancreatic edema, necrosis and inflammation at 48 h after Arg administration. KSG-504 administration did not exert any beneficial effect on the development of histopathological changes neither modified the serum amylase or cytokine levels. Oxygen-derived free radicals and cytokines are involved, while endogenous CCK does not seem to play a role in the pathogenesis of Arg-induced acute pancreatitis.

MeSH terms

  • Allopurinol / pharmacology
  • Amylases / blood
  • Animals
  • Arginine*
  • Catalase / metabolism
  • Cholecystokinin / blood
  • Cholecystokinin / physiology*
  • Cytokines / blood
  • Cytokines / physiology
  • Enzyme Inhibitors / pharmacology
  • Glutathione Peroxidase / metabolism
  • Hormone Antagonists / pharmacology
  • Inflammation Mediators / physiology*
  • Male
  • Naphthalenes / pharmacology
  • Pancreas / pathology
  • Pancreatitis, Acute Necrotizing / chemically induced*
  • Pancreatitis, Acute Necrotizing / enzymology
  • Pancreatitis, Acute Necrotizing / pathology
  • Pentanoic Acids / pharmacology
  • Rats
  • Rats, Wistar
  • Reactive Oxygen Species / physiology
  • Superoxide Dismutase / metabolism

Substances

  • Cytokines
  • Enzyme Inhibitors
  • Hormone Antagonists
  • Inflammation Mediators
  • Naphthalenes
  • Pentanoic Acids
  • Reactive Oxygen Species
  • KSG 504
  • Allopurinol
  • Cholecystokinin
  • Arginine
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Amylases