Neutrophils and NADPH oxidase mediate intrapancreatic trypsin activation in murine experimental acute pancreatitis

Gastroenterology. 2002 Apr;122(4):974-84. doi: 10.1053/gast.2002.32409.


Background & aims: Intrapancreatic activation of digestive enzymes is a key event in the parenchymal cell injury of pancreatitis. We hypothesized that neutrophils recruited to the pancreas during pancreatitis may contribute to such activation.

Methods: To cause experimental pancreatitis, rats and mice were treated with high doses of cerulein. Activation of the digestive enzyme, trypsin, was measured in pancreatic homogenates using a fluorogenic assay and localized immunocytochemically with antibody to trypsin-activation peptide (TAP).

Results: Compared with controls, rats depleted of neutrophils with antineutrophil serum exhibited a marked attenuation in intrapancreatic trypsin activation and acinar cell TAP labeling induced by high-dose cerulein. To examine the mechanism, mice deficient in either nicontinamide adenine dinucleotide phosphate (NADPH) oxidase, or myeloperoxidase (MPO) were studied for trypsin activation. Mice deficient in NADPH oxidase exhibited attenuation of the cerulein-induced trypsin activation, but those deficient in MPO did not. Using measurements of Western blot analysis, generation of reactive oxygen species, and immunocytochemistry, we demonstrated the NADPH oxidase activity is in neutrophils and not pancreatic acinar tissue.

Conclusions: The results demonstrate a novel role for neutrophils infiltrating the pancreas in pathologic activation of digestive enzymes in acute pancreatitis and indicate that this effect is mediated by products of NADPH oxidase.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies / pharmacology
  • Ceruletide
  • Enzyme Activation / physiology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • NADPH Oxidases / genetics
  • NADPH Oxidases / metabolism*
  • Neutrophils / enzymology*
  • Neutrophils / immunology
  • Pancreas / enzymology
  • Pancreatitis, Acute Necrotizing / chemically induced
  • Pancreatitis, Acute Necrotizing / immunology*
  • Pancreatitis, Acute Necrotizing / metabolism*
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Trypsin / metabolism*


  • Antibodies
  • Phosphoproteins
  • Ceruletide
  • NADPH Oxidases
  • neutrophil cytosolic factor 1
  • Trypsin