Int J Angiol 2000; 9(4): 236-240
DOI: 10.1007/BF01623901
Original Articles

© Georg Thieme Verlag KG Stuttgart · New York

Cytokine suppressive agent prevents pancreatic injuries induced by ischemia-reperfusion in rats

Tetsuya Hirano
  • Department of Surgery, Hirano Clinic, Izumisano, Osaka, Japan
Further Information

Publication History

Publication Date:
24 April 2011 (online)

Abstract

This study was designed to evaluate the possible role of cytokines (IL-1 and TNF-α) in the pathogenesis of pancreatic injuries induced by pancreatic ischemia-reperfusion and to evaluate the protective effect of the cytokine suppressive agent, FR167653, against pancreatic injuries. Pancreatic ischemia-reperfusion was induced in rats by ligating the celiac and caudate mesenteric arteries by small metallic clips for 45 min, after this ischemia, the metal clips were removed. Four hours after removing the metal clips, the animals were used for the experiments. In this model, mild hyperamylsemia and significant increases in pancreatic water and trypsin content were observed. Significant increases in serum IL-1 and TNF-α were also observed, as compared with the control rats. Pancreatic subcellular redistribution of lysosomal enzyme cathepsin B from the lysosomal fraction to the zymogen fraction was also observed. However, treatment with FR167653 at a dose of 0.5 mg/kg.hr significantly prevented all these pancreatic injuries. These results indicate that cytokines such as IL-1 and TNF-α might be involved in the pathogenesis of pancreatic injuries induced by ischemia-reperfusion, and that a cytokine suppressive agent might be of therapeutic value for the treatment of pancreatic ischemia.

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