Protective effects of gabexate mesilate on acute pancreatitis induced by tacrolimus (FK-506) in rats in which the pancreas was stimulated by caerulein
Autor: | Hajime Nawapa, Masayoshi Goto, Tetsuhide Ito, Itsuro Nakano, Hiroya Yamaguchi, Masayuki Furukawa, Toshinari Kimura |
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Rok vydání: | 1994 |
Předmět: |
Male
medicine.medical_specialty Gabexate Tacrolimus chemistry.chemical_compound Internal medicine medicine Animals Amylase Rats Wistar Pancreas Pancreatic elastase Ceruletide Pancreatic Elastase biology business.industry Gastroenterology medicine.disease Rats Endocrinology medicine.anatomical_structure Pancreatitis chemistry Vacuolization Amylases biology.protein Acute pancreatitis business |
Zdroj: | Journal of Gastroenterology. 29:305-313 |
ISSN: | 1435-5922 0944-1174 |
Popis: | We investigated the acute effects of the immunosuppressive agent, tacrolimus (FK-506), on the exocrine pancreas, in rats with or without stimulation of the pancreas, and evaluated the protective effects exerted by gabexate mesilate (FOY). While an intravenous injection of FK-506 did not change serum amylase levels during the 5-h observation period, this agent increased pancreatic amylase and protein content, and decreased the content of pancreatic DNA. Histologically, we observed intra-acinar vacuolization and individual cell necrosis. When the pancreas was stimulated by two intraperitoneal injections of caerulein (5 micrograms/kg) at 1-h intervals, however, which treatment did not induce any evident pancreatic change, FK-506 significantly increased serum amylase, pancreatic wet weight, and pancreatic amylase and protein, and decreased pancreatic DNA. Histologically, there were significant dose-related differences in the severity of intra-acinar vacuolization, interstitial edema, neutrophil infiltration, individual cell necrosis, and hemorrhage. Levels of intrapancreatic elastase were elevated and local pancreatic blood flow was reduced. Treatment with FOY improved the FK-506-induced acute pancreatitis, but did not increase the pancreatic blood flow. These findings indicate that FK-506 enhances abnormal pancreatic enzyme secretion and suggest that therapeutic doses of this agent can induce acute pancreatitis when the pancreas is stimulated. A protease inhibitor may protect the exocrine pancreas in patients who receive FK-506 after organ transplantation. |
Databáze: | OpenAIRE |
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