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Original Article
124 (
6
); 709-714
doi:
10.25259/IJMR_20061246_709

The role of allopurinol in experimental acute necrotizing pancreatitis

Department of Internal Medicine, Gulhane School of Medicine, Ankara, Turkey
Department of Pharmacology, Gulhane School of Medicine, Ankara, Turkey
Department of Surgery, Yuksek Ihtisas Hospital, Ankara, Turkey
Department of Anatomy, Baskent University, Ankara, Turkey

Reprint requests: Dr Ahmet Turan Isik, GATA Ic Hastaliklari A.D., 06010 Etlik, Ankara, Turkey e-mail: ahmetturanisik@yahoo.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background & objectives:

Acute pancreatitis (AP) in its severe form can lead to severe complications and death. Translocation of bacteria from the gut is one of the most important factors in the development of septic complications and mortality in acute pancreatitis. Oxygen-derived free radicals have been suggested to play a major role in the pathogenesis of AP. Xanthine oxidase enzyme is an important source of reactive oxygen metabolites. We undertook this study to evaluate the effect of allopurinol on bacterial translocation, oxidative stress and the course of AP in a rat model.

Methods:

Male Sprague-Dawley rats (n=48) were randomly allocated into three equal groups. Acute pancreatitis (AP) was induced in group II (AP+Saline), and group III (AP+allopurinol) by retrograde infusion of taurocholate into the common biliopancreatic duct. Group I rats (Sham) received normal saline infusion into the common biliopancreatic duct for mimicking pressure effect. Group III rats were treated with allopurinol intraperitoneally for 48 h after induction of pancreatitis. Blood samples were drawn from all animals for biochemical analyses and pancreatic tissues were examined for bacterial translocation.

Results:

Acute pancreatitis was developed in all groups, but not in group I (Sham), as indicated by microscopic parenchymal necrosis, fat necrosis and abundant turbid peritoneal fluid. Pathologic score of the pancreatitis in the allopurinol group (14.0 ± 0.5) was lower when compared with group II (19.2 ± 0.6) (P<0.001). Bacterial translocation to pancreas in group treated with allopurinol was significantly lower when compared with control group (p<0.02). Plasma glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) levels were higher and malondialdehyde (MDA) levels were lower in allopurinol group when compared with those in control groups.

Interpretation & conclusion:

Our findings suggested that addition of allopurinol to the treatment protocol in the acute pancreatitis might improve the pathologic score, bacterial translocation and oxidative stress parameters. However, more studies need to be done to confirm these findings.

Keywords

Acute necrotizing pancreatitis
allopurinol
bacterial translocation

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