Basic Research
Copyright ©2006 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Oct 28, 2006; 12(40): 6458-6463
Published online Oct 28, 2006. doi: 10.3748/wjg.v12.i40.6458
Peroxisome proliferator-activated receptor γ agonist reduces the severity of post-ERCP pancreatitis in rats
Emma Folch-Puy, Susana Granell, Juan L Iovanna, Marc Barthet, Daniel Closa
Emma Folch-Puy, Susana Granell, Daniel Closa, Department of Experimental Pathology, IIBB-CSIC, IDIBAPS, Barcelona, Spain
Juan L Iovanna, Marc Barthet, INSERM, U.624, Stress Cellulaire, Marseille, France
Supported by FIS grant PI020286 and PI050599 and Ramón y Cajal contract to Emma Folch-Puy. Susana Granell was a recipient for an IDIBAPS grant
Correspondence to: Dr. Daniel Closa, Experimental Pathology Department, Institut d’Investigacions Biomèdiques de Barcelona-Consejo Superior de Investigaciones Científicas; Institut d’Investigacions Biomèdiques August Pi i Sunyer), c/Rosselló 161, 7º, Barcelona 08036, Spain. dcabam@iibb.csic.es
Telephone: +34-93-3638307 Fax: +34-93-3638301
Received: December 29, 2005
Revised: February 18, 2006
Accepted: April 21, 2006
Published online: October 28, 2006
Abstract

AIM: To determine the effects of prophylactic peroxi-some proliferator-activated receptor (PPARγ) agonist administration in an experimental model of post-endoscopic retrograde cholangiopancreatography (post-ERCP) acute pancreatitis.

METHODS: Post-ERCP pancreatitis was induced in male Wistar rats by infusion of contrast medium into the pancreatic duct. In additional group, rosiglitazone, a PPARγ agonist, was administered 1 h before infusion of contrast medium. Plasma and pancreas samples were obtained 6 h after the infusion.

RESULTS: Infusion of contrast medium into the pan-creatic duct resulted in an inflammatory process characterized by increased lipase levels in plasma, and edema and myeloperoxidase activity (MPO) in pancreas. This result correlated with the activation of nuclear factor κB (NFκB) and the inducible NO synthase (iNOS) expression in pancreatic cells. Rosiglitazone reduced the increase in lipase and the level of edema and the increase in myeloperoxidase as well as the activation of NFκB and iNOS expression.

CONCLUSION: A single oral dose of rosiglitazone, given 1 h before post-ERCP pancreatitis induction is effective in reducing the severity of the subsequent inflammatory process. The protective effect of rosiglitazone was associated with NFκB inhibition and the blockage of leukocyte infiltration in pancreas.

Keywords: Peroxisome proliferator-activated receptor γ, Pancreatitis, Endoscopic retrograde cholangio pancreatography, Inflammation, Nuclear factor κB