Basic Research
Copyright ©The Author(s) 2002. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Aug 15, 2002; 8(4): 707-711
Published online Aug 15, 2002. doi: 10.3748/wjg.v8.i4.707
Stimulation of p38 MAPK by hormal preconditioning with atrial natriuretic peptide
Alexandra K. Kiemer, Stefanie Kulhanek-Heinze, Tobias Gerwig, Alexander L. Gerbes, Angelika M. Vollmar
Alexandra K. Kiemer, Stefanie Kulhanek-Heinze, Tobias Gerwig, Angelika M. Vollmar, Department of Pharmacy, Center of Drug Research, University of Munich, Munich 81377, Germany
Alexandra K. Kiemer, Stefanie Kulhanek-Heinze, Tobias Gerwig, Alexander L. Gerbes, Department of Medicine II, Klinikum Grosshadern, University of Munich, Munich 81377, Germany
Author contributions: All authors contributed equally to the work.
Supported by the Deutsche Forschungsgemeinschaft (DFG: Ge 576/14-2 and FOR 440/1-2: KI 702/2). A.K.K. is a recipient of the "Bayerischer Habilitationsfoderpreis".
Correspondence to: Alexandra K. Kiemer, Ph.D., Department of Pharmacy, Center of Drug Research, Butenandtstr.5-13, 81377 Munich, Germany. alexandra.kiemer@cup.uni-muenchen.de
Telephone: +49-89-2180-7165 Fax: +49-89-2180-7170
Received: May 20, 2002
Revised: June 1, 2002
Accepted: June 3, 2002
Published online: August 15, 2002
Abstract

AIM: Stress-activated signaling pathways responsible for hepatic ischemia reperfusion injury and their modulation by protective interventions are widely unknown. Preconditioning of rat livers with Atrial Natriuretic Peptide (ANP) attenuates ischemia reperfusion injury (Gerbes et al[21]Hepatology 1998, 28:1309-1317). Since ANP has recently been shown to be a regulator of the p38 MAPK pathway in endothelial cells (Kiemer et al[25]Circ Res 2002, 90:874-881), aim of this study was to investigate activities of MAPK during ischemia and reperfusion and effects of ANP on MAPK.

METHODS: Rat livers were perfused with KH-buffer in the presence or absence of ANP for 20 min, kept in cold UW solution for 24 h, and reperfused for up to 120 min. Activities of p38 MAPK and JNK was determined by in vitro phosphorylation assays using MBP and c-jun as substrates. After SDS/PAGE electrophoresis, gels were quantified by phosphorimaging.

RESULTS: Activity of p38 MAPK in control organs decreased in the course of ischemia and reperfusion by 85%, whereas ANP increased p38 activity by up to 30-fold. JNK activation of control livers increased in the course of ischemia and reperfusion by up to three-fold. This increase in JNK activity was slightly elevated in ANP preconditioned organs.

CONCLUSION: This work represents a systematic investigation of MAPK activation during liver ischemia and reperfusion. Employing ANP, for the first time a pharmacological approach to modulate these central signal transduction molecules is presented.

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