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Grape seed extract treatment reduces hepatic ischemia‐reperfusion injury in rats
Author(s) -
Şehirli Özer,
Ozel Yahya,
Dulundu Ender,
Topaloglu Umit,
Ercan Feriha,
Şener Goksel
Publication year - 2008
Publication title -
phytotherapy research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.019
H-Index - 129
eISSN - 1099-1573
pISSN - 0951-418X
DOI - 10.1002/ptr.2256
Subject(s) - reperfusion injury , medicine , ischemia , phytotherapy , pharmacognosy , traditional medicine , liver injury , pharmacology , biology , pathology , biological activity , in vitro , alternative medicine , biochemistry
Abstract This study was designed to determine the possible protective effect of grape seed extract (GSE), a widely used antioxidant dietary supplement, on hepatic ischemia/reperfusion (I/R) injury. Wistar albino rats were subjected to 45 min of hepatic ischemia, followed by a 60 min reperfusion period. GSE was administered in a dose of 50 mg/kg/day orally for 15 days before I/R injury and repeated before the reperfusion period. Liver samples were taken for histological examination or determination of hepatic malondialdehyde (MDA), glutathione (GSH) and myeloperoxidase (MPO) activity. Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels were determined to assess liver functions. Lactate dehydrogenase (LDH) and cytokines (TNF‐ α and IL‐1 β ) were also assayed in serum samples for the evaluation of generalized tissue damage. Ischemia/reperfusion caused a significant decrease in hepatic GSH, and significant increases in MDA level, and MPO activity. Serum AST and ALT levels, as well as LDH activity and plasma TNF‐ α and IL‐1 β levels were also elevated in the I/R group. Treatment with GSE reversed all these biochemical parameters as well as histological alterations induced by I/R. In conclusion, GSE reduced I/R‐induced organ injury through its ability to balance the oxidant–antioxidant status, to inhibit neutrophil infiltration and to regulate the release of inflammatory mediators. Copyright © 2007 John Wiley & Sons, Ltd.