| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2688539 | Clinical Nutrition | 2009 | 7 Pages |
SummaryBackground & aimsGlutamine and vitamin E may prevent hepatic ischemia–reperfusion (I/R) injuries. Our aim was to investigate the effects of glutamine, either alone or combined with vitamin E, against I/R in the isolated perfused rat liver.MethodsFour groups of 8 livers from male Sprague-Dawley rats were isolated and submitted to a 45-min no-flow ischemia and reperfusion in the presence of alanine 2 mM, alanine 2 mM plus vitamin E 150 μM, Alanyl-Glutamine (AlaGln) 2 mM, or AlaGln 2 mM plus vitamin E 150 μM. Six non-perfused livers were studied in parallel. Liver function, metabolic parameters, oxidative stress and inflammatory parameters have been studied.ResultsAlaGln was rapidly cleared from the perfusate (436 ± 41 nmol min−1 g−1) and lowered transaminase release during reperfusion (ALT: −59%), significantly so in the AlaGln + Vit E group (ALT: −65%, p < 0.05). The association of glutamine with vitamin E led to lower °NO (−83%, p < 0.05) production, better preserved hepatic glutathione content and, as with vitamin E alone, preserved hepatic vitamin A and significantly decreased malondialdehyde (−85%, p < 0.05).ConclusionBoth glutamine, by attenuating inflammatory response, and vitamin E, via its antioxidative properties, showed complementary protective effects against I/R-induced hepatic injury. These data emphasize the potential benefit of combining glutamine and vitamin E supplementation in hepatic I/R injury.
