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Alanine minimises hepatocyte injury after ischemia-reperfusion in an ex vivo rat liver model

Berengere PAPEGAY1, *, Michaela STADLER1, Vincent Nuyens1, Isabelle SALMON2, Veronique KRUYS3, Jean G. BOOGAERTS1

1 Laboratory of Experimental Medicine (ULB unit 222), University Hospital Centre, Charleroi, Belgium
2 I. Salmon Laboratory of Pathological Anatomy (ULB unit 724), Free University of Brussels, Brussels, Belgium
3 V. Kruys Laboratory of Molecular Biology of the Gene, Department of Molecular Biology, Free University of Brussels (ULB), Gosselies, Belgium.

* Address correspondence to: Berengere Papegay, email

BIOCELL 2014, 38(1), 25-32. https://doi.org/10.32604/biocell.2014.38.025

Abstract

Ischemia-reperfusion injury is a determinant in liver injury occurring during surgery, ischemic states and multiple organ failure. The pre-existing nutritional status of the liver, i.e., fasting, might contribute to the extent of tissue injury. This study investigated whether alanine, an amino acid precursor of glucose, could protect ex vivo perfused livers of fasting rats from reperfusion injury. The portal vein was cannulated, the liver removed and perfused in a closed ex vivo system. Isolated livers were perfused either with glucose 1 g/L and 10 g/L, or with equal concentrations of alanine (n = 10 in each group). The experiment consisted of perfusion for 15 min, ischemia for 60 min, and reoxygenation during 60 min. Enzymes, glucose, lactate and bilirubin were analysed in perfusate samples. The proportion of glycogen as well as activation of caspase 3 was determined in biopsies. Alanine at a concentration of 10 g/L attenuated enzymes release in the perfusate during reoxygenation when compared to glucose-treated groups. Lactate level in the perfusate was lowest in alanine groups. Ischemia-reperfusion and mainly alanine activated apoptosis, specifically in Kupffer and endothelial cells. Alanine presents a protective effect on normothermic ischemia-reperfusion injury of the fasting rat liver when compared to glucose

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APA Style
PAPEGAY, B., STADLER, M., Nuyens, V., SALMON, I., KRUYS, V. et al. (2014). Alanine minimises hepatocyte injury after ischemia-reperfusion in an ex vivo rat liver model . BIOCELL, 38(1), 25-32. https://doi.org/10.32604/biocell.2014.38.025
Vancouver Style
PAPEGAY B, STADLER M, Nuyens V, SALMON I, KRUYS V, BOOGAERTS JG. Alanine minimises hepatocyte injury after ischemia-reperfusion in an ex vivo rat liver model . BIOCELL . 2014;38(1):25-32 https://doi.org/10.32604/biocell.2014.38.025
IEEE Style
B. PAPEGAY, M. STADLER, V. Nuyens, I. SALMON, V. KRUYS, and J.G. BOOGAERTS, “Alanine minimises hepatocyte injury after ischemia-reperfusion in an ex vivo rat liver model ,” BIOCELL , vol. 38, no. 1, pp. 25-32, 2014. https://doi.org/10.32604/biocell.2014.38.025

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cc Copyright © 2014 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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