Artigo Produção Nacional Revisado por pares

The Effects of Allopurinol in Hepatic Ischemia and Reperfusion: Experimental Study in Rats

2000; Karger Publishers; Volume: 32; Issue: 4 Linguagem: Inglês

10.1159/000008767

ISSN

1421-9921

Autores

Ernani Luı́s Rhoden, Luiz Pereira-Lima, M Lucas, Marcelo Mauri, Cláudia Ramos Rhoden, J.C. Pereira-Lima, Cláudio Galeano Zettler, Leonardo Petteffi, Adriane Belló‐Klein,

Tópico(s)

Metabolism and Genetic Disorders

Resumo

<i>Background/Aims:</i> Some studies have shown that postischemic hepatic dysfunction is mainly due to oxygen free radicals that are generated by xanthine oxidase. The present study was undertaken to determine the effect of allopurinol, an inhibitor of xanthine oxidase, on oxidative stress, liver injury and histologic alterations induced by hepatic ischemia-reperfusion in rats. <i>Methods:</i> One hundred and sixty Wistar rats were used and divided into three groups. Group 1: sham operation; group 2: 50 min of ischemia followed by 1 h of reperfusion, and group 3: pretreatment with allopurinol and 50 min of ischemia followed by 1 h of reperfusion. The effect of allopurinol was evaluated by plasma levels of alanine aminotransferase and aspartate aminotransferase, histopathologic studies, and lipid peroxidation measured by the thiobarbituric acid reactive substances method and chemiluminescence initiated by tert-butyl hydroperoxide technique. <i>Results:</i> Ischemia followed by reperfusion promoted an increase in lipid peroxidation of the hepatic cells when compared to the sham-operated group (p < 0.05). This increase was attenuated in the group treated with allopurinol (p < 0.05). Allopurinol also showed a protective effect on hepatocellular necrosis (p < 0.05), and the plasma levels of liver enzymes returned earlier to the normal range in rats pretreated with allopurinol in comparison to those that did not receive the drug (p < 0.05). <i>Conclusions:</i> Allopurinol exerted a protective effect on hepatic ischemia and reperfusion in rats. The administration of this drug prior to liver operations should be considered to be submitted to trials in humans.

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