细胞凋亡
肝移植
缺血
再灌注损伤
免疫印迹
缺氧(环境)
医学
移植
内分泌学
男科
生物
内科学
化学
基因
生物化学
有机化学
氧气
作者
Raffaele Cursio,C. Miele,Nathalie Filippa,E Van Obberghen,Jean Gugenheim
标识
DOI:10.1016/j.transproceed.2008.05.037
摘要
Apoptosis plays an important role in ischemia-reperfusion (I-R) injury during liver transplantation. The hypoxia-inducible factor alpha (HIF-1α) may trigger liver apoptosis following I-R through the induction of hypoxically regulated genes. The aim of this study was to evaluate the effect of normothermic liver I-R on HIF-1α expression and apoptosis in rats. Segmental normothermic ischemia of the liver was induced in rats for 120 minutes. Liver extracts from either ischemic or nonischemic lobes were prepared at 0, 1, 3, and 6 hours after reperfusion. Liver HIF-1α protein expression was examined by Western blot analysis. Liver apoptosis was quantified using terminal deoxynucleotide transferase-mediated deoxyuridine triphosphate nick end labeling assay. Normothermic I-R resulted in a significant (P < .05) increase in liver HIF-1α protein levels 1 and 3 hours after reperfusion. Liver apoptosis was significantly (P < .005) increased at 3 and 6 hours after reperfusion. In conclusion, normothermic liver I-R leads to increased liver expression of HIF-1α and apoptosis.
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