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引用次数: 1
摘要
在临床缺血/再灌注损伤中,氧化和亚硝化应激引起的损伤通常被认为是移植物功能的关键。然而,越来越多的证据表明,包括原位肝移植(OLT)在内的现代临床移植与器官再氧化应激和亚硝化应激升高无关。我们测量了8例终末期肝病患者在整个OLT期间血浆中的两种目前使用的氧化应激生物标志物,即15(S)-8-异-前列腺素f2a (15(S)-8-异- pgf 2a)和顺式-环氧十八烷酸(顺式- epoa)。15(S)-8- iso - pgf 2a和顺式- epoa浓度未见明显变化,提示氧化应激缺乏。先前,我们发现在相同的患者中,亚硝化应激,测量为3-硝基酪氨酸和3-硝基酪氨酸白蛋白。然而,由于15(S)-8- iso - pgf 2a、顺式- epoa和3-硝基酪氨酸都是通过化学反应和酶促反应产生的,因此目前关于氧化应激和亚硝化应激的概念需要重新考虑。
Does Oxidative Stress Change During Orthotopic Liver Transplantation
In clinical ischemia/reperfusion injury, damage resulting from oxidative and nitrosative stress is generally considered crucial for graft functioning. Yet, there is increasing evidence that modern clinical transplantation including orthotopic liver transplantation (OLT) is not associated with elevation of oxidative and nitrosative stress upon organ reoxygenation. We measured two currently used biomarkers of oxidative stress, i.e., 15( S )-8- iso -prostaglandin F 2a (15( S )-8- iso -PGF 2a ) and cis -epoxyoctadecanoic acid ( cis -EpOA), in human plasma during the entire time duration of OLT in eight patients suffering from end-stage liver disease. No considerable concentration changes of 15( S )-8- iso -PGF 2a and cis -EpOA were observed, indicating lack of oxidative stress. Previously, we found in the same patients that nitrosative stress, measured as 3-nitrotyrosine and 3-nitrotyrosinoalbumin. Yet, as 15( S )-8- iso -PGF 2a , cis -EpOA and 3-nitrotyrosine are produced both by chemical and enzymatic reactions, the current concepts of oxidative and nitrosative stress require reconsideration.