Chen C F, Hsueh C W, Tang T S, Wang D, Shen C Y, Pei J S
Department of Internal Medicine, Cheng Hsin General Hospital, Taipei, Taiwan.
Transplant Proc. 2007 May;39(4):858-60. doi: 10.1016/j.transproceed.2007.02.018.
Reperfusion of the ischemic liver results in the generation of oxygen radicals. In this study, we analyzed if the mRNA and protein expressions of superoxide dismutase (SOD) and catalase increased after ischemia (I) and reperfusion (R) of the rat liver.
Ischemia was induced by clamping off the common hepatic artery and portal vein of rats for 40 minutes, which were then reperfused for 90 minutes. Blood samples collected prior to I and after R were analyzed for hydroxyl radical (.OH), nitric oxide (NO), and alanine transferase (ALT). Liver tissues were used to analyze the SOD and catalase mRNA and protein expressions by real-time polymerase chain reaction and Western blot.
The results showed that this protocol resulted in elevation of the blood ALT, NO, and .OH levels (P<.001). mRNA (P<.01) and protein expressions (P<.05) of SOD and catalase were all increased. Pretreatment with antioxidant, N-acetyl cysteine, attenuated the liver injury.
These results indicate that reperfusion of the ischemic liver induced antioxidant enzymes expressions so that oxygen radicals are scavenged. Oxygen radical scavenger could further attenuate the I/R-induced liver injury.
缺血肝脏再灌注会导致氧自由基的产生。在本研究中,我们分析了大鼠肝脏缺血(I)和再灌注(R)后超氧化物歧化酶(SOD)和过氧化氢酶的mRNA及蛋白表达是否增加。
通过夹闭大鼠肝总动脉和门静脉40分钟诱导缺血,随后再灌注90分钟。在缺血前和再灌注后采集血样,分析其中的羟自由基(·OH)、一氧化氮(NO)和丙氨酸转氨酶(ALT)。肝组织用于通过实时聚合酶链反应和蛋白质印迹法分析SOD和过氧化氢酶的mRNA及蛋白表达。
结果显示,该方案导致血ALT、NO和·OH水平升高(P<0.001)。SOD和过氧化氢酶的mRNA(P<0.01)及蛋白表达(P<0.05)均增加。用抗氧化剂N-乙酰半胱氨酸预处理可减轻肝损伤。
这些结果表明,缺血肝脏再灌注诱导了抗氧化酶的表达,从而清除了氧自由基。氧自由基清除剂可进一步减轻缺血/再灌注诱导的肝损伤。