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首页> 外文期刊>Oncology letters >Intestinal NF-E2-related factor-2 expression and antioxidant activity changes in rats undergoing orthotopic liver autotransplantation
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Intestinal NF-E2-related factor-2 expression and antioxidant activity changes in rats undergoing orthotopic liver autotransplantation

机译:肝原位移植大鼠肠道NF-E2相关因子2的表达及抗氧化活性的变化

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Liver transplantation is known to trigger intestinal injuries. Oxidative damage that is induced by reactive oxygen species (ROS) plays a crucial role in ischemia-reperfusion injuries. NF-E2-related factor-2 (Nrf2) and its modulated antioxidant enzymes form the critical endogenous antioxidant system to scavenge ROS. The present study investigated the dynamic changes of intestinal ROS levels, Nrf2 expression and antioxidant enzyme activity following orthotopic liver autotransplantation (OLAT). Sprague-Dawley rats were randomly divided into five groups consisting of one sham group and four groups with rats that underwent OLAT and were evaluated following 4, 8, 16 and 24 h, respectively. The intestinal specimens were collected for histopathological examination and the detection of hydrogen peroxide (H2O2), hydroxyl radical (?OH), malondialdehyde (MDA), reduced glutathione (GSH), superoxide dismutase (SOD) and catalase (CAT) levels and the expression of Nrf2. The present study demonstrated that OLAT resulted in severe intestinal injury, which manifested as a significant change in the intestine pathological scores as early as 4 h and peaking at 8 h post-treatment. Oxidative stress was also revealed by the increase of the H2O2, ?OH and MDA levels. Significant decreases were observed in the activity of SOD and CAT and a dramatic decrease occurred in the levels of GSH at 4 and 8 h post-treatment. All the parameters were restored gradually at 16 and 24 h post-treatment. The expression of Nrf2 in the intestinal tissues increased significantly at 4, 16 and 24 h following OLAT. The present study shows that an imbalance between oxidants and antioxidants contributes to intestinal oxidative injury, and that the upregulation of Nrf2 is not sufficient to withstand intestinal oxidative injury following OLAT.
机译:众所周知,肝移植会引起肠道损伤。活性氧(ROS)引起的氧化损伤在缺血再灌注损伤中起关键作用。 NF-E2相关因子2(Nrf2)及其调节的抗氧化剂酶形成了清除ROS的关键内源性抗氧化剂系统。本研究调查了原位肝自体移植(OLAT)后肠道ROS水平,Nrf2表达和抗氧化酶活性的动态变化。将Sprague-Dawley大鼠随机分为5组,每组分别由假手术组和四组大鼠分别进行OLAT,并在4、8、16和24小时后进行评估。收集肠道标本进行组织病理学检查,并检测过氧化氢(H2O2),羟基自由基(?OH),丙二醛(MDA),还原型谷胱甘肽(GSH),超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的水平和表达Nrf2。本研究表明,OLAT会导致严重的肠道损伤,这表现为肠道病理学评分的显着变化早于4 h,并在治疗后8 h达到峰值。 H2O2,?OH和MDA含量的增加也揭示了氧化应激。在处理后4小时和8小时,SOD和CAT的活性显着下降,GSH水平显着下降。在治疗后16和24小时,所有参数逐渐恢复。 OLAT后4、16和24小时,肠组织中Nrf2的表达显着增加。本研究表明,氧化剂和抗氧化剂之间的不平衡会导致肠道氧化损伤,而Nrf2的上调不足以抵抗OLAT后的肠道氧化损伤。

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