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首页> 外文期刊>Journal of investigative surgery: The official journal of the Academy of Surgical Research >Free Radical Scavengers Improve Liver Function but Not Morphological Changes Induced by Reperfusion Injury
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Free Radical Scavengers Improve Liver Function but Not Morphological Changes Induced by Reperfusion Injury

机译:自由基清除剂可改善肝脏功能,但不能改善再灌注损伤所致的形态变化

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Objective: Reperfusion injury (RI) is associated with high generation of reactive oxygen species (ROS), but the extent of involvement of these agents in the injury remains controversial. The present study aimed to examine the effectiveness of ROS scavengers against hepatic reperfusion injury in the rat. Methods: The RI was induced in the liver using an isolated slow-flow, reflow perfused rat liver in both anterograde and retrograde perfusion. The effects of gentisic acid, N-acetyl cysteine, and trolox C on the superoxide production, liver function, and morphological changes were examined using different biochemical and histological assays. Results: The hepatic RI caused a significant (p < 0.05) increase in superoxide production and enzyme releases and a decrease in bile flow in both directions. Histological changes induced by RI include apoptosis, necrosis, pale cytoplasm, cell vacuolation, and attenuation of cell cords. Although the production of superoxide in retrograde direction was significantly less than the anterograde, the extent of the injury in the retrograde was greater than the anterograde direction. Pretreatment of the livers with each of the test compounds significantly reduced the release of lactate dehydrogenase and aspartate aminotransferase and improved bile flow in the liver exposed to hypoxia/reperfusion. However, they failed to protect the liver against the structural alterations induced by RI. Conclusion: ROS scavengers can reduce superoxide-induced damage and improve the liver function, but they are not able to prevent the structural changes. It shows that ROS are not the sole causative mechanism of hepatic RI and other mechanisms and mediators may be involved.
机译:目的:再灌注损伤(RI)与活性氧(ROS)的大量产生有关,但是这些药物参与损伤的程度仍存在争议。本研究旨在检查活性氧清除剂对大鼠肝再灌注损伤的有效性。方法:在顺行和逆行灌注中,使用隔离的慢流,回流灌注大鼠肝脏在肝脏中诱导RI。用不同的生化和组织学方法检查了龙胆酸,N-乙酰基半胱氨酸和trolox C对超氧化物生成,肝功能和形态变化的影响。结果:肝RI导致两个方向的超氧化物生成和酶释放显着(p <0.05)增加,并且胆汁流量减少。 RI引起的组织学变化包括细胞凋亡,坏死,胞浆苍白,细胞空泡化和细胞线衰减。尽管逆行方向的超氧化物生成量明显少于顺行方向,但逆行方向的损伤程度却大于顺行方向。用每种测试化合物对肝脏进行预处理可显着减少乳酸脱氢酶和天冬氨酸转氨酶的释放,并改善暴露于缺氧/再灌注的肝脏中的胆汁流量。但是,他们未能保护肝脏免受RI诱导的结构改变。结论:ROS清除剂可以减少超氧化物诱导的损伤并改善肝功能,但不能阻止其结构改变。结果表明,ROS不是肝RI的唯一病因机制,可能涉及其他机制和介体。

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