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脂质过氧化介导的U937细胞毒性和DNA损伤。

Lipid peroxidation-mediated cytotoxicity and DNA damage in U937 cells.

作者信息

Park Ji Eun, Yang Joon-Hyuck, Yoon Seon Joo, Lee Jin-Hyup, Yang Eun Sun, Park Jeen-Woo

机构信息

Department of Biochemistry, College of Natural Sciences, Kyungpook National University, Taegu 702-701, Republic of Korea.

出版信息

Biochimie. 2002 Dec;84(12):1199-205. doi: 10.1016/s0300-9084(02)00039-1.

Abstract

Membrane lipid peroxidation processes yield products that may react with DNA and proteins to cause oxidative modifications. In the present study, we evaluated lipid peroxidation-mediated cytotoxicity and oxidative DNA damage in U937 cells. Upon exposure of U937 cells to tert-butylhydroperoxide (t-BOOH) and 2,2'-azobis (2-amidinopropane) hydrochloride (AAPH), which induce lipid peroxidation in membranes, the cells exhibited a reduction in viability and an increase in the endogenous production of reactive oxygen species (ROS), as measured by the oxidation of 2',7'-dichlorodihydrofluorescein. In addition, a significant decrease in the intracellular GSH level and the activities of major antioxidant enzymes were observed. We also observed lipid peroxidation-mediated oxidative DNA damage, reflected by an increase in 8-OH-dG level and loss of the ability of DNA to renature. When the cells were pretreated with the antioxidant N-acetylcysteine (NAC) or the spin trap alpha-phenyl-N-t-butylnitrone (PBN), lipid peroxidation-mediated cytotoxicity in U937 cells was protected. This effect seems to be due to the ability of NAC and PBN to reduce ROS generation induced by lipid peroxidation. These results suggest that lipid peroxidation resulted in a pro-oxidant condition of U937 cells by the depletion of GSH and inactivation of antioxidant enzymes, which consequently leads to a decrease in survival and oxidative damage to DNA. The results indicate that the peroxidation of lipid is probably one of the important intermediary events in oxidative stress-induced cellular damage.

摘要

膜脂质过氧化过程会产生一些产物,这些产物可能与DNA和蛋白质发生反应,从而引起氧化修饰。在本研究中,我们评估了脂质过氧化介导的U937细胞毒性和氧化性DNA损伤。当U937细胞暴露于能诱导膜脂质过氧化的叔丁基过氧化氢(t-BOOH)和2,2'-偶氮二(2-脒基丙烷)盐酸盐(AAPH)时,细胞活力降低,活性氧(ROS)的内源性生成增加,这是通过2',7'-二氯二氢荧光素的氧化来测定的。此外,还观察到细胞内谷胱甘肽(GSH)水平和主要抗氧化酶活性显著下降。我们还观察到脂质过氧化介导的氧化性DNA损伤,表现为8-羟基脱氧鸟苷(8-OH-dG)水平升高以及DNA复性能力丧失。当细胞用抗氧化剂N-乙酰半胱氨酸(NAC)或自旋捕获剂α-苯基-N-叔丁基硝酮(PBN)预处理时,U937细胞中脂质过氧化介导的细胞毒性得到了保护。这种作用似乎是由于NAC和PBN能够减少脂质过氧化诱导的ROS生成。这些结果表明,脂质过氧化通过消耗GSH和使抗氧化酶失活,导致U937细胞处于促氧化状态,进而导致细胞存活率下降和DNA氧化损伤。结果表明,脂质过氧化可能是氧化应激诱导细胞损伤的重要中间事件之一。

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