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自由基与脂质的相互作用及其病理后果。

Free radical-lipid interactions and their pathological consequences.

作者信息

Rice-Evans C, Burdon R

机构信息

Free Radical Research Group, United Medical School of Guy's Hospital, University of London, U.K.

出版信息

Prog Lipid Res. 1993;32(1):71-110. doi: 10.1016/0163-7827(93)90006-i.

Abstract

In this review we have tried to present the current thinking on the consequences for lipids of their interactions with free radicals and the pathological implications. In particular, atherosclerosis and cancer have been addressed. In the case of the former, it is not clear whether the initial oxidative event is an enzymic or free radical-mediated process as yet. However, the importance of the antioxidants in controlling LDL oxidation, macrophage uptake of oxidatively modified LDL and progression of atheroma in animal models certainly suggests an important propagative role for free radical-mediated events. With regard to cancer, oxidative modification of cell lipids has potential consequences for tumour cell proliferation. Whilst lipid hydroperoxides can serve as an origin of prostaglandins with tumour inhibitor (or immunosuppressive) properties, they may also influence cellular growth regulatory proteins normally dependent on membrane lipid integrity. Alternatively, they may function as a source of aldehydic breakdown products capable of 'down-regulating' cell proliferation through covalent modification of regulatory proteins. Oils rich in n-3 polyunsaturated fatty acids have toxic effects towards tumour cells. This toxicity is not mediated by prostaglandins but rather through the capacity of such agents to elevate the levels of lipid peroxides. This may be enhanced by active oxygen species released constitutively from tumour cells.

摘要

在本综述中,我们试图阐述目前关于脂质与自由基相互作用的后果及其病理意义的观点。特别讨论了动脉粥样硬化和癌症。就前者而言,目前尚不清楚初始氧化事件是酶促过程还是自由基介导的过程。然而,抗氧化剂在控制低密度脂蛋白氧化、巨噬细胞摄取氧化修饰的低密度脂蛋白以及动物模型中动脉粥样硬化进展方面的重要性,无疑表明自由基介导的事件具有重要的传播作用。关于癌症,细胞脂质的氧化修饰对肿瘤细胞增殖可能产生影响。虽然脂质氢过氧化物可作为具有肿瘤抑制(或免疫抑制)特性的前列腺素的来源,但它们也可能影响通常依赖膜脂质完整性的细胞生长调节蛋白。或者,它们可能作为醛类分解产物的来源,通过对调节蛋白的共价修饰来“下调”细胞增殖。富含n-3多不饱和脂肪酸的油对肿瘤细胞具有毒性作用。这种毒性不是由前列腺素介导的,而是通过此类物质提高脂质过氧化物水平的能力来介导的。肿瘤细胞持续释放的活性氧可能会增强这种毒性。

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