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氮氧化物超氧化物歧化酶模拟物:作用方式。

Nitroxide SOD-mimics: modes of action.

作者信息

Samuni A, Mitchell J B, DeGraff W, Krishna C M, Samuni U, Russo A

机构信息

Radiation Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

Free Radic Res Commun. 1991;12-13 Pt 1:187-94. doi: 10.3109/10715769109145785.

Abstract

Low molecular weight superoxide dismutase mimics have been shown to afford protection from oxidative damage. Such SOD-mimics can readily permeate cell membrane achieving sufficiently high levels both inside and outside the cell to effectively detoxify intracellular O2-.. Preliminary findings also indicated that metal-based and metal-free SOD-mimics can protect hypoxic cells from H2O2-induced damage. The present study explored the possibility that SOD-mimics such as desferrioxamine-Mn(III) chelate [DF-Mn] or cyclic nitroxide stable free radicals could protect from O2-.-independent damage. Killing of monolayered V79 Chinese hamster cells was induced by H2O2 or by t-butyl hydroperoxide (t-BHP) and assayed clonogenically. Neither catalase nor native SOD protected the cells from t-BHP. In contrast, both DF-Mn and cyclic nitroxides protected suggesting cytotoxic processes independent of O2-. or of O2-.-derived active species. The inhibition of the damage by both metal-free and metal-based SOD mimics is attributable to either SOD-mimic reacting with reduced transition metal to block the Fenton reaction and/or intercepting and detoxifying intracellular organic free radicals.

摘要

低分子量超氧化物歧化酶模拟物已被证明能提供抗氧化损伤的保护作用。这类超氧化物歧化酶模拟物能够轻易穿透细胞膜,在细胞内外达到足够高的水平,从而有效地清除细胞内的超氧阴离子。初步研究结果还表明,基于金属和不含金属的超氧化物歧化酶模拟物能够保护缺氧细胞免受过氧化氢诱导的损伤。本研究探讨了诸如去铁胺 - 锰(III)螯合物[DF-Mn]或环状氮氧化物稳定自由基等超氧化物歧化酶模拟物能否保护细胞免受与超氧阴离子无关的损伤的可能性。通过过氧化氢或叔丁基过氧化氢(t-BHP)诱导单层V79中国仓鼠细胞死亡,并进行克隆形成分析。过氧化氢酶和天然超氧化物歧化酶均不能保护细胞免受t-BHP的损伤。相比之下,DF-Mn和环状氮氧化物均具有保护作用,这表明细胞毒性过程与超氧阴离子或超氧阴离子衍生的活性物质无关。不含金属和基于金属的超氧化物歧化酶模拟物对损伤的抑制作用,要么归因于超氧化物歧化酶模拟物与还原态过渡金属反应以阻断芬顿反应,和/或拦截并清除细胞内有机自由基。

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