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在NADPH氧化过程中,肝微粒体会产生羟基自由基:与乙醇代谢的关系。

Hydroxyl radicals are generated by hepatic microsomes during NADPH oxidation: relationship to ethanol metabolism.

作者信息

McCay P B, Reinke L A, Rau J M

机构信息

Molecular Toxicology Program, Oklahoma Medical Research Foundation, Oklahoma City 73104.

出版信息

Free Radic Res Commun. 1992;15(6):335-46. doi: 10.3109/10715769209049149.

Abstract

Ethanol is metabolized to acetaldehyde by hepatic microsomes in a reaction that requires cytochrome P-450, and a role for hydroxyl radicals has been implicated in this process. However, previous spin trapping experiments have failed to demonstrate the production of hydroxyl radicals by liver microsomes unless iron or other metal catalysts have been added. The spin trapping experiments described in this report provide unambiguous evidence that liver microsomes form hydroxyl radicals during oxidation of NADPH, that the addition of exogenous iron is unnecessary for this process, and that hydroxyl radicals participate in the metabolism of ethanol. Liver microsomes are known to metabolize ethanol to the 1-hydroxyethyl radical, and our experimental data support the conclusion that a significant part of the production of the 1-hydroxethyl radical occurs as a consequence of hydroxyl radical attack on ethanol. Lack of previous observation of microsomal hydroxyl radical production in spin trapping experiments is shown to be related to the contamination of the microsomes with catalase.

摘要

乙醇在肝脏微粒体中通过一种需要细胞色素P - 450的反应代谢为乙醛,并且羟自由基在这个过程中被认为起到了一定作用。然而,之前的自旋捕获实验未能证明肝脏微粒体产生羟自由基,除非添加了铁或其他金属催化剂。本报告中描述的自旋捕获实验提供了明确的证据,表明肝脏微粒体在NADPH氧化过程中形成羟自由基,此过程无需添加外源铁,且羟自由基参与乙醇的代谢。已知肝脏微粒体将乙醇代谢为1 - 羟乙基自由基,我们的实验数据支持这样的结论:1 - 羟乙基自由基的大量产生是羟自由基攻击乙醇的结果。自旋捕获实验中先前未观察到微粒体产生羟自由基,表明这与微粒体被过氧化氢酶污染有关。

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