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[邻苯醌衍生物在四氯化碳诱导的大鼠肝脂质过氧化过程中的抗氧化作用]

[Antioxidative effect of o-benzoquinone derivatives during CCl4-induced lipid peroxidation in the rat liver].

作者信息

Potapovich A I, Kostiuk V A

出版信息

Biokhimiia. 1988 Feb;53(2):233-7.

PMID:3370249
Abstract

It was found that o-benzoquinones (oBQ) inhibit the CCl4-dependent lipid peroxidation (LPO) in rat liver microsomes in vitro. The experimental data suggest that the antioxidant effect of oBQ is not due to the ability of these substances to shunt the NADPH-dependent electron transport pathways. More likely, oBQ inhibit LPO due to the ability of their reduced forms to scavenge the free radicals which induce LPO. Based on the experimental data, it was concluded that the increasing absorption of liver lipids at 230-236 nm after administration of CCl4 is due to the accumulation of reduced hydroperoxides. This process was shown to be inhibited by oBQ.

摘要

研究发现,邻苯醌(oBQ)在体外可抑制大鼠肝微粒体中四氯化碳依赖性脂质过氧化(LPO)。实验数据表明,oBQ的抗氧化作用并非源于这些物质分流NADPH依赖性电子传递途径的能力。更有可能的是,oBQ抑制LPO是因其还原形式具有清除诱导LPO的自由基的能力。基于实验数据得出结论,四氯化碳给药后肝脏脂质在230 - 236 nm处吸收增加是由于还原型氢过氧化物的积累。该过程被证明可被oBQ抑制。

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