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Glutathione disulfide formation during naproxen metabolism in the isolated rat hepatocytes.

机译:在分离的大鼠肝细胞中萘普生代谢过程中谷胱甘肽二硫化物的形成。

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As naproxen was found to induce lipid peroxidation in liver microsomes and isolated hepatocytes of rats during its oxidative metabolism, we studied changes of glutathione on its metabolism. Intracellular oxidized glutathione (GSSG) content increased in isolated rat hepatocytes during naproxen metabolism. The intracellular GSSG increased preceding the production of thiobarbituric acid reactive substances (TBARS) and the release of lactate dehydrogenase (LDH). The glutathione-depleted hepatocytes treated with diethymaleate (DEM) enhanced TBARS production and LDH release, compared to the untreated hepatocytes. The production of GSSG may possibly be an early stage of the naproxen-induced oxidative stress which leads to lipid peroxidation and lethal cell injury.
机译:由于发现萘普生在其氧化代谢过程中会诱导大鼠肝微粒体和离体的肝细胞中脂质过氧化,因此我们研究了谷胱甘肽对其代谢的变化。在萘普生代谢过程中,离体大鼠肝细胞中的细胞内氧化型谷胱甘肽(GSSG)含量增加。细胞内GSSG在产生硫代巴比妥酸反应性物质(TBARS)和释放乳酸脱氢酶(LDH)之前增加。与未处理的肝细胞相比,用二甲基马来酸酯(DEM)处理的减少了谷胱甘肽的肝细胞提高了TBARS产生和LDH释放。 GSSG的产生可能是萘普生诱导的氧化应激的早期阶段,导致脂质过氧化和致命的细胞损伤。

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