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硒缺乏会增强百草枯诱导的离体灌注大鼠肺组织脂质过氧化反应。

Selenium deficiency potentiates paraquat-induced lipid peroxidation in isolated perfused rat lung.

作者信息

Glass M, Sutherland M W, Forman H J, Fisher A B

出版信息

J Appl Physiol (1985). 1985 Aug;59(2):619-22. doi: 10.1152/jappl.1985.59.2.619.

Abstract

Glutathione peroxidase (GSHPx), a seleno-enzyme, reduces lipid hydroperoxides while producing oxidized glutathione (GSSG), which can efflux from cells. To study the role of GSHPx in antioxidant defense, isolated lungs from selenium-deficient rats were perfused for 2 h with or without 1 mM paraquat. Perfusate GSSG was measured as an index of GSHPx activity, and malondialdehyde (MDA) as an index of lipid peroxidation. Selenium deficiency decreased lung GSHPx activity 75-80%. During perfusion control lungs showed GSSG efflux of 8.5 +/- 4.5 nmol/h and with paraquat 49.1 +/- 12.1 nmol/h. Selenium-deficient lungs with or without paraquat showed GSSG efflux of 16.4 +/- 5.3 and 13.7 +/- 8.9 nmol/h, respectively. MDA efflux occurred only in paraquat-perfused selenium-deficient lungs (7.8 +/- 2.7 nmol/h). Lung homogenates from this group had lower GSH + GSSG than the other three groups. These results indicate an inverse correlation between GSSG efflux and MDA accumulation from paraquat-perfused lungs and suggest that increased turnover of the GSHPx reaction protects paraquat-perfused lungs from lipid peroxidation.

摘要

谷胱甘肽过氧化物酶(GSHPx)是一种含硒酶,可还原脂质氢过氧化物,同时产生氧化型谷胱甘肽(GSSG),后者可从细胞中流出。为研究GSHPx在抗氧化防御中的作用,用或不用1 mM百草枯对缺硒大鼠分离出的肺进行2小时灌注。测定灌注液中的GSSG作为GSHPx活性指标,测定丙二醛(MDA)作为脂质过氧化指标。缺硒使肺GSHPx活性降低75 - 80%。在灌注过程中,对照肺的GSSG流出量为8.5±4.5 nmol/h,使用百草枯时为49.1±12.1 nmol/h。无论有无百草枯,缺硒肺的GSSG流出量分别为16.4±5.3和13.7±8.9 nmol/h。MDA仅在灌注百草枯的缺硒肺中流出(7.8±2.7 nmol/h)。该组肺匀浆中的GSH + GSSG低于其他三组。这些结果表明,百草枯灌注肺中GSSG流出与MDA积累呈负相关,提示GSHPx反应周转率增加可保护百草枯灌注肺免受脂质过氧化。

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