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地西泮在大鼠脑内的亚细胞水平诱导早期氧化变化。

Diazepam induced early oxidative changes at the subcellular level in rat brain.

作者信息

Musavi S, Kakkar P

机构信息

Ecotoxicology Division, Industrial Toxicology Research Centre, M.G. Marg, Lucknow, India.

出版信息

Mol Cell Biochem. 1998 Jan;178(1-2):41-6. doi: 10.1023/a:1006834706117.

Abstract

Studies were conducted to ascertain any involvement of free radical mediated prooxidative processes in different brain regions following diazepam administration. A significant decrease in TBA reactive substance formation was observed in cerebral cortex, cerebellum and brain stem regions after single doses of 1.5, 3 and 6 mg/kg b.wt. For further studies rats were given diazepam (i.p.) at 3 mg/kg body weight dose and sacrificed after 1 h to follow changes in the pro/antioxidant status. An enhancement in the TBARS formation was found in the mitochondrial fractions from cerebral cortex and brain stem. This effect was highest in brain stem being 107% as compared to controls. In the post mitochondrial fraction, cerebellum showed 49% enhancement whereas decreased formation of thiobarbituric acid reactive substances was observed in cerebral cortex and brain stem. Isozymes of superoxide dismutase showed a decrease in activity which was region dependent. Even though, total thiols were not significantly altered, free thiols showed depletion in cerebellum (39.8%) and brain stem (50%). Glutathione reductase activity was also decreased in cerebellum and brain stem. The results indicate that a single dose of diazepam causes free radical mediated changes and the modulatory response of antioxidant defences appears to be region specific.

摘要

开展了多项研究,以确定地西泮给药后不同脑区中自由基介导的促氧化过程是否有任何参与。在单剂量给予1.5、3和6mg/kg体重的地西泮后,观察到大脑皮层、小脑和脑干区域中TBA反应性物质的形成显著减少。为了进一步研究,给大鼠腹腔注射3mg/kg体重剂量的地西泮,并在1小时后处死,以追踪抗氧化/促氧化状态的变化。在大脑皮层和脑干的线粒体部分中发现丙二醛(TBARS)的形成有所增加。这种效应在脑干中最为明显,与对照组相比增加了107%。在后线粒体部分中,小脑显示增加了49%,而在大脑皮层和脑干中观察到硫代巴比妥酸反应性物质的形成减少。超氧化物歧化酶的同工酶活性呈现出下降,且具有区域依赖性。尽管总硫醇没有显著改变,但游离硫醇在小脑(39.8%)和脑干(50%)中显示出消耗。小脑和脑干中的谷胱甘肽还原酶活性也降低。结果表明,单剂量的地西泮会导致自由基介导的变化,并且抗氧化防御的调节反应似乎具有区域特异性。

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