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喹啉酸对大鼠纹状体内源性抗氧化剂的影响。

Effect of quinolinic acid on endogenous antioxidants in rat corpus striatum.

作者信息

Rodríguez-Martínez E, Camacho A, Maldonado P D, Pedraza-Chaverrí J, Santamaría D, Galván-Arzate S, Santamaría A

机构信息

Department of Neurochemistry, National Institute of Neurology and Neurosurgery Manuel Velasco Suárez, SSA, Av. Insurgentes Sur # 3877, Mexico City, Mexico.

出版信息

Brain Res. 2000 Mar 10;858(2):436-9. doi: 10.1016/s0006-8993(99)02474-9.

Abstract

The response of endogenous antioxidants to the N-methyl-D-aspartate (NMDA) receptor agonist and excitotoxin, quinolinic acid (QUIN), was investigated in rat corpus striatum. Animals treated with QUIN (240 nmol/microl), were sacrificed at 120 min after a single intrastriatal injection to examine the alterations in the levels of both reduced (GSH) and oxidized (GSSG) glutathione, and the activities of the antioxidant enzymes, superoxide dismutase (SOD) and glutathione peroxidase (Gpx). Changes in the rate of lipid peroxidation (LP) were also measured after exposure to different doses of QUIN (60, 120, 240 and 480 nmol/microl) as an index of oxidative stress. When compared to control, lipid peroxidation was increased at QUIN doses of 240 and 480 nmol/microl. Striatal levels of GSH and GSSG were decreased and increased, respectively, after QUIN injection; whereas GPx activity was unchanged. Cytosolic copper/zinc SOD (CuZn-SOD) activity decreased after treatment, while mitochondrial manganese SOD (Mn-SOD) was unchanged. The alterations observed on these antioxidant systems suggest that QUIN toxicity is mediated by specific mechanisms leading to oxidative stress.

摘要

研究了大鼠纹状体内源性抗氧化剂对N-甲基-D-天冬氨酸(NMDA)受体激动剂及兴奋性毒素喹啉酸(QUIN)的反应。单次纹状体内注射QUIN(240 nmol/μl)的动物,在注射后120分钟处死,以检测还原型谷胱甘肽(GSH)和氧化型谷胱甘肽(GSSG)水平的变化,以及抗氧化酶超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(Gpx)的活性。作为氧化应激指标,在给予不同剂量的QUIN(60、120、240和480 nmol/μl)后,还测量了脂质过氧化(LP)速率的变化。与对照组相比,在QUIN剂量为240和480 nmol/μl时脂质过氧化增加。注射QUIN后,纹状体内GSH水平降低,GSSG水平升高;而Gpx活性未改变。处理后胞质铜/锌超氧化物歧化酶(CuZn-SOD)活性降低,而线粒体锰超氧化物歧化酶(Mn-SOD)未改变。在这些抗氧化系统上观察到的变化表明,QUIN毒性是由导致氧化应激的特定机制介导的。

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