Santamaría A, Galván-Arzate S, Lisý V, Ali S F, Duhart H M, Osorio-Rico L, Ríos C, St'astný F
Department of Neurochemistry, National Institute of Neurology and Neurosurgery Manuel Velasco Suárez SSA, Insurgentes Sur, Mexico DF, Mexico.
Neuroreport. 2001 Mar 26;12(4):871-4. doi: 10.1097/00001756-200103260-00049.
The oxidative action of quinolinic acid (QUIN), and the protective effects of glutathione (GSH), and 2-amino-5-phosphonovaleric acid (APV), were tested in rat brain synaptosomes, Reactive oxygen species (ROS) formation was quantified after the exposure of synaptosomes to increasing concentrations of QUIN (25-500 microM). The potency of QUIN to induce lipid peroxidation (LP) was tested as a regional index of thiobarbituric acid-reactive substances (TBARS) production, and the antioxidant actions of both GSH (50 microM) and APV (250 microM) on QUIN-induced LP were evaluated in synaptosomes prepared from different brain regions. QUIN induced concentration-dependent increases in ROS formation and TBARS in all regions analyzed, but increased production of fluorescent peroxidized lipids only in the striatum and the hippocampus, whereas both GSH and APV decreased this index. These results suggest that the excitotoxic action of QUIN involves regional selectivity in the oxidative status of brain synaptosomes, and may be prevented by substances exhibiting antagonism at the NMDA receptor.
在大鼠脑突触体中测试了喹啉酸(QUIN)的氧化作用以及谷胱甘肽(GSH)和2-氨基-5-磷酸戊酸(APV)的保护作用。将突触体暴露于浓度不断增加的QUIN(25 - 500微摩尔)后,对活性氧(ROS)的形成进行了定量分析。以硫代巴比妥酸反应性物质(TBARS)的产生作为区域指标,测试了QUIN诱导脂质过氧化(LP)的能力,并在从不同脑区制备的突触体中评估了GSH(50微摩尔)和APV(250微摩尔)对QUIN诱导的LP的抗氧化作用。在所有分析区域中,QUIN均诱导ROS形成和TBARS呈浓度依赖性增加,但仅在纹状体和海马体中增加了荧光过氧化脂质的产生,而GSH和APV均降低了该指标。这些结果表明,QUIN的兴奋性毒性作用涉及脑突触体氧化状态的区域选择性,并且可能被在N-甲基-D-天冬氨酸(NMDA)受体处表现出拮抗作用的物质所阻止。