Martins Márcio R, Petronilho Fabrícia C, Gomes Karin M, Dal-Pizzol Felipe, Streck Emilio L, Quevedo João
Laboratório de Neurociencias, Programa de Pós-graduacao em Cicecias da Saúde, Universidade do Extremo Sul Catarinense, 88806-000 Criciúma, SC, Brazil.
Neurotox Res. 2008 Jan;13(1):63-9. doi: 10.1007/BF03033368.
Typical and atypical antipsychotic drugs have been shown to have different clinical and behavioral profiles. Haloperidol (HAL) is a typical neuroleptic that acts primarily as a D(2) dopamine receptor antagonist. It has been proposed that reactive oxygen species play a causative role in neurotoxic effects induced by HAL. We evaluated oxidative damage in rat brain induced by chronic (28 days) HAL, clozapine (CLO), olanzapine (OLZ) or aripiprazole (ARI) administration. Adult male Wistar rats received daily injections of HAL (1.5 mg/kg), CLO (25 mg/kg), OLZ (2.5, 5 or 10 mg/kg) or ARI (2, 10 or 20 mg/kg); control animals received vehicle (Tween 1% solution). Thiobarbituric acid reactive substances (TBARS) and protein carbonylation were measured in the prefrontal cortex, hippocampus, striatum and cerebral cortex. The results showed that TBARS were increased in the striatum after HAL treatment. On the other hand, TBARS were diminished in the prefrontal cortex by OLZ and ARI. Our results also showed that all drugs tested in this work decreased TBARS levels in the cerebral cortex. In hippocampus, TBARS levels were not altered by any drug. Protein carbonyl content after HAL and CLO treatment was increased in the hippocampus. Moreover, OLZ and ARI did not alter protein carbonyl content when compared to control group. ARI chronic administration (20 mg/kg) also increased mitochondrial superoxide in the prefrontal cortex and striatum. ARI did not alter mitochondrial superoxide in the hippocampus and cerebral cortex. Moreover, HAL, OLZ and CLO did not cause significant alterations in mitochondrial superoxide in rat brain. Our findings demonstrate that OLZ and ARI do not induce oxidative damage in rat brain as observed after HAL and CLO treatment.
典型和非典型抗精神病药物已被证明具有不同的临床和行为特征。氟哌啶醇(HAL)是一种典型的抗精神病药物,主要作为D(2)多巴胺受体拮抗剂起作用。有人提出,活性氧在HAL诱导的神经毒性作用中起因果作用。我们评估了慢性(28天)给予HAL、氯氮平(CLO)、奥氮平(OLZ)或阿立哌唑(ARI)对大鼠脑氧化损伤的影响。成年雄性Wistar大鼠每天注射HAL(1.5mg/kg)、CLO(25mg/kg)、OLZ(2.5、5或10mg/kg)或ARI(2、10或20mg/kg);对照动物注射赋形剂(1%吐温溶液)。测定前额叶皮质、海马、纹状体和大脑皮质中的硫代巴比妥酸反应物质(TBARS)和蛋白质羰基化水平。结果表明,HAL治疗后纹状体中的TBARS增加。另一方面,OLZ和ARI使前额叶皮质中的TBARS减少。我们的结果还表明,本研究中测试的所有药物均降低了大脑皮质中的TBARS水平。在海马中,任何药物均未改变TBARS水平。HAL和CLO治疗后海马中的蛋白质羰基含量增加。此外,与对照组相比,OLZ和ARI未改变蛋白质羰基含量。长期给予ARI(20mg/kg)也增加了前额叶皮质和纹状体中的线粒体超氧化物。ARI未改变海马和大脑皮质中的线粒体超氧化物。此外,HAL、OLZ和CLO未引起大鼠脑线粒体超氧化物的显著改变。我们的研究结果表明,与HAL和CLO治疗后观察到的情况不同,OLZ和ARI不会在大鼠脑中诱导氧化损伤。