Faculty of Medicine Estácio of Juazeiro do Norte (Estácio FMJ), Juazeiro do Norte, Brazil; Faculty of Medicine of the Federal University of Ceará (UFC), Fortaleza, Brazil.
Faculty of Medicine Estácio of Juazeiro do Norte (Estácio FMJ), Juazeiro do Norte, Brazil.
Pharmacol Biochem Behav. 2018 Apr;167:17-28. doi: 10.1016/j.pbb.2018.02.001. Epub 2018 Feb 13.
Valproic acid (VA) is an antiepileptic that is also used for the treatment of bipolar disorders. The objective was to evaluate the neuroprotective effects of VA on a brain ischemia model. The groups of male Wistar rats were: SO (sham-operated), ischemic and ischemic treated with VA (25, 50 and 100 mg/kg, p.o.). After anesthesia with ketamine and xilazine, the animals were subjected to clamping of carotid arteries (30 min) and reperfusion. Except for the carotid clamping, the SO group was submitted to the same procedure. On the 7th day, the animals were behaviorally evaluated, euthanized and had their brain dissected for neurochemical and immunohistochemical assays. The data were analyzed by ANOVA and Tukey as the post hoc test. The results showed that VA reversed partly or completely the behavioral (locomotor activity and memory deficits), neurochemical (striatal DA and DOPAC levels, brain nitrite and lipid peroxidation) and immunohistochemical alterations (iNOS, COX-2, HDAC and GSK3) observed in the untreated ischemic group. VA neuroprotective effects are probably related to its anti-inflammatory and antioxidant properties, as well as to HDAC and GSK3 inhibitory effects. These findings stimulate translational studies focusing on VA as a neuroprotective drug to be potentially used in the clinic for several neurological conditions.
丙戊酸(VA)是一种抗癫痫药,也用于治疗双相情感障碍。本研究旨在评估 VA 对脑缺血模型的神经保护作用。雄性 Wistar 大鼠分为:假手术(SO)组、缺血组和缺血后用 VA(25、50 和 100mg/kg,po)处理组。在氯胺酮和甲苯噻嗪麻醉后,动物的颈动脉被夹闭(30min)并再灌注。除了颈动脉夹闭,SO 组接受相同的处理。在第 7 天,对动物进行行为评估,安乐死后对大脑进行神经化学和免疫组织化学分析。数据采用 ANOVA 和 Tukey 作为事后检验进行分析。结果表明,VA 部分或完全逆转了未经处理的缺血组观察到的行为(运动活性和记忆缺陷)、神经化学(纹状体 DA 和 DOPAC 水平、脑亚硝酸盐和脂质过氧化)和免疫组织化学改变(iNOS、COX-2、HDAC 和 GSK3)。VA 的神经保护作用可能与其抗炎和抗氧化特性以及对 HDAC 和 GSK3 的抑制作用有关。这些发现促进了针对 VA 作为神经保护药物的转化研究,该药物可能在临床上用于多种神经疾病。