Department of Physiology and Pharmacology, Federal University of Pernambuco, Recife, Pernambuco, 50670-901, Brazil.
Psychopharmacology (Berl). 2013 May;227(2):209-19. doi: 10.1007/s00213-012-2951-2. Epub 2012 Dec 29.
There is extensive evidence indicating the influence of seizures on emotional responses observed in human and animals, but so far few studies are focusing on the behavioral profile of animals that do not have seizures despite being treated with convulsant agents.
We aimed to establish the behavioral profile, biochemical, and electrographic features of rats submitted to the pilocarpine model of temporal lobe epilepsy
Rats treated with pilocarpine (20 to 350 mg/kg, i.p.) that did not develop status epilepticus or spontaneous recurrent seizures were evaluated 1 month later in the elevated plus maze (EPM), T-maze (ETM), open-field (OF), and step-down avoidance tests. Electroencephalographic (EEG), glutamate uptake, and hippocampal neuronal death assays were also performed
Pilocarpine (150 or 350 mg/kg) promoted anxiogenic-like effects in rats evaluated in the EPM, ETM, and OF tests, whereas only the highest dose evoked spike-wave discharges during EEG recordings. Hippocampal theta rhythm was increased by pilocarpine 150 or 350 mg/kg and only the highest dose reduced the L-[(3)H]-glutamate uptake and cell viability on hippocampal slices.
Subconvulsant doses of pilocarpine promote long-lasting alterations on neural circuitry, reflected by an increased theta activity in the hippocampus and an anxiety-like profile of rats evaluated 1 month after the treatment which is independent of seizure occurrence and is not related to changes in glutamate uptake or hippocampal damage. These results prompt us to suggest that a systemic administration of subconvulsant doses of pilocarpine could be useful as a new tool to model trait anxiety in rats.
有大量证据表明,癫痫发作对人类和动物观察到的情绪反应有影响,但到目前为止,很少有研究关注尽管使用致惊厥剂治疗但仍未发生癫痫发作的动物的行为特征。
我们旨在建立接受匹鲁卡品颞叶癫痫模型的大鼠的行为特征、生化和脑电图特征。
在 1 个月后,对未发生癫痫持续状态或自发性反复癫痫发作的匹鲁卡品(20 至 350mg/kg,ip)治疗大鼠进行高架十字迷宫(EPM)、T 迷宫(ETM)、旷场(OF)和避错试验评估。还进行了脑电图(EEG)、谷氨酸摄取和海马神经元死亡测定。
匹鲁卡品(150 或 350mg/kg)在 EPM、ETM 和 OF 试验中引起大鼠焦虑样效应,而只有最高剂量在 EEG 记录中诱发尖波-慢波放电。匹鲁卡品 150 或 350mg/kg 增加了海马的θ节律,只有最高剂量降低了海马切片上的 L-[(3)H]-谷氨酸摄取和细胞活力。
亚惊厥剂量的匹鲁卡品可促进神经回路的长期改变,表现为海马中θ活动增加和大鼠在治疗 1 个月后表现出焦虑样特征,这与发作发生无关,也与谷氨酸摄取或海马损伤的变化无关。这些结果提示我们,全身给予亚惊厥剂量的匹鲁卡品可能是在大鼠中模拟特质焦虑的一种新工具。