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反复乙醇戒断会延迟海马点燃模型中局灶性癫痫发作的发展。

Repeated ethanol withdrawal delays development of focal seizures in hippocampal kindling.

作者信息

Veatch L M, Gonzalez L P

机构信息

Department of Psychiatry and Behavioral Sciences, University of Oklahoma Health Sciences Center, Oklahoma City 73190-3000, USA.

出版信息

Alcohol Clin Exp Res. 1999 Jul;23(7):1145-50.

Abstract

Clinical studies report an increase in the prevalence of alcohol withdrawal-related seizures in patients with a history of multiple detoxifications. In order to investigate the alcohol withdrawal-related alterations in neural activity that lead to this increase in seizure propensity, basic researchers have examined both spontaneous and elicited seizures in animals undergoing withdrawal from chronic ethanol. This study was designed to further examine alcohol withdrawal-related seizure activity in a rodent model by assessing the development of electrical kindling after chronic ethanol exposure administered in multiple or single treatment episodes. Laboratory rats were exposed to either five periods of 3 days of ethanol, one 15-day period of continuous ethanol, or a period of control handling with no ethanol exposure. Ten days after a final withdrawal episode, all animals were surgically prepared with recording and stimulating electrodes. Twenty days after final withdrawal from ethanol or an equivalent period of similar handling, daily electrical stimulation of hippocampal area CA3 was initiated. Animals exposed to ethanol required more daily stimulations to become fully kindled than did ethanol-naive controls, with those animals experiencing five withdrawals requiring the most stimulations overall and more stimulations to progress from focal to generalized seizure behaviors. These results indicate that chronic ethanol exposure and withdrawal alter neuronal mechanisms important for hippocampal kindling in a manner that persists long after cessation of ethanol exposure, and they indicate that this effect is increased by exposure to repeated withdrawal episodes.

摘要

临床研究报告称,有多次戒酒经历的患者中,与酒精戒断相关的癫痫发作患病率有所增加。为了研究导致癫痫发作倾向增加的与酒精戒断相关的神经活动变化,基础研究人员检查了慢性乙醇戒断动物的自发性和诱发性癫痫发作。本研究旨在通过评估多次或单次治疗期给予慢性乙醇暴露后电点燃的发展情况,进一步研究啮齿动物模型中与酒精戒断相关的癫痫活动。将实验大鼠暴露于五个为期3天的乙醇期、一个为期15天的连续乙醇期或一个无乙醇暴露的对照处理期。在最后一次戒断期后10天,所有动物均通过手术植入记录和刺激电极。在从乙醇最终戒断或同等时长的类似处理20天后,开始每日对海马体CA3区进行电刺激。与未接触过乙醇的对照动物相比,接触过乙醇的动物每天需要更多次刺激才能完全点燃,其中经历五次戒断的动物总体上需要的刺激最多,并且从局灶性癫痫发作行为发展为全身性癫痫发作行为需要更多刺激。这些结果表明,慢性乙醇暴露和戒断会改变对海马体点燃很重要的神经元机制,且这种改变在乙醇暴露停止后仍会持续很长时间,并且表明这种效应会因反复经历戒断期而增强。

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