Ribak C E, Hunt C A, Bakay R A, Oertel W H
Brain Res. 1986 Jan 15;363(1):78-90. doi: 10.1016/0006-8993(86)90660-8.
Previous studies have indicated that a loss of GABAergic terminals occurs at epileptic foci. The present study was undertaken to investigate if this loss is associated with a loss of GABAergic neuronal somata. Seven juvenile monkeys (M. mulatta) received alumina gel injections to the pre-central gyrus of the left cerebral hemisphere to produce epileptic foci. Four of these monkeys were chosen for further quantitative study. One was sacrificed prior to seizure onset ('pre-seizure'), one had seizures for 3 days ('acute'), and two had a seizure record of one month ('chronic'). Sections of tissue from the epileptic cortex and from the contralateral, non-epileptic cortex were processed for glutamate decarboxylase (GAD) immunocytochemistry at the light microscopic level. Quantitative analysis revealed that a loss of GAD-positive neuronal somata ranging from 24 to 52% occurred at epileptic foci for all monkeys. This decrease was significant (P less than 0.01) for the two chronic monkeys. There was also a slight decrease in GAD-positive neurons 1 cm distal to the focus ('parafocus') in the chronic monkeys, but not in the acute or pre-seizure animals. In addition, small GAD-positive somata (50-150 micron2) were more severely decreased in number at epileptic foci than larger ones (200-250 micron2). As an experimental control, an additional monkey was given a surgical lesion in area 4 of one cerebral hemisphere. It did not display seizure activity prior to sacrifice and did not show a loss of GAD-positive neurons proximal to the control lesions. The results of this study indicate that a loss of GABAergic neuronal somata is associated with a loss of GABAergic terminals at epileptic foci, and that this loss may be more specific for the small GABAergic neurons.
以往的研究表明,癫痫病灶处存在γ-氨基丁酸能(GABAergic)终末的丧失。本研究旨在探讨这种丧失是否与GABA能神经元胞体的丧失有关。七只幼年猕猴(恒河猴)接受了向左侧大脑半球中央前回注射氧化铝凝胶以产生癫痫病灶。其中四只猴子被选作进一步的定量研究。一只在癫痫发作前处死(“发作前”),一只癫痫发作3天(“急性”),两只癫痫发作记录为1个月(“慢性”)。对癫痫皮质和对侧非癫痫皮质的组织切片进行光镜下谷氨酸脱羧酶(GAD)免疫细胞化学处理。定量分析显示,所有猴子癫痫病灶处GAD阳性神经元胞体丧失24%至52%。对于两只慢性猴子,这种减少具有显著性(P小于0.01)。在慢性猴子中,病灶远端1厘米处(“病灶旁”)的GAD阳性神经元也略有减少,但急性或发作前动物中未出现这种情况。此外,癫痫病灶处小的GAD阳性胞体(50 - 150平方微米)数量减少比大的(200 - 250平方微米)更严重。作为实验对照,另一只猴子在一个大脑半球的4区进行了手术损伤。它在处死前未表现出癫痫活动,且对照损伤近端未显示GAD阳性神经元的丧失。本研究结果表明,癫痫病灶处GABA能神经元胞体的丧失与GABA能终末的丧失有关,且这种丧失可能对小的GABA能神经元更具特异性。