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大鼠荷包牡丹碱致痫作用

Bicuculline epileptogenesis in the rat.

作者信息

Campbell A M, Holmes O

出版信息

Brain Res. 1984 Dec 10;323(2):239-46. doi: 10.1016/0006-8993(84)90294-4.

Abstract

Bicuculline has been applied electrophoretically from a fluid filled microelectrode at different depths within the primary somatosensory area of the cerebral cortex of rats anaesthetized with urethane. The delay between onset of drug application at a constant rate and onset of spontaneous focal interictal epileptiform discharges (FIEDs), detected by a nearby recording microelectrode, was least when bicuculline was applied at a depth of 0.65 mm below the pial surface. The subsequent frequency of FIEDs and their voltage excursion were also greatest at this depth. The relationship between the delay of onset of epileptiform spiking and the depth of drug application was very similar to that previously determined for penicillin. This similarity of the sensitivity profiles suggests that the epileptogenic actions of the two agents may be attributable to a common mechanism. At low concentrations, both agents specifically block GABAergic inhibitory synaptic transmission in brain tissue. This is likely to be the mechanism of their epileptogenic effects. Other synaptic and non-synaptic mechanisms cannot, however, be ruled out because of the high concentrations which are achieved locally when a chemical is applied from a point source.

摘要

荷包牡丹碱已通过充满液体的微电极在氨基甲酸乙酯麻醉的大鼠大脑皮层初级体感区的不同深度进行电泳施加。以恒定速率施加药物开始至附近记录微电极检测到自发局灶性发作间期癫痫样放电(FIEDs)开始之间的延迟,在软脑膜表面以下0.65毫米深度施加荷包牡丹碱时最短。在此深度,随后的FIEDs频率及其电压偏移也最大。癫痫样尖峰发作延迟与药物施加深度之间的关系与先前针对青霉素确定的关系非常相似。这种敏感性分布的相似性表明,这两种药物的致痫作用可能归因于共同机制。在低浓度时,这两种药物都特异性阻断脑组织中的GABA能抑制性突触传递。这可能是它们致痫作用的机制。然而,由于从点源施加化学物质时在局部达到的高浓度,其他突触和非突触机制不能排除。

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