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孕酮及其代谢产物对猫大脑皮质发作间期癫痫样放电的影响。

The effect of progesterone and its metabolites on the interictal epileptiform discharge in the cat's cerebral cortex.

作者信息

Landgren S, Aasly J, Bäckström T, Dubrovsky B, Danielsson E

机构信息

Department of Physiology, University of Umeå, Sweden.

出版信息

Acta Physiol Scand. 1987 Sep;131(1):33-42. doi: 10.1111/j.1748-1716.1987.tb08202.x.

DOI:10.1111/j.1748-1716.1987.tb08202.x
PMID:3673611
Abstract

The antiepileptic effect of progesterone, 5-alpha-pregnane-3,20-dione, 3-alpha-hydroxy-5-alpha-pregnane-20-one, and 3-alpha-hydroxy-5-beta-pregnane-20-one were tested in an experimental animal model, and compared with the effect of clonazepam. The steroids were dissolved in serum from ovariectomized cats. Ovariectomized adult cats were used and spontaneous epileptic discharges were generated by placing small pieces of penicillin-soaked filter papers on the ipsi and contralateral cerebral cortex. The frequency and amplitude of the interictal epileptiform spikes were recorded, and analysed in a computer. The changes in frequency and amplitudes were calculated. The drugs were infused during 20-s periods into one cerebral hemisphere via the ipsilateral lingual artery with speeds of 1.1, 3.4 and 6.3 ml min-1. A penicillin focus on the contralateral hemisphere served as a simultaneous control. Progesterone and clonazepam showed similar inhibitory effects on epileptiform interictal spiking (median reduction of spike frequency 21%, cf. Table I). The 5-alpha-pregnane-3, 20-dione was generally less potent than progesterone (median reduction 9%) and the 5-alpha- and 5-beta-pregnanolones were two to three times more potent than progesterone (54-66% reduction). The latency of the inhibitory effect was 4-10 s measured from the entrance of the infusion into the lingual artery. The depression lasted 10-20 min. It is concluded that the pregnanolones have strong antiepileptic properties. The rapid onset of effect indicates that the steroids may interact with the neuronal function at the membrane or synaptic levels.

摘要

在实验动物模型中测试了孕酮、5α-孕烷-3,20-二酮、3α-羟基-5α-孕烷-20-酮和3α-羟基-5β-孕烷-20-酮的抗癫痫作用,并与氯硝西泮的作用进行了比较。这些类固醇溶解在去卵巢猫的血清中。使用去卵巢成年猫,通过在同侧和对侧大脑皮层放置小块浸有青霉素的滤纸来产生自发性癫痫放电。记录发作间期癫痫样棘波的频率和幅度,并在计算机上进行分析。计算频率和幅度的变化。通过同侧舌动脉以1.1、3.4和6.3 ml min-1的速度在20秒内将药物注入一个大脑半球。对侧半球的青霉素病灶作为同步对照。孕酮和氯硝西泮对癫痫样发作间期棘波显示出相似的抑制作用(棘波频率中位数降低21%,见表I)。5α-孕烷-3,20-二酮的效力通常低于孕酮(中位数降低9%),5α-和5β-孕烷醇酮的效力比孕酮高两到三倍(降低54-66%)。从药物注入舌动脉开始测量,抑制作用的潜伏期为4-10秒。抑制持续10-20分钟。结论是孕烷醇酮具有很强的抗癫痫特性。作用起效迅速表明这些类固醇可能在膜或突触水平与神经元功能相互作用。

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