NEUROACTIVE STEROID MODULATION OF [H-3] MUSCIMOL BINDING TO THE GABA(A) RECEPTOR COMPLEX IN RAT CORTEX

被引:32
作者
GOODNOUGH, DB
HAWKINSON, JE
机构
[1] Department of Biochemical Pharmacology, CoCensys, Inc., Irvine, CA 92718
来源
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION | 1995年 / 288卷 / 02期
关键词
EPALON; NEUROACTIVE STEROID; GABA(A) RECEPTOR; H-3] MUSCIMOL; 3-ALPHA-HYDROXY-5-ALPHA-PREGNAN-20-ONE;
D O I
10.1016/0922-4106(95)90190-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Epalons are a subclass of neuroactive steroids which are positive allosteric modulators of the GABA(A) receptor acting via a unique site on the receptor complex. Enhancement of [H-3]muscimol binding to the GABA recognition site was observed to be either full (> 150%) or limited (110-135%) and specific for epalons. Both one and two component modulation was observed. Saturation studies performed in the presence of 3 alpha-hydroxy-5 alpha-pregnan-20-one (3 alpha,5 alpha-P) showed that 3 alpha,5 alpha-P increased the density of high affinity [H-3]muscimol sites and doubled the affinity of low affinity sites. 3 alpha,5 alpha-P had no effect on the affinity of the high affinity site or the density of the low affinity site. These data indicate that: (1) epalons are potent, stereoselective enhancers of [H-3]muscimol binding; (2) epalons display varying levels of efficacy and some exhibit two-component enhancement; and (3) 3 alpha,5 alpha-P enhancement of [H-3]muscimol binding results from both an increased density of high affinity sites and an increased affinity for low affinity sites.
引用
收藏
页码:157 / 162
页数:6
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