Recent developments in structure-activity relationships for steroid modulators of GABAA receptors

被引:66
作者
Covey, DF
Evers, AS
Mennerick, S
Zorumski, CF
Purdy, RH
机构
[1] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Anesthesiol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[5] Scripps Res Inst, Dept Neurobiol, La Jolla, CA 92037 USA
关键词
ligand gated ion channels; functional modulation; benz[e]indenes; intravenous anesthetic; neuroactive steroid; neurosteroid enantiomer; GABA(A) receptor; NMDA receptor;
D O I
10.1016/S0165-0173(01)00126-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
GABAergic neurotransmission can be both positively and negatively modulated by steroids. The steroid effects are thought to be mediated by binding of steroids to specific sites on GABA(A) receptors. It appears that the receptor sites for positive and negative modulatory steroids are different. Thus far, the location and number of binding sites for steroids on these receptors have not been established. In this brief review, we concentrate largely on results from our own structure-activity studies. Novel analogues have been studied to further delineate the structural features required for compounds to modulate receptor function via steroid binding sites. Non-naturally occurring enantiomers of both positive and negative modulators have been studied to provide further evidence for the existence of specific steroid binding sites on the receptors. (C) 2001 Elsevier Science BY. All rights reserved.
引用
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页码:91 / 97
页数:7
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