Distinct sites for inverse modulation of N-methyl-D-aspartate receptors by sulfated steroids

被引:192
作者
Park-Chung, M
Wu, FS
Purdy, RH
Malayev, AA
Gibbs, TT
Farb, DH
机构
[1] Boston Univ, Sch Med, Dept Pharmacol, Mol Neurobiol Lab, Boston, MA 02118 USA
[2] Univ Calif San Diego, Sch Med, Dept Psychiat, San Diego, CA 92161 USA
关键词
D O I
10.1124/mol.52.6.1113
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Steroid sulfation Occurs in nervous tissue and endogenous sulfated steroids can act as positive or negative modulators of N-methyl-D-aspartate (NMDA) receptor function. In the current study, structure-activity relationships for sulfated steroids were examined in voltage-clamped chick spinal cord and rat hippocampal neurons in culture and in Xenopus laevis oocytes expressing NR1(100) and NR2A subunits. The ability of pregnenolone sulfate (a positive modulator) and epipregnanolone sulfate (a negative modulator) to compete with each another, as well as with other known classes of NMDA receptor modulators, was examined. The results show that steroid positive and negative modulators act at specific, extracellularly directed sites that are distinct from one another and from the spermine, redox, glycine, Mg2+, MK-801, and arachidonic acid sites. Sulfated steroids are effective as modulators of ongoing glutamate-mediated synaptic transmission, which is consistent with their possible role as endogenous neuromodulators in the CNS.
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页码:1113 / 1123
页数:11
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