Anthraquinone polyamines:: novel channel blockers of N-methyl-D-aspartate receptors

被引:7
|
作者
Kashiwagi, K.
Williams, K.
Igarashi, K.
机构
[1] Chiba Inst Sci, Fac Pharm, Chiba 2880025, Japan
[2] SUNY Hlth Sci Ctr, Dept Physiol & Pharmacol, Brooklyn, NY 11203 USA
[3] Chiba Univ, Grad Sch Pharmaceut Sci, Chiba, Japan
关键词
polyamine derivatives; glutamate receptor; NMDA receptor; channel blocker;
D O I
10.1007/s00726-007-0520-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polyamines, in particular spermine, as well as some natural and synthetic polyamine derivatives have been found to be blockers of N-methyl-D-aspartate receptors. We developed novel, polyamine-based channel blockers to analyze the structure of NMDA receptors. Anthraquinone polyamines block NMDA receptors with some selectivity compared to other glutamate receptors. Results using mutant NR1 and NR2 subunits identified amino acid residues that influence blockade by anthraquinone polyamines. The head group (anthraquinone) may be positioned at the selectivity filter/narrowest constriction of the channel and the polyamine tail penetrates this constriction into the inner vestibule below the level of the selectivity filter. The results are consistent with other work showing that NR1 (Asn616) and NR2B (Asn616), but not NR2B (Asn615), make the narrowest constriction of NMDA channel, and that the M3 segments from the two subunits, which form the outer vestibule, are likely staggered relative to each other in the vertical axis of the channel.
引用
收藏
页码:299 / 304
页数:6
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