THE BEHAVIORAL PHARMACOLOGY OF NMDA RECEPTOR ANTAGONISTS

被引:338
作者
WILLETTS, J
BALSTER, RL
LEANDER, JD
机构
[1] VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,DEPT PHARMACOL & TOXICOL,RICHMOND,VA 23298
[2] ELI LILLY INT CORP,LILLY RES LABS,INDIANAPOLIS,IN 46285
关键词
( )-6-phosphonomethyl-decahydroisoquinoline-3-carboxylicacid; 1-(cis-2-carboxypiperidine-4-yl)-methyl-l-phosphonic acid; 2-amino-4; 2-amino-5-phosphonovalerate; 2-arnino-7-phosphonoheptanoate; 2-cyclohexyl)-7-phosphonoheptanoic acid; 3-([±]-2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid; 5-(l; AF5; AP7; CGP37849; CGS19755; cis-(±)-4-(2H-tetrazol-5-yl)methylpiperidine-2-carboxylicacid; CPP; d; l-(E)-2-amino-4-methyl-5-phosphono-3-pentanoic acid; LY233053; LY274614; NPC12626;
D O I
10.1016/0165-6147(90)90150-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
There is considerable interest in the development of NMDA antagonists as potential therapeutic agents in the treatment of convulsant, neurodegenerative and anxiety disorders. Because the clinical use of phencyclidine (PCP) has been precluded by its psychotomimetic effects and abuse potential, there has been concern that other NMDA antagonists including those acting competitively might produce similar untoward effects. However, the studies in animals, reviewed here by Joyce Willetts, Robert Balster and David Leander, suggest that while there are certain similarities in the behavioral effects of PCP-like and competitive antagonists, there are also differences. These differences have implications for the development of NMDA antagonists with less likelihood for producing PCP-like side-effects. © 1990.
引用
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页码:423 / 428
页数:6
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