ANTIDEPRESSANT-LIKE ACTIONS OF THE POLYAMINE SITE NMDA ANTAGONIST, ELIPRODIL (SL-82.0715)

被引:113
作者
LAYER, RT
POPIK, P
OLDS, T
SKOLNICK, P
机构
[1] Laboratory of Neuroscience, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda
关键词
ELIPRODIL; SL-82.0715; ANTIDEPRESSANTS; NMDA RECEPTORS; BETA-ADRENOCEPTORS; FORCED SWIM TEST;
D O I
10.1016/0091-3057(95)00155-P
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Functional N-methyl-D-aspartate (NMDA) antagonists including competitive antagonists, glycine partial agonists, and use-dependent channel blockers exhibit antidepressant-like actions in preclinical models. The present study examined the effects of eliprodil (SL-82.0715), an NMDA antagonist acting at polyamine sites, in behavioral and neurochemical tests predictive of antidepressant activity. In mice, eliprodil produced a dose-dependent reduction in immobility in the forced swim test, but was inactive in the tail suspension test. Chronic treatment with eliprodil produced both a significant downregulation of beta-adrenoceptors and a reduction in the potency of glycine to inhibit [H-3]5,7-dichlorokynurenic acid binding to strychnine-insensitive glycine receptors in neocortical membranes. In toto, these data indicate that like other NMDA antagonists, eliprodil possesses antidepressant-like actions in preclinical tests predictive of clinical efficacy.
引用
收藏
页码:621 / 627
页数:7
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