Suppr超能文献

[在抑郁症模型中,NMDA受体多胺结合位点某些配体缺乏抗抑郁样活性]

[Lack of antidepresant-like activity of some ligands of polyamine binding sites of NMDA receptors in models of depression].

作者信息

Zin'kovskaia L Ia, Kidin Iu V, Komissarov I V, Obraztsova O G

出版信息

Eksp Klin Farmakol. 2006 Jan-Feb;69(1):3-5.

Abstract

Arcain and a series of the partial modulators of polyamine binding sites of NMDA receptors (spermine- and adamantyl-containing polyamines IEM-1460, IEM-1490, IEM-1592, IEM-1755) do not display (in contrast to melipramine and memantine) antidepressant-like action in the forced swimming test and reserpine-induced depression test in rats. Compounds IEM-1460, IEM-1490, IEM-1592 increase the total time of immobilization in the Porsolt test, probably, by facilitating the development of stress-induced depression. It is supposed that the prodepressant activity of these compounds is mediated by NMDA-receptors having NR1/NR2C and NR1/NR2D subunit composition.

摘要

与丙咪嗪和美金刚不同,阿卡因以及一系列NMDA受体多胺结合位点的部分调节剂(含精胺和金刚烷基的多胺IEM-1460、IEM-1490、IEM-1592、IEM-1755)在大鼠强迫游泳试验和利血平诱导的抑郁试验中未表现出抗抑郁样作用。化合物IEM-1460、IEM-1490、IEM-1592可能通过促进应激诱导抑郁的发展,增加了波索尔特试验中的总不动时间。据推测,这些化合物的促抑郁活性是由具有NR1/NR2C和NR1/NR2D亚基组成的NMDA受体介导的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验