Suppr超能文献

特定的α2-肾上腺素受体拮抗剂可诱发大鼠的行为激活。

Specific α2-adrenoreceptor antagonists induce behavioural activation in the rat.

机构信息

Reckitt and Colman Psychopharmacology Unit, The School of Medical Sciences, University Walk, Bristol, BS8 1TD.

出版信息

J Psychopharmacol. 1990 Jan;4(2):90-9. doi: 10.1177/026988119000400207.

Abstract

The behavioural effects of the specific and selective α(2)-adrenoreceptor antagonists, idazoxan, efaroxan and RX811059, have been investigated in the rat. All three drugs induced periods of behavioural activation characterized by increased locomotion and exploration (rearing and hole dipping). However, these effects were only apparent in animals which were fully habituated to their environments and thus displayed low baseline activity. The behaviour observed lay within the normal range of activity and was not apparent under conditions when exploration was stimulated such as in a novel environment. α( 2)-Adrenoreceptor antagonist- induced activation was a weak response when compared with the intense and prolonged hyperactivity, in both novel and non-novel environments, induced by the amine releaser D- amphetamine. Possible mechanisms involving a direct action of noradrenaline at postsynaptic α( 1)-adrenoreceptors (subsequent to enhanced presynaptic α(2)-receptor feedback blockade) or an indirect action of α(2)-antagonists on dopamine function in mesolimbic pathways are discussed.

摘要

已经在大鼠身上研究了特定和选择性的α(2)-肾上腺素受体拮抗剂伊达唑兰、埃法罗辛和 RX811059 的行为效应。这三种药物都诱导了行为激活期,表现为运动和探索(站立和洞穴探测)增加。然而,这些效应仅在完全适应环境且基础活动水平较低的动物中明显。观察到的行为处于正常活动范围内,在刺激探索的情况下(例如在新环境中)并不明显。与胺释放剂 D-苯丙胺在新环境和非新环境中引起的强烈和持久的过度兴奋相比,α(2)-受体拮抗剂诱导的激活是一种较弱的反应。讨论了涉及去甲肾上腺素在后突触α(1)-肾上腺素受体上的直接作用(继发于增强的突触前α(2)-受体反馈阻断)或α(2)-拮抗剂对中脑边缘多巴胺功能的间接作用的可能机制。

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