Suppr超能文献

阿扑吗啡作为人类自我抑制性多巴胺受体的优先刺激剂。

Apomorphine as a preferential stimulant of self-inhibitory dopamine receptors in man.

作者信息

Corsini G U, Del Zompo M, Piccardi M P, Mangoni A, Gessa G L

出版信息

Ann Ist Super Sanita. 1978;14(1):123-30.

PMID:756167
Abstract

In man, non emetic doses of apomorphine elicit a series of behavioural, neurological and psychological changes which are difficult to ascribe to the stimulation of postsynaptic dopamine receptors. Since similar effects are elicited by neuroleptic drugs, the functional changes induced by apomorphine in man might be interpreted as being the result of a decreased dopaminergic activity. The sedation and sleep, the improvement of choreic movements and the antipsychotic effect induced by non emetic doses of apomorphine are prevented by specific dopamine receptor blockers. These responses therefore are mediated through a stimulation of dopamine receptors leading to a decreased dopaminergic transmission. This new type of receptors might be identified with the so called "self-inhibitory" dopamine receptors.

摘要

在人类中,非催吐剂量的阿扑吗啡会引发一系列行为、神经和心理变化,这些变化很难归因于对突触后多巴胺受体的刺激。由于抗精神病药物也会引发类似的效应,因此阿扑吗啡在人类中诱导的功能变化可能被解释为多巴胺能活性降低的结果。非催吐剂量的阿扑吗啡所诱导的镇静、睡眠、舞蹈样运动的改善以及抗精神病作用,可被特定的多巴胺受体阻滞剂所阻断。因此,这些反应是通过刺激多巴胺受体介导的,从而导致多巴胺能传递减少。这种新型受体可能与所谓的“自我抑制性”多巴胺受体相同。

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