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多巴胺“稳定剂”(-)-OSU6162对体外多巴胺D2受体功能的刺激和抑制作用

Stimulating and inhibitory effects of the dopamine "stabilizer" (-)-OSU6162 on dopamine D2 receptor function in vitro.

作者信息

Lahti R A, Tamminga C A, Carlsson A

机构信息

Maryland Psychiatric Research Center, University of Maryland, Baltimore, MD, USA.

出版信息

J Neural Transm (Vienna). 2007 Sep;114(9):1143-6. doi: 10.1007/s00702-007-0784-7. Epub 2007 Jul 6.

Abstract

The effect of (-)-OSU6162 on the incorporation of GTPgammaS(35) in the membranes of hD(2l)-transfected CHO cells was investigated. In the absence of dopamine the compound exerted a slight but significant stimulating action, suggesting a weak partial agonism. In the presence of dopamine, low concentrations (10 to 100 nM) enhanced the stimulating action of dopamine. This enhancing effect was reversed by higher concentrations of (-)-OSU6162 in a complex biphasic manner. The dopamine-enhancing action is proposed to be mediated by binding to an allosteric site with high affinity and the inhibitory component by a low-affinity binding to the orthosteric site of the dopamine receptor.

摘要

研究了(-)-OSU6162对转染人D2L型多巴胺受体的中国仓鼠卵巢(CHO)细胞膜中GTPγS(35)掺入的影响。在无多巴胺的情况下,该化合物发挥了轻微但显著的刺激作用,提示存在弱部分激动作用。在有多巴胺存在时,低浓度(10至100 nM)增强了多巴胺的刺激作用。较高浓度的(-)-OSU6162以复杂的双相方式逆转了这种增强作用。多巴胺增强作用被认为是通过高亲和力结合变构位点介导的,而抑制成分则是通过低亲和力结合多巴胺受体的正构位点介导的。

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