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纹状体多巴胺D2受体调节中的多种膜内受体-受体相互作用

Multiple intramembrane receptor-receptor interactions in the regulation of striatal dopamine D2 receptors.

作者信息

Rimondini R, Fuxe K, Ferré S

机构信息

Department of Neuroscience, Karolinska Institute, Stockholm, Sweden.

出版信息

Neuroreport. 1999 Jul 13;10(10):2051-4. doi: 10.1097/00001756-199907130-00011.

Abstract

Adenosine A2A, group I mGlu and neurotensin receptors have been previously found to modulate the binding characteristics of dopamine D2 receptors in membrane preparations from rat striatum. In the present study it is shown that stimulation of different combinations of striatal A2A, group I mGlu and neurotensin receptors induce different effects on the modulation of D2 receptor binding to those obtained when they are separately stimulated using maximal effective concentrations. In competitive inhibition experiments of dopamine versus the D2 receptor antagonist [3H]raclopride the addition of the A2A receptor agonist CGS 21680, the group I mGlu receptor agonist DHPG or neurotensin induced a decrease in the affinity of the high affinity state of the dopamine D2 receptors for dopamine. When added together CGS 21680 plus neurotensin induced the same effect as when administered alone, CGS 21680 plus DHPG induced a synergistic effect and DHPG plus neurotensin lost their modulating effect on D2 receptor binding. These results demonstrate the existence of multiple intramembrane receptor-receptor interactions in the regulation of striatal D2 receptors.

摘要

腺苷A2A、I组代谢型谷氨酸(mGlu)和神经降压素受体先前已被发现可调节大鼠纹状体膜制剂中多巴胺D2受体的结合特性。在本研究中发现,刺激纹状体A2A、I组mGlu和神经降压素受体的不同组合,对D2受体结合的调节作用与使用最大有效浓度分别刺激时所获得的不同。在多巴胺与D2受体拮抗剂[3H]雷氯必利的竞争性抑制实验中,添加A2A受体激动剂CGS 21680、I组mGlu受体激动剂DHPG或神经降压素会导致多巴胺D2受体高亲和力状态对多巴胺的亲和力降低。当CGS 21680与神经降压素一起添加时,诱导的效果与单独给药时相同;CGS 21680与DHPG一起添加时,诱导协同效应;而DHPG与神经降压素一起添加时,则失去了对D2受体结合的调节作用。这些结果证明在纹状体D2受体的调节中存在多种膜内受体 - 受体相互作用。

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