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腺苷A1受体激活对多巴胺D1受体脱敏的增强作用。

The enhancement of dopamine D1 receptor desensitization by adenosine A1 receptor activation.

作者信息

Cao Yan, Xie Ke-Qiang, Zhu Xing-Zu

机构信息

Department of Pharmacology, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, PR China.

出版信息

Eur J Pharmacol. 2007 May 7;562(1-2):34-8. doi: 10.1016/j.ejphar.2007.01.090. Epub 2007 Feb 16.

Abstract

The present study was designed to examine the effects of adenosine A(1) receptor on dopamine D(1) receptor desensitization in a human embryonic kidney 293 cell line stably cotransfected with human adenosine A(1) receptor and dopamine D(1) receptor cDNAs (A(1)D(1) cells) by means of cAMP accumulation assay. Long-term exposure of A(1)D(1) cells to dopamine D(1) receptor agonist (+/-)-1-phenyl-2,3,4,5-tetrahydro-(1H)-3-benzazepine-7,8-diol hydrochloride (SKF38393) caused a rapid desensitization of dopamine D(1) receptor. Coadministration of adenosine A(1) receptor agonist N(6)-cyclopentyladenosine (CPA) potentiated the effect of SKF38393. This enhancement effect of CPA was blocked by adenosine A(1) receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX) but not by pertussis toxin, indicating that this effect of CPA was mediated by adenosine A(1) receptor and was G(i) protein independent. Furthermore, the blockade of endogenous adenosine by adenosine deaminase or DPCPX attenuated dopamine D(1) receptor desensitization. Collectively, these results suggest that adenosine A(1) receptor plays an important role in the regulation of dopamine D(1) receptor by potentiating ligand-induced desensitization.

摘要

本研究旨在通过环磷酸腺苷(cAMP)积累试验,检测腺苷A(1)受体对稳定共转染人腺苷A(1)受体和多巴胺D(1)受体cDNA的人胚肾293细胞系(A(1)D(1)细胞)中多巴胺D(1)受体脱敏的影响。将A(1)D(1)细胞长期暴露于多巴胺D(1)受体激动剂(±)-1-苯基-2,3,4,5-四氢-(1H)-3-苯并氮杂卓-7,8-二醇盐酸盐(SKF38393)会导致多巴胺D(1)受体迅速脱敏。同时给予腺苷A(1)受体激动剂N(6)-环戊基腺苷(CPA)可增强SKF38393的作用。CPA的这种增强作用被腺苷A(1)受体拮抗剂8-环戊基-1,3-二丙基黄嘌呤(DPCPX)阻断,但不被百日咳毒素阻断,这表明CPA的这种作用是由腺苷A(1)受体介导的,且与G(i)蛋白无关。此外,腺苷脱氨酶或DPCPX对内源性腺苷的阻断减弱了多巴胺D(1)受体的脱敏。总的来说,这些结果表明腺苷A(1)受体通过增强配体诱导的脱敏作用,在多巴胺D(1)受体的调节中发挥重要作用。

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