Xie Zhihua, Miller Gregory M
New England Primate Research Center, Harvard Medical School, One Pine Hill Drive, Southborough, MA 01772, USA.
J Pharmacol Exp Ther. 2009 Jul;330(1):316-25. doi: 10.1124/jpet.109.153775. Epub 2009 Apr 13.
This study reveals a novel receptor mechanism for methamphetamine action in dopamine transporter (DAT) regulation. Trace amine-associated receptor 1 (TAAR1) is expressed in brain dopaminergic nuclei and is activated by methamphetamine in vitro. Here, we show that methamphetamine interaction with TAAR1 inhibits [(3)H]dopamine uptake, enhances or induces [(3)H]dopamine efflux, and triggers DAT internalization. In time course assays in which methamphetamine and [(3)H]dopamine were concurrently loaded into cells or synaptosomes or in pretreatment assays in which methamphetamine was washed away before [(3)H]dopamine loading, methamphetamine caused a distinct inhibition in [(3)H]dopamine uptake in TAAR1 + DAT-cotransfected cells and in wild-type mouse and rhesus monkey striatal synaptosomes. This distinct uptake inhibition was not observed in DAT-only transfected cells or in TAAR1 knockout mouse striatal synaptosomes. In [(3)H]dopamine efflux assays using the same cell and synaptosome preparations, methamphetamine enhanced [(3)H]dopamine efflux at a high loading concentration of [(3)H]dopamine (1 muM) or induced [(3)H]dopamine efflux at a low loading concentration of [(3)H]dopamine (10 nM) in a TAAR1-dependent manner. In DAT biotinylation assays using the same cell and synaptosome preparations, we observed that 1 muM methamphetamine induced DAT internalization in a TAAR1-dependent manner. All these TAAR1-mediated effects of methamphetamine were blocked by the protein kinase inhibitors H89 [N-[2-(4-bromocinnamylamino)ethyl]-5-isoquinoline] and/or 2-{8-[(dimethylamino) methyl]-6,7,8,9-tetrahydropyrido[1,2-a]indol-3-yl}-3-(1-methylindol-3-yl)maleimide (Ro32-0432), suggesting that methamphetamine interaction with TAAR1 triggers cellular phosphorylation cascades and leads to the observed effects of methamphetamine on DAT. These findings demonstrate a mediatory role of TAAR1 in methamphetamine action in DAT regulation and implicate this receptor as a potential target of therapeutics drugs for methamphetamine addiction.
本研究揭示了甲基苯丙胺在多巴胺转运体(DAT)调节中的一种新型受体机制。痕量胺相关受体1(TAAR1)在脑多巴胺能核中表达,并在体外被甲基苯丙胺激活。在此,我们表明甲基苯丙胺与TAAR1的相互作用抑制[³H]多巴胺摄取,增强或诱导[³H]多巴胺外流,并触发DAT内化。在甲基苯丙胺和[³H]多巴胺同时加载到细胞或突触体中的时间进程分析中,或在[³H]多巴胺加载前将甲基苯丙胺洗脱的预处理分析中,甲基苯丙胺在TAAR1 + DAT共转染细胞以及野生型小鼠和恒河猴纹状体突触体中对[³H]多巴胺摄取产生明显抑制。在仅转染DAT的细胞或TAAR1基因敲除小鼠纹状体突触体中未观察到这种明显的摄取抑制。在使用相同细胞和突触体制备的[³H]多巴胺外流分析中,甲基苯丙胺在高加载浓度的[³H]多巴胺(1μM)下增强[³H]多巴胺外流,或在低加载浓度的[³H]多巴胺(10 nM)下以TAAR1依赖的方式诱导[³H]多巴胺外流。在使用相同细胞和突触体制备的DAT生物素化分析中,我们观察到1μM甲基苯丙胺以TAAR1依赖的方式诱导DAT内化。甲基苯丙胺的所有这些由TAAR1介导的效应均被蛋白激酶抑制剂H89 [N-[2-(4-溴肉桂酰胺基)乙基]-5-异喹啉]和/或2-{8-[(二甲基氨基)甲基]-6,7,8,9-四氢吡啶并[1,2-a]吲哚-3-基}-3-(1-甲基吲哚-3-基)马来酰亚胺(Ro32-0432)阻断,这表明甲基苯丙胺与TAAR1的相互作用触发细胞磷酸化级联反应,并导致甲基苯丙胺对DAT产生观察到的效应。这些发现证明了TAAR1在甲基苯丙胺对DAT调节作用中的介导作用,并表明该受体是甲基苯丙胺成瘾治疗药物的潜在靶点。