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Cellular and Molecular Aspects of Monoamine Neurotransmitter Transporters

机译:单胺神经递质转运蛋白的细胞和分子方面

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References(126) Cited-By(25) Neurotransmitter transporters terminate synaptic neurotransmission by accumulating neurotransmitters once again after release in a sodium- and chloride-dependent fashion. The availability of the cloned neurotransmitter transporters has allowed investigation into the roles of these transporters in neuronal function. Molecular biological and protein engineering studies including in vitro site-directed mutagenesis, chimera formation of several transporter clones, or epitope-tagging various regions of transporter proteins, have revealed the topology and functionally mapped the transporter proteins. Monoamine neurotransmitter transporters such as those for dopamine, norepinephrine and serotonin are of interest, since they are a target of drugs of abuse and are involved in neuronal disorders including Parkinson''s disease and depression. Therefore, elucidating the molecular basis of these transporters may clarify these problems and help develop treatments with which to combat these disorders and drug abuse.
机译:参考文献(126)被引用的(25)神经递质转运蛋白通过以钠和氯化物依赖性方式释放后再次积累神经递质来终止突触神经传递。克隆的神经递质转运蛋白的可用性已允许调查这些转运蛋白在神经元功能中的作用。分子生物学和蛋白质工程研究包括体外定点诱变,几种转运蛋白克隆的嵌合体形成或转运蛋白各个区域的表位标记,揭示了拓扑结构并在功能上定位了转运蛋白。单胺神经递质转运蛋白,例如多巴胺,去甲肾上腺素和5-羟色胺的转运蛋白,是令人感兴趣的,因为它们是滥用药物的靶标,并涉及神经元疾病,包括帕金森氏症和抑郁症。因此,阐明这些转运蛋白的分子基础可能会澄清这些问题,并有助于开发与这些疾病和药物滥用作斗争的治疗方法。

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