Trace amine receptor in GtoPdb v.2023.1

T. Bonner, A. Davenport, S. Foord, J. Maguire, William A. E. Parker
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引用次数: 1

Abstract

Trace amine-associated receptors were discovered from a search for novel 5-HT receptors [9], where 15 mammalian orthologues were identified and divided into two families. The TA1 receptor (nomenclature as agreed by the NC-IUPHAR Subcommittee for the Trace amine receptor [58]) has affinity for the endogenous trace amines tyramine, β-phenylethylamine and octopamine in addition to the classical amine dopamine [9]. Emerging evidence suggests that TA1 is a modulator of monoaminergic activity in the brain [94] with TA1 and dopamine D2 receptors shown to form constitutive heterodimers when co-expressed [30]. In addition to trace amines, receptors can be activated by amphetamine-like psychostimulants, and endogenous thyronamines.
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GtoPdb v.2023.1中微量胺受体
在寻找新的5-HT受体的过程中发现了微量胺相关受体[9],其中鉴定了15种哺乳动物同源物,并将其分为两个科。TA1受体(由NC-IUPHAR小组委员会商定的微量胺受体命名法[58])除了对经典胺多巴胺具有亲和力外,还对内源性微量胺如酪胺、β-苯乙胺和章鱼胺具有亲和力[9]。新出现的证据表明,TA1是大脑中单胺能活性的调节剂[94],TA1和多巴胺D2受体在共表达时形成组成性异二聚体[30]。除了微量胺,受体还可以被苯丙胺类精神兴奋剂和内源性甲状腺胺激活。
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