Schafer Martin K-H, Weihe Eberhard, Eiden Lee E
Institute of Anatomy and Cell Biology, Philipps-University Marburg, Marburg, Germany.
Adv Pharmacol. 2013;68:319-34. doi: 10.1016/B978-0-12-411512-5.00015-4.
VMAT2 is the vesicular monoamine transporter that allows DA, NE, Epi, His, and 5-HT uptake into neurons and endocrine cells. A second isoform, VMAT1, has similar structure and function, but does not recognize histamine as a substrate. VMAT1 is absent from neurons, and its major function appears to be in endocrine cells, that is, enterochromaffin cells, which scavenge 5-HT, but not histamine, from dietary sources. This chapter provides an update on the neuroanatomical distribution of VMAT2 across various mammalian species, including human, primate, pig, rat, and mouse. When necessary, VMAT1 expression is provided as a contrast. The main purpose of this chapter is to allow clinicians, in particular endocrinologists and diagnosing neuroradiologists and neuropathologists, an acquaintanceship with the possibilities for VMAT2 as a target for in vivo imaging, and drug development, based on this updated information.
VMAT2是囊泡单胺转运体,可使多巴胺、去甲肾上腺素、肾上腺素、组胺和5-羟色胺摄取到神经元和内分泌细胞中。第二种亚型VMAT1具有相似的结构和功能,但不将组胺识别为底物。VMAT1在神经元中不存在,其主要功能似乎存在于内分泌细胞中,即肠嗜铬细胞,其从饮食来源清除5-羟色胺,但不清除组胺。本章提供了VMAT2在包括人类、灵长类动物、猪、大鼠和小鼠在内的各种哺乳动物物种中的神经解剖分布的最新信息。必要时,将提供VMAT1的表达作为对照。本章的主要目的是让临床医生,特别是内分泌学家、诊断神经放射学家和神经病理学家,基于这些最新信息了解VMAT2作为体内成像靶点和药物开发的可能性。