Kitayama Shigeo, Sogawa Chiharu
Department of Dental Pharmacology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 5-1 Shikata-cho, 2-chome, Okayama 700-8525, Japan.
J Pharmacol Sci. 2005 Oct;99(2):121-7. doi: 10.1254/jphs.cpj05003x. Epub 2005 Oct 8.
Termination of neurotransmission at catecholaminergic synapses is well documented by the transporters for dopamine and norepinephrine, members of the Na(+)/Cl(-)-dependent neurotransmitter transporter family, which accumulates released transmitters within their nerve endings, respectively. Although somatodendritic expression of the transporters and the effects of cocaine and amphetamine on those have been reported, their role is still obscure. Recent findings of the transporter function as an ion channel and/or its reverse transport property provide a clue to identify the role of these transporters in the somatodendrites and their consequential interaction with uptake inhibitors. Differences in ionic environment and maturity of the release machinery in the somatodendrites at developmental stages influence the transporter functions, resulting in the formation of both positive and negative feedback loop of catecholaminergic neurons.
多巴胺和去甲肾上腺素转运体对儿茶酚胺能突触处神经传递的终止作用已有充分记录,它们是Na(+)/Cl(-)依赖性神经递质转运体家族的成员,分别在神经末梢内积累释放的递质。尽管已有报道称转运体在树突体上的表达以及可卡因和苯丙胺对其的影响,但其作用仍不清楚。转运体作为离子通道的功能及其反向转运特性的最新发现为确定这些转运体在树突体中的作用及其与摄取抑制剂的相互作用提供了线索。发育阶段树突体中离子环境和释放机制成熟度的差异会影响转运体功能,从而导致儿茶酚胺能神经元形成正反馈和负反馈回路。