Zahniser Nancy R, Sorkin Alexander
Department of Pharmacology, University of Colorado Denver, Aurora, CO 80045, USA.
Semin Cell Dev Biol. 2009 Jun;20(4):411-7. doi: 10.1016/j.semcdb.2009.01.004. Epub 2009 Jan 22.
Brain dopamine (DA) plays a pivotal role in drug addiction. Since the plasma membrane DA transporter (DAT) is critical for terminating DA neurotransmission, it is important to understand how DATs are regulated and this regulation impacts drug addiction. The number of cell surface DATs is controlled by constitutive and regulated endocytic trafficking. Psychostimulants impact this trafficking. Amphetamines, DAT substrates, cause rapid up-regulation and slower down-regulation of DAT whereas cocaine, a DAT inhibitor, increases surface DATs. Recent reports have begun to elucidate the molecular mechanisms of these psychostimulant effects and link changes in DAT trafficking to psychostimulant-induced reward/reinforcement in animal models.
脑多巴胺(DA)在药物成瘾中起关键作用。由于质膜多巴胺转运体(DAT)对于终止多巴胺神经传递至关重要,因此了解DAT如何被调节以及这种调节如何影响药物成瘾很重要。细胞表面DAT的数量由组成型和调节型内吞转运控制。精神兴奋剂会影响这种转运。苯丙胺类,即DAT底物,会导致DAT快速上调和缓慢下调,而可卡因,一种DAT抑制剂,则会增加表面DAT的数量。最近的报告已开始阐明这些精神兴奋剂作用的分子机制,并将DAT转运的变化与动物模型中精神兴奋剂诱导的奖赏/强化联系起来。