Jayanthi Lankupalle D, Ramamoorthy Sammanda
Department of Neurosciences, Medical University of South Carolina, Charleston, SC 29425, USA.
AAPS J. 2005 Oct 27;7(3):E728-38. doi: 10.1208/aapsj070373.
Synaptic neurotransmission in the central nervous system (CNS) requires the precise control of the duration and the magnitude of neurotransmitter action at specific molecular targets. At the molecular level, neurotransmitter signaling is dynamically regulated by a diverse set of macromolecules including biosynthetic enzymes, secretory proteins, ion channels, pre- and postsynaptic receptors and transporters. Monoamines, 5-hydroxytryptamine or serotonin (5-HT), norepinephrine (NE), and dopamine (DA) play an important modulatory role in the CNS and are involved in numerous physiological functions and pathological conditions. Presynaptic plasma membrane transporters for 5-HT (SERT), NE (NET), and DA (DAT), respectively, control synaptic actions of these monoamines by rapidly clearing the released amine. Monoamine transporters are the sites of action for widely used antidepressants and are high affinity molecular targets for drugs of abuse including cocaine, amphetamine, and 3,4-methylenedioxymetamphetamine (MDMA) "Ecstasy." Monoamine transporters also serve as molecular gateways for neurotoxins. Emerging evidence indicates that regulation of transporter function and surface expression can be rapidly modulated by "intrinsic" transporter activity itself, and antidepressant and psychostimulant drugs that block monoamine transport have a profound effect on transporter regulation. Therefore, disregulations in the functioning of monoamine transporters may underlie many disorders of transmitter imbalance such as depression, attention deficit hyperactivity disorder, and schizophrenia. This review integrates recent progress in understanding the molecular mechanisms of monoamine transporter regulation, in particular, posttranscriptional regulation by phosphorylation and trafficking linked to cellular protein kinases, protein phosphatases, and transporter interacting proteins. The review also discusses the possible role of psychostimulants and antidepressants in influencing monoamine transport regulation.
中枢神经系统(CNS)中的突触神经传递需要精确控制神经递质在特定分子靶点处作用的持续时间和强度。在分子水平上,神经递质信号传导受到多种大分子的动态调节,这些大分子包括生物合成酶、分泌蛋白、离子通道、突触前和突触后受体以及转运体。单胺类物质,如5-羟色胺或血清素(5-HT)、去甲肾上腺素(NE)和多巴胺(DA),在中枢神经系统中发挥重要的调节作用,并参与众多生理功能和病理状况。5-HT(SERT)、NE(NET)和DA(DAT)的突触前质膜转运体分别通过快速清除释放的胺来控制这些单胺类物质的突触作用。单胺转运体是广泛使用的抗抑郁药的作用位点,也是包括可卡因、安非他明和3,4-亚甲基二氧甲基苯丙胺(摇头丸)等滥用药物的高亲和力分子靶点。单胺转运体还充当神经毒素的分子通道。新出现的证据表明,转运体功能和表面表达的调节可由“内在”转运体活性本身快速调节,而阻断单胺转运的抗抑郁药和精神兴奋药对转运体调节有深远影响。因此,单胺转运体功能失调可能是许多递质失衡疾病的基础,如抑郁症、注意力缺陷多动障碍和精神分裂症。本综述整合了在理解单胺转运体调节分子机制方面的最新进展,特别是与细胞蛋白激酶、蛋白磷酸酶和转运体相互作用蛋白相关的磷酸化和转运的转录后调节。本综述还讨论了精神兴奋药和抗抑郁药在影响单胺转运调节方面的可能作用。