Zhou F C, Tao-Cheng J H, Segu L, Patel T, Wang Y
Department of Anatomy and Medical Neurobiology Program, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, IN 46202, USA.
Brain Res. 1998 Sep 14;805(1-2):241-54. doi: 10.1016/s0006-8993(98)00691-x.
The serotonin (5-HT) transporter (5-HTT) is known to play a role in depression and many 5-HT related diseases, and is the target site for drugs of abuse, such as cocaine, MDMA, and methamphetamine. The major role of the 5-HTT has long been considered to be to inactivate serotonin transmission through the elimination of serotonin at release sites. However, immunocytochemistry using an antibody against the N-terminal of the 5-HTT at the light microscopic (LM) level indicates that the 5-HTT is associated not only with 5-HT varicosities but also with axons. Electron microscopy (EM) reveals that the majority of the 5-HTTs exist on the axolemma outside the synaptic junctions. In studying whether axonal 5-HTTs are involved in the uptake of 5-HT, we found with autoradiography that [3H]citalopram bound to all major 5-HT fibers, not only in the terminal regions, but also in 5-HT axonal bundles such as the cingulum bundle and medial forebrain bundle. Furthermore, voltammetry recordings indicated that serotonin axonal bundles were actively engaged in high affinity serotonin uptake. The evidence indicates that 5-HTTs on 5-HT axons away from the synapse are likely to be functional in a manner similar to the terminal 5-HTT for serotonin uptake. It also suggests that the role of the 5-HTT may not only be for the termination of synaptic transmission, but also for the regulation of 5-HT through extrasynaptic (volume) transmission. Our findings may also impact the understanding of the sites of action of selective serotonin reuptake inhibitors and drug entry into serotonin neurons via the numerous axonal sites.
血清素(5-羟色胺,5-HT)转运体(5-HTT)在抑郁症及许多与5-羟色胺相关的疾病中发挥作用,并且是可卡因、摇头丸和甲基苯丙胺等滥用药物的作用靶点。长期以来,5-HTT的主要作用被认为是通过消除释放部位的血清素来使血清素传递失活。然而,在光学显微镜(LM)水平使用针对5-HTT N端的抗体进行免疫细胞化学研究表明,5-HTT不仅与5-羟色胺曲张体相关,还与轴突相关。电子显微镜(EM)显示,大多数5-HTT存在于突触连接外部的轴膜上。在研究轴突5-HTT是否参与5-羟色胺的摄取时,我们通过放射自显影发现,[3H]西酞普兰不仅与所有主要的5-羟色胺纤维结合,不仅在终末区域,而且在5-羟色胺轴突束如扣带束和内侧前脑束中也有结合。此外,伏安法记录表明,5-羟色胺轴突束积极参与高亲和力的5-羟色胺摄取。证据表明,远离突触的5-羟色胺轴突上的5-HTT在摄取5-羟色胺方面可能以类似于终末5-HTT的方式发挥作用。这也表明,5-HTT的作用可能不仅在于终止突触传递,还在于通过突触外(容积)传递来调节5-羟色胺。我们的发现也可能影响对选择性5-羟色胺再摄取抑制剂作用位点的理解以及药物通过众多轴突位点进入5-羟色胺神经元的认识。