Svingos A L, Clarke C L, Pickel V M
Department of Neurology and Neuroscience, Division of Neurobiology, Cornell University Medical College, New York, New York, 10021, USA.
J Neurosci. 1998 Mar 1;18(5):1923-33. doi: 10.1523/JNEUROSCI.18-05-01923.1998.
The shell compartment of the nucleus accumbens (AcbSh) is prominently involved in the rewarding aspects of delta-opioid receptor (DOR) agonists, including one of its putative endogenous ligands, Met5-enkephalin (Enk). We examined the ultrastructural immunocytochemical localization of an antipeptide DOR antiserum and an antibody against Enk to determine the major cellular sites for DOR activation and the spatial relationship between DOR and Enk in this region. Sixty percent of DOR-immunoreactive profiles were axon terminals and small unmyelinated axons, whereas the remainder were mainly dendrites and dendritic spines. In axons and terminals, DOR labeling was distributed along plasma and vesicular membranes. DOR-containing terminals were mainly large and primarily formed symmetric synapses or occasionally asymmetric synapses. DOR immunoreactivity also was associated with terminals that were small and formed punctate symmetric or nonrecognizable synapses. Dual immunoperoxidase and immunogold labeling showed that 35% of DOR-labeled axons apposed other terminals that contained Enk. In addition, 25% of the DOR-labeled terminals contained Enk. Thirty-five percent of DOR labeling was observed within dendrites and dendritic spines. DOR-labeled spines showed intense immunoreactivity within asymmetric postsynaptic junctions, which were formed by terminals that lacked Enk immunoreactivity. DOR-labeled spines, however, were apposed to Enk-containing terminals in 13% of all associations between dually labeled profiles. These results provide ultrastructural evidence that activation of DOR in the AcbSh is primarily involved in modulating the presynaptic release of mainly inhibitory, but also excitatory, neurotransmitters. These data also suggest that DOR plays a role in determining the postsynaptic response to excitatory afferents.
伏隔核壳部(AcbSh)显著参与δ-阿片受体(DOR)激动剂的奖赏效应,包括其一种假定的内源性配体,甲硫氨酸脑啡肽(Enk)。我们检测了抗肽DOR抗血清和抗Enk抗体的超微结构免疫细胞化学定位,以确定该区域DOR激活的主要细胞位点以及DOR与Enk之间的空间关系。60%的DOR免疫反应性轮廓为轴突终末和无髓小轴突,其余主要为树突和树突棘。在轴突和终末中,DOR标记沿质膜和囊泡膜分布。含DOR的终末主要较大,主要形成对称性突触,偶尔形成非对称性突触。DOR免疫反应性也与小的、形成点状对称性或不可识别突触的终末相关。双重免疫过氧化物酶和免疫金标记显示,35%的DOR标记轴突与其他含Enk的终末相邻。此外,25%的DOR标记终末含有Enk。在树突和树突棘内观察到35%的DOR标记。DOR标记的树突棘在由缺乏Enk免疫反应性的终末形成的非对称性突触后连接内显示出强烈的免疫反应性。然而,在双重标记轮廓的所有关联中,13%的DOR标记树突棘与含Enk的终末相邻。这些结果提供了超微结构证据,表明AcbSh中DOR的激活主要参与调节主要为抑制性但也有兴奋性神经递质的突触前释放。这些数据还表明DOR在决定对兴奋性传入的突触后反应中起作用。