Cheng P Y, Liu-Chen L Y, Pickel V M
Department of Neurology, Cornell University Medical College, New York, NY 10021, USA.
Brain Res. 1997 Dec 19;778(2):367-80. doi: 10.1016/s0006-8993(97)00891-3.
The delta opioid receptor (DOR) and mu opioid receptor (MOR) are abundantly distributed in the dorsal horn of the spinal cord. Simultaneous activation of each receptor by selective opiate agonists has been shown to result in synergistic analgesic effects. To determine the cellular basis for these functional associations, we examined the electron microscopic immunocytochemical localization of DOR and MOR in single sections through the superficial layers of the dorsal horn in the adult rat spinal cord (C2-C4). From a total of 270 DOR-labeled profiles, 49% were soma and dendrites, 46% were axon terminals and small unmyelinated axons, and 5% were glial processes. 6% of the DOR-labeled soma and dendrites, and < 1% of the glial processes also showed MOR-like immunoreactivity (MOR-LI). Of 339 MOR-labeled profiles, 87% were axon terminals and small unmyelinated axons, 12% were soma and dendrites, and 2% were glial processes. 21% of the MOR-labeled soma and dendrites, but none of the axon terminals also contain DOR-LI. The subcellular distributions of MOR and DOR were distinct in axon terminals. In axon terminals, both DOR-LI and MOR-LI were detected along the plasmalemma, but only DOR-LI was associated with large dense core vesicles. DOR-labeled terminals formed synapses with dendrites containing MOR and conversely, MOR-labeled terminals formed synapses with DOR-labeled dendrites. These results suggest that the synergistic actions of selective MOR- and DOR-agonists may be attributed to dual modulation of the same or synaptically linked neurons in the superficial layers of the spinal cord.
δ阿片受体(DOR)和μ阿片受体(MOR)大量分布于脊髓背角。选择性阿片类激动剂同时激活每种受体已被证明可产生协同镇痛作用。为了确定这些功能关联的细胞基础,我们通过成年大鼠脊髓(C2 - C4)背角浅层的单切片,研究了DOR和MOR的电子显微镜免疫细胞化学定位。在总共270个DOR标记的形态结构中,49%为胞体和树突,46%为轴突终末和无髓小轴突,5%为胶质细胞突起。6%的DOR标记的胞体和树突,以及<1%的胶质细胞突起也显示出MOR样免疫反应性(MOR-LI)。在339个MOR标记的形态结构中,87%为轴突终末和无髓小轴突,12%为胞体和树突,2%为胶质细胞突起。21%的MOR标记的胞体和树突含有DOR-LI,但轴突终末均未含有。MOR和DOR在轴突终末的亚细胞分布不同。在轴突终末,DOR-LI和MOR-LI均沿质膜检测到,但只有DOR-LI与大的致密核心囊泡相关。DOR标记的终末与含有MOR的树突形成突触,反之,MOR标记的终末与DOR标记的树突形成突触。这些结果表明,选择性MOR和DOR激动剂的协同作用可能归因于脊髓浅层同一或突触连接神经元的双重调节。