Wang H, Moriwaki A, Wang J B, Uhl G R, Pickel V M
Department of Neurology and Neuroscience, Cornell University Medical College, New York, New York 10021, USA.
J Comp Neurol. 1996 Nov 25;375(4):659-74. doi: 10.1002/(SICI)1096-9861(19961125)375:4<659::AID-CNE7>3.0.CO;2-0.
To delineate the cellular sites for the motor effects of opiates acting at the mu opioid receptor (MOR) in the rat caudate-putamen nucleus, we examined the ultrastructural immunogold and immunoperoxidase labeling of an antipeptide antiserum specific for the MOR. We also combined these labeling methods to examine the subcellular relationship between the MOR and the endogenous opioid peptide, Leu5-enkephalin (LE). By light microscopy, MOR-labeling was seen in a heterogeneous patchy distribution. Electron microscopic analysis of these patches showed that more than 80% of the total neuronal profiles (n = 1,586) containing MOR-like immunoreactivity (MOR-IR) were dendrites and dendritic spines. The remaining labeled profiles included a few perikarya and many axon terminals. MOR-IR was predominantly localized to extrasynaptic plasma membranes of dendrites, and to both synaptic vesicles and plasma membranes in terminals. Ten percent of the total MOR-labeled terminals (n = 272) formed asymmetric synapses with unlabeled or MOR-labeled dendritic spines. Terminals containing LE-IR formed synapses, in almost equal proportions, on MOR-labeled dendrites and dendritic spines, while over 80% of the unlabeled terminals formed synapses on MOR-labeled dendritic spines. Moreover, colocalization of MOR- and LE-IR was often seen in both dendrites and terminals. These results indicate that in patch compartments of the caudate-putamen nucleus, the MOR is mainly involved in extrasynaptic modulation of spiny neurons, including those that contain LE. In addition, the findings provide a cellular basis for presynaptic opioid modulation of neurotransmitter release through MOR located on axon terminals.
为了确定阿片类药物作用于大鼠尾状核 - 壳核中μ阿片受体(MOR)产生运动效应的细胞位点,我们检测了一种针对MOR的抗肽抗血清的超微结构免疫金标和免疫过氧化物酶标记。我们还结合这些标记方法来研究MOR与内源性阿片肽亮氨酸脑啡肽(LE)之间的亚细胞关系。通过光学显微镜观察,MOR标记呈异质性斑片状分布。对这些斑块的电子显微镜分析表明,含有MOR样免疫反应性(MOR-IR)的神经元轮廓总数(n = 1586)中,超过80%是树突和树突棘。其余标记的轮廓包括一些胞体和许多轴突终末。MOR-IR主要定位于树突的突触外质膜,以及终末的突触小泡和质膜。在总共MOR标记的终末中(n = 272),10%与未标记或MOR标记的树突棘形成不对称突触。含有LE-IR的终末以几乎相等的比例在MOR标记的树突和树突棘上形成突触,而超过80%的未标记终末在MOR标记的树突棘上形成突触。此外,在树突和终末中经常可见MOR-IR和LE-IR的共定位。这些结果表明,在尾状核 - 壳核的斑块区域,MOR主要参与对棘状神经元的突触外调节,包括那些含有LE的神经元。此外,这些发现为通过位于轴突终末的MOR进行神经递质释放的突触前阿片调节提供了细胞基础。