Speciale S G, Manaye K F, Sadeq M, German D C
Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas.
J Neural Transm Gen Sect. 1993;91(1):53-66. doi: 10.1007/BF01244918.
Opiates and opioid peptides are known to influence the dopaminergic (DA) neurons in the midbrain. The purpose of this study was to map and quantify the density of kappa and delta opioid receptor subtypes in the retrorubral field, substantia nigra, and ventral tegmental area and related nuclei, which contain DA nuclei A8, A9, and A10, respectively. Sections through the rostral-caudal extent of the rat midbrain were stained with an antibody against tyrosine hydroxylase, as a DA cell marker, and comparable sections were processed for in vitro receptor autoradiography using the kappa-selective ligand, U-69593, and the delta-selective ligand, D-Pen2, D-Pen5-enkephalin. In general, both kappa and delta ligands exhibited low levels of specific binding in regions occupied by the midbrain DA neurons. Kappa binding (4-8 fmol/mg tissue) was high throughout the rostral-caudal extent of the substantia nigra, in rostral portions of the ventral tegmental area, and in the nucleus paranigralis; low binding occurred in the retrorubral field and central linear nucleus raphe. Delta binding (6-18 fmol/mg tissue) was high in the caudal portion of the substantia nigra pars reticulata, and in the medial terminal nucleus of the accessory optic system (a region previously shown to contain DA dendrites). The kappa and delta receptor binding is heterogeneously distributed in regions occupied by midbrain dopaminergic neurons, and several fold lower than the binding of mu opioid receptors in the same brain regions.
已知阿片类药物和阿片肽会影响中脑的多巴胺能(DA)神经元。本研究的目的是绘制并量化红核后区、黑质、腹侧被盖区及相关核团中κ和δ阿片受体亚型的密度,这些核团分别包含DA核团A8、A9和A10。通过大鼠中脑的头-尾范围制作切片,用抗酪氨酸羟化酶抗体染色,作为DA细胞标记物,同时对可比切片进行体外受体放射自显影,使用κ选择性配体U-69593和δ选择性配体D-Pen2,D-Pen5-脑啡肽。总体而言,κ和δ配体在中脑DA神经元占据的区域均表现出低水平的特异性结合。κ结合(4 - 8 fmol/mg组织)在黑质的整个头-尾范围、腹侧被盖区的前部以及黑质旁核中较高;在红核后区和中缝中央线性核中结合较低。δ结合(6 - 18 fmol/mg组织)在黑质网状部的尾部以及副视系统内侧终核(先前显示该区域含有DA树突的区域)中较高。κ和δ受体结合在中脑多巴胺能神经元占据的区域呈异质性分布,且比同一脑区中μ阿片受体的结合低几倍。