Bausch S B, Patterson T A, Ehrengruber M U, Lester H A, Davidson N, Chavkin C
Department of Pharmacology, University of Washington, Seattle 98195-7280, USA.
Recept Channels. 1995;3(3):221-41.
Affinity-purified anti-peptide antibodies generated against the carboxy-terminal region of the mu opioid receptor and the GIRK1 (Kir 3.1) ion channel were used to localize these two proteins in the rat brain. Mu opioid receptor immunoreactivity was detected in brain regions that were previously found to contain mu opioid binding sites using autoradiography. The distribution of GIRK1 immunoreactivity in the brain correlated well with a previous in situ hybridization study. Confocal microscopy of rat brain sections double-labelled with anti-mu opioid receptor and anti-GIRK1 antibodies revealed colocalization of GIRK1 and mu opioid receptor immunoreactivities in somata of subpopulations of neurons in the cerebral cortex, anterior olfactory nucleus, nucleus accumbens, globus pallidus, substantia nigra, peripeduncular nucleus, hippocampal formation, diagonal band, thalamus, locus coeruleus, dorsal raphe, red nucleus, nucleus of the trapezoid body, reticular nucleus, vestibular nucleus, inferior colliculus and the mesencephalic trigeminal nucleus. These anatomical findings suggest that the mu opioid receptor may couple to GIRK1 in some but not all regions of the rat brain.
针对μ阿片受体羧基末端区域和GIRK1(Kir 3.1)离子通道产生的亲和纯化抗肽抗体,用于在大鼠脑中定位这两种蛋白质。使用放射自显影法在先前发现含有μ阿片结合位点的脑区中检测到μ阿片受体免疫反应性。脑中GIRK1免疫反应性的分布与先前的原位杂交研究结果高度相关。用抗μ阿片受体和抗GIRK1抗体双重标记的大鼠脑切片的共聚焦显微镜检查显示,GIRK1和μ阿片受体免疫反应性在大脑皮层、前嗅核、伏隔核、苍白球、黑质、脚周核、海马结构、斜角带、丘脑、蓝斑、中缝背核、红核、梯形核、网状核、前庭核、下丘和中脑三叉神经核的部分神经元胞体中共定位。这些解剖学发现表明,μ阿片受体可能在大鼠脑的某些但不是所有区域与GIRK1偶联。