Delfs J M, Kong H, Mestek A, Chen Y, Yu L, Reisine T, Chesselet M F
Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia 19104.
J Comp Neurol. 1994 Jul 1;345(1):46-68. doi: 10.1002/cne.903450104.
The mu (mu) opioid receptors, which mediate the effects of morphine, are widely distributed in brain. We have examined the distribution of mRNA encoding a mu opioid receptor in rat brain with in situ hybridization histochemistry at the single-cell level to obtain information about the cell types synthesizing this receptor. Only neurons, not glia, were labeled in discrete brain regions. High levels of labeling were detected in the thalamus, striosomes of the caudate-putamen, globus pallidus, and brain regions involved in nociception, arousal, respiratory control, and, possibly, addiction. The general distribution of the receptor mRNA paralleled that of mu opioid binding sites with some notable exceptions. These include the cerebral cortex, which contains binding sites, but very few labeled neurons. No labeling was observed in the cerebellum, a region devoid of mu binding sites. Three main findings emerged from these experiments: 1) the mRNA was present in regions mediating both the therapeutic (analgesia) and the unwanted (respiratory depression, addiction) effects of morphine, 2) the mRNA was very densely expressed by neurons known to receive dense enkephalin-containing inputs, and 3) the dissociation between the presence of binding sites and absence of mRNA in some brain regions supports a presynaptic localization of mu opioid receptors in these areas. Alternatively, other subtypes of mu opioid receptors may be encoded by a different mRNA. These results provide new insights into the receptor types and neuronal circuits involved in the effects of endogenous opioids and morphine.
介导吗啡作用的μ阿片受体广泛分布于脑内。我们采用单细胞水平的原位杂交组织化学方法研究了大鼠脑中编码μ阿片受体的mRNA的分布,以获取有关合成该受体的细胞类型的信息。在离散的脑区中,只有神经元被标记,而非神经胶质细胞。在丘脑、尾状核 - 壳核的纹状体、苍白球以及参与痛觉感受、觉醒、呼吸控制以及可能与成瘾相关的脑区中检测到高水平的标记。受体mRNA的总体分布与μ阿片结合位点的分布相似,但也有一些显著的例外。这些例外包括大脑皮层,其中含有结合位点,但标记的神经元很少。在小脑(一个没有μ结合位点的区域)未观察到标记。这些实验得出了三个主要发现:1)mRNA存在于介导吗啡治疗作用(镇痛)和不良作用(呼吸抑制、成瘾)的区域;2)已知接受密集含脑啡肽输入的神经元中mRNA表达非常密集;3)某些脑区中结合位点的存在与mRNA的缺失之间的分离支持了这些区域中μ阿片受体的突触前定位。或者,μ阿片受体的其他亚型可能由不同的mRNA编码。这些结果为内源性阿片类物质和吗啡作用所涉及的受体类型和神经回路提供了新的见解。