Guttenberg N D, Klop H, Minami M, Satoh M, Voorn P
Vrije Universiteit, Department of Anatomy and Embryology, Amsterdam, The Netherlands.
Neuroreport. 1996 Sep 2;7(13):2119-24. doi: 10.1097/00001756-199609020-00011.
Using a combination of radioactive and non-radioactive in situ hybridization, the mu opioid receptor mRNA was localized in enkephalin as well as dynorphin neurones of the rat striatum. The proportion of enkephalin neurones showing co-localized mu opioid receptor mRNA was dependent on the rostrocaudal level (17-39% in rostral/intermediate levels vs 0.4-5% caudally) but did not differ between striatal subregions. For dynorphin neurones the reverse was true, with consistently higher levels of co-localization in the caudate-putamen (56-77%) than the nucleus accumbens (15-43%), but no differences along the rostrocaudal axis. Furthermore, the degree of enkephalin/mu co-localization was significantly lower than that of dynorphin/mu. These results suggest a fine-grained topological differentiation of mu receptor modulation of striatal opioid systems.
运用放射性和非放射性原位杂交相结合的方法,μ阿片受体mRNA定位于大鼠纹状体的脑啡肽能神经元以及强啡肽能神经元中。显示μ阿片受体mRNA共定位的脑啡肽能神经元比例取决于 rostrocaudal 水平(在 Rostral/中间水平为17 - 39%,而在尾侧为0.4 - 5%),但在纹状体亚区域之间没有差异。对于强啡肽能神经元,情况则相反,尾壳核中的共定位水平始终高于伏隔核(分别为56 - 77%和15 - 43%),但沿 rostrocaudal 轴没有差异。此外,脑啡肽/μ的共定位程度明显低于强啡肽/μ。这些结果表明纹状体阿片系统的μ受体调节存在精细的拓扑分化。