Sari Y, Miquel M C, Brisorgueil M J, Ruiz G, Doucet E, Hamon M, Vergé D
Département de Neurobiologie des Signaux Intercellulaires, Institut des Neurosciences, CNRS URA 1488, Université Pierre et Marie Curie, Paris, France.
Neuroscience. 1999;88(3):899-915. doi: 10.1016/s0306-4522(98)00256-5.
The localization of 5-hydroxytryptamine1B receptors in the rat central nervous system was investigated using anti-peptide antibodies that recognize a selective portion of the third intracytoplasmic loop of the receptor protein. At the light microscope level the densest 5-hydroxytryptamine1B receptor-like immunoreactivity was observed in ventral pallidum, globus pallidus, substantia nigra and dorsal subiculum. In addition, moderate immunoreactivity was found in the entopeduncular nucleus, the superficial gray layer of the superior colliculus, the caudate-putamen and the deep nuclei of the cerebellum. This distribution matched perfectly that previously described from radioligand binding studies. At the ultrastructural level, 5-hydroxytryptamine1B receptor-like immunoreactivity was associated with axons and axon terminals in the three areas examined: substantia nigra, globus pallidus and superficial gray layer of the superior colliculus. In all cases, immunostaining was located on the plasma membrane of unmyelinated axon terminals and in the cytoplasm close to the plasmalemma. Synaptic differentiations were never labelled but, in some cases, 5-hydroxytryptamine1B receptor-like immunoreactivity was found in their close vicinity. Injection of kainic acid into the neostriatum resulted in a marked decrease in receptor-like immunoreactivity in the globus pallidus and the substantia nigra, consistent with the location of 5-hydroxytryptamine1B receptors on terminals of striatopallidal and striatonigral fibres, respectively. A reduction in 5-hydroxytryptamine1B receptor-like immunoreactivity was also noted in the superficial gray layer of the superior colliculus after contralateral enucleation, as expected of the location of 5-hydroxytryptamine1B receptors on the terminals of retinocollicular fibres. In both lesion experiments, immunolabelled degenerating terminals were observed in the projection areas. Anterograde labelling experiments coupled with immunocytochemical detection further showed that 5-hydroxytryptamine1B receptors in the substantia nigra are located on axons of striatal neurons. These data provide anatomical support for the idea that 5-hydroxytryptamine1B receptors act as terminal receptors involved in presynaptic regulation of the release of various neurotransmitters, including 5-hydroxytryptamine itself.
利用识别受体蛋白第三胞质内环特定区域的抗肽抗体,研究了大鼠中枢神经系统中5-羟色胺1B受体的定位。在光学显微镜水平,在腹侧苍白球、苍白球、黑质和背侧海马下托观察到最密集的5-羟色胺1B受体样免疫反应性。此外,在内侧缰核、上丘浅层灰质、尾状核-壳核和小脑深部核团中发现中等免疫反应性。这种分布与先前放射性配体结合研究描述的完全一致。在超微结构水平,在检查的三个区域:黑质、苍白球和上丘浅层灰质中,5-羟色胺1B受体样免疫反应性与轴突和轴突终末相关。在所有情况下,免疫染色位于无髓轴突终末的质膜上以及靠近质膜的细胞质中。突触分化从未被标记,但在某些情况下,在其附近发现了5-羟色胺1B受体样免疫反应性。向新纹状体注射 kainic 酸导致苍白球和黑质中受体样免疫反应性显著降低,这分别与5-羟色胺1B受体在纹状体苍白球纤维和纹状体黑质纤维终末的定位一致。在对侧眼球摘除后,上丘浅层灰质中5-羟色胺1B受体样免疫反应性也降低,这与5-羟色胺1B受体在视网膜-上丘纤维终末的定位预期相符。在这两个损伤实验中,在投射区域观察到免疫标记的变性终末。顺行标记实验与免疫细胞化学检测相结合进一步表明,黑质中的5-羟色胺1B受体位于纹状体神经元的轴突上。这些数据为5-羟色胺1B受体作为参与包括5-羟色胺自身在内的各种神经递质释放的突触前调节的终末受体这一观点提供了解剖学支持。