Goldman S, Pélaprat D, Van Reeth O, Roques B P, Vanderhaeghen J J
Laboratory of Neuropathology and Neuropeptide Research, Clinique de Neuropathologie Hôpital Erasme et Brugmann, Université Libre de Bruxelles, 808 route de Lennik, bât C, B-1070 Brussels, Belgium.
Neurochem Int. 1987;10(4):467-71. doi: 10.1016/0197-0186(87)90073-8.
Carboxyl-terminal cholecystokinin octapeptide (CCK8) binding sites were studied in the human cerebellar system by autoradiography. High affinity CCK8 binding sites were demonstrated in the main cerebellar afferent nuclei, namely the inferior olivary complex and the pontine nuclei. This localization of CCK8 binding sites was partly correlated with already described CCK containing terminals. In the cerebellar cortex, high affinity CCK8 binding sites were detected with a laminar distribution. Levels were higher in the granular layer (mostly in the superficial part) and lower in the white matter and the Purkinje cell layer. The non-specific binding was homogenous and particularly low (9%) in the cerebellar cortex but a non-specific binding was selectively localized in the deep cerebellar nuclei. Those results illustrate the species variability of CCK binding sites in the cerebellum and are briefly discussed in relation with the low level of CCK immunoreactivity in this structure. The presence of CCK8 binding sites in cerebellar afferent nuclei and cortex suggests a role of CCK in human cerebellar physiology and particularly in the modulation of afferent inputs to the cerebellum.
通过放射自显影术研究了人小脑系统中羧基末端胆囊收缩素八肽(CCK8)结合位点。在主要的小脑传入核,即下橄榄复合体和脑桥核中,证实存在高亲和力CCK8结合位点。CCK8结合位点的这种定位与已描述的含CCK终末部分相关。在小脑皮质中,检测到高亲和力CCK8结合位点呈层状分布。颗粒层(主要在表层)中的水平较高,而白质和浦肯野细胞层中的水平较低。小脑皮质中的非特异性结合是均匀的,且特别低(9%),但非特异性结合选择性地定位于小脑深部核团。这些结果说明了小脑CCK结合位点的物种变异性,并结合该结构中CCK免疫反应性的低水平进行了简要讨论。小脑传入核和皮质中存在CCK8结合位点表明CCK在人类小脑生理学中发挥作用,特别是在调节小脑传入输入方面。