Kalil K
J Comp Neurol. 1981 Jan 1;195(1):25-50. doi: 10.1002/cne.901950105.
Projections from the cerebellar and dorsal column nuclei to the midbrain and thalamus of the rhesus monkey were traced with anterograde autoradiographic techniques, or, in a few cases, with the Fink-Heimer method. The cerebellar nuclei give rise to a massive projection to the contralateral midbrain and thalamus via the ascending limb of the superior cerebellar peduncle. Cerebellar efferent fibers terminate contralaterally in both divisions of the red nucleus, and bilaterally in the interstitial nucleus of Cajal, the nucleus of Darkschewitsch, the oculomotor nucleus, and the central gray. All the deep cerebellar nuclei project upon a broad area of the contralateral ventral thalamus as well as certain intralaminar nuclei. Corresponding ipsilateral thalamic terminations are sparse. The topographic organization of cerebellothalamic fibers does not correspond to individual cerebellar nuclei or to cytoarchitectonic divisions of the ventral thalamic nuclei. Rather there are longitudinally oriented strips of terminal labeling which extend through all divisions of the ventral lateral nucleus, i.e., the VLps, the VLc, the VLo, as well as nucleus X, the oral division of the ventral posterolateral nucleus (VPLo), the central lateral nucleus (CL), and the most caudal region of the ventral anterior nucleus (VA). The topography of the cerebellothalamic fibers is arranged in a mediolateral pattern with fibers originating from anterior zones of the dentate and interpositus ending most laterally and those from posterior dentate and interpositus terminating most medially. The fastigial contribution is relatively sparse. The longitudinal strips of terminal labeling in the ventral thalamic nuclei are made up of still smaller terminal units consisting of disk-like aggregates of silver grains separated from one another by grain-free spaces. The dorsal column nuclei terminate primarily in the contralateral caudal division of the VPL (VPLc) and never extend rostrally into VPLo. These results demonstrate a segregation of cerebellar and dorsal columnar inputs to motor and sensory regions of the thalamus, respectively. Since these regions are separate and discrete in their cortical associations as well (Kalil, '76), it seems unlikely that fast afferent pathways relaying to motor cortex (Lemon and Porter, '76) could arise from the dorsal column nuclei.
运用顺行性放射自显影技术,或在少数情况下运用芬克 - 海默法,追踪了恒河猴小脑和薄束核向中脑和丘脑的投射。小脑核通过小脑上脚的升支向对侧中脑和丘脑发出大量投射。小脑传出纤维在对侧红核的两个部分终止,在 Cajal 间质核、Darkschewitsch 核、动眼神经核和中央灰质中双侧终止。所有小脑深部核团都投射到对侧腹侧丘脑的广泛区域以及某些板内核。相应的同侧丘脑终末较为稀疏。小脑丘脑纤维的拓扑组织并不对应于单个小脑核或腹侧丘脑核的细胞构筑分区。相反,有纵向排列的终末标记带,其延伸穿过腹外侧核的所有分区,即 VLps、VLc、VLo,以及 X 核、腹后外侧核的嘴侧部(VPLo)、中央外侧核(CL)和腹前核最尾侧区域(VA)。小脑丘脑纤维的拓扑结构呈内外侧模式排列,来自齿状核和间位核前部区域的纤维在最外侧终止,而来自齿状核后部和间位核的纤维在最内侧终止。顶核的投射相对较少。腹侧丘脑核中的纵向终末标记带由更小的终末单位组成,这些终末单位由盘状银粒聚集体构成,彼此之间由无颗粒空间分隔。薄束核主要终止于对侧 VPL 的尾侧部(VPLc),从不向嘴侧延伸至 VPLo。这些结果表明,小脑和薄束核的输入分别在丘脑的运动和感觉区域存在分离。由于这些区域在其皮质联系中也是分开且离散的(卡利尔,1976 年),因此传递至运动皮层的快速传入通路(莱蒙和波特,1976 年)似乎不太可能起源于薄束核。