Brodal P
Neuroscience. 1983 Nov;10(3):621-38. doi: 10.1016/0306-4522(83)90207-5.
In 13 cats injections of horseradish peroxidase-wheat germ agglutinin in various parts of the cerebral cortex were combined with injections in the cerebellar crus II in the same animal in order to study the cortical regions that may influence the crus II via the pontine nuclei. In 2 cats lesions in the cerebral cortex were combined with horseradish peroxidase injections in the crus II. In the pons terminal regions (anterogradely labelled from the cerebral cortex or containing terminal degeneration) and cell groups retrogradely labelled from crus II were carefully plotted. The pontocerebellar projection to crus II is mainly crossed, on the average 26% of the labelled cells were found in the ipsilateral pons. Some overlap between sites of ending of cortical fibres and sites of origin of fibres to crus II was present in all cases, but the degree of overlap varied considerably, depending on which cortical region was injected. Typically, partial overlap between terminal patches and groups of labelled cells occurred at multiple sites in the pontine nuclei. A major input to crus II appears to come from the parietal region. Experiments with bilateral cortical injections showed that the pontine projection from the parietal region is topographically organized in a precise mosaic pattern of adjacent but apparently non-overlapping patches of termination. Area 6 also has strong connections with crus II, while only very few of the corticopontine fibres from the sensorimotor region overlap with cell groups labelled from crus II. The second somatosensory area and the visual cortex both seem able to influence a small but significant proportion of cells projecting to crus II. In contrast to other cortical regions, the auditory cortex appears to send fibres mainly to cell groups projecting to the ipsilateral crus II. It is concluded that the input to crus II originates in wide areas of the cerebral cortex. Small subgroups of neurons projecting to crus II can be differentiated on the basis of their cortical afferents. It appears likely that each subgroup receives fibres mainly or in some instances only from one cortical site. The corticopontocerebellar projection to crus II probably exhibits a high degree of spatial order providing a specific pattern of convergence and divergence in the cerebellar cortex, in agreement with recent physiological evidence from micromapping studies.
为了研究可能通过脑桥核影响小脑脚Ⅱ的皮质区域,对13只猫在大脑皮质的不同部位注射辣根过氧化物酶-小麦胚凝集素,并在同一只动物的小脑脚Ⅱ进行注射。对2只猫进行大脑皮质损伤并在小脑脚Ⅱ注射辣根过氧化物酶。在脑桥中,仔细描绘了终末区域(从大脑皮质顺行标记或含有终末变性的区域)以及从小脑脚Ⅱ逆行标记的细胞群。脑桥小脑投射到小脑脚Ⅱ主要是交叉性的,平均有26%的标记细胞在同侧脑桥中被发现。在所有情况下,皮质纤维终末部位与投射到小脑脚Ⅱ的纤维起始部位之间都存在一定程度的重叠,但重叠程度差异很大,这取决于注射的是哪个皮质区域。典型的情况是,终末小体与标记细胞群之间的部分重叠在脑桥核的多个部位出现。小脑脚Ⅱ的主要输入似乎来自顶叶区域。双侧皮质注射的实验表明,来自顶叶区域的脑桥投射在地形上以相邻但明显不重叠的终末小斑块的精确镶嵌模式组织起来。6区与小脑脚Ⅱ也有很强的联系,而来自感觉运动区的皮质脑桥纤维中只有极少数与从小脑脚Ⅱ标记的细胞群重叠。第二躯体感觉区和视觉皮质似乎都能够影响投射到小脑脚Ⅱ的一小部分但数量可观的细胞。与其他皮质区域不同,听觉皮质似乎主要将纤维发送到投射到同侧小脑脚Ⅱ的细胞群。结论是,小脑脚Ⅱ的输入起源于大脑皮质的广泛区域。根据其皮质传入神经,可以区分出投射到小脑脚Ⅱ的小神经元亚群。似乎每个亚群主要或在某些情况下仅从一个皮质部位接收纤维。皮质脑桥小脑投射到小脑脚Ⅱ可能表现出高度的空间秩序,在小脑皮质中提供特定的会聚和发散模式,这与最近微区映射研究的生理学证据一致。