Batini C, Bernard J F, Buisseret-Delmas C, Horcholle-Bossavit G
Exp Brain Res. 1983;52(3):400-10. doi: 10.1007/BF00238033.
The cerebellar output function was studied using cerebellopetal proprioceptive stimulation which produces simple and complex excitatory discharges as well as inhibitory activity in the Purkinje cells. The activity of the intracerebellar nuclei (and of the entire brain stem) was measured by the energy consumption as revealed with the [14C )-2-deoxyglucose method. The stimulations consisted of repetitive (1-20 c/s) electrical excitation of the nerve leading to the inferior oblique, to the masseteric and to the gastrocnemius soleus muscle. Compared to a group of non-stimulated controls, heavy bilateral labeling was obtained in the posterior pole of the fastigial nucleus. This was not observed with stimulation of the vibrissal pad which, however, produced a clear increase of [14C]-2-deoxyglucose uptake in the secondary trigeminal complex. Labeling of the posterior part of the fastigial nuclei was suppressed by ablation or pharmacologic inactivation of the overlying cerebellar cortex which suppresses the inhibitory activity of the Purkinje cells into the nuclear cells. Labeling of the posterior fastigial nuclei was also decreased in animals not stimulated but with ablation or pharmacologic inactivation of the overlying cerebellar cortex. The hypothesis proposed is that the marking results are the consequence of an increased activity in the Purkinje cell terminals. The activity of the Purkinje cells was also recorded extracellulary both before and during repetitive stimulation of a muscle nerve. The discharge activity of those in the cerebellar vermis and giving axons to the posterior fastigial nucleus was increased by the stimulation, whereas the activity of those of the hemispheral parts remained unchanged. Units in the fastigial nucleus were also recorded. Their activity was found to be deeply depressed so that only a few units were encountered and no further decrease of their discharge could be detected with the stimulation of a muscle nerve. Nevertheless, using the present data and those previously obtained, the conclusion is advanced that the cerebellar output function is actually decreased during afferent cerebellar stimulation.
利用向小脑的本体感觉刺激来研究小脑的输出功能,这种刺激会在浦肯野细胞中产生简单和复杂的兴奋性放电以及抑制性活动。小脑内神经核(以及整个脑干)的活动通过[14C] -2-脱氧葡萄糖法所揭示的能量消耗来测量。刺激包括对通向眼外下直肌、咬肌和腓肠肌比目鱼肌的神经进行重复(1 - 20次/秒)电刺激。与一组未受刺激的对照组相比,在顶核后极获得了大量双侧标记。刺激触须垫时未观察到这种情况,然而,触须垫刺激会使三叉神经二级复合体中[14C] -2-脱氧葡萄糖摄取明显增加。顶核后部的标记会因覆盖其上的小脑皮质的切除或药物失活而受到抑制,这会抑制浦肯野细胞对核细胞的抑制性活动。在未受刺激但覆盖其上的小脑皮质被切除或药物失活的动物中,顶核后部的标记也会减少。提出的假设是标记结果是浦肯野细胞终末活动增加的结果。在重复刺激肌肉神经之前和期间,还通过细胞外记录了浦肯野细胞的活动。刺激会增加小脑蚓部那些向顶核后部发出轴突的细胞的放电活动,而半球部分细胞的活动保持不变。也记录了顶核中的单位。发现它们的活动深度抑制,以至于只能遇到少数单位,并且在刺激肌肉神经时无法检测到它们放电的进一步减少。尽管如此,根据目前的数据和先前获得的数据,得出的结论是在小脑传入刺激期间小脑的输出功能实际上是下降的。