Pierrot-Deseilligny C, Gaymard B
Service de Neurologie, Unité INSERM 289, Hôpital de la Salpêtrière, Paris, France.
Baillieres Clin Neurol. 1992 Aug;1(2):435-54.
Smooth pursuit is a relatively recent eye movement which has developed in frontal-eyed species. The smooth pursuit system is involved during foveal smooth pursuit, the 'rapid' component of OKN slow phase and VOR suppression. The cortical areas controlling smooth pursuit (at the temporo-parieto-occipital junction and in the FEF) send ipsilateral projections onto the pontine nuclei, mainly the DLPN, passing through the anterior part of the midbrain. A midbrain or DLPN lesion results in ipsilateral smooth pursuit impairment (i.e. decreased gain) (Table 1). After the pontine nuclei, all smooth pursuit pathways pass through the cerebellum. They project onto the flocculus, mainly contralaterally (first decussation of the lateral smooth pursuit circuitry), and bilaterally onto the posterior vermis. Eye velocity is encoded in the activity of the floccular Purkinje cells, whereas target velocity is encoded in that of the vermal Purkinje cells. Unilateral floccular lesions and posterior vermal lesions (involving both sides of this structure) result in ipsilateral and bilateral smooth pursuit impairment, respectively. The flocculus sends an ipsilateral inhibitory projection onto the MVN, the y-group nucleus and the SVN, controlling contralateral, upward and perhaps downward smooth pursuit, respectively. Alternatively, the downward smooth pursuit pathway could pass through the dentate nuclei. The MVN sends a contralateral excitatory projection onto the abducens nucleus (second decussation of the lateral smooth pursuit circuitry). These anatomical and physiological characteristics of lateral smooth pursuit pathways, in addition to the results of lesion studies, suggest that, besides the floccular inhibitory Purkinje cell, there is another inhibitory neurone in the circuitry preceding this cell, perhaps within the flocculus itself. The posterior vermis projects onto the fastigial nuclei, which also control smooth pursuit. These nuclei could send efferents to those periabducens cells involved in ipsilateral smooth pursuit. The final part of the pathways involved in vertical smooth pursuit could pass mainly through the BC, originating in the y-group nucleus for upward movement and in the SVN or the dentate nuclei for downward movement. Alternatively, a ventral tegmental tract could transmit upward smooth pursuit signals between the y-group nucleus and the oculomotor nucleus. The MLF also belongs to this vestibulo-oculomotor circuitry, but does not appear to be crucial for vertical smooth pursuit since this eye movement is only partially impaired after MLF lesions. Lastly, parallel to the direct vestibulo-ocular motor nuclei pathways, there are other pathways passing through the brain stem integrators, converting eye velocity signals to eye position signals during all eye movements, including smooth pursuit.(ABSTRACT TRUNCATED AT 400 WORDS)
平稳跟踪是一种相对较新的眼球运动,在双眼向前的物种中进化而来。在中央凹平稳跟踪、视动性眼震慢相的“快速”成分以及前庭眼反射抑制过程中,平稳跟踪系统会发挥作用。控制平稳跟踪的皮质区域(位于颞顶枕交界处和额眼区)发出同侧投射到脑桥核,主要是背外侧脑桥核,投射经过中脑前部。中脑或背外侧脑桥核损伤会导致同侧平稳跟踪功能受损(即增益降低)(表1)。脑桥核之后,所有平稳跟踪通路都经过小脑。它们投射到绒球,主要是对侧投射(外侧平稳跟踪回路的第一次交叉),并双侧投射到小脑蚓后部。眼球速度由绒球浦肯野细胞的活动编码,而目标速度由蚓部浦肯野细胞的活动编码。单侧绒球损伤和小脑蚓后部损伤(涉及该结构的两侧)分别导致同侧和双侧平稳跟踪功能受损。绒球向内侧前庭核、y组核和舌下神经核发出同侧抑制性投射,分别控制对侧、向上以及可能向下的平稳跟踪。或者,向下的平稳跟踪通路可能经过齿状核。内侧前庭核向展神经核发出对侧兴奋性投射(外侧平稳跟踪回路的第二次交叉)。外侧平稳跟踪通路的这些解剖和生理特征,以及损伤研究的结果表明,除了绒球抑制性浦肯野细胞外,在该细胞之前的回路中还存在另一种抑制性神经元,可能就在绒球本身内部。小脑蚓后部投射到顶核,顶核也控制平稳跟踪。这些核可能向参与同侧平稳跟踪的展神经周围细胞发出传出纤维。垂直平稳跟踪所涉及通路的最后部分可能主要经过结合臂,向上运动起源于y组核,向下运动起源于舌下神经核或齿状核。或者,一条腹侧被盖束可以在y组核和动眼神经核之间传递向上的平稳跟踪信号。内侧纵束也属于这个前庭眼动回路,但对于垂直平稳跟踪似乎并非至关重要,因为在其损伤后这种眼球运动只是部分受损。最后,与直接的前庭眼动神经核通路平行,还有其他通路经过脑干整合器,在包括平稳跟踪在内的所有眼球运动过程中将眼球速度信号转换为眼球位置信号。(摘要截断于400字)