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在人类视觉引导的扫视过程中,对小脑后部进行经颅磁刺激。

Transcranial magnetic stimulation over the posterior cerebellum during visually guided saccades in man.

作者信息

Hashimoto M, Ohtsuka K

机构信息

Department of Ophthalmology, School of Medicine, Sapporo Medical University, Japan.

出版信息

Brain. 1995 Oct;118 ( Pt 5):1185-93. doi: 10.1093/brain/118.5.1185.

DOI:10.1093/brain/118.5.1185
PMID:7496779
Abstract

Recent intensive neurophysiological experiments in the monkey have demonstrated the function of the cerebellum in the control of saccadic eye movements. Microstimulation studies on monkeys have determined that the cerebellar cortex, which is specifically involved in the control of saccades, is located in vermal lobules VIc and VII. The Purkinje-cell axons arising from this vermal area terminate almost exclusively in an ellipsoidal region which protrudes dorsocaudally from the fastigial nucleus. Saccade-related cells in the fastigial nucleus are located exclusively in the ellipsoidal region. Microstimulation of the vermis modulated the activity of saccade-related cells in the fastigial nucleus, and then produced dysmetric saccades. In this study, we investigated effects of cerebellar stimulation on saccade metrics in man using a transcranial magnetic stimulation (TMS) device. Focal TMS was applied over the posterior cerebellum at an area approximately 7 mm lateral and caudal to the inion during horizontal visually guided saccades in six normal subjects. The TMS device was triggered after the onset of saccades with a latency of 0, 20, 40 or 60 ms. We investigated the effect of TMS on the amplitude and velocity of saccadic eye movements. For visually guided saccades directed contralateral to the stimulation side, TMS of the posterior cerebellum with the latency of 0 ms produced hypometric saccades followed by corrective saccades. Transcranial magnetic stimulation with latencies of 20, 40 and 60 ms had no effect on saccade metrics. On the other hand, for ipsilateral saccades, TMS with latencies of 0, 20 and 40 ms produced hypermetric saccades followed by postsaccadic drift.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

最近在猴子身上进行的密集神经生理学实验已经证明了小脑在控制眼球快速运动中的作用。对猴子的微刺激研究已经确定,专门参与控制快速扫视的小脑皮质位于蚓部小叶VIc和VII。源自这个蚓部区域的浦肯野细胞轴突几乎完全终止于一个从顶核向背尾侧突出的椭圆形区域。顶核中与快速扫视相关的细胞仅位于椭圆形区域。对蚓部的微刺激调节了顶核中与快速扫视相关细胞的活动,然后产生了测量不准的快速扫视。在这项研究中,我们使用经颅磁刺激(TMS)设备研究了小脑刺激对人类快速扫视指标的影响。在六名正常受试者进行水平视觉引导的快速扫视期间,将聚焦TMS应用于小脑后部,该区域位于枕外隆凸外侧和尾侧约7毫米处。TMS设备在快速扫视开始后0、20、40或60毫秒的潜伏期触发。我们研究了TMS对眼球快速运动的幅度和速度的影响。对于指向刺激侧对侧的视觉引导快速扫视,潜伏期为0毫秒的小脑后部TMS产生了幅度减小的快速扫视,随后是校正性快速扫视。潜伏期为20、40和60毫秒的经颅磁刺激对快速扫视指标没有影响。另一方面,对于同侧快速扫视,潜伏期为0、20和40毫秒的TMS产生了幅度增大的快速扫视,随后是扫视后漂移。(摘要截断于250字)

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