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小脑动眼蚓部的复合锋电位活动:扫视运动学习的矢量误差信号?

Complex spike activity in the oculomotor vermis of the cerebellum: a vectorial error signal for saccade motor learning?

作者信息

Soetedjo Robijanto, Kojima Yoshiko, Fuchs Albert F

机构信息

Department of Physiology, 1959 NE Pacific St., HSB I421, Washington National Primate Research Center, Box 357330, University of Washington, Seattle, WA 98195-7330, USA.

出版信息

J Neurophysiol. 2008 Oct;100(4):1949-66. doi: 10.1152/jn.90526.2008. Epub 2008 Jul 23.

Abstract

Brain stem signals that generate saccadic eye movements originate in the superior colliculus. They reach the pontine burst generator for horizontal saccades via short-latency pathways and a longer pathway through the oculomotor vermis (OMV) of the cerebellum. Lesion studies implicate the OMV in the adaptation of saccade amplitude that occurs when saccades become inaccurate because of extraocular muscle weakness or behavioral manipulations. We studied the nature of the possible error signal that might drive adaptation by examining the complex spike (CS) activity of vermis Purkinje (P-) cells in monkeys. We produced a saccade error by displacing the target as a saccade was made toward it; a corrective saccade approximately 200 ms later eliminated the resulting error. In most P-cells, the probability of CS firing changed, but only in the error interval between the primary and corrective saccade. For most P-cells, CSs occurred in a tight cluster approximately 100 ms after error onset. The probability of CS occurrence depended on both error direction and size. Across our sample, all error directions were represented; most had a horizontal component. In more than one half of our P-cells, the probability of CS occurrence was greatest for error sizes<5 degrees and less for larger errors. In the remaining cells, there was a uniform increased probability of CS occurrence for all errors<or=7-9 degrees. CS responses disappeared when the target was extinguished during a saccade. We discuss the properties of this putative CS error signal in the context of the characteristics of saccade adaptation produced by the target displacement paradigm.

摘要

产生眼球快速跳动的脑干信号起源于上丘。它们通过短潜伏期通路以及一条经过小脑动眼蚓部(OMV)的较长通路到达脑桥爆发发生器以产生水平眼球快速跳动。损伤研究表明,当由于眼外肌无力或行为操作导致眼球快速跳动不准确时,OMV参与了眼球快速跳动幅度的适应性调节。我们通过研究猴子动眼蚓部浦肯野(P-)细胞的复合动作电位(CS)活动,来探究可能驱动适应性调节的误差信号的本质。当向目标进行眼球快速跳动时,我们通过移动目标来产生眼球快速跳动误差;大约200毫秒后产生的纠正性眼球快速跳动消除了由此产生的误差。在大多数P-细胞中,CS发放的概率发生了变化,但仅在初次和纠正性眼球快速跳动之间的误差区间内。对于大多数P-细胞,CS在误差出现后约100毫秒紧密成簇出现。CS出现的概率取决于误差方向和大小。在我们的样本中,所有误差方向都有体现;大多数具有水平分量。在超过一半的P-细胞中,误差大小<5度时CS出现的概率最大,而较大误差时概率较小。在其余细胞中,对于所有<或=7 - 9度的误差,CS出现的概率均均匀增加。当在眼球快速跳动期间目标消失时,CS反应消失。我们根据目标位移范式产生的眼球快速跳动适应性调节的特征,讨论了这种假定的CS误差信号的特性。

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