Kojima Yoshiko, Fuchs Albert F, Soetedjo Robijanto
Department of Physiology and Biophysics and Washington National Primate Research Center, University of Washington, Seattle, Washington.
J Neurophysiol. 2015 Jul;114(1):125-37. doi: 10.1152/jn.00212.2015. Epub 2015 Apr 8.
Shifts in the direction of gaze are accomplished by different kinds of saccades, which are elicited under different circumstances. Saccade types include targeting saccades to simple jumping targets, delayed saccades to visible targets after a waiting period, memory-guided (MG) saccades to remembered target locations, scanning saccades to stationary target arrays, and express saccades after very short latencies. Studies of human cases and neurophysiological experiments in monkeys suggest that separate pathways, which converge on a common locus that provides the motor command, generate these different types of saccade. When behavioral manipulations in humans cause targeting saccades to have persistent dysmetrias as might occur naturally from growth, aging, and injury, they gradually adapt to reduce the dysmetria. Although results differ slightly between laboratories, this adaptation generalizes or transfers to all the other saccade types mentioned above. Also, when one of the other types of saccade undergoes adaptation, it often transfers to another saccade type. Similar adaptation and transfer experiments, which allow inferences to be drawn about the site(s) of adaptation for different saccade types, have yet to be done in monkeys. Here we show that simian targeting and MG saccades adapt more than express, scanning, and delayed saccades. Adaptation of targeting saccades transfers to all the other saccade types. However, the adaptation of MG saccades transfers only to delayed saccades. These data suggest that adaptation of simian targeting saccades occurs on the pathway common to all saccade types. In contrast, only the delayed saccade command passes through the adaptation site of the MG saccade.
目光注视方向的改变是通过不同类型的扫视来完成的,这些扫视在不同情况下引发。扫视类型包括针对简单跳跃目标的目标导向扫视、等待一段时间后对可见目标的延迟扫视、对记忆中目标位置的记忆引导(MG)扫视、对静止目标阵列的扫描扫视以及潜伏期极短的快速扫视。对人类病例的研究和猴子的神经生理学实验表明,不同的通路汇聚于一个共同的位点,该位点提供运动指令,从而产生这些不同类型的扫视。当人类的行为操作导致目标导向扫视出现持续性的度量障碍,如自然生长、衰老和损伤可能引发的情况时,它们会逐渐适应以减少度量障碍。尽管不同实验室的结果略有差异,但这种适应会推广或转移到上述所有其他扫视类型。此外,当其他类型的扫视之一进行适应时,它通常会转移到另一种扫视类型。类似的适应和转移实验,可用于推断不同扫视类型的适应位点,尚未在猴子身上进行。在这里,我们表明猕猴的目标导向扫视和MG扫视比快速扫视、扫描扫视和延迟扫视更易适应。目标导向扫视的适应会转移到所有其他扫视类型。然而,MG扫视的适应仅转移到延迟扫视。这些数据表明,猕猴目标导向扫视的适应发生在所有扫视类型共有的通路上。相比之下,只有延迟扫视指令会通过MG扫视的适应位点。