Guitton D, Douglas R M, Volle M
J Neurophysiol. 1984 Dec;52(6):1030-50. doi: 10.1152/jn.1984.52.6.1030.
Gaze is the position of the visual axis in space and is the sum of the eye movement relative to the head plus head movement relative to space. In monkeys, a gaze shift is programmed with a single saccade that will, by itself, take the eye to a target, irrespective of whether the head moves. If the head turns simultaneously, the saccade is correctly reduced in size (to prevent gaze overshoot) by the vestibuloocular reflex (VOR). Cats have an oculomotor range (OMR) of only about +/- 25 degrees, but their field of view extends to about +/- 70 degrees. The use of the monkey's motor strategy to acquire targets lying beyond +/- 25 degrees requires the programming of saccades that cannot be physically made. We have studied, in cats, rapid horizontal gaze shifts to visual targets within and beyond the OMR. Heads were either totally unrestrained or attached to an apparatus that permitted short unexpected perturbations of the head trajectory. Qualitatively, similar rapid gaze shifts of all sizes up to at least 70 degrees could be accomplished with the classic single-eye saccade and a saccade-like head movement. For gaze shifts greater than 30 degrees, this classic pattern frequently was not observed, and gaze shifts were accomplished with a series of rapid eye movements whose time separation decreased, frequently until they blended into each other, as head velocity increased. Between discrete rapid eye movements, gaze continued in constant velocity ramps, controlled by signals added to the VOR-induced compensatory phase that followed a saccade. When the head was braked just prior to its onset in a 10 degrees gaze shift, the eye attained the target. This motor strategy is the same as that reported for monkeys. However, for larger target eccentricities (e.g., 50 degrees), the gaze shift was interrupted by the brake and the average saccade amplitude was 12-15 degrees, well short of the target and the OMR. Gaze shifts were completed by vestibularly driven eye movements when the head was released. Braking the head during either quick phases driven by passive head displacements or visually triggered saccades resulted in an acceleration of the eye, thereby implying interaction between the VOR and these rapid-eye-movement signals. Head movements possessed a characteristic but task-dependent relationship between maximum velocity and amplitude. Head movements terminated with the head on target. The eye saccade usually lagged the head displacement.(ABSTRACT TRUNCATED AT 400 WORDS)
注视是视轴在空间中的位置,是眼球相对于头部的运动加上头部相对于空间的运动的总和。在猴子中,一次扫视就可规划一次注视转移,这本身就能使眼睛看向目标,而不论头部是否移动。如果头部同时转动,前庭眼反射(VOR)会正确地减小扫视幅度(以防止注视超调)。猫的动眼范围(OMR)仅约为±25度,但其视野范围可延伸至约±70度。要运用猴子的运动策略来获取位于±25度范围之外的目标,就需要规划出实际上无法做出的扫视。我们研究了猫对OMR范围内及范围外的视觉目标的快速水平注视转移。头部要么完全不受约束,要么连接到一个装置上,该装置允许对头部轨迹进行短暂的意外扰动。定性地说,通过经典的单眼扫视和类似扫视的头部运动,可以完成至少70度的各种大小的类似快速注视转移。对于大于30度的注视转移,这种经典模式常常未被观察到,注视转移是通过一系列快速眼动完成的,随着头部速度增加,这些眼动之间的时间间隔减小,常常直至相互融合。在离散的快速眼动之间,注视以恒定速度斜坡持续,由添加到扫视后VOR诱导的补偿阶段的信号控制。当头部在10度注视转移开始前被制动时,眼睛到达目标。这种运动策略与报道的猴子的运动策略相同。然而,对于更大的目标偏心度(例如50度),注视转移会被制动打断,平均扫视幅度为12 - 15度,远未达到目标和OMR。当头部被释放时,注视转移通过前庭驱动的眼动完成。在由被动头部位移驱动的快速阶段或视觉触发的扫视过程中制动头部,会导致眼睛加速,从而意味着VOR与这些快速眼动信号之间存在相互作用。头部运动在最大速度和幅度之间具有一种特征性但依赖于任务的关系。头部运动在头部到达目标时终止。眼扫视通常滞后于头部位移。(摘要截取自400字)