Werner Reichardt Centre for Integrative Neuroscience,
Hertie Institute for Clinical Brain Research, and.
J Neurosci. 2019 Apr 3;39(14):2709-2721. doi: 10.1523/JNEUROSCI.2178-18.2019. Epub 2019 Feb 1.
The oculomotor system integrates a variety of visual signals into appropriate motor plans, but such integration can have widely varying time scales. For example, smooth pursuit eye movements to follow a moving target are slower and longer lasting than saccadic eye movements and it has been suggested that initiating a smooth pursuit eye movement involves an obligatory "open-loop" interval in which new visual motion signals presumably cannot influence the ensuing motor plan for up to 100 ms after movement initiation. However, this view is contrary to the idea that the oculomotor periphery has privileged access to short-latency visual signals. Here, we show that smooth pursuit initiation is sensitive to visual inputs, even in open-loop intervals. We instructed male rhesus macaque monkeys to initiate saccade-free smooth pursuit eye movements and injected a transient, instantaneous eye position error signal at different times relative to movement initiation. We found robust short-latency modulations in eye velocity and acceleration, starting only ∼50 ms after transient signal occurrence and even during open-loop pursuit initiation. Critically, the spatial direction of the injected position error signal had predictable effects on smooth pursuit initiation, with forward errors increasing eye acceleration and backward errors reducing it. Catch-up saccade frequencies and amplitudes were also similarly altered ∼50 ms after transient signals, much like the well known effects on microsaccades during fixation. Our results demonstrate that smooth pursuit initiation is highly sensitive to visual signals and that catch-up saccade generation is reset after a visual transient. Smooth pursuit eye movements allow us to track moving objects. The first ∼100 ms of smooth pursuit initiation are characterized by smooth eye acceleration and are overwhelmingly described as being "open-loop"; that is, unmodifiable by new visual motion signals. We found that all phases of smooth pursuit, including the so-called open-loop intervals, are reliably modifiable by visual signals. We injected transient flashes resulting in very brief, spatially specific position error signals to smooth pursuit and observed very short-latency changes in smooth eye movements to minimize such errors. Our results highlight the flexibility of the oculomotor system in reacting to environmental events and suggest a functional role for the pervasiveness of visual sensitivity in oculomotor control brain regions.
动眼系统将各种视觉信号整合到适当的运动计划中,但这种整合的时间尺度可能有很大差异。例如,为了跟踪移动的目标,平滑追踪眼球运动比眼跳运动更慢且持续时间更长,人们认为启动平滑追踪眼球运动涉及一个强制性的“开环”间隔,在运动开始后 100 毫秒内,新的视觉运动信号大概无法影响随后的运动计划。然而,这种观点与动眼系统外围具有优先获取短潜伏期视觉信号的观点相矛盾。在这里,我们表明,即使在开环间隔内,平滑追踪的启动也对视觉输入敏感。我们指示雄性恒河猴发起无眼跳的平滑追踪眼球运动,并在相对于运动启动的不同时间注入一个短暂的、瞬时的眼位误差信号。我们发现,在瞬态信号发生后仅约 50 毫秒,甚至在开环追踪启动期间,眼速和加速度都出现了强大的短潜伏期调制。关键的是,注入的位置误差信号的空间方向对平滑追踪的启动具有可预测的影响,正向误差增加眼加速度,而反向误差减小眼加速度。捕捉性眼跳的频率和幅度也在瞬态信号后约 50 毫秒时类似地发生改变,就像在注视时对微眼跳的影响一样明显。我们的结果表明,平滑追踪的启动对视觉信号非常敏感,并且在视觉瞬变后重新设置捕捉性眼跳的生成。平滑追踪眼球运动使我们能够跟踪移动的物体。平滑追踪启动的最初约 100 毫秒的特征是平滑的眼加速,并且绝大多数被描述为“开环”,即不能被新的视觉运动信号改变。我们发现,平滑追踪的所有阶段,包括所谓的开环间隔,都可以被视觉信号可靠地改变。我们向平滑追踪注入短暂的闪光,产生非常短暂、空间特定的位置误差信号,并观察到平滑眼运动的非常短潜伏期变化,以最小化这些误差。我们的结果突出了动眼系统对环境事件的反应灵活性,并表明视觉敏感性在动眼控制脑区中的普遍性具有功能作用。