Otero-Millan Jorge, Optican Lance M, Macknik Stephen L, Martinez-Conde Susana
Department of Neurology, Johns Hopkins University, Baltimore, MD, United States.
Laboratory of Sensorimotor Research, National Eye Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, United States.
Front Neurol. 2018 May 28;9:346. doi: 10.3389/fneur.2018.00346. eCollection 2018.
When we explore a static visual scene, our eyes move in a sequence of fast eye movements called saccades, which are separated by fixation periods of relative eye stability. Based on uncertain sensory and cognitive inputs, the oculomotor system must decide, at every moment, whether to initiate a saccade or to remain in the fixation state. Even when we attempt to maintain our gaze on a small spot, small saccades, called microsaccades, intrude on fixation once or twice per second. Because microsaccades occur at the boundary of the decision to maintain fixation versus starting a saccade, they offer a unique opportunity to study the mechanisms that control saccadic triggering. Abnormal saccadic intrusions can occur during attempted fixation in patients with neurodegenerative disorders. We have implemented a model of the triggering mechanism of saccades, based on known anatomy and physiology, that successfully simulates the generation of saccades of any size-including microsaccades in healthy observers, and the saccadic intrusions that interrupt attempted fixation in parkinsonian patients. The model suggests that noisy neuronal activity in the superior colliculus controls the state of a mutually inhibitory network in the brain stem formed by burst neurons and omnipause neurons. When the neuronal activity is centered at the rostral pole, the system remains at a state of fixation. When activity is perturbed away from this center, a saccade is triggered. This perturbation can be produced either by the intent to move one's gaze or by random fluctuations in activity.
当我们探索一个静态视觉场景时,我们的眼睛会以一系列快速眼动(称为扫视)移动,这些扫视之间由相对眼稳定的注视期隔开。基于不确定的感官和认知输入,动眼系统必须时刻决定是发起扫视还是保持注视状态。即使我们试图将目光固定在一个小点上,每秒也会有一两次称为微扫视的小扫视打断注视。由于微扫视发生在维持注视与开始扫视的决策边界,它们为研究控制扫视触发的机制提供了独特的机会。神经退行性疾病患者在试图注视时可能会出现异常的扫视侵入。我们基于已知的解剖学和生理学原理,实现了一个扫视触发机制模型,该模型成功地模拟了任何大小的扫视的产生——包括健康观察者的微扫视,以及打断帕金森病患者试图注视的扫视侵入。该模型表明,上丘中嘈杂的神经元活动控制着由爆发神经元和全暂停神经元在脑干中形成的相互抑制网络的状态。当神经元活动集中在吻侧极时,系统保持在注视状态。当活动偏离这个中心受到干扰时,就会触发扫视。这种干扰可以由移动目光的意图或活动中的随机波动产生。