Daroff-Dell'Osso Ocular Motility Laboratory, Department of Neurology, Louis Stokes Cleveland VA Medical Center, Cleveland, OH, United States; School of Medicine, Case Western Reserve University, Cleveland, OH, United States; Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, United States.
Department of Neurology, University of Catania, Catania, Italy.
Prog Brain Res. 2019;249:329-344. doi: 10.1016/bs.pbr.2019.04.021. Epub 2019 Jun 6.
Internuclear ophthalmoparesis (INO) in multiple sclerosis (MS) is due to demyelination of the medial longitudinal fasciculus (MLF). INO is typically modeled as an increased peak-velocity and peak-acceleration ratio of abducting to adducting eye (pulse-size ratio, PSR). PSR can be affected by fatigue during prolonged ocular-motor tasks (ocular-motor fatigue). We propose that an important component of horizontal disconjugacy in INO is due to a delayed delivery of the saccadic pulse to the adducting eye (pulse-time delay, PTD). We expanded a control-system model to account for both abnormal PSR and PTD reflecting faulty axonal transmission in INO and to provide a better understanding of possible changes induced by fatigue. Saccades were measured in 19 MS patients with INO and 10 controls, using a 10-min saccadic "fatigue test" consisting of repetitive back-to-back 20° saccades. In the horizontal saccades model the unitary MLF connection was partitioned into parallel sub-tracts representing progressive degrees of disease effect. INO patients showed baseline abnormal PSR and PTD with some changes during the fatigue test. Manipulations of gain and transmission delay in the model provided simulated saccades that closely resembled those of INO. Ocular-motor fatigue may be a heterogeneous phenomenon that involves inter-saccadic fluctuation of PSR and PTD and adaptation during demanding ocular-motor tasks. INO as a model of abnormal axonal conduction has a potential role in assessing efficacy of reparative therapies in MS.
多发性硬化症(MS)中的核间眼肌麻痹(INO)是由于内侧纵束(MLF)脱髓鞘所致。INO 通常表现为外展和内收眼球的最大速度和最大加速度比值增加(脉冲大小比,PSR)。PSR 可能会受到长时间眼球运动任务(眼球运动疲劳)期间的疲劳影响。我们提出,INO 中水平分离的一个重要组成部分是由于眼球扫视脉冲传递到内收眼球的延迟(脉冲时间延迟,PTD)。我们扩展了一个控制系统模型,以解释异常 PSR 和 PTD,这反映了 INO 中轴突传输的故障,并提供对疲劳引起的可能变化的更好理解。我们使用包括重复的 20°扫视的 10 分钟扫视“疲劳测试”,测量了 19 名 INO 患者和 10 名对照者的扫视。在水平扫视模型中,单一的 MLF 连接被分成代表疾病进展程度的平行子部分。INO 患者在基线时表现出异常的 PSR 和 PTD,并且在疲劳测试期间有一些变化。模型中的增益和传输延迟的操作提供了与 INO 非常相似的模拟扫视。眼球运动疲劳可能是一种异质现象,涉及 PSR 和 PTD 的扫视间波动以及在要求苛刻的眼球运动任务期间的适应。INO 作为异常轴突传导的模型,在评估 MS 修复治疗的疗效方面具有潜在作用。