Department of Neurology, The Johns Hopkins University, Baltimore, MD 21287, USA.
Brain. 2010 Mar;133(Pt 3):923-40. doi: 10.1093/brain/awp323. Epub 2010 Jan 15.
The inferior olivary nuclei clearly play a role in creating oculopalatal tremor, but the exact mechanism is unknown. Oculopalatal tremor develops some time after a lesion in the brain that interrupts inhibition of the inferior olive by the deep cerebellar nuclei. Over time the inferior olive gradually becomes hypertrophic and its neurons enlarge developing abnormal soma-somatic gap junctions. However, results from several experimental studies have confounded the issue because they seem inconsistent with a role for the inferior olive in oculopalatal tremor, or because they ascribe the tremor to other brain areas. Here we look at 3D binocular eye movements in 15 oculopalatal tremor patients and compare their behaviour to the output of our recent mathematical model of oculopalatal tremor. This model has two mechanisms that interact to create oculopalatal tremor: an oscillator in the inferior olive and a modulator in the cerebellum. Here we show that this dual mechanism model can reproduce the basic features of oculopalatal tremor and plausibly refute the confounding experimental results. Oscillations in all patients and simulations were aperiodic, with a complicated frequency spectrum showing dominant components from 1 to 3 Hz. The model's synchronized inferior olive output was too small to induce noticeable ocular oscillations, requiring amplification by the cerebellar cortex. Simulations show that reducing the influence of the cerebellar cortex on the oculomotor pathway reduces the amplitude of ocular tremor, makes it more periodic and pulse-like, but leaves its frequency unchanged. Reducing the coupling among cells in the inferior olive decreases the oscillation's amplitude until they stop (at approximately 20% of full coupling strength), but does not change their frequency. The dual-mechanism model accounts for many of the properties of oculopalatal tremor. Simulations suggest that drug therapies designed to reduce electrotonic coupling within the inferior olive or reduce the disinhibition of the cerebellar cortex on the deep cerebellar nuclei could treat oculopalatal tremor. We conclude that oculopalatal tremor oscillations originate in the hypertrophic inferior olive and are amplified by learning in the cerebellum.
橄榄下核显然在产生眼-腭震颤中起作用,但确切机制尚不清楚。眼-腭震颤在大脑中损伤后一段时间发展,该损伤中断了小脑深部核对橄榄下核的抑制。随着时间的推移,橄榄下核逐渐出现肥大,其神经元增大,形成异常的胞体-胞体缝隙连接。然而,几项实验研究的结果使问题变得复杂,因为它们似乎与橄榄下核在眼-腭震颤中的作用不一致,或者因为它们将震颤归因于其他脑区。在这里,我们观察了 15 例眼-腭震颤患者的 3D 双眼运动,并将其行为与我们最近的眼-腭震颤数学模型的输出进行了比较。该模型有两个相互作用产生眼-腭震颤的机制:一个是橄榄下核中的振荡器,另一个是小脑中的调制器。在这里,我们表明,这个双机制模型可以再现眼-腭震颤的基本特征,并合理地反驳混淆的实验结果。所有患者和模拟的振荡都是非周期性的,具有复杂的频谱,显示出 1 至 3 Hz 的主要成分。模型的同步橄榄下核输出太小,无法引起明显的眼球振荡,需要小脑皮层放大。模拟表明,降低小脑皮层对眼动通路的影响会降低眼球震颤的幅度,使其更具周期性和脉冲状,但频率不变。降低橄榄下核细胞之间的耦合会降低振荡的幅度,直到它们停止(大约是完全耦合强度的 20%),但不会改变它们的频率。双机制模型解释了眼-腭震颤的许多特性。模拟表明,旨在降低橄榄下核内电紧张耦合或降低小脑皮层对小脑深部核的去抑制作用的药物治疗可能治疗眼-腭震颤。我们的结论是,眼-腭震颤的振荡起源于肥大的橄榄下核,并通过小脑的学习得到放大。