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A Cerebellar Learning Model of Vestibulo-Ocular Reflex Adaptation in Wild-Type and Mutant Mice

机译:野生型和突变型小鼠的动眼反射适应的小脑学习模型。

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摘要

Mechanisms of cerebellar motor learning are still poorly understood. The standard Marr–Albus–Ito theory posits that learning involves plasticity at the parallel fiber to Purkinje cell synapses under control of the climbing fiber input, which provides an error signal as in classical supervised learning paradigms. However, a growing body of evidence challenges this theory, in that additional sites of plasticity appear to contribute to motor adaptation. Here, we consider phase-reversal training of the vestibulo-ocular reflex (VOR), a simple form of motor learning for which a large body of experimental data is available in wild-type and mutant mice, in which the excitability of granule cells or inhibition of Purkinje cells was affected in a cell-specific fashion. We present novel electrophysiological recordings of Purkinje cell activity measured in naive wild-type mice subjected to this VOR adaptation task. We then introduce a minimal model that consists of learning at the parallel fibers to Purkinje cells with the help of the climbing fibers. Although the minimal model reproduces the behavior of the wild-type animals and is analytically tractable, it fails at reproducing the behavior of mutant mice and the electrophysiology data. Therefore, we build a detailed model involving plasticity at the parallel fibers to Purkinje cells' synapse guided by climbing fibers, feedforward inhibition of Purkinje cells, and plasticity at the mossy fiber to vestibular nuclei neuron synapse. The detailed model reproduces both the behavioral and electrophysiological data of both the wild-type and mutant mice and allows for experimentally testable predictions.
机译:小脑运动学习的机制仍知之甚少。标准的Marr-Albus-Ito理论认为,学习涉及在攀爬纤维输入的控制下,与Purkinje细胞突触平行的纤维在可塑性上的可塑性,这在传统的监督学习范例中提供了一个误差信号。但是,越来越多的证据对这一理论提出了挑战,因为其他可塑性部位似乎有助于运动适应。在这里,我们考虑对前庭眼反射(VOR)进行相逆训练,这是一种简单的运动学习形式,在野生型和突变型小鼠中可获得大量的实验数据,其中颗粒细胞或浦肯野细胞的抑制作用以细胞特异性方式受到影响。我们目前在接受此VOR适应任务的天真野生型小鼠中测量的Purkinje细胞活性的新型电生理记录。然后,我们引入一个最小模型,该模型包括借助攀爬纤维在与浦肯野细胞平行的纤维上学习。尽管最小模型再现了野生型动物的行为并且在分析上易于处理,但是它无法再现突变小鼠的行为和电生理数据。因此,我们建立了一个详细的模型,涉及由攀爬纤维引导的平行纤维对浦肯野细胞突触的可塑性,前馈抑制浦肯野细胞以及在苔藓纤维对前庭核神经元突触的可塑性。详细的模型复制了野生型和突变型小鼠的行为和电生理数据,并允许进行实验测试的预测。

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