Neural Learning Rules for the Vestibulo-Ocular Reflex

Mechanisms for the induction of motor learning in the vestibulo-ocular reflex (VOR) were evaluated by recording the patterns of neural activity elicited in the cerebellum by a range of stimuli that induce learning. Patterns of climbing-fiber, vestibular, and Purkinje cell simple-spike signals were e...

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Veröffentlicht in:The Journal of neuroscience 1998-11, Vol.18 (21), p.9112-9129
Hauptverfasser: Raymond, Jennifer L, Lisberger, Stephen G
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container_title The Journal of neuroscience
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creator Raymond, Jennifer L
Lisberger, Stephen G
description Mechanisms for the induction of motor learning in the vestibulo-ocular reflex (VOR) were evaluated by recording the patterns of neural activity elicited in the cerebellum by a range of stimuli that induce learning. Patterns of climbing-fiber, vestibular, and Purkinje cell simple-spike signals were examined during sinusoidal head movement paired with visual image movement at stimulus frequencies from 0.5 to 10 Hz. A comparison of simple-spike and vestibular signals contained the information required to guide learning only at low stimulus frequencies, and a comparison of climbing-fiber and simple-spike signals contained the information required to guide learning only at high stimulus frequencies. Learning could be guided by comparison of climbing-fiber and vestibular signals at all stimulus frequencies tested, but only if climbing fiber responses were compared with the vestibular signals present 100 msec earlier. Computational analysis demonstrated that this conclusion is valid even if there is a broad range of vestibular signals at the site of plasticity. Simulations also indicated that the comparison of vestibular and climbing-fiber signals across the 100 msec delay must be implemented by a subcellular "eligibility" trace rather than by neural circuits that delay the vestibular inputs to the site of plasticity. The results suggest two alternative accounts of learning in the VOR. Either there are multiple mechanisms of learning that use different combinations of neural signals to drive plasticity, or there is a single mechanism tuned to climbing-fiber activity that follows activity in vestibular pathways by approximately 100 msec.
doi_str_mv 10.1523/jneurosci.18-21-09112.1998
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source MEDLINE; NASA Technical Reports Server; PubMed Central; EZB Electronic Journals Library
subjects Animals
Electrophysiology
Evoked Potentials, Visual
Learning - physiology
Life Sciences (General)
Macaca mulatta
Male
Models, Biological
Neuronal Plasticity
Posture
Purkinje Cells - physiology
Reflex, Vestibulo-Ocular - physiology
Space life sciences
title Neural Learning Rules for the Vestibulo-Ocular Reflex
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