Literature DB >> 28444617

Computational Theory Underlying Acute Vestibulo-ocular Reflex Motor Learning with Cerebellar Long-Term Depression and Long-Term Potentiation.

Keiichiro Inagaki1, Yutaka Hirata2.   

Abstract

The vestibulo-ocular reflex (VOR) can be viewed as an adaptive control system that maintains compensatory eye movements during head motion. As the cerebellar flocculus is intimately involved in this adaptive motor control of the VOR, the VOR has been a popular model system for investigating cerebellar motor learning. Long-term depression (LTD) and long-term potentiation (LTP) at the parallel fiber-Purkinje cell synapses are considered to play major roles in cerebellar motor learning. A recent study using mutant mice demonstrated cerebellar motor learning with hampered LTD; the study concluded that the parallel fiber-Purkinje cell LTD is not essential. More recently, multiple forms of plasticity have been found in the cerebellum, and they are believed to contribute to cerebellar motor learning. However, it is still unclear how synaptic plasticity modifies the signal processing that underlies motor learning in the flocculus. A computational simulation suggested that the plasticity present in mossy fiber-granule cell synapses improves VOR-related sensory-motor information transferred into granule cells, whereas the plasticity in the molecular layer stores this information as a memory under guidance from climbing fiber teaching signals. Thus, motor learning and memory are thought to be induced mainly by LTD and LTP at parallel fiber-Purkinje cell synapses and by rebound potentiation at molecular interneuron-Purkinje cell synapses among the multiple forms of plasticity in the cerebellum. In this study, we focused on the LTD and LTP at parallel fiber-Purkinje cell synapses. Based on our simulation, we propose that acute VOR motor learning accomplishes by simultaneous enhancement of eye movement signals via LTP and suppression of vestibular signals via LTD to increase VOR gain (gain-up learning). To decrease VOR gain (gain-down learning), these two signals are modified in the opposite directions; namely, LTD suppresses eye movement signals, whereas LTP enhances vestibular signals.

Entities:  

Keywords:  Cerebellar flocculus; Computer simulation; Signal selection; Spike timing-dependent plasticity; Spiking neuron network model

Mesh:

Year:  2017        PMID: 28444617     DOI: 10.1007/s12311-017-0857-6

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  60 in total

1.  Temporal specificity of long-term depression in parallel fiber--Purkinje synapses in rat cerebellar slice.

Authors:  C Chen; R F Thompson
Journal:  Learn Mem       Date:  1995 May-Aug       Impact factor: 2.460

2.  Capacity of vertical VOR adaptation in squirrel monkey.

Authors:  Y Hirata; J M Lockard; S M Highstein
Journal:  J Neurophysiol       Date:  2002-12       Impact factor: 2.714

3.  Synaptic excitation produces a long-lasting rebound potentiation of inhibitory synaptic signals in cerebellar Purkinje cells.

Authors:  M Kano; U Rexhausen; J Dreessen; A Konnerth
Journal:  Nature       Date:  1992-04-16       Impact factor: 49.962

Review 4.  Timing and plasticity in the cerebellum: focus on the granular layer.

Authors:  Egidio D'Angelo; Chris I De Zeeuw
Journal:  Trends Neurosci       Date:  2008-10-30       Impact factor: 13.837

5.  Role of granule-cell transmission in memory trace of cerebellum-dependent optokinetic motor learning.

Authors:  Norio Wada; Kazuo Funabiki; Shigetada Nakanishi
Journal:  Proc Natl Acad Sci U S A       Date:  2014-03-24       Impact factor: 11.205

6.  Simulation of adaptive modification of the vestibulo-ocular reflex with an adaptive filter model of the cerebellum.

Authors:  M Fujita
Journal:  Biol Cybern       Date:  1982       Impact factor: 2.086

Review 7.  Cerebellar long-term depression: characterization, signal transduction, and functional roles.

Authors:  M Ito
Journal:  Physiol Rev       Date:  2001-07       Impact factor: 37.312

Review 8.  LTD, RP, and Motor Learning.

Authors:  Tomoo Hirano; Yoshito Yamazaki; Yoji Nakamura
Journal:  Cerebellum       Date:  2016-02       Impact factor: 3.847

9.  Temporal firing patterns of Purkinje cells in the cerebellar ventral paraflocculus during ocular following responses in monkeys II. Complex spikes.

Authors:  Y Kobayashi; K Kawano; A Takemura; Y Inoue; T Kitama; H Gomi; M Kawato
Journal:  J Neurophysiol       Date:  1998-08       Impact factor: 2.714

10.  Inhibitory synaptic currents in stellate cells of rat cerebellar slices.

Authors:  I Llano; H M Gerschenfeld
Journal:  J Physiol       Date:  1993-08       Impact factor: 5.182

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  4 in total

1.  Effect of convergence on the horizontal VOR in normal subjects and patients with peripheral and central vestibulopathy.

Authors:  Ammar L Ujjainwala; Callum D Dewar; Laurel Fifield; Caroline Rayburn; Emily Buenting; Jordan Boyle; Jorge C Kattah
Journal:  Neurol Sci       Date:  2022-03-04       Impact factor: 3.307

2.  Time Is Cerebellum.

Authors:  Hiroshi Mitoma; Mario Manto; Christiane S Hampe
Journal:  Cerebellum       Date:  2018-08       Impact factor: 3.847

3.  Occurrence of long-term depression in the cerebellar flocculus during adaptation of optokinetic response.

Authors:  Takuma Inoshita; Tomoo Hirano
Journal:  Elife       Date:  2018-03-27       Impact factor: 8.140

4.  World Statistics Drive Learning of Cerebellar Internal Models in Adaptive Feedback Control: A Case Study Using the Optokinetic Reflex.

Authors:  Sean R Anderson; John Porrill; Paul Dean
Journal:  Front Syst Neurosci       Date:  2020-03-25
  4 in total

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