Literature DB >> 24985239

Spike-coding mechanisms of cerebellar temporal processing in classical conditioning and voluntary movements.

Kenji Yamaguchi1, Yoshio Sakurai.   

Abstract

Time is a fundamental and critical factor in daily life. Millisecond timing, which is the underlying temporal processing for speaking, dancing, and other activities, is reported to rely on the cerebellum. In this review, we discuss the cerebellar spike-coding mechanisms for temporal processing. Although the contribution of the cerebellum to both classical conditioning and voluntary movements is well known, the difference of the mechanisms for temporal processing between classical conditioning and voluntary movements is not clear. Therefore, we review the evidence of cerebellar temporal processing in studies of classical conditioning and voluntary movements and report the similarities and differences between them. From some studies, which used tasks that can change some of the temporal properties (e.g., the duration of interstimulus intervals) with keeping identical movements, we concluded that classical conditioning and voluntary movements may share a common spike-coding mechanism because simple spikes in Purkinje cells decrease at predicted times for responses regardless of the intervals between responses or stimulation.

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Year:  2014        PMID: 24985239     DOI: 10.1007/s12311-014-0580-5

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


  68 in total

1.  Evidence that climbing fibers control an intrinsic spike generator in cerebellar Purkinje cells.

Authors:  Nadia L Cerminara; John A Rawson
Journal:  J Neurosci       Date:  2004-05-12       Impact factor: 6.167

2.  Mechanisms of synchronous activity in cerebellar Purkinje cells.

Authors:  Andrew K Wise; Nadia L Cerminara; Dilwyn E Marple-Horvat; Richard Apps
Journal:  J Physiol       Date:  2010-05-04       Impact factor: 5.182

Review 3.  What makes us tick? Functional and neural mechanisms of interval timing.

Authors:  Catalin V Buhusi; Warren H Meck
Journal:  Nat Rev Neurosci       Date:  2005-10       Impact factor: 34.870

4.  Effect of conditioned stimulus parameters on timing of conditioned Purkinje cell responses.

Authors:  Pär Svensson; Dan-Anders Jirenhed; Fredrik Bengtsson; Germund Hesslow
Journal:  J Neurophysiol       Date:  2009-12-23       Impact factor: 2.714

5.  Bidirectional plasticity of Purkinje cells matches temporal features of learning.

Authors:  Daniel Z Wetmore; Dan-Anders Jirenhed; Anders Rasmussen; Fredrik Johansson; Mark J Schnitzer; Germund Hesslow
Journal:  J Neurosci       Date:  2014-01-29       Impact factor: 6.167

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Authors:  J P Welsh; E J Lang; I Suglhara; R Llinás
Journal:  Nature       Date:  1995-03-30       Impact factor: 49.962

7.  Ultradian rhythms in the mobility and behavior of rhesus monkeys.

Authors:  J M Delgado-García; C Grau; P DeFeudis; F del Pozo; J M Jimenez; J M Delgado
Journal:  Exp Brain Res       Date:  1976-05-10       Impact factor: 1.972

8.  Climbing fibre induced depression of both mossy fibre responsiveness and glutamate sensitivity of cerebellar Purkinje cells.

Authors:  M Ito; M Sakurai; P Tongroach
Journal:  J Physiol       Date:  1982-03       Impact factor: 5.182

9.  Somatosensory receptive fields of single units in cat cerebellar cortex.

Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1967-07       Impact factor: 2.714

10.  Strength and timing of motor responses mediated by rebound firing in the cerebellar nuclei after Purkinje cell activation.

Authors:  Laurens Witter; Cathrin B Canto; Tycho M Hoogland; Jornt R de Gruijl; Chris I De Zeeuw
Journal:  Front Neural Circuits       Date:  2013-08-21       Impact factor: 3.492

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  1 in total

1.  Inactivation of Cerebellar Cortical Crus II Disrupts Temporal Processing of Absolute Timing but not Relative Timing in Voluntary Movements.

Authors:  Kenji Yamaguchi; Yoshio Sakurai
Journal:  Front Syst Neurosci       Date:  2016-02-24
  1 in total

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