Literature DB >> 20032243

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

Pär Svensson1, Dan-Anders Jirenhed, Fredrik Bengtsson, Germund Hesslow.   

Abstract

Pavlovian eyeblink conditioning is a useful experimental model for studying adaptive timing, an important aspect of skilled movements. The conditioned response (CR) is precisely timed to occur just before the onset of the expected unconditioned stimulus (US). The timing can be changed immediately, however, by varying parameters of the conditioned stimulus (CS). It has previously been shown that increasing the intensity of a peripheral CS or the frequency of a CS consisting of a train of stimuli to the mossy fibers shortens the latency of the CR. The adaptive timing of behavioral CRs probably reflects the timing of an underlying learned inhibitory response in cerebellar Purkinje cells. It is not known how the latency of this Purkinje cell CR is controlled. We have recorded form Purkinje cells in conditioned decerebrate ferrets while increasing the intensity of a peripheral CS or the frequency of a mossy fiber CS. We observe changes in the timing of the Purkinje cell CR that match the behavioral effects. The results are consistent with the effect of CS parameters on behavioral CR latency being caused by corresponding changes in Purkinje cell CRs. They suggest that synaptic temporal summation may be one of several mechanisms underlying adaptive timing of movements.

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Year:  2009        PMID: 20032243     DOI: 10.1152/jn.00524.2009

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  16 in total

1.  Timing and causality in the generation of learned eyelid responses.

Authors:  Raudel Sánchez-Campusano; Agnès Gruart; José M Delgado-García
Journal:  Front Integr Neurosci       Date:  2011-08-30

2.  Time course of classically conditioned Purkinje cell response is determined by initial part of conditioned stimulus.

Authors:  Dan-Anders Jirenhed; Germund Hesslow
Journal:  J Neurosci       Date:  2011-06-22       Impact factor: 6.167

3.  Learning stimulus intervals--adaptive timing of conditioned purkinje cell responses.

Authors:  Dan-Anders Jirenhed; Germund Hesslow
Journal:  Cerebellum       Date:  2011-09       Impact factor: 3.847

4.  Relating cerebellar purkinje cell activity to the timing and amplitude of conditioned eyelid responses.

Authors:  Hunter E Halverson; Andrei Khilkevich; Michael D Mauk
Journal:  J Neurosci       Date:  2015-05-20       Impact factor: 6.167

Review 5.  Spike-coding mechanisms of cerebellar temporal processing in classical conditioning and voluntary movements.

Authors:  Kenji Yamaguchi; Yoshio Sakurai
Journal:  Cerebellum       Date:  2014-10       Impact factor: 3.847

6.  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

7.  Memory trace and timing mechanism localized to cerebellar Purkinje cells.

Authors:  Fredrik Johansson; Dan-Anders Jirenhed; Anders Rasmussen; Riccardo Zucca; Germund Hesslow
Journal:  Proc Natl Acad Sci U S A       Date:  2014-09-29       Impact factor: 11.205

8.  Climbing fiber activity reduces 14-3-3-θ regulated GABA(A) receptor phosphorylation in cerebellar Purkinje cells.

Authors:  Z Qian; M Micorescu; V Yakhnitsa; N H Barmack
Journal:  Neuroscience       Date:  2011-11-17       Impact factor: 3.590

9.  Cerebellar structure and function in male Wistar-Kyoto hyperactive rats.

Authors:  Alexandra Thanellou; John T Green
Journal:  Behav Neurosci       Date:  2013-02-11       Impact factor: 1.912

10.  A computational mechanism for unified gain and timing control in the cerebellum.

Authors:  Tadashi Yamazaki; Soichi Nagao
Journal:  PLoS One       Date:  2012-03-13       Impact factor: 3.240

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