Literature DB >> 10727626

The human cerebellum and associative learning: dissociation between the acquisition, retention and extinction of conditioned eyeblinks.

V Bracha1, L Zhao, K B Irwin, J R Bloedel.   

Abstract

The present paper is part of a systematic exploration of the neural substrates of conditioned eyeblink responses in humans. Normal subjects and patients with lesions restricted to the cerebellum were examined for their ability to acquire new classically conditioned eyeblinks to an auditory conditioned stimulus and whether they were able to perform and extinguish a previously learned natural anticipatory eyeblink response - the kinesthetic threat eyeblink response (KTER). In classical conditioning to an auditory conditioned stimulus, cerebellar patients failed to acquire new conditioned responses. In contrast to this impairment, in the KTER task both cerebellar patients and control subjects exhibited a high incidence of anticipatory eyeblinks which were initiated before the forehead tap. These results indicate that the cerebellar circuits, which are critical for the acquisition of new conditioned responses, are not essential for the storage and expression of naturally acquired conditioned responses. In the extinction experiment, cerebellar patients failed to extinguish their KTERs. This finding suggests that in humans, the acquisition of new and the extinction of previously learned conditioned responses depends on a similar set of cerebellar circuits.

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Year:  2000        PMID: 10727626     DOI: 10.1016/s0006-8993(00)01995-8

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  24 in total

1.  Stimulus-response versus stimulus-stimulus-response learning in cerebellar patients.

Authors:  S Richter; K Matthies; T Ohde; A Dimitrova; E Gizewski; A Beck; V Aurich; D Timmann
Journal:  Exp Brain Res       Date:  2004-06-18       Impact factor: 1.972

2.  Dynamic changes in the cerebellar-interpositus/red-nucleus-motoneuron pathway during motor learning.

Authors:  Raudel Sánchez-Campusano; Agnès Gruart; José M Delgado-García
Journal:  Cerebellum       Date:  2011-12       Impact factor: 3.847

3.  Forebrain-Cerebellar Interactions During Learning.

Authors:  Craig Weiss; Aldis P Weible; Roberto Galvez; John F Disterhoft
Journal:  Cellscience       Date:  2006-10-27

Review 4.  Consolidation of motor memory.

Authors:  John W Krakauer; Reza Shadmehr
Journal:  Trends Neurosci       Date:  2005-11-14       Impact factor: 13.837

5.  Trace eyeblink conditioning in human subjects with cerebellar lesions.

Authors:  M Gerwig; K Haerter; K Hajjar; A Dimitrova; M Maschke; F P Kolb; A F Thilmann; E R Gizewski; D Timmann
Journal:  Exp Brain Res       Date:  2005-11-18       Impact factor: 1.972

6.  The cerebellar interpositus nucleus and the dynamic control of learned motor responses.

Authors:  Raudel Sánchez-Campusano; Agnès Gruart; José M Delgado-García
Journal:  J Neurosci       Date:  2007-06-20       Impact factor: 6.167

7.  Spontaneous recovery of motor memory during saccade adaptation.

Authors:  Vincent Ethier; David S Zee; Reza Shadmehr
Journal:  J Neurophysiol       Date:  2008-03-19       Impact factor: 2.714

8.  Extinction and Renewal of Conditioned Eyeblink Responses in Focal Cerebellar Disease.

Authors:  Katharina M Steiner; Yvonne Gisbertz; Dae-In Chang; Björn Koch; Ellen Uslar; Jens Claassen; Elke Wondzinski; Thomas M Ernst; Sophia L Göricke; Mario Siebler; Dagmar Timmann
Journal:  Cerebellum       Date:  2019-04       Impact factor: 3.847

9.  Role of cerebellar interpositus nucleus in the genesis and control of reflex and conditioned eyelid responses.

Authors:  Lydia Jiménez-Díaz; Juan de Dios Navarro-López; Agnès Gruart; José M Delgado-García
Journal:  J Neurosci       Date:  2004-10-13       Impact factor: 6.167

10.  Classically conditioned postural reflex in cerebellar patients.

Authors:  F P Kolb; S Lachauer; M Maschke; D Timmann
Journal:  Exp Brain Res       Date:  2004-05-29       Impact factor: 1.972

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