Literature DB >> 1482542

Rabbit classically conditioned eyelid responses do not reappear after interpositus nucleus lesion and extensive post-lesion training.

J E Steinmetz1, S F Logue, S S Steinmetz.   

Abstract

The left eyelid responses of four rabbits were classical conditioned by pairing a tone conditioned stimulus and air puff unconditioned stimulus. After conditioned responses were well-established, the left interpositus nucleus was lesioned and 150-200 post-lesion training sessions, distributed over 10 months, were given. In three of the rabbits, no anticipatory conditioned responses were observed on paired trials and responses were at or below spontaneous blinking rates on 2,500 ms CS-alone trials that were also presented. Post-lesion conditioned responses were present when the right side was trained. The fourth rabbit showed few post-lesion conditioned responses on paired trials but eventually showed 80% conditioned responses on tone-alone trials. Histological analysis of the lesion extents indicate that a portion of the anterior interpositus nucleus was spared in this rabbit. These results argue that unlike other cerebellar lesion effects reported in the literature, where some recovery of function is normally noted, the effects of interpositus nucleus lesions are somewhat unique in that conditioned response abolition is seen as long as 10 months after the lesion.

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Year:  1992        PMID: 1482542     DOI: 10.1016/s0166-4328(05)80317-1

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  16 in total

1.  Cerebellar cortical inhibition and classical eyeblink conditioning.

Authors:  Shaowen Bao; Lu Chen; Jeansok J Kim; Richard F Thompson
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-22       Impact factor: 11.205

Review 2.  Parallel neural systems for classical conditioning: support from computational modeling.

Authors:  M T Allen; C E Myers; M A Gluck
Journal:  Integr Physiol Behav Sci       Date:  2001 Jan-Mar

Review 3.  Neuroscience and learning: lessons from studying the involvement of a region of cerebellar cortex in eyeblink classical conditioning.

Authors:  Ronald P Villarreal; Joseph E Steinmetz
Journal:  J Exp Anal Behav       Date:  2005-11       Impact factor: 2.468

4.  Metabolic mapping of the rat cerebellum during delay and trace eyeblink conditioning.

Authors:  Bethany Plakke; John H Freeman; Amy Poremba
Journal:  Neurobiol Learn Mem       Date:  2007-04-30       Impact factor: 2.877

5.  Abnormal classical eye-blink conditioning in autism.

Authors:  L L Sears; P R Finn; J E Steinmetz
Journal:  J Autism Dev Disord       Date:  1994-12

6.  Absence of an association between motor coordination and spatial orientation in lurcher mutant mice.

Authors:  R Lalonde; S Thifault
Journal:  Behav Genet       Date:  1994-11       Impact factor: 2.805

Review 7.  Neural circuitry and plasticity mechanisms underlying delay eyeblink conditioning.

Authors:  John H Freeman; Adam B Steinmetz
Journal:  Learn Mem       Date:  2011-10-03       Impact factor: 2.460

8.  Examination of bilateral eyeblink conditioning in rats.

Authors:  Matthew M Campolattaro; John H Freeman
Journal:  Behav Neurosci       Date:  2009-12       Impact factor: 1.912

9.  Localization of the cerebellar cortical zone mediating acquisition of eyeblink conditioning in rats.

Authors:  Adam B Steinmetz; John H Freeman
Journal:  Neurobiol Learn Mem       Date:  2014-06-13       Impact factor: 2.877

10.  Impaired cerebellar-dependent eyeblink conditioning in first-degree relatives of individuals with schizophrenia.

Authors:  Amanda R Bolbecker; Jerillyn S Kent; Isaac T Petersen; Mallory J Klaunig; Jennifer K Forsyth; Josselyn M Howell; Daniel R Westfall; Brian F O'Donnell; William P Hetrick
Journal:  Schizophr Bull       Date:  2013-08-20       Impact factor: 9.306

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