Literature DB >> 1335267

Reversible lesions of the cerebellar interpositus nucleus during acquisition and retention of a classically conditioned behavior.

R E Clark1, A A Zhang, D G Lavond.   

Abstract

Previous lesion, recording, and stimulation studies have implicated the cerebellum and its associated circuitry as essentially involved in classical conditioning of discrete, somatic muscle responses. In 2 experiments, the interpositus nucleus of the cerebellum was assessed for the plasticity associated with learning and memory of the nictitating membrane (NM) response by using local cooling as a reversible lesion technique. In well-trained animals (Experiment 1), NM conditioned responses (CRs) were abolished during cooling of the interpositus but reappeared when the interpositus returned to body temperature. This cooling-warming protocol could be repeated many times. Cooling could be prolonged (one session, approximately 1 hr) with recovery of NM CRs as tested on the next day. Multiple-unit recordings related to learning were also absent in the interpositus and red nucleus during cooling. In naive animals (Experiment 2), both behavioral and unit CRs did not develop while training with cooling. There was no evidence of savings when training continued without cooling: Behavioral and unit CRs developed as if the animals were still naive. These results support the idea that the interpositus nucleus of the cerebellum is the critical locus for learning and memory of this classical CR.

Mesh:

Year:  1992        PMID: 1335267     DOI: 10.1037//0735-7044.106.6.879

Source DB:  PubMed          Journal:  Behav Neurosci        ISSN: 0735-7044            Impact factor:   1.912


  36 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

3.  A trigeminal conditioned stimulus yields fast acquisition of cerebellum-dependent conditioned eyeblinks.

Authors:  Andrew J Carrel; Svitlana Zbarska; Gary D Zenitsky; Vlastislav Bracha
Journal:  Behav Brain Res       Date:  2011-09-12       Impact factor: 3.332

Review 4.  Using eyeblink classical conditioning as a test of the functional consequences of exposure of the developing cerebellum to alcohol.

Authors:  John T Green
Journal:  Integr Physiol Behav Sci       Date:  2003 Jan-Mar

5.  Developmental changes in eyeblink conditioning and neuronal activity in the pontine nuclei.

Authors:  John H Freeman; Adam S Muckler
Journal:  Learn Mem       Date:  2003 Sep-Oct       Impact factor: 2.460

6.  Cerebellar norepinephrine modulates learning of delay classical eyeblink conditioning: evidence for post-synaptic signaling via PKA.

Authors:  M Claire Cartford; Amy Samec; Mathew Fister; Paula C Bickford
Journal:  Learn Mem       Date:  2004-11-10       Impact factor: 2.460

7.  Hippocampus and remote spatial memory in rats.

Authors:  Robert E Clark; Nicola J Broadbent; Larry R Squire
Journal:  Hippocampus       Date:  2005       Impact factor: 3.899

Review 8.  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

9.  Neonatal eyelid conditioning during sleep.

Authors:  Amanda R Tarullo; Joseph R Isler; Carmen Condon; Kimon Violaris; Peter D Balsam; William P Fifer
Journal:  Dev Psychobiol       Date:  2016-11       Impact factor: 3.038

10.  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

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