Literature DB >> 9554999

Microinjections of anisomycin into the intermediate cerebellum during learning affect the acquisition of classically conditioned responses in the rabbit.

V Bracha1, K B Irwin, M L Webster, D A Wunderlich, M K Stachowiak, J R Bloedel.   

Abstract

The purpose of this study was to examine the effects of protein synthesis inhibition in the intermediate cerebellum on the acquisition and expression of classically conditioned nictitating membrane responses in the rabbit. Animals were conditioned for three days in a standard delay paradigm. Before each training session, either a solution of anisomycin (a protein synthesis inhibitor) or vehicle was bilaterally injected into the interposed cerebellar nuclear. Following these three training sessions, rabbits were tested to determine whether the previous training under the influence of anisomycin or vehicle resulted in the acquisition of conditioned responses. In this test, animals that were injected previously with the protein synthesis inhibitor exhibited significantly less retention of conditioned responses than rabbits injected with vehicle. Additional experiments demonstrated that anisomycin does not block the expression of conditioned responses during conditioning or in well-trained animals. Microinjections of muscimol at the same sites of the previous drug infusions suppressed the expression of conditioned responses, indicating that the protein synthesis inhibitor was applied to the eyeblink-related parts of cerebellar circuits. The obtained data are the first to demonstrate that a manipulation of cerebellar circuits, which does not affect the performance of learned behavior, can affect the process of learning. These results suggest that the synthesis of new proteins in the intermediate cerebellum participates in the formation of plastic changes responsible for eyeblink conditioning. Copyright 1998 Elsevier Science B.V.

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Year:  1998        PMID: 9554999     DOI: 10.1016/s0006-8993(97)01535-7

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


  20 in total

1.  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

2.  On-line compensation for perturbations of a reaching movement is cerebellar dependent: support for the task dependency hypothesis.

Authors:  Yury Shimansky; Jian-Jun Wang; Richard A Bauer; Vlastislav Bracha; James R Bloedel
Journal:  Exp Brain Res       Date:  2003-12-03       Impact factor: 1.972

3.  Synapse formation is associated with memory storage in the cerebellum.

Authors:  Jeffrey A Kleim; John H Freeman; Rochelle Bruneau; Brian C Nolan; Natalie R Cooper; Alison Zook; Drew Walters
Journal:  Proc Natl Acad Sci U S A       Date:  2002-09-16       Impact factor: 11.205

4.  Molecular evidence for two-stage learning and partial laterality in eyeblink conditioning of mice.

Authors:  Jin-Sung Park; Takashi Onodera; Shin-ichi Nishimura; Richard F Thompson; Shigeyoshi Itohara
Journal:  Proc Natl Acad Sci U S A       Date:  2006-03-28       Impact factor: 11.205

5.  Eye-blink conditioning is associated with changes in synaptic ultrastructure in the rabbit interpositus nuclei.

Authors:  Andrew C W Weeks; Steve Connor; Richard Hinchcliff; Janelle C LeBoutillier; Richard F Thompson; Ted L Petit
Journal:  Learn Mem       Date:  2007-06-05       Impact factor: 2.460

6.  A new rapid protocol for eyeblink conditioning to assess cerebellar motor learning.

Authors:  Kyoichi Emi; Kazuhisa Kohda; Wataru Kakegawa; Sakae Narumi; Michisuke Yuzaki
Journal:  Neurochem Res       Date:  2011-01-09       Impact factor: 3.996

7.  Inactivation of cerebellar output axons impairs acquisition of conditioned eyeblinks.

Authors:  W U Nilaweera; G D Zenitsky; V Bracha
Journal:  Brain Res       Date:  2006-10-24       Impact factor: 3.252

8.  Expression of the immediate-early gene-encoded protein Egr-1 (zif268) during in vitro classical conditioning.

Authors:  Maxim Mokin; Joyce Keifer
Journal:  Learn Mem       Date:  2005 Mar-Apr       Impact factor: 2.460

Review 9.  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

10.  Ethanol-exposed neonatal rats are impaired as adults in classical eyeblink conditioning at multiple unconditioned stimulus intensities.

Authors:  Derick H Lindquist; Greta Sokoloff; Joseph E Steinmetz
Journal:  Brain Res       Date:  2007-03-06       Impact factor: 3.252

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