Literature DB >> 12802552

Abducens conditioning in in vitro turtle brain stem without cerebellum requires NMDA receptors and involves upregulation of GluR4-containing AMPA receptors.

Joyce Keifer1, Timothy G Clark.   

Abstract

Previous work showed that in vitro abducens eyeblink classical conditioning of turtle brain stem-cerebellum preparations involved NMDA-mediated mechanisms and redistribution of GluR4-containing AMPA receptors in the abducens motor nuclei. Since conditioning can be obtained in brain stem preparations without the cerebellum, we examined whether similar mechanisms were involved during conditioning of the brain stem alone. The results showed that conditioning could not be induced in the presence of the NMDA receptor antagonist dl-2-amino-5-phosphonovaleric acid (AP-5) and that abducens nerve conditioned responses, once initiated in normal saline, were significantly attenuated in the presence of AP-5. The effects of AP-5 did not generally depress physiological responsiveness of preparations because some abducens nerve reflexes were not significantly reduced by the compound. GluR4-containing AMPA receptors in the abducens motor nuclei were significantly upregulated and positively correlated with the levels of conditioning similar to that of preparations having an intact cerebellum. Furthermore, increased GluR4 subunits after brain stem conditioning was confirmed by Western blot analysis. These results suggest that NMDA receptor-mediated mechanisms and GluR4 upregulation may mediate in vitro abducens eyeblink classical conditioning and that these mechanisms reside in the brain stem eyeblink circuitry.

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Year:  2003        PMID: 12802552     DOI: 10.1007/s00221-003-1494-5

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  16 in total

1.  Role for calbindin-D28K in in vitro classical conditioning of abducens nerve responses in turtles.

Authors:  Joyce Keifer; Boone T Brewer; Phillip E Meehan; Richard J Brue; Timothy G Clark
Journal:  Synapse       Date:  2003-08       Impact factor: 2.562

2.  The cerebellum and red nucleus are not required for In vitro classical conditioning of the turtle abducens nerve response.

Authors:  C W Anderson; J Keifer
Journal:  J Neurosci       Date:  1997-12-15       Impact factor: 6.167

3.  Evidence for a photosensitive region in the caudal mesencephalon of the turtle brain.

Authors:  C W Anderson; J Keifer
Journal:  Exp Brain Res       Date:  1998-04       Impact factor: 1.972

4.  In vitro eye-blink reflex model: role of excitatory amino acids and labeling of network activity with sulforhodamine.

Authors:  J Keifer
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

5.  Immunocytochemical localization of glutamate receptor subunits in the brain stem and cerebellum of the turtle Chrysemys picta.

Authors:  J Keifer; M T Carr
Journal:  J Comp Neurol       Date:  2000-11-20       Impact factor: 3.215

6.  Properties of conditioned abducens nerve responses in a highly reduced in vitro brain stem preparation from the turtle.

Authors:  C W Anderson; J Keifer
Journal:  J Neurophysiol       Date:  1999-03       Impact factor: 2.714

7.  In vitro eye-blink classical conditioning is NMDA receptor dependent and involves redistribution of AMPA receptor subunit GluR4.

Authors:  J Keifer
Journal:  J Neurosci       Date:  2001-04-01       Impact factor: 6.167

8.  Classical conditioning of the eyeblink reflex in the decerebrate-decerebellate rabbit.

Authors:  T M Kelly; C C Zuo; J R Bloedel
Journal:  Behav Brain Res       Date:  1990-04-16       Impact factor: 3.332

9.  In vitro classical conditioning of abducens nerve discharge in turtles.

Authors:  J Keifer; K E Armstrong; J C Houk
Journal:  J Neurosci       Date:  1995-07       Impact factor: 6.167

10.  Classical conditioning with auditory discrimination of the eye blink in decerebrate cats.

Authors:  R J Norman; J S Buchwald; J R Villablanca
Journal:  Science       Date:  1977-04-29       Impact factor: 47.728

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  8 in total

1.  Characterization of a novel reptilian tolloid-like gene in the pond turtle, Pseudemys scripta elegans.

Authors:  Boris E Sabirzhanov; Joyce Keifer; Timothy G Clark
Journal:  Brain Res       Date:  2007-04-06       Impact factor: 3.252

2.  Coordinate action of pre- and postsynaptic brain-derived neurotrophic factor is required for AMPAR trafficking and acquisition of in vitro classical conditioning.

Authors:  W Li; J Keifer
Journal:  Neuroscience       Date:  2008-06-25       Impact factor: 3.590

3.  Protein kinase C-dependent and independent signaling pathways regulate synaptic GluR1 and GluR4 AMPAR subunits during in vitro classical conditioning.

Authors:  Z Zheng; J Keifer
Journal:  Neuroscience       Date:  2008-08-27       Impact factor: 3.590

4.  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

5.  Functional Organization of Vestibulo-Ocular Responses in Abducens Motoneurons.

Authors:  Haike Dietrich; Stefan Glasauer; Hans Straka
Journal:  J Neurosci       Date:  2017-03-14       Impact factor: 6.167

6.  Synaptic localization of GluR4-containing AMPARs and Arc during acquisition, extinction, and reacquisition of in vitro classical conditioning.

Authors:  Joyce Keifer; Zhaoqing Zheng; Maxim Mokin
Journal:  Neurobiol Learn Mem       Date:  2008-06-02       Impact factor: 2.877

7.  BDNF-induced synaptic delivery of AMPAR subunits is differentially dependent on NMDA receptors and requires ERK.

Authors:  Wei Li; Joyce Keifer
Journal:  Neurobiol Learn Mem       Date:  2008-11-17       Impact factor: 2.877

8.  Analysis of the potential role of GluA4 carboxyl-terminus in PDZ interactions.

Authors:  Sarah K Coleman; Chunlin Cai; Nisse Kalkkinen; Esa R Korpi; Kari Keinänen
Journal:  PLoS One       Date:  2010-01-14       Impact factor: 3.240

  8 in total

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