Literature DB >> 8921297

Brain structure and task-specific increase in expression of the gene encoding syntaxin 1B during learning in the rat: a potential molecular marker for learning-induced synaptic plasticity in neural networks.

S Davis1, J Rodger, A Hicks, J Mallet, S Laroche.   

Abstract

The mRNAs encoding the synaptic vesicle proteins syntaxin 1B and synapsin I were measured using in situ hybridization in several brain regions--the dentate gyrus, CA3 and CA1 of the hippocampus, the parietal, the motor and prefrontal cortices and the core and shell of the accumbens--of rats that were learning a spatial reference or working memory task on a radial arm maze. The mRNA encoding syntaxin 1B was significantly increased in all hippocampal regions in rats learning the working memory task, whereas it was increased in the prelimbic area of the prefrontal cortex and the shell of the accumbens in rats learning the spatial reference memory task. No change in mRNA encoding syntaxin 1B was observed in the motor and parietal and cortices or the core of the accumbens, and the mRNA encoding synapsin I was not significantly different from that of naive caged controls or rats running the maze for continuous reinforcement in any of the brain structures examined. These results demonstrate that the gene encoding a key member of synaptic vesicle function is up-regulated in a task- and brain-specific manner during learning. They are discussed in terms of the potential role this protein may play in trans-synaptic propagation of plasticity within specific neural networks as a function of the information required in the laying down of different types of memory.

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Year:  1996        PMID: 8921297     DOI: 10.1111/j.1460-9568.1996.tb00727.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  8 in total

1.  Increase in syntaxin 1B mRNA in hippocampal and cortical circuits during spatial learning reflects a mechanism of trans-synaptic plasticity involved in establishing a memory trace.

Authors:  S Davis; J Rodger; A Stéphan; A Hicks; J Mallet; S Laroche
Journal:  Learn Mem       Date:  1998 Sep-Oct       Impact factor: 2.460

2.  Dynamics of Hippocampal Protein Expression During Long-term Spatial Memory Formation.

Authors:  Natalia Borovok; Elimelech Nesher; Yishai Levin; Michal Reichenstein; Albert Pinhasov; Izhak Michaelevski
Journal:  Mol Cell Proteomics       Date:  2015-11-23       Impact factor: 5.911

3.  Changes in Synaptic Proteins Precede Neurodegeneration Markers in Preclinical Alzheimer's Disease Cerebrospinal Fluid.

Authors:  Alberto Lleó; Raúl Núñez-Llaves; Daniel Alcolea; Cristina Chiva; Daniel Balateu-Paños; Martí Colom-Cadena; Gemma Gomez-Giro; Laia Muñoz; Marta Querol-Vilaseca; Jordi Pegueroles; Lorena Rami; Albert Lladó; José L Molinuevo; Mikel Tainta; Jordi Clarimón; Tara Spires-Jones; Rafael Blesa; Juan Fortea; Pablo Martínez-Lage; Raquel Sánchez-Valle; Eduard Sabidó; Àlex Bayés; Olivia Belbin
Journal:  Mol Cell Proteomics       Date:  2019-01-03       Impact factor: 5.911

Review 4.  MAPK, CREB and zif268 are all required for the consolidation of recognition memory.

Authors:  Bruno Bozon; Aine Kelly; Sheena A Josselyn; Alcino J Silva; Sabrina Davis; Serge Laroche
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2003-04-29       Impact factor: 6.237

5.  Prefrontal cortical GABAergic dysfunction contributes to age-related working memory impairment.

Authors:  Cristina Bañuelos; B Sofia Beas; Joseph A McQuail; Ryan J Gilbert; Charles J Frazier; Barry Setlow; Jennifer L Bizon
Journal:  J Neurosci       Date:  2014-03-05       Impact factor: 6.167

Review 6.  Cholinergic and glutamatergic alterations beginning at the early stages of Alzheimer disease: participation of the phospholipase A2 enzyme.

Authors:  Evelin L Schaeffer; Wagner F Gattaz
Journal:  Psychopharmacology (Berl)       Date:  2008-02-19       Impact factor: 4.530

7.  Transsynaptic Long-Term Potentiation in the Hippocampus of Behaving Mice.

Authors:  Maria Teresa Romero-Barragán; Agnes Gruart; José M Delgado-García
Journal:  Front Synaptic Neurosci       Date:  2022-01-20

8.  Sustained increase of spontaneous input and spike transfer in the CA3-CA1 pathway following long-term potentiation in vivo.

Authors:  Antonio Fernández-Ruiz; Valeri A Makarov; Oscar Herreras
Journal:  Front Neural Circuits       Date:  2012-10-05       Impact factor: 3.492

  8 in total

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