Literature DB >> 15723058

Restoration of spatial working memory by genetic rescue of GluR-A-deficient mice.

W B Schmitt1, R Sprengel, V Mack, R W Draft, P H Seeburg, R M J Deacon, J N P Rawlins, D M Bannerman.   

Abstract

Gene-targeted mice lacking the AMPA receptor subunit GluR-A (also called GluR1 encoded by the gene Gria1,) have deficits in hippocampal CA3-CA1 long-term potentiation (LTP) and have profoundly impaired hippocampus-dependent spatial working memory (SWM) tasks, although their spatial reference memory remains normal. Here we show that forebrain-localized expression of GFP-tagged GluR-A subunits in GluR-A-deficient mice rescues SWM, paralleling its rescue of CA3-CA1 LTP. This provides powerful new evidence linking hippocampal GluR-A-dependent synaptic plasticity to rapid, flexible memory processing.

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Year:  2005        PMID: 15723058     DOI: 10.1038/nn1412

Source DB:  PubMed          Journal:  Nat Neurosci        ISSN: 1097-6256            Impact factor:   24.884


  53 in total

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Review 5.  Running to stand still: ionotropic receptor dynamics at central and peripheral synapses.

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Journal:  Mol Neurobiol       Date:  2006-10       Impact factor: 5.590

6.  Pharmacological inactivation of the small GTPase Rac1 impairs long-term plasticity in the mouse hippocampus.

Authors:  Luis A Martinez; Maria V Tejada-Simon
Journal:  Neuropharmacology       Date:  2011-05-05       Impact factor: 5.250

7.  Ras signaling mechanisms underlying impaired GluR1-dependent plasticity associated with fragile X syndrome.

Authors:  Hailan Hu; Yi Qin; Genrieta Bochorishvili; Yinghua Zhu; Linda van Aelst; J Julius Zhu
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Review 8.  History of the Concept of Disconnectivity in Schizophrenia.

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9.  Mechanisms underlying cognitive enhancement and reversal of cognitive deficits in nonhuman primates by the ampakine CX717.

Authors:  R E Hampson; R A España; G A Rogers; L J Porrino; S A Deadwyler
Journal:  Psychopharmacology (Berl)       Date:  2008-11-05       Impact factor: 4.530

10.  A single early-life seizure impairs short-term memory but does not alter spatial learning, recognition memory, or anxiety.

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