Potentiation of GluN2C/D NMDA Receptor Subtypes in the Amygdala Facilitates the Retention of Fear and Extinction Learning in Mice
NMDA receptors are glutamate receptor ion channels that contribute to synaptic plasticity and are important for many forms of learning and memory. In the amygdala, NMDA receptors are critical for the acquisition, retention, and extinction of classically conditioned fear responses. Although the GluN2...
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description | NMDA receptors are glutamate receptor ion channels that contribute to synaptic plasticity and are important for many forms of learning and memory. In the amygdala, NMDA receptors are critical for the acquisition, retention, and extinction of classically conditioned fear responses. Although the GluN2B subunit has been implicated in both the acquisition and extinction of conditioned fear, GluN2C-knockout mice show reduced conditioned fear responses. Moreover, D-cycloserine (DCS), which facilitates fear extinction, selectively enhances the activity of GluN2C-containing NMDA receptors. To further define the contribution of GluN2C receptors to fear learning, we infused the GluN2C/GluN2D-selective potentiator CIQ bilaterally into the basolateral amygdala (3, 10, or 30 μg/side) following either fear conditioning or fear extinction training. CIQ both increased the expression of conditioned fear 24 h later and enhanced the extinction of the previously conditioned fear response. These results support a critical role for GluN2C receptors in the amygdala in the consolidation of learned fear responses and suggest that increased activity of GluN2C receptors may underlie the therapeutic actions of DCS. |
doi_str_mv | 10.1038/npp.2013.241 |
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These results support a critical role for GluN2C receptors in the amygdala in the consolidation of learned fear responses and suggest that increased activity of GluN2C receptors may underlie the therapeutic actions of DCS.</description><identifier>ISSN: 0893-133X</identifier><identifier>EISSN: 1740-634X</identifier><identifier>DOI: 10.1038/npp.2013.241</identifier><identifier>PMID: 24008353</identifier><identifier>CODEN: NEROEW</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing Group</publisher><subject>Amygdala ; Amygdala - drug effects ; Amygdala - metabolism ; Animals ; Anxiety disorders ; Area Under Curve ; Benzimidazoles - pharmacology ; Biological and medical sciences ; Conditioning (Psychology) - drug effects ; Conditioning (Psychology) - physiology ; Dose-Response Relationship, Drug ; Extinction (Learning) ; Extinction, Psychological - drug effects ; Extinction, Psychological - physiology ; Fear & phobias ; Fear - drug effects ; Fear - physiology ; Gene Expression Regulation - drug effects ; Male ; Maze Learning - drug effects ; Medical sciences ; Memory ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Microinjections ; Motor Activity - drug effects ; Neurosciences ; Oocytes ; Original ; Receptors, N-Methyl-D-Aspartate - genetics ; Receptors, N-Methyl-D-Aspartate - metabolism ; Retention ; Retention (Psychology) - drug effects ; Retention (Psychology) - physiology ; Xenopus</subject><ispartof>Neuropsychopharmacology (New York, N.Y.), 2014-02, Vol.39 (3), p.625-637</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Feb 2014</rights><rights>Copyright © 2014 American College of Neuropsychopharmacology 2014 American College of Neuropsychopharmacology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-808188264ed5b77f25b390bf3691a42aac3511929fb42ce41344387671056aac3</citedby><cites>FETCH-LOGICAL-c475t-808188264ed5b77f25b390bf3691a42aac3511929fb42ce41344387671056aac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895240/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895240/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28283134$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24008353$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>OGDEN, Kevin K</creatorcontrib><creatorcontrib>KHATRI, Alpa</creatorcontrib><creatorcontrib>TRAYNELIS, Stephen F</creatorcontrib><creatorcontrib>HELDT, Scott A</creatorcontrib><title>Potentiation of GluN2C/D NMDA Receptor Subtypes in the Amygdala Facilitates the Retention of Fear and Extinction Learning in Mice</title><title>Neuropsychopharmacology (New York, N.Y.)</title><addtitle>Neuropsychopharmacology</addtitle><description>NMDA receptors are glutamate receptor ion channels that contribute to synaptic plasticity and are important for many forms of learning and memory. 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In the amygdala, NMDA receptors are critical for the acquisition, retention, and extinction of classically conditioned fear responses. Although the GluN2B subunit has been implicated in both the acquisition and extinction of conditioned fear, GluN2C-knockout mice show reduced conditioned fear responses. Moreover, D-cycloserine (DCS), which facilitates fear extinction, selectively enhances the activity of GluN2C-containing NMDA receptors. To further define the contribution of GluN2C receptors to fear learning, we infused the GluN2C/GluN2D-selective potentiator CIQ bilaterally into the basolateral amygdala (3, 10, or 30 μg/side) following either fear conditioning or fear extinction training. CIQ both increased the expression of conditioned fear 24 h later and enhanced the extinction of the previously conditioned fear response. 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subjects | Amygdala Amygdala - drug effects Amygdala - metabolism Animals Anxiety disorders Area Under Curve Benzimidazoles - pharmacology Biological and medical sciences Conditioning (Psychology) - drug effects Conditioning (Psychology) - physiology Dose-Response Relationship, Drug Extinction (Learning) Extinction, Psychological - drug effects Extinction, Psychological - physiology Fear & phobias Fear - drug effects Fear - physiology Gene Expression Regulation - drug effects Male Maze Learning - drug effects Medical sciences Memory Mice Mice, Inbred C57BL Mice, Knockout Microinjections Motor Activity - drug effects Neurosciences Oocytes Original Receptors, N-Methyl-D-Aspartate - genetics Receptors, N-Methyl-D-Aspartate - metabolism Retention Retention (Psychology) - drug effects Retention (Psychology) - physiology Xenopus |
title | Potentiation of GluN2C/D NMDA Receptor Subtypes in the Amygdala Facilitates the Retention of Fear and Extinction Learning in Mice |
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