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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neuropsychopharmacology (New York, N.Y.) N.Y.), 2014-02, Vol.39 (3), p.625-637
Hauptverfasser: OGDEN, Kevin K, KHATRI, Alpa, TRAYNELIS, Stephen F, HELDT, Scott A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 637
container_issue 3
container_start_page 625
container_title Neuropsychopharmacology (New York, N.Y.)
container_volume 39
creator OGDEN, Kevin K
KHATRI, Alpa
TRAYNELIS, Stephen F
HELDT, Scott A
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
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3895240</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3181584041</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-808188264ed5b77f25b390bf3691a42aac3511929fb42ce41344387671056aac3</originalsourceid><addsrcrecordid>eNpdkc9rFDEYhoModm29eZaACB6cbX7NJHMpLNtuFbatVIXeQiab2abMJmOSEffof26mu63VU-B7Hx6-fC8AbzCaYkTFsev7KUGYTgnDz8AEc4aKirKb52CCRE0LTOnNAXgV4x1CuOSVeAkOCENI0JJOwO8vPhmXrErWO-hbeN4Nl2R-fAovL05n8Npo0ycf4NehSdveRGgdTLcGzjbb9Up1Ci6Utp1NKuVsDK7NvW8nWxgVoHIrePYrWafvx8s8c9atR9OF1eYIvGhVF83r_XsIvi_Ovs0_Fcur88_z2bLQjJepEEhgIUjFzKpsOG9J2dAaNS2taqwYUUrTEuOa1G3DiDYMU8ao4BXHqKzG9BCc7Lz90GzMSuctg-pkH-xGha30ysp_E2dv5dr_lFTUZT5YFnzYC4L_MZiY5MZGbbpOOeOHKDGrK1HXnI7ou__QOz8El7-XKc4Z5YzxTH3cUTr4GINpH5fBSI7dytytHLuVuduMv336gUf4ocwMvN8DKmrVtUE5beNfThBB81noH7auq_g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1477437447</pqid></control><display><type>article</type><title>Potentiation of GluN2C/D NMDA Receptor Subtypes in the Amygdala Facilitates the Retention of Fear and Extinction Learning in Mice</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>SpringerLink Journals - AutoHoldings</source><creator>OGDEN, Kevin K ; KHATRI, Alpa ; TRAYNELIS, Stephen F ; HELDT, Scott A</creator><creatorcontrib>OGDEN, Kevin K ; KHATRI, Alpa ; TRAYNELIS, Stephen F ; HELDT, Scott A</creatorcontrib><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.</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 &amp; 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&amp;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. 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.</description><subject>Amygdala</subject><subject>Amygdala - drug effects</subject><subject>Amygdala - metabolism</subject><subject>Animals</subject><subject>Anxiety disorders</subject><subject>Area Under Curve</subject><subject>Benzimidazoles - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Conditioning (Psychology) - drug effects</subject><subject>Conditioning (Psychology) - physiology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Extinction (Learning)</subject><subject>Extinction, Psychological - drug effects</subject><subject>Extinction, Psychological - physiology</subject><subject>Fear &amp; phobias</subject><subject>Fear - drug effects</subject><subject>Fear - physiology</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Male</subject><subject>Maze Learning - drug effects</subject><subject>Medical sciences</subject><subject>Memory</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Microinjections</subject><subject>Motor Activity - drug effects</subject><subject>Neurosciences</subject><subject>Oocytes</subject><subject>Original</subject><subject>Receptors, N-Methyl-D-Aspartate - genetics</subject><subject>Receptors, N-Methyl-D-Aspartate - metabolism</subject><subject>Retention</subject><subject>Retention (Psychology) - drug effects</subject><subject>Retention (Psychology) - physiology</subject><subject>Xenopus</subject><issn>0893-133X</issn><issn>1740-634X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkc9rFDEYhoModm29eZaACB6cbX7NJHMpLNtuFbatVIXeQiab2abMJmOSEffof26mu63VU-B7Hx6-fC8AbzCaYkTFsev7KUGYTgnDz8AEc4aKirKb52CCRE0LTOnNAXgV4x1CuOSVeAkOCENI0JJOwO8vPhmXrErWO-hbeN4Nl2R-fAovL05n8Npo0ycf4NehSdveRGgdTLcGzjbb9Up1Ci6Utp1NKuVsDK7NvW8nWxgVoHIrePYrWafvx8s8c9atR9OF1eYIvGhVF83r_XsIvi_Ovs0_Fcur88_z2bLQjJepEEhgIUjFzKpsOG9J2dAaNS2taqwYUUrTEuOa1G3DiDYMU8ao4BXHqKzG9BCc7Lz90GzMSuctg-pkH-xGha30ysp_E2dv5dr_lFTUZT5YFnzYC4L_MZiY5MZGbbpOOeOHKDGrK1HXnI7ou__QOz8El7-XKc4Z5YzxTH3cUTr4GINpH5fBSI7dytytHLuVuduMv336gUf4ocwMvN8DKmrVtUE5beNfThBB81noH7auq_g</recordid><startdate>20140201</startdate><enddate>20140201</enddate><creator>OGDEN, Kevin K</creator><creator>KHATRI, Alpa</creator><creator>TRAYNELIS, Stephen F</creator><creator>HELDT, Scott A</creator><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>5PM</scope></search><sort><creationdate>20140201</creationdate><title>Potentiation of GluN2C/D NMDA Receptor Subtypes in the Amygdala Facilitates the Retention of Fear and Extinction Learning in Mice</title><author>OGDEN, Kevin K ; KHATRI, Alpa ; TRAYNELIS, Stephen F ; HELDT, Scott A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-808188264ed5b77f25b390bf3691a42aac3511929fb42ce41344387671056aac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Amygdala</topic><topic>Amygdala - drug effects</topic><topic>Amygdala - metabolism</topic><topic>Animals</topic><topic>Anxiety disorders</topic><topic>Area Under Curve</topic><topic>Benzimidazoles - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Conditioning (Psychology) - drug effects</topic><topic>Conditioning (Psychology) - physiology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Extinction (Learning)</topic><topic>Extinction, Psychological - drug effects</topic><topic>Extinction, Psychological - physiology</topic><topic>Fear &amp; phobias</topic><topic>Fear - drug effects</topic><topic>Fear - physiology</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Male</topic><topic>Maze Learning - drug effects</topic><topic>Medical sciences</topic><topic>Memory</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Microinjections</topic><topic>Motor Activity - drug effects</topic><topic>Neurosciences</topic><topic>Oocytes</topic><topic>Original</topic><topic>Receptors, N-Methyl-D-Aspartate - genetics</topic><topic>Receptors, N-Methyl-D-Aspartate - metabolism</topic><topic>Retention</topic><topic>Retention (Psychology) - drug effects</topic><topic>Retention (Psychology) - physiology</topic><topic>Xenopus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>OGDEN, Kevin K</creatorcontrib><creatorcontrib>KHATRI, Alpa</creatorcontrib><creatorcontrib>TRAYNELIS, Stephen F</creatorcontrib><creatorcontrib>HELDT, Scott A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neuropsychopharmacology (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>OGDEN, Kevin K</au><au>KHATRI, Alpa</au><au>TRAYNELIS, Stephen F</au><au>HELDT, Scott A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potentiation of GluN2C/D NMDA Receptor Subtypes in the Amygdala Facilitates the Retention of Fear and Extinction Learning in Mice</atitle><jtitle>Neuropsychopharmacology (New York, N.Y.)</jtitle><addtitle>Neuropsychopharmacology</addtitle><date>2014-02-01</date><risdate>2014</risdate><volume>39</volume><issue>3</issue><spage>625</spage><epage>637</epage><pages>625-637</pages><issn>0893-133X</issn><eissn>1740-634X</eissn><coden>NEROEW</coden><abstract>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.</abstract><cop>Basingstoke</cop><pub>Nature Publishing Group</pub><pmid>24008353</pmid><doi>10.1038/npp.2013.241</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0893-133X
ispartof Neuropsychopharmacology (New York, N.Y.), 2014-02, Vol.39 (3), p.625-637
issn 0893-133X
1740-634X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3895240
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; SpringerLink Journals - AutoHoldings
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T07%3A14%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Potentiation%20of%20GluN2C/D%20NMDA%20Receptor%20Subtypes%20in%20the%20Amygdala%20Facilitates%20the%20Retention%20of%20Fear%20and%20Extinction%20Learning%20in%20Mice&rft.jtitle=Neuropsychopharmacology%20(New%20York,%20N.Y.)&rft.au=OGDEN,%20Kevin%20K&rft.date=2014-02-01&rft.volume=39&rft.issue=3&rft.spage=625&rft.epage=637&rft.pages=625-637&rft.issn=0893-133X&rft.eissn=1740-634X&rft.coden=NEROEW&rft_id=info:doi/10.1038/npp.2013.241&rft_dat=%3Cproquest_pubme%3E3181584041%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1477437447&rft_id=info:pmid/24008353&rfr_iscdi=true