Loading…

Enantiomers of 2-methylglutamate and 2-methylglutamine selectively impact mouse brain metabolism and behavior

Imbalance of excitatory and inhibitory neurotransmission is implicated in a wide range of psychiatric and neurologic disorders. Here we tested the hypothesis that insertion of a methyl group on the stereogenic alpha carbon of l -Glu or l -Gln would impact the γ-aminobutyric acid (GABA) shunt and the...

Full description

Saved in:
Bibliographic Details
Published in:Scientific reports 2021-04, Vol.11 (1), p.8138-8138, Article 8138
Main Authors: Wawro, Adam M., Gajera, Chandresh R., Baker, Steven A., Leśniak, Robert K., Fischer, Curt R., Saw, Nay L., Shamloo, Mehrdad, Montine, Thomas J.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c540t-dce56d72a4789b1f4a2b259ecb1e9c7084a77da6a506f763d9ee0b35f7cc507d3
cites cdi_FETCH-LOGICAL-c540t-dce56d72a4789b1f4a2b259ecb1e9c7084a77da6a506f763d9ee0b35f7cc507d3
container_end_page 8138
container_issue 1
container_start_page 8138
container_title Scientific reports
container_volume 11
creator Wawro, Adam M.
Gajera, Chandresh R.
Baker, Steven A.
Leśniak, Robert K.
Fischer, Curt R.
Saw, Nay L.
Shamloo, Mehrdad
Montine, Thomas J.
description Imbalance of excitatory and inhibitory neurotransmission is implicated in a wide range of psychiatric and neurologic disorders. Here we tested the hypothesis that insertion of a methyl group on the stereogenic alpha carbon of l -Glu or l -Gln would impact the γ-aminobutyric acid (GABA) shunt and the glutamate-glutamine cycle. ( S )-2-methylglutamate, or ( S )-2MeGlu, was efficiently transported into brain and synaptosomes where it was released by membrane depolarization in a manner equivalent to endogenous l -Glu. ( R )-2MeGlu was transported less efficiently into brain and synaptosomes but was not released by membrane depolarization. Each enantiomer of 2MeGlu had limited activity across a panel of over 30 glutamate and GABA receptors. While neither enantiomer of 2MeGlu was metabolized along the GABA shunt, ( S )-2MeGlu was selectively converted to ( S )-2-methylglutamine, or ( S )-2MeGln, which was subsequently slowly hydrolyzed back to ( S )-2MeGlu in brain. rac-2MeGln was also transported into brain, with similar efficiency as ( S )-2MeGlu. A battery of behavioral tests in young adult wild type mice showed safety with up to single 900 mg/kg dose of ( R )-2MeGlu, ( S )-2MeGlu, or rac-2MeGln, suppressed locomotor activity with single ≥ 100 mg/kg dose of ( R )-2MeGlu or ( S )-2MeGlu. No effect on anxiety or hippocampus-dependent learning was evident. Enantiomers of 2MeGlu and 2MeGln show promise as potential pharmacologic agents and imaging probes for cells that produce or transport l -Gln.
doi_str_mv 10.1038/s41598-021-87569-1
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_0b1cf771b7094dddbe45b3302eac42de</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_0b1cf771b7094dddbe45b3302eac42de</doaj_id><sourcerecordid>2513246635</sourcerecordid><originalsourceid>FETCH-LOGICAL-c540t-dce56d72a4789b1f4a2b259ecb1e9c7084a77da6a506f763d9ee0b35f7cc507d3</originalsourceid><addsrcrecordid>eNp9kk1v1DAQhiMEolXpH-CAInHhkuLPOLkgoarQSpW4wNka25NdrxJ7sbMr7b_Huyml7QFfbM0888549FbVe0quKOHd5yyo7LuGMNp0SrZ9Q19V54wI2TDO2Osn77PqMucNKUeyXtD-bXXGeScF5fS8mm4ChNnHCVOu41CzZsJ5fRhX426GCWasIbgXUR-wzjiinf0ex0Ptpy3YuZ7iLmNtEvhQFxxMHH2eTvUG17D3Mb2r3gwwZrx8uC-qX99ufl7fNvc_vt9df71vrBRkbpxF2TrFQKiuN3QQwAyTPVpDsbeKdAKUctCCJO2gWu56RGK4HJS1kijHL6q7RddF2Oht8hOkg47g9SkQ00pDmr0dURND7aAUNYr0wjlnUEjDOWEIVjCHRevLorXdmQnLaGFOMD4TfZ4Jfq1Xca87IhShtAh8ehBI8fcO86wnny2OIwQsK9NMUs5E23JZ0I8v0E3cpVBWdaQY71rJSKHYQtkUc044PA5DiT6aQy_m0MUc-mQOfZziw9NvPJb8tUIB-ALkkgorTP96_0f2D9e7x4g</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2512386520</pqid></control><display><type>article</type><title>Enantiomers of 2-methylglutamate and 2-methylglutamine selectively impact mouse brain metabolism and behavior</title><source>Publicly Available Content Database</source><source>PubMed Central(OpenAccess)</source><source>Free Full-Text Journals in Chemistry</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Wawro, Adam M. ; Gajera, Chandresh R. ; Baker, Steven A. ; Leśniak, Robert K. ; Fischer, Curt R. ; Saw, Nay L. ; Shamloo, Mehrdad ; Montine, Thomas J.</creator><creatorcontrib>Wawro, Adam M. ; Gajera, Chandresh R. ; Baker, Steven A. ; Leśniak, Robert K. ; Fischer, Curt R. ; Saw, Nay L. ; Shamloo, Mehrdad ; Montine, Thomas J.</creatorcontrib><description>Imbalance of excitatory and inhibitory neurotransmission is implicated in a wide range of psychiatric and neurologic disorders. Here we tested the hypothesis that insertion of a methyl group on the stereogenic alpha carbon of l -Glu or l -Gln would impact the γ-aminobutyric acid (GABA) shunt and the glutamate-glutamine cycle. ( S )-2-methylglutamate, or ( S )-2MeGlu, was efficiently transported into brain and synaptosomes where it was released by membrane depolarization in a manner equivalent to endogenous l -Glu. ( R )-2MeGlu was transported less efficiently into brain and synaptosomes but was not released by membrane depolarization. Each enantiomer of 2MeGlu had limited activity across a panel of over 30 glutamate and GABA receptors. While neither enantiomer of 2MeGlu was metabolized along the GABA shunt, ( S )-2MeGlu was selectively converted to ( S )-2-methylglutamine, or ( S )-2MeGln, which was subsequently slowly hydrolyzed back to ( S )-2MeGlu in brain. rac-2MeGln was also transported into brain, with similar efficiency as ( S )-2MeGlu. A battery of behavioral tests in young adult wild type mice showed safety with up to single 900 mg/kg dose of ( R )-2MeGlu, ( S )-2MeGlu, or rac-2MeGln, suppressed locomotor activity with single ≥ 100 mg/kg dose of ( R )-2MeGlu or ( S )-2MeGlu. No effect on anxiety or hippocampus-dependent learning was evident. Enantiomers of 2MeGlu and 2MeGln show promise as potential pharmacologic agents and imaging probes for cells that produce or transport l -Gln.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-021-87569-1</identifier><identifier>PMID: 33854131</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/45/882 ; 639/638/11/296 ; 639/638/309/436 ; Alzheimer's disease ; Carbon ; Dehydrogenases ; Depolarization ; Enantiomers ; Glutamine ; Humanities and Social Sciences ; Hypotheses ; Locomotor activity ; Membrane potential ; Metabolism ; Metabolites ; multidisciplinary ; Neuroimaging ; Neurotransmission ; Science ; Science (multidisciplinary) ; Synaptosomes ; γ-Aminobutyric acid ; γ-Aminobutyric acid receptors</subject><ispartof>Scientific reports, 2021-04, Vol.11 (1), p.8138-8138, Article 8138</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-dce56d72a4789b1f4a2b259ecb1e9c7084a77da6a506f763d9ee0b35f7cc507d3</citedby><cites>FETCH-LOGICAL-c540t-dce56d72a4789b1f4a2b259ecb1e9c7084a77da6a506f763d9ee0b35f7cc507d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2512386520/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2512386520?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33854131$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wawro, Adam M.</creatorcontrib><creatorcontrib>Gajera, Chandresh R.</creatorcontrib><creatorcontrib>Baker, Steven A.</creatorcontrib><creatorcontrib>Leśniak, Robert K.</creatorcontrib><creatorcontrib>Fischer, Curt R.</creatorcontrib><creatorcontrib>Saw, Nay L.</creatorcontrib><creatorcontrib>Shamloo, Mehrdad</creatorcontrib><creatorcontrib>Montine, Thomas J.</creatorcontrib><title>Enantiomers of 2-methylglutamate and 2-methylglutamine selectively impact mouse brain metabolism and behavior</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Imbalance of excitatory and inhibitory neurotransmission is implicated in a wide range of psychiatric and neurologic disorders. Here we tested the hypothesis that insertion of a methyl group on the stereogenic alpha carbon of l -Glu or l -Gln would impact the γ-aminobutyric acid (GABA) shunt and the glutamate-glutamine cycle. ( S )-2-methylglutamate, or ( S )-2MeGlu, was efficiently transported into brain and synaptosomes where it was released by membrane depolarization in a manner equivalent to endogenous l -Glu. ( R )-2MeGlu was transported less efficiently into brain and synaptosomes but was not released by membrane depolarization. Each enantiomer of 2MeGlu had limited activity across a panel of over 30 glutamate and GABA receptors. While neither enantiomer of 2MeGlu was metabolized along the GABA shunt, ( S )-2MeGlu was selectively converted to ( S )-2-methylglutamine, or ( S )-2MeGln, which was subsequently slowly hydrolyzed back to ( S )-2MeGlu in brain. rac-2MeGln was also transported into brain, with similar efficiency as ( S )-2MeGlu. A battery of behavioral tests in young adult wild type mice showed safety with up to single 900 mg/kg dose of ( R )-2MeGlu, ( S )-2MeGlu, or rac-2MeGln, suppressed locomotor activity with single ≥ 100 mg/kg dose of ( R )-2MeGlu or ( S )-2MeGlu. No effect on anxiety or hippocampus-dependent learning was evident. Enantiomers of 2MeGlu and 2MeGln show promise as potential pharmacologic agents and imaging probes for cells that produce or transport l -Gln.</description><subject>631/45/882</subject><subject>639/638/11/296</subject><subject>639/638/309/436</subject><subject>Alzheimer's disease</subject><subject>Carbon</subject><subject>Dehydrogenases</subject><subject>Depolarization</subject><subject>Enantiomers</subject><subject>Glutamine</subject><subject>Humanities and Social Sciences</subject><subject>Hypotheses</subject><subject>Locomotor activity</subject><subject>Membrane potential</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>multidisciplinary</subject><subject>Neuroimaging</subject><subject>Neurotransmission</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Synaptosomes</subject><subject>γ-Aminobutyric acid</subject><subject>γ-Aminobutyric acid receptors</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kk1v1DAQhiMEolXpH-CAInHhkuLPOLkgoarQSpW4wNka25NdrxJ7sbMr7b_Huyml7QFfbM0888549FbVe0quKOHd5yyo7LuGMNp0SrZ9Q19V54wI2TDO2Osn77PqMucNKUeyXtD-bXXGeScF5fS8mm4ChNnHCVOu41CzZsJ5fRhX426GCWasIbgXUR-wzjiinf0ex0Ptpy3YuZ7iLmNtEvhQFxxMHH2eTvUG17D3Mb2r3gwwZrx8uC-qX99ufl7fNvc_vt9df71vrBRkbpxF2TrFQKiuN3QQwAyTPVpDsbeKdAKUctCCJO2gWu56RGK4HJS1kijHL6q7RddF2Oht8hOkg47g9SkQ00pDmr0dURND7aAUNYr0wjlnUEjDOWEIVjCHRevLorXdmQnLaGFOMD4TfZ4Jfq1Xca87IhShtAh8ehBI8fcO86wnny2OIwQsK9NMUs5E23JZ0I8v0E3cpVBWdaQY71rJSKHYQtkUc044PA5DiT6aQy_m0MUc-mQOfZziw9NvPJb8tUIB-ALkkgorTP96_0f2D9e7x4g</recordid><startdate>20210414</startdate><enddate>20210414</enddate><creator>Wawro, Adam M.</creator><creator>Gajera, Chandresh R.</creator><creator>Baker, Steven A.</creator><creator>Leśniak, Robert K.</creator><creator>Fischer, Curt R.</creator><creator>Saw, Nay L.</creator><creator>Shamloo, Mehrdad</creator><creator>Montine, Thomas J.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><general>Nature Portfolio</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</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>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20210414</creationdate><title>Enantiomers of 2-methylglutamate and 2-methylglutamine selectively impact mouse brain metabolism and behavior</title><author>Wawro, Adam M. ; Gajera, Chandresh R. ; Baker, Steven A. ; Leśniak, Robert K. ; Fischer, Curt R. ; Saw, Nay L. ; Shamloo, Mehrdad ; Montine, Thomas J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-dce56d72a4789b1f4a2b259ecb1e9c7084a77da6a506f763d9ee0b35f7cc507d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>631/45/882</topic><topic>639/638/11/296</topic><topic>639/638/309/436</topic><topic>Alzheimer's disease</topic><topic>Carbon</topic><topic>Dehydrogenases</topic><topic>Depolarization</topic><topic>Enantiomers</topic><topic>Glutamine</topic><topic>Humanities and Social Sciences</topic><topic>Hypotheses</topic><topic>Locomotor activity</topic><topic>Membrane potential</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>multidisciplinary</topic><topic>Neuroimaging</topic><topic>Neurotransmission</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Synaptosomes</topic><topic>γ-Aminobutyric acid</topic><topic>γ-Aminobutyric acid receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wawro, Adam M.</creatorcontrib><creatorcontrib>Gajera, Chandresh R.</creatorcontrib><creatorcontrib>Baker, Steven A.</creatorcontrib><creatorcontrib>Leśniak, Robert K.</creatorcontrib><creatorcontrib>Fischer, Curt R.</creatorcontrib><creatorcontrib>Saw, Nay L.</creatorcontrib><creatorcontrib>Shamloo, Mehrdad</creatorcontrib><creatorcontrib>Montine, Thomas J.</creatorcontrib><collection>SpringerOpen (Open Access)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</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)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Publicly Available Content 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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wawro, Adam M.</au><au>Gajera, Chandresh R.</au><au>Baker, Steven A.</au><au>Leśniak, Robert K.</au><au>Fischer, Curt R.</au><au>Saw, Nay L.</au><au>Shamloo, Mehrdad</au><au>Montine, Thomas J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enantiomers of 2-methylglutamate and 2-methylglutamine selectively impact mouse brain metabolism and behavior</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2021-04-14</date><risdate>2021</risdate><volume>11</volume><issue>1</issue><spage>8138</spage><epage>8138</epage><pages>8138-8138</pages><artnum>8138</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Imbalance of excitatory and inhibitory neurotransmission is implicated in a wide range of psychiatric and neurologic disorders. Here we tested the hypothesis that insertion of a methyl group on the stereogenic alpha carbon of l -Glu or l -Gln would impact the γ-aminobutyric acid (GABA) shunt and the glutamate-glutamine cycle. ( S )-2-methylglutamate, or ( S )-2MeGlu, was efficiently transported into brain and synaptosomes where it was released by membrane depolarization in a manner equivalent to endogenous l -Glu. ( R )-2MeGlu was transported less efficiently into brain and synaptosomes but was not released by membrane depolarization. Each enantiomer of 2MeGlu had limited activity across a panel of over 30 glutamate and GABA receptors. While neither enantiomer of 2MeGlu was metabolized along the GABA shunt, ( S )-2MeGlu was selectively converted to ( S )-2-methylglutamine, or ( S )-2MeGln, which was subsequently slowly hydrolyzed back to ( S )-2MeGlu in brain. rac-2MeGln was also transported into brain, with similar efficiency as ( S )-2MeGlu. A battery of behavioral tests in young adult wild type mice showed safety with up to single 900 mg/kg dose of ( R )-2MeGlu, ( S )-2MeGlu, or rac-2MeGln, suppressed locomotor activity with single ≥ 100 mg/kg dose of ( R )-2MeGlu or ( S )-2MeGlu. No effect on anxiety or hippocampus-dependent learning was evident. Enantiomers of 2MeGlu and 2MeGln show promise as potential pharmacologic agents and imaging probes for cells that produce or transport l -Gln.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33854131</pmid><doi>10.1038/s41598-021-87569-1</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2045-2322
ispartof Scientific reports, 2021-04, Vol.11 (1), p.8138-8138, Article 8138
issn 2045-2322
2045-2322
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_0b1cf771b7094dddbe45b3302eac42de
source Publicly Available Content Database; PubMed Central(OpenAccess); Free Full-Text Journals in Chemistry; Springer Nature - nature.com Journals - Fully Open Access
subjects 631/45/882
639/638/11/296
639/638/309/436
Alzheimer's disease
Carbon
Dehydrogenases
Depolarization
Enantiomers
Glutamine
Humanities and Social Sciences
Hypotheses
Locomotor activity
Membrane potential
Metabolism
Metabolites
multidisciplinary
Neuroimaging
Neurotransmission
Science
Science (multidisciplinary)
Synaptosomes
γ-Aminobutyric acid
γ-Aminobutyric acid receptors
title Enantiomers of 2-methylglutamate and 2-methylglutamine selectively impact mouse brain metabolism and behavior
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T04%3A35%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Enantiomers%20of%202-methylglutamate%20and%202-methylglutamine%20selectively%20impact%20mouse%20brain%20metabolism%20and%20behavior&rft.jtitle=Scientific%20reports&rft.au=Wawro,%20Adam%20M.&rft.date=2021-04-14&rft.volume=11&rft.issue=1&rft.spage=8138&rft.epage=8138&rft.pages=8138-8138&rft.artnum=8138&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/s41598-021-87569-1&rft_dat=%3Cproquest_doaj_%3E2513246635%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c540t-dce56d72a4789b1f4a2b259ecb1e9c7084a77da6a506f763d9ee0b35f7cc507d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2512386520&rft_id=info:pmid/33854131&rfr_iscdi=true