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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...
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Published in: | Scientific reports 2021-04, Vol.11 (1), p.8138-8138, Article 8138 |
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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 |
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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. ; 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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> |
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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 |
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