Metabolomics of cerebrospinal fluid reveals changes in the central nervous system metabolism in a rat model of multiple sclerosis
Experimental Autoimmune Encephalomyelitis (EAE) is the most commonly used animal model for Multiple Sclerosis (MScl). CSF metabolomics in an acute EAE rat model was investigated using targetted LC–MS and GC–MS. Acute EAE in Lewis rats was induced by co-injection of Myelin Basic Protein with Complete...
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creator | Noga, Marek J. Dane, Adrie Shi, Shanna Attali, Amos van Aken, Hans Suidgeest, Ernst Tuinstra, Tinka Muilwijk, Bas Coulier, Leon Luider, Theo Reijmers, Theo H. Vreeken, Rob J. Hankemeier, Thomas |
description | Experimental Autoimmune Encephalomyelitis (EAE) is the most commonly used animal model for Multiple Sclerosis (MScl). CSF metabolomics in an acute EAE rat model was investigated using targetted LC–MS and GC–MS. Acute EAE in Lewis rats was induced by co-injection of Myelin Basic Protein with Complete Freund’s Adjuvant. CSF samples were collected at two time points: 10 days after inoculation, which was during the onset of the disease, and 14 days after inoculation, which was during the peak of the disease. The obtained metabolite profiles from the two time points of EAE development show profound differences between onset and the peak of the disease, suggesting significant changes in CNS metabolism over the course of MBP-induced neuroinflammation. Around the onset of EAE the metabolome profile shows significant decreases in arginine, alanine and branched amino acid levels, relative to controls. At the peak of the disease, significant increases in concentrations of multiple metabolites are observed, including glutamine,
O
-phosphoethanolamine, branched-chain amino acids and putrescine. Observed changes in metabolite levels suggest profound changes in CNS metabolism over the course of EAE. Affected pathways include nitric oxide synthesis, altered energy metabolism, polyamine synthesis and levels of endogenous antioxidants. |
doi_str_mv | 10.1007/s11306-011-0306-3 |
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O
-phosphoethanolamine, branched-chain amino acids and putrescine. Observed changes in metabolite levels suggest profound changes in CNS metabolism over the course of EAE. Affected pathways include nitric oxide synthesis, altered energy metabolism, polyamine synthesis and levels of endogenous antioxidants.</description><identifier>ISSN: 1573-3882</identifier><identifier>EISSN: 1573-3890</identifier><identifier>DOI: 10.1007/s11306-011-0306-3</identifier><identifier>PMID: 22448154</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Developmental Biology ; Life Sciences ; Molecular Medicine ; Original ; Original Article</subject><ispartof>Metabolomics, 2012-04, Vol.8 (2), p.253-263</ispartof><rights>The Author(s) 2011</rights><rights>Springer Science+Business Media, LLC 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c568t-3cc40f0874a05aa643665a2dae5be7e530c3ed5ae8050d50c7c49f6be5acb61f3</citedby><cites>FETCH-LOGICAL-c568t-3cc40f0874a05aa643665a2dae5be7e530c3ed5ae8050d50c7c49f6be5acb61f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11306-011-0306-3$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11306-011-0306-3$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22448154$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Noga, Marek J.</creatorcontrib><creatorcontrib>Dane, Adrie</creatorcontrib><creatorcontrib>Shi, Shanna</creatorcontrib><creatorcontrib>Attali, Amos</creatorcontrib><creatorcontrib>van Aken, Hans</creatorcontrib><creatorcontrib>Suidgeest, Ernst</creatorcontrib><creatorcontrib>Tuinstra, Tinka</creatorcontrib><creatorcontrib>Muilwijk, Bas</creatorcontrib><creatorcontrib>Coulier, Leon</creatorcontrib><creatorcontrib>Luider, Theo</creatorcontrib><creatorcontrib>Reijmers, Theo H.</creatorcontrib><creatorcontrib>Vreeken, Rob J.</creatorcontrib><creatorcontrib>Hankemeier, Thomas</creatorcontrib><title>Metabolomics of cerebrospinal fluid reveals changes in the central nervous system metabolism in a rat model of multiple sclerosis</title><title>Metabolomics</title><addtitle>Metabolomics</addtitle><addtitle>Metabolomics</addtitle><description>Experimental Autoimmune Encephalomyelitis (EAE) is the most commonly used animal model for Multiple Sclerosis (MScl). CSF metabolomics in an acute EAE rat model was investigated using targetted LC–MS and GC–MS. Acute EAE in Lewis rats was induced by co-injection of Myelin Basic Protein with Complete Freund’s Adjuvant. CSF samples were collected at two time points: 10 days after inoculation, which was during the onset of the disease, and 14 days after inoculation, which was during the peak of the disease. The obtained metabolite profiles from the two time points of EAE development show profound differences between onset and the peak of the disease, suggesting significant changes in CNS metabolism over the course of MBP-induced neuroinflammation. Around the onset of EAE the metabolome profile shows significant decreases in arginine, alanine and branched amino acid levels, relative to controls. At the peak of the disease, significant increases in concentrations of multiple metabolites are observed, including glutamine,
O
-phosphoethanolamine, branched-chain amino acids and putrescine. Observed changes in metabolite levels suggest profound changes in CNS metabolism over the course of EAE. Affected pathways include nitric oxide synthesis, altered energy metabolism, polyamine synthesis and levels of endogenous antioxidants.</description><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Developmental Biology</subject><subject>Life Sciences</subject><subject>Molecular Medicine</subject><subject>Original</subject><subject>Original Article</subject><issn>1573-3882</issn><issn>1573-3890</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkkuL1TAUx4sozkM_gBsJrtxUT97tRpBBHWHEja5Dmp7OzZA216S9MEu_uSm9Xh8guMqB_M7_vP5V9YzCKwqgX2dKOagaKK1hDfiD6pxKzWvetPDwFDfsrLrI-Q5AiFbD4-qMMSEaKsV59f0TzraLIY7eZRIH4jBhl2Le-8kGMoTF9yThAW3IxO3sdIuZ-InMOyzoNKcCTZgOcckk3-cZRzJuij6PK2hJsjMZY49hlR-XMPt9QJJdwFLG5yfVo6GI49Pje1l9ff_uy9V1ffP5w8ertze1k6qZa-6cgAEaLSxIa5XgSknLeouyQ42Sg-PYS4sNSOglOO1EO6gOpXWdogO_rN5suvulG7E_Nm_2yY823ZtovfnzZ_I7cxsPhrOWNpwVgZdHgRS_LZhnM_rsMAQ7YRnf0Ea2SosW_gPV0FKlGVcFffEXeheXVHafTcukllywtkB0g1xZWU44nNqmYFYrmM0KpljBrFYwvOQ8_33eU8bP2xeAbUAuX-Wu6Vflf6v-AARvwfY</recordid><startdate>20120401</startdate><enddate>20120401</enddate><creator>Noga, Marek J.</creator><creator>Dane, Adrie</creator><creator>Shi, Shanna</creator><creator>Attali, Amos</creator><creator>van Aken, Hans</creator><creator>Suidgeest, Ernst</creator><creator>Tuinstra, Tinka</creator><creator>Muilwijk, Bas</creator><creator>Coulier, Leon</creator><creator>Luider, Theo</creator><creator>Reijmers, Theo H.</creator><creator>Vreeken, Rob J.</creator><creator>Hankemeier, Thomas</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</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>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120401</creationdate><title>Metabolomics of cerebrospinal fluid reveals changes in the central nervous system metabolism in a rat model of multiple sclerosis</title><author>Noga, Marek J. ; 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CSF metabolomics in an acute EAE rat model was investigated using targetted LC–MS and GC–MS. Acute EAE in Lewis rats was induced by co-injection of Myelin Basic Protein with Complete Freund’s Adjuvant. CSF samples were collected at two time points: 10 days after inoculation, which was during the onset of the disease, and 14 days after inoculation, which was during the peak of the disease. The obtained metabolite profiles from the two time points of EAE development show profound differences between onset and the peak of the disease, suggesting significant changes in CNS metabolism over the course of MBP-induced neuroinflammation. Around the onset of EAE the metabolome profile shows significant decreases in arginine, alanine and branched amino acid levels, relative to controls. At the peak of the disease, significant increases in concentrations of multiple metabolites are observed, including glutamine,
O
-phosphoethanolamine, branched-chain amino acids and putrescine. Observed changes in metabolite levels suggest profound changes in CNS metabolism over the course of EAE. Affected pathways include nitric oxide synthesis, altered energy metabolism, polyamine synthesis and levels of endogenous antioxidants.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>22448154</pmid><doi>10.1007/s11306-011-0306-3</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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title | Metabolomics of cerebrospinal fluid reveals changes in the central nervous system metabolism in a rat model of multiple sclerosis |
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