Assay of the Human Liver Citric Acid Cycle Probe Phenylacetylglutamine and of Phenylacetate in Plasma by Gas Chromatography-Mass Spectrometry

Phenylacetate, derived from phenylalanine, is converted in human and primate liver to phenylacetylglutamine. The latter has been used to assess the labeling pattern of liver citric acid cycle intermediates. We present gas chromatographic-mass spectrometric assays of phenylacetylglutamine, Phenylacet...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Analytical biochemistry 1993-07, Vol.212 (1), p.277-282
Hauptverfasser: Yang, D.W., Beylot, M., Agarwal, K.C., Soloviev, M.V., Brunengraber, H.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 282
container_issue 1
container_start_page 277
container_title Analytical biochemistry
container_volume 212
creator Yang, D.W.
Beylot, M.
Agarwal, K.C.
Soloviev, M.V.
Brunengraber, H.
description Phenylacetate, derived from phenylalanine, is converted in human and primate liver to phenylacetylglutamine. The latter has been used to assess the labeling pattern of liver citric acid cycle intermediates. We present gas chromatographic-mass spectrometric assays of phenylacetylglutamine, Phenylacetate, and phenylalanine in biological fluids. The compounds are derivatized with dimethylformamide dimethyl acetal. Limits of detection are 0.1 nmol for phenylacetylglutamine and phenylacetate and 2 nmol for phenylalanine. Baseline plasma concentrations of phenylacetate and phenylacetylglutamine are 1 and 3 μM, respectively. The 24-h urinary excretions of phenylacetate and phenylacetylglutamine are about 4 μmol and 1 mmol, respectively. Ingestion of phenylalanine (in the form of aspartame) by a human is followed by sequential increases in phenylacetate and phenylacetylglutamine concentrations in plasma and urine. This assay opens the way to noninvasive probing of the 13C-labeling pattern of liver citric acid cycle intermediates in humans.
doi_str_mv 10.1006/abio.1993.1323
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_75930983</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0003269783713230</els_id><sourcerecordid>75930983</sourcerecordid><originalsourceid>FETCH-LOGICAL-c368t-30c0ac00ea172d2d5fbc4584194b9a0462227c79fee3da72c80976dd4eeb505a3</originalsourceid><addsrcrecordid>eNp1kE2LFDEQhoMo6-zq1ZuQg3jrsdLprxyHQXcXRlxQz6E6qd6J9MeYpBf6R_ifTTPDevKSgrxPvRQPY-8EbAVA9QlbN22FUnIrZC5fsI0AVWUgQb1kGwCQWV6p-jW7DuEXgBBFWV2xq0ZWTQlyw_7sQsCFTx2PR-J384AjP7gn8nzvoneG74yzfL-YnviDn9r0HmlcejQUl_6xnyMObiSOo11L_oUYibuRP_QYBuTtwm8x8P3RTwPG6dHj6bhkXzEE_v1EJqZvin55w1512Ad6e5k37OeXzz_2d9nh2-39fnfITLo7ZhIMoAEgFHVuc1t2rSnKphCqaBVCUeV5XptadUTSYp2bBlRdWVsQtSWUKG_Yx3PvyU-_ZwpRDy4Y6nscaZqDrkuVBDYygdszaPwUgqdOn7wb0C9agF7969W_Xv3r1X9aeH9pntuB7DN-EZ7yD5ccg8G-8zgaF56xoqlkJfKENWeMkoUnR14H42g0ZJ1PurSd3P8u-Asc4aLd</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>75930983</pqid></control><display><type>article</type><title>Assay of the Human Liver Citric Acid Cycle Probe Phenylacetylglutamine and of Phenylacetate in Plasma by Gas Chromatography-Mass Spectrometry</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Yang, D.W. ; Beylot, M. ; Agarwal, K.C. ; Soloviev, M.V. ; Brunengraber, H.</creator><creatorcontrib>Yang, D.W. ; Beylot, M. ; Agarwal, K.C. ; Soloviev, M.V. ; Brunengraber, H.</creatorcontrib><description>Phenylacetate, derived from phenylalanine, is converted in human and primate liver to phenylacetylglutamine. The latter has been used to assess the labeling pattern of liver citric acid cycle intermediates. We present gas chromatographic-mass spectrometric assays of phenylacetylglutamine, Phenylacetate, and phenylalanine in biological fluids. The compounds are derivatized with dimethylformamide dimethyl acetal. Limits of detection are 0.1 nmol for phenylacetylglutamine and phenylacetate and 2 nmol for phenylalanine. Baseline plasma concentrations of phenylacetate and phenylacetylglutamine are 1 and 3 μM, respectively. The 24-h urinary excretions of phenylacetate and phenylacetylglutamine are about 4 μmol and 1 mmol, respectively. Ingestion of phenylalanine (in the form of aspartame) by a human is followed by sequential increases in phenylacetate and phenylacetylglutamine concentrations in plasma and urine. This assay opens the way to noninvasive probing of the 13C-labeling pattern of liver citric acid cycle intermediates in humans.</description><identifier>ISSN: 0003-2697</identifier><identifier>EISSN: 1096-0309</identifier><identifier>DOI: 10.1006/abio.1993.1323</identifier><identifier>PMID: 8368503</identifier><identifier>CODEN: ANBCA2</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Adult ; Analytical, structural and metabolic biochemistry ; Biological and medical sciences ; Citric Acid Cycle ; Evaluation Studies as Topic ; Fundamental and applied biological sciences. Psychology ; Gas Chromatography-Mass Spectrometry - methods ; Gas Chromatography-Mass Spectrometry - statistics &amp; numerical data ; Glutamine - analogs &amp; derivatives ; Glutamine - analysis ; Glutamine - blood ; Humans ; Intermediary metabolites. Miscellaneous ; Liver - metabolism ; Molecular Probes ; Other biological molecules ; Phenylacetates - analysis ; Phenylacetates - blood ; Phenylalanine - analysis ; Phenylalanine - blood ; Sensitivity and Specificity</subject><ispartof>Analytical biochemistry, 1993-07, Vol.212 (1), p.277-282</ispartof><rights>1993 Academic Press</rights><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-30c0ac00ea172d2d5fbc4584194b9a0462227c79fee3da72c80976dd4eeb505a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/abio.1993.1323$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4863612$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8368503$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, D.W.</creatorcontrib><creatorcontrib>Beylot, M.</creatorcontrib><creatorcontrib>Agarwal, K.C.</creatorcontrib><creatorcontrib>Soloviev, M.V.</creatorcontrib><creatorcontrib>Brunengraber, H.</creatorcontrib><title>Assay of the Human Liver Citric Acid Cycle Probe Phenylacetylglutamine and of Phenylacetate in Plasma by Gas Chromatography-Mass Spectrometry</title><title>Analytical biochemistry</title><addtitle>Anal Biochem</addtitle><description>Phenylacetate, derived from phenylalanine, is converted in human and primate liver to phenylacetylglutamine. The latter has been used to assess the labeling pattern of liver citric acid cycle intermediates. We present gas chromatographic-mass spectrometric assays of phenylacetylglutamine, Phenylacetate, and phenylalanine in biological fluids. The compounds are derivatized with dimethylformamide dimethyl acetal. Limits of detection are 0.1 nmol for phenylacetylglutamine and phenylacetate and 2 nmol for phenylalanine. Baseline plasma concentrations of phenylacetate and phenylacetylglutamine are 1 and 3 μM, respectively. The 24-h urinary excretions of phenylacetate and phenylacetylglutamine are about 4 μmol and 1 mmol, respectively. Ingestion of phenylalanine (in the form of aspartame) by a human is followed by sequential increases in phenylacetate and phenylacetylglutamine concentrations in plasma and urine. This assay opens the way to noninvasive probing of the 13C-labeling pattern of liver citric acid cycle intermediates in humans.</description><subject>Adult</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Biological and medical sciences</subject><subject>Citric Acid Cycle</subject><subject>Evaluation Studies as Topic</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gas Chromatography-Mass Spectrometry - methods</subject><subject>Gas Chromatography-Mass Spectrometry - statistics &amp; numerical data</subject><subject>Glutamine - analogs &amp; derivatives</subject><subject>Glutamine - analysis</subject><subject>Glutamine - blood</subject><subject>Humans</subject><subject>Intermediary metabolites. Miscellaneous</subject><subject>Liver - metabolism</subject><subject>Molecular Probes</subject><subject>Other biological molecules</subject><subject>Phenylacetates - analysis</subject><subject>Phenylacetates - blood</subject><subject>Phenylalanine - analysis</subject><subject>Phenylalanine - blood</subject><subject>Sensitivity and Specificity</subject><issn>0003-2697</issn><issn>1096-0309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE2LFDEQhoMo6-zq1ZuQg3jrsdLprxyHQXcXRlxQz6E6qd6J9MeYpBf6R_ifTTPDevKSgrxPvRQPY-8EbAVA9QlbN22FUnIrZC5fsI0AVWUgQb1kGwCQWV6p-jW7DuEXgBBFWV2xq0ZWTQlyw_7sQsCFTx2PR-J384AjP7gn8nzvoneG74yzfL-YnviDn9r0HmlcejQUl_6xnyMObiSOo11L_oUYibuRP_QYBuTtwm8x8P3RTwPG6dHj6bhkXzEE_v1EJqZvin55w1512Ad6e5k37OeXzz_2d9nh2-39fnfITLo7ZhIMoAEgFHVuc1t2rSnKphCqaBVCUeV5XptadUTSYp2bBlRdWVsQtSWUKG_Yx3PvyU-_ZwpRDy4Y6nscaZqDrkuVBDYygdszaPwUgqdOn7wb0C9agF7969W_Xv3r1X9aeH9pntuB7DN-EZ7yD5ccg8G-8zgaF56xoqlkJfKENWeMkoUnR14H42g0ZJ1PurSd3P8u-Asc4aLd</recordid><startdate>19930701</startdate><enddate>19930701</enddate><creator>Yang, D.W.</creator><creator>Beylot, M.</creator><creator>Agarwal, K.C.</creator><creator>Soloviev, M.V.</creator><creator>Brunengraber, H.</creator><general>Elsevier Inc</general><general>Elsevier</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>7X8</scope></search><sort><creationdate>19930701</creationdate><title>Assay of the Human Liver Citric Acid Cycle Probe Phenylacetylglutamine and of Phenylacetate in Plasma by Gas Chromatography-Mass Spectrometry</title><author>Yang, D.W. ; Beylot, M. ; Agarwal, K.C. ; Soloviev, M.V. ; Brunengraber, H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-30c0ac00ea172d2d5fbc4584194b9a0462227c79fee3da72c80976dd4eeb505a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Adult</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Biological and medical sciences</topic><topic>Citric Acid Cycle</topic><topic>Evaluation Studies as Topic</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gas Chromatography-Mass Spectrometry - methods</topic><topic>Gas Chromatography-Mass Spectrometry - statistics &amp; numerical data</topic><topic>Glutamine - analogs &amp; derivatives</topic><topic>Glutamine - analysis</topic><topic>Glutamine - blood</topic><topic>Humans</topic><topic>Intermediary metabolites. Miscellaneous</topic><topic>Liver - metabolism</topic><topic>Molecular Probes</topic><topic>Other biological molecules</topic><topic>Phenylacetates - analysis</topic><topic>Phenylacetates - blood</topic><topic>Phenylalanine - analysis</topic><topic>Phenylalanine - blood</topic><topic>Sensitivity and Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, D.W.</creatorcontrib><creatorcontrib>Beylot, M.</creatorcontrib><creatorcontrib>Agarwal, K.C.</creatorcontrib><creatorcontrib>Soloviev, M.V.</creatorcontrib><creatorcontrib>Brunengraber, H.</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>MEDLINE - Academic</collection><jtitle>Analytical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, D.W.</au><au>Beylot, M.</au><au>Agarwal, K.C.</au><au>Soloviev, M.V.</au><au>Brunengraber, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assay of the Human Liver Citric Acid Cycle Probe Phenylacetylglutamine and of Phenylacetate in Plasma by Gas Chromatography-Mass Spectrometry</atitle><jtitle>Analytical biochemistry</jtitle><addtitle>Anal Biochem</addtitle><date>1993-07-01</date><risdate>1993</risdate><volume>212</volume><issue>1</issue><spage>277</spage><epage>282</epage><pages>277-282</pages><issn>0003-2697</issn><eissn>1096-0309</eissn><coden>ANBCA2</coden><abstract>Phenylacetate, derived from phenylalanine, is converted in human and primate liver to phenylacetylglutamine. The latter has been used to assess the labeling pattern of liver citric acid cycle intermediates. We present gas chromatographic-mass spectrometric assays of phenylacetylglutamine, Phenylacetate, and phenylalanine in biological fluids. The compounds are derivatized with dimethylformamide dimethyl acetal. Limits of detection are 0.1 nmol for phenylacetylglutamine and phenylacetate and 2 nmol for phenylalanine. Baseline plasma concentrations of phenylacetate and phenylacetylglutamine are 1 and 3 μM, respectively. The 24-h urinary excretions of phenylacetate and phenylacetylglutamine are about 4 μmol and 1 mmol, respectively. Ingestion of phenylalanine (in the form of aspartame) by a human is followed by sequential increases in phenylacetate and phenylacetylglutamine concentrations in plasma and urine. This assay opens the way to noninvasive probing of the 13C-labeling pattern of liver citric acid cycle intermediates in humans.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>8368503</pmid><doi>10.1006/abio.1993.1323</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0003-2697
ispartof Analytical biochemistry, 1993-07, Vol.212 (1), p.277-282
issn 0003-2697
1096-0309
language eng
recordid cdi_proquest_miscellaneous_75930983
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Adult
Analytical, structural and metabolic biochemistry
Biological and medical sciences
Citric Acid Cycle
Evaluation Studies as Topic
Fundamental and applied biological sciences. Psychology
Gas Chromatography-Mass Spectrometry - methods
Gas Chromatography-Mass Spectrometry - statistics & numerical data
Glutamine - analogs & derivatives
Glutamine - analysis
Glutamine - blood
Humans
Intermediary metabolites. Miscellaneous
Liver - metabolism
Molecular Probes
Other biological molecules
Phenylacetates - analysis
Phenylacetates - blood
Phenylalanine - analysis
Phenylalanine - blood
Sensitivity and Specificity
title Assay of the Human Liver Citric Acid Cycle Probe Phenylacetylglutamine and of Phenylacetate in Plasma by Gas Chromatography-Mass Spectrometry
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T16%3A10%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Assay%20of%20the%20Human%20Liver%20Citric%20Acid%20Cycle%20Probe%20Phenylacetylglutamine%20and%20of%20Phenylacetate%20in%20Plasma%20by%20Gas%20Chromatography-Mass%20Spectrometry&rft.jtitle=Analytical%20biochemistry&rft.au=Yang,%20D.W.&rft.date=1993-07-01&rft.volume=212&rft.issue=1&rft.spage=277&rft.epage=282&rft.pages=277-282&rft.issn=0003-2697&rft.eissn=1096-0309&rft.coden=ANBCA2&rft_id=info:doi/10.1006/abio.1993.1323&rft_dat=%3Cproquest_cross%3E75930983%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=75930983&rft_id=info:pmid/8368503&rft_els_id=S0003269783713230&rfr_iscdi=true