<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schroeder MA</submitter><funding>British Heart Foundation</funding><funding>NIBIB NIH HHS</funding><funding>Medical Research Council</funding><funding>Wellcome Trust</funding><pagination>201-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3378498</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Carnitine acetyltransferase catalyzes the reversible conversion of acetyl-coenzyme A (CoA) into acetylcarnitine. The aim of this study was to use the metabolic tracer hyperpolarized [2-(13)C]pyruvate with magnetic resonance spectroscopy to determine whether carnitine acetyltransferase facilitates carbohydrate oxidation in the heart.&lt;h4>Methods and results&lt;/h4>Ex vivo, following hyperpolarized [2-(13)C]pyruvate infusion, the [1-(13)C]acetylcarnitine resonance was saturated with a radiofrequency pulse, and the effect of this saturation on [1-(13)C]citrate and [5-(13)C]glutamate was observed. In vivo, [2-(13)C]pyruvate was infused into 3 groups of fed male Wistar rats: (1) controls, (2) rats in which dichloroacetate enhanced pyruvate dehydrogenase flux, and (3) rats in whic</pubmed_abstract><journal>Circulation. Cardiovascular imaging</journal><pubmed_title>The cycling of acetyl-coenzyme A through acetylcarnitine buffers cardiac substrate supply: a hyperpolarized 13C magnetic resonance study.</pubmed_title><pmcid>PMC3378498</pmcid><funding_grant_id>F31 EB006692</funding_grant_id><funding_grant_id>PS/02/002/14893</funding_grant_id><funding_grant_id>G0601490</funding_grant_id><funding_grant_id>RG/07/004/22659</funding_grant_id><funding_grant_id>FS/10/002/28078</funding_grant_id><funding_grant_id>089010</funding_grant_id><funding_grant_id>PG/07/070/23365</funding_grant_id><funding_grant_id>1-F31-EB006692-01A1</funding_grant_id><pubmed_authors>Clarke K</pubmed_authors><pubmed_authors>Tyler DJ</pubmed_authors><pubmed_authors>Atherton HJ</pubmed_authors><pubmed_authors>Lee P</pubmed_authors><pubmed_authors>Schroeder MA</pubmed_authors><pubmed_authors>Dodd MS</pubmed_authors><pubmed_authors>Radda GK</pubmed_authors><pubmed_authors>Cochlin LE</pubmed_authors></additional><is_claimable>false</is_claimable><name>The cycling of acetyl-coenzyme A through acetylcarnitine buffers cardiac substrate supply: a hyperpolarized 13C magnetic resonance study.</name><description>&lt;h4>Background&lt;/h4>Carnitine acetyltransferase catalyzes the reversible conversion of acetyl-coenzyme A (CoA) into acetylcarnitine. The aim of this study was to use the metabolic tracer hyperpolarized [2-(13)C]pyruvate with magnetic resonance spectroscopy to determine whether carnitine acetyltransferase facilitates carbohydrate oxidation in the heart.&lt;h4>Methods and results&lt;/h4>Ex vivo, following hyperpolarized [2-(13)C]pyruvate infusion, the [1-(13)C]acetylcarnitine resonance was saturated with a radiofrequency pulse, and the effect of this saturation on [1-(13)C]citrate and [5-(13)C]glutamate was observed. In vivo, [2-(13)C]pyruvate was infused into 3 groups of fed male Wistar rats: (1) controls, (2) rats in which dichloroacetate enhanced pyruvate dehydrogenase flux, and (3) rats in whic</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Mar</publication><modification>2025-04-04T18:56:08.5Z</modification><creation>2019-03-26T23:49:24Z</creation></dates><accession>S-EPMC3378498</accession><cross_references><pubmed>22238215</pubmed><doi>10.1161/circimaging.111.969451</doi><doi>10.1161/CIRCIMAGING.111.969451</doi></cross_references></HashMap>