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Hyperpolarized Butyrate: A Metabolic Probe of Short Chain Fatty Acid Metabolism in the Heart
PURPOSE: Butyrate, a short chain fatty acid, was studied as a novel hyperpolarized substrate for use in dynamic nuclear polarization enhanced magnetic resonance spectroscopy experiments, to define the pathways of short chain fatty acid and ketone body metabolism in real time. METHODS: Butyrate was p...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238803/ https://www.ncbi.nlm.nih.gov/pubmed/23798473 http://dx.doi.org/10.1002/mrm.24849 |
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author | Ball, Daniel R Rowlands, Ben Dodd, Michael S Le Page, Lydia Ball, Vicky Carr, Carolyn A Clarke, Kieran Tyler, Damian J |
author_facet | Ball, Daniel R Rowlands, Ben Dodd, Michael S Le Page, Lydia Ball, Vicky Carr, Carolyn A Clarke, Kieran Tyler, Damian J |
author_sort | Ball, Daniel R |
collection | PubMed |
description | PURPOSE: Butyrate, a short chain fatty acid, was studied as a novel hyperpolarized substrate for use in dynamic nuclear polarization enhanced magnetic resonance spectroscopy experiments, to define the pathways of short chain fatty acid and ketone body metabolism in real time. METHODS: Butyrate was polarized via the dynamic nuclear polarization process and subsequently dissolved to generate an injectable metabolic substrate. Metabolism was initially assessed in the isolated perfused rat heart, followed by evaluation in the in vivo rat heart. RESULTS: Hyperpolarized butyrate was generated with a polarization level of 7% and was shown to have a T(1) relaxation time of 20 s. These physical characteristics were sufficient to enable assessment of multiple steps in its metabolism, with the ketone body acetoacetate and several tricarboxylic acid cycle intermediates observed both in vitro and in vivo. Metabolite to butyrate ratios of 0.1–0.4% and 0.5–2% were observed in vitro and in vivo respectively, similar to levels previously observed with hyperpolarized [2-(13)C]pyruvate. CONCLUSIONS: In this study, butyrate has been demonstrated to be a suitable hyperpolarized substrate capable of revealing multi-step metabolism in dynamic nuclear polarization experiments and providing information on the metabolism of fatty acids not currently achievable with other hyperpolarized substrates. Magn Reson Med 71:1663–1669, 2014. © 2013 Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-4238803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42388032014-11-28 Hyperpolarized Butyrate: A Metabolic Probe of Short Chain Fatty Acid Metabolism in the Heart Ball, Daniel R Rowlands, Ben Dodd, Michael S Le Page, Lydia Ball, Vicky Carr, Carolyn A Clarke, Kieran Tyler, Damian J Magn Reson Med Spectroscopic Methodology—Notes PURPOSE: Butyrate, a short chain fatty acid, was studied as a novel hyperpolarized substrate for use in dynamic nuclear polarization enhanced magnetic resonance spectroscopy experiments, to define the pathways of short chain fatty acid and ketone body metabolism in real time. METHODS: Butyrate was polarized via the dynamic nuclear polarization process and subsequently dissolved to generate an injectable metabolic substrate. Metabolism was initially assessed in the isolated perfused rat heart, followed by evaluation in the in vivo rat heart. RESULTS: Hyperpolarized butyrate was generated with a polarization level of 7% and was shown to have a T(1) relaxation time of 20 s. These physical characteristics were sufficient to enable assessment of multiple steps in its metabolism, with the ketone body acetoacetate and several tricarboxylic acid cycle intermediates observed both in vitro and in vivo. Metabolite to butyrate ratios of 0.1–0.4% and 0.5–2% were observed in vitro and in vivo respectively, similar to levels previously observed with hyperpolarized [2-(13)C]pyruvate. CONCLUSIONS: In this study, butyrate has been demonstrated to be a suitable hyperpolarized substrate capable of revealing multi-step metabolism in dynamic nuclear polarization experiments and providing information on the metabolism of fatty acids not currently achievable with other hyperpolarized substrates. Magn Reson Med 71:1663–1669, 2014. © 2013 Wiley Periodicals, Inc. BlackWell Publishing Ltd 2014-01 2013-06-24 /pmc/articles/PMC4238803/ /pubmed/23798473 http://dx.doi.org/10.1002/mrm.24849 Text en Copyright © 2013 Wiley Periodicals, Inc. |
spellingShingle | Spectroscopic Methodology—Notes Ball, Daniel R Rowlands, Ben Dodd, Michael S Le Page, Lydia Ball, Vicky Carr, Carolyn A Clarke, Kieran Tyler, Damian J Hyperpolarized Butyrate: A Metabolic Probe of Short Chain Fatty Acid Metabolism in the Heart |
title | Hyperpolarized Butyrate: A Metabolic Probe of Short Chain Fatty Acid Metabolism in the Heart |
title_full | Hyperpolarized Butyrate: A Metabolic Probe of Short Chain Fatty Acid Metabolism in the Heart |
title_fullStr | Hyperpolarized Butyrate: A Metabolic Probe of Short Chain Fatty Acid Metabolism in the Heart |
title_full_unstemmed | Hyperpolarized Butyrate: A Metabolic Probe of Short Chain Fatty Acid Metabolism in the Heart |
title_short | Hyperpolarized Butyrate: A Metabolic Probe of Short Chain Fatty Acid Metabolism in the Heart |
title_sort | hyperpolarized butyrate: a metabolic probe of short chain fatty acid metabolism in the heart |
topic | Spectroscopic Methodology—Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238803/ https://www.ncbi.nlm.nih.gov/pubmed/23798473 http://dx.doi.org/10.1002/mrm.24849 |
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