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Evaluation of Active Brown Adipose Tissue by the Use of Hyperpolarized [1-(13)C]Pyruvate MRI in Mice
The capacity to increase energy expenditure makes brown adipose tissue (BAT) a putative target for treatment of metabolic diseases such as obesity. Presently, investigation of BAT in vivo is mainly performed by fluoro-d-glucose positron emission tomography (FDG PET)/CT. However, non-radioactive meth...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164296/ https://www.ncbi.nlm.nih.gov/pubmed/30200469 http://dx.doi.org/10.3390/ijms19092597 |
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author | Riis-Vestergaard, Mette Ji Breining, Peter Pedersen, Steen Bønløkke Laustsen, Christoffer Stødkilde-Jørgensen, Hans Borghammer, Per Jessen, Niels Richelsen, Bjørn |
author_facet | Riis-Vestergaard, Mette Ji Breining, Peter Pedersen, Steen Bønløkke Laustsen, Christoffer Stødkilde-Jørgensen, Hans Borghammer, Per Jessen, Niels Richelsen, Bjørn |
author_sort | Riis-Vestergaard, Mette Ji |
collection | PubMed |
description | The capacity to increase energy expenditure makes brown adipose tissue (BAT) a putative target for treatment of metabolic diseases such as obesity. Presently, investigation of BAT in vivo is mainly performed by fluoro-d-glucose positron emission tomography (FDG PET)/CT. However, non-radioactive methods that add information on, for example, substrate metabolism are warranted. Thus, the aim of this study was to evaluate the potential of hyperpolarized [1-(13)C]pyruvate Magnetic Resonance Imaging (HP-MRI) to determine BAT activity in mice following chronic cold exposure. Cold (6 °C) and thermo-neutral (30 °C) acclimated mice were scanned with HP-MRI for assessment of the interscapular BAT (iBAT) activity. Comparable mice were scanned with the conventional method FDG PET/MRI. Finally, iBAT was evaluated for gene expression and protein levels of the specific thermogenic marker, uncoupling protein 1 (UCP1). Cold exposure increased the thermogenic capacity 3–4 fold (p < 0.05) as measured by UCP1 gene and protein analysis. Furthermore, cold exposure as compared with thermo-neutrality increased iBAT pyruvate metabolism by 5.5-fold determined by HP-MRI which is in good agreement with the 5-fold increment in FDG uptake (p < 0.05) measured by FDG PET/MRI. iBAT activity is detectable in mice using HP-MRI in which potential changes in intracellular metabolism may add useful information to the conventional FDG PET studies. HP-MRI may also be a promising radiation-free tool for repetitive BAT studies in humans. |
format | Online Article Text |
id | pubmed-6164296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61642962018-10-10 Evaluation of Active Brown Adipose Tissue by the Use of Hyperpolarized [1-(13)C]Pyruvate MRI in Mice Riis-Vestergaard, Mette Ji Breining, Peter Pedersen, Steen Bønløkke Laustsen, Christoffer Stødkilde-Jørgensen, Hans Borghammer, Per Jessen, Niels Richelsen, Bjørn Int J Mol Sci Article The capacity to increase energy expenditure makes brown adipose tissue (BAT) a putative target for treatment of metabolic diseases such as obesity. Presently, investigation of BAT in vivo is mainly performed by fluoro-d-glucose positron emission tomography (FDG PET)/CT. However, non-radioactive methods that add information on, for example, substrate metabolism are warranted. Thus, the aim of this study was to evaluate the potential of hyperpolarized [1-(13)C]pyruvate Magnetic Resonance Imaging (HP-MRI) to determine BAT activity in mice following chronic cold exposure. Cold (6 °C) and thermo-neutral (30 °C) acclimated mice were scanned with HP-MRI for assessment of the interscapular BAT (iBAT) activity. Comparable mice were scanned with the conventional method FDG PET/MRI. Finally, iBAT was evaluated for gene expression and protein levels of the specific thermogenic marker, uncoupling protein 1 (UCP1). Cold exposure increased the thermogenic capacity 3–4 fold (p < 0.05) as measured by UCP1 gene and protein analysis. Furthermore, cold exposure as compared with thermo-neutrality increased iBAT pyruvate metabolism by 5.5-fold determined by HP-MRI which is in good agreement with the 5-fold increment in FDG uptake (p < 0.05) measured by FDG PET/MRI. iBAT activity is detectable in mice using HP-MRI in which potential changes in intracellular metabolism may add useful information to the conventional FDG PET studies. HP-MRI may also be a promising radiation-free tool for repetitive BAT studies in humans. MDPI 2018-09-01 /pmc/articles/PMC6164296/ /pubmed/30200469 http://dx.doi.org/10.3390/ijms19092597 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Riis-Vestergaard, Mette Ji Breining, Peter Pedersen, Steen Bønløkke Laustsen, Christoffer Stødkilde-Jørgensen, Hans Borghammer, Per Jessen, Niels Richelsen, Bjørn Evaluation of Active Brown Adipose Tissue by the Use of Hyperpolarized [1-(13)C]Pyruvate MRI in Mice |
title | Evaluation of Active Brown Adipose Tissue by the Use of Hyperpolarized [1-(13)C]Pyruvate MRI in Mice |
title_full | Evaluation of Active Brown Adipose Tissue by the Use of Hyperpolarized [1-(13)C]Pyruvate MRI in Mice |
title_fullStr | Evaluation of Active Brown Adipose Tissue by the Use of Hyperpolarized [1-(13)C]Pyruvate MRI in Mice |
title_full_unstemmed | Evaluation of Active Brown Adipose Tissue by the Use of Hyperpolarized [1-(13)C]Pyruvate MRI in Mice |
title_short | Evaluation of Active Brown Adipose Tissue by the Use of Hyperpolarized [1-(13)C]Pyruvate MRI in Mice |
title_sort | evaluation of active brown adipose tissue by the use of hyperpolarized [1-(13)c]pyruvate mri in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164296/ https://www.ncbi.nlm.nih.gov/pubmed/30200469 http://dx.doi.org/10.3390/ijms19092597 |
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