Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease.

The recent discovery of active brown fat in human adults has led to renewed interest in the role of this key metabolic tissue. This is particularly true for neurodegenerative conditions like Huntington disease (HD), an adult-onset heritable disorder with a prominent energy deficit phenotype. Current...

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Autores principales: Katrin S Lindenberg, Patrick Weydt, Hans-Peter Müller, Axel Bornstedt, Albert C Ludolph, G Bernhard Landwehrmeyer, Wolfgang Rottbauer, Jan Kassubek, Volker Rasche
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Publicado: Public Library of Science (PLoS) 2014
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spelling oai:doaj.org-article:cc4968a994c54fe38c0855de15fcb15f2021-11-25T06:03:45ZTwo-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease.1932-620310.1371/journal.pone.0105556https://doaj.org/article/cc4968a994c54fe38c0855de15fcb15f2014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/25144457/?tool=EBIhttps://doaj.org/toc/1932-6203The recent discovery of active brown fat in human adults has led to renewed interest in the role of this key metabolic tissue. This is particularly true for neurodegenerative conditions like Huntington disease (HD), an adult-onset heritable disorder with a prominent energy deficit phenotype. Current methods for imaging brown adipose tissue (BAT) are in limited use because they are equipment-wise demanding and often prohibitively expensive. This prompted us to explore how a standard MRI set-up can be modified to visualize BAT in situ by taking advantage of its characteristic fat/water content ratio to differentiate it from surrounding white fat. We present a modified MRI protocol for use on an 11.7 T small animal MRI scanner to visualize and quantify BAT in wild-type and disease model laboratory mice. In this application study using the R6/2 transgenic mouse model of HD we demonstrate a significantly reduced BAT volume in HD mice vs. matched controls (n = 5 per group). This finding provides a plausible structural explanation for the previously described temperature phenotype of HD mice and underscores the significance of peripheral tissue pathology for the HD phenotype. On a more general level, the results demonstrate the feasibility of MR-based BAT imaging in rodents and open the path towards transferring this imaging approach to human patients. Future studies are needed to determine if this method can be used to track disease progression in HD and other disease entities associated with BAT abnormalities, including metabolic conditions such as obesity, cachexia, and diabetes.Katrin S LindenbergPatrick WeydtHans-Peter MüllerAxel BornstedtAlbert C LudolphG Bernhard LandwehrmeyerWolfgang RottbauerJan KassubekVolker RaschePublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 8, p e105556 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Katrin S Lindenberg
Patrick Weydt
Hans-Peter Müller
Axel Bornstedt
Albert C Ludolph
G Bernhard Landwehrmeyer
Wolfgang Rottbauer
Jan Kassubek
Volker Rasche
Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease.
description The recent discovery of active brown fat in human adults has led to renewed interest in the role of this key metabolic tissue. This is particularly true for neurodegenerative conditions like Huntington disease (HD), an adult-onset heritable disorder with a prominent energy deficit phenotype. Current methods for imaging brown adipose tissue (BAT) are in limited use because they are equipment-wise demanding and often prohibitively expensive. This prompted us to explore how a standard MRI set-up can be modified to visualize BAT in situ by taking advantage of its characteristic fat/water content ratio to differentiate it from surrounding white fat. We present a modified MRI protocol for use on an 11.7 T small animal MRI scanner to visualize and quantify BAT in wild-type and disease model laboratory mice. In this application study using the R6/2 transgenic mouse model of HD we demonstrate a significantly reduced BAT volume in HD mice vs. matched controls (n = 5 per group). This finding provides a plausible structural explanation for the previously described temperature phenotype of HD mice and underscores the significance of peripheral tissue pathology for the HD phenotype. On a more general level, the results demonstrate the feasibility of MR-based BAT imaging in rodents and open the path towards transferring this imaging approach to human patients. Future studies are needed to determine if this method can be used to track disease progression in HD and other disease entities associated with BAT abnormalities, including metabolic conditions such as obesity, cachexia, and diabetes.
format article
author Katrin S Lindenberg
Patrick Weydt
Hans-Peter Müller
Axel Bornstedt
Albert C Ludolph
G Bernhard Landwehrmeyer
Wolfgang Rottbauer
Jan Kassubek
Volker Rasche
author_facet Katrin S Lindenberg
Patrick Weydt
Hans-Peter Müller
Axel Bornstedt
Albert C Ludolph
G Bernhard Landwehrmeyer
Wolfgang Rottbauer
Jan Kassubek
Volker Rasche
author_sort Katrin S Lindenberg
title Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease.
title_short Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease.
title_full Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease.
title_fullStr Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease.
title_full_unstemmed Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease.
title_sort two-point magnitude mri for rapid mapping of brown adipose tissue and its application to the r6/2 mouse model of huntington disease.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/cc4968a994c54fe38c0855de15fcb15f
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