Thyroid hormone status defines brown adipose tissue activity and browning of white adipose tissues in mice

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作者
Juliane Weiner
Mathias Kranz
Nora Klöting
Anne Kunath
Karen Steinhoff
Eddy Rijntjes
Josef Köhrle
Vilia Zeisig
Mohammed Hankir
Claudia Gebhardt
Winnie Deuther-Conrad
John T. Heiker
Susan Kralisch
Michael Stumvoll
Matthias Blüher
Osama Sabri
Swen Hesse
Peter Brust
Anke Tönjes
Kerstin Krause
机构
[1] University Hospital,Department of Endocrinology and Nephrology
[2] Helmholtz-Zentrum Dresden-Rossendorf,Department of Neuroradiopharmaceuticals
[3] Institute of Radiopharmaceutical Cancer Research,Department of Nuclear Medicine
[4] Research Site Leipzig,undefined
[5] University of Leipzig,undefined
[6] IFB Adiposity Diseases,undefined
[7] German Center for Diabetes Research (DZD),undefined
[8] University Hospital,undefined
[9] Institute of Experimental Endocrinology,undefined
[10] Charité University Hospital,undefined
来源
Scientific Reports | / 6卷
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摘要
The present study aimed to determine the effect of thyroid hormone dysfunction on brown adipose tissue activity and white adipose tissue browning in mice. Twenty randomized female C57BL/6NTac mice per treatment group housed at room temperature were rendered hypothyroid or hyperthyroid. In-vivo small animal 18F-FDG PET/MRI was performed to determine the effects of hypo- and hyperthyroidism on BAT mass and BAT activity. Ex-vivo14C-acetate loading assay and assessment of thermogenic gene and protein expression permitted analysis of oxidative and thermogenic capacities of WAT and BAT of eu-, hyper and hypothyroid mice. 18F-FDG PET/MRI revealed a lack of brown adipose tissue activity in hypothyroid mice, whereas hyperthyroid mice displayed increased BAT mass alongside enhanced 18F-FDG uptake. In white adipose tissue of both, hyper- and hypothyroid mice, we found a significant induction of thermogenic genes together with multilocular adipocytes expressing UCP1. Taken together, these results suggest that both the hyperthyroid and hypothyroid state stimulate WAT thermogenesis most likely as a consequence of enhanced adrenergic signaling or compensation for impaired BAT function, respectively.
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