| Autor: |
Julia Calzada-Wack, D. S. Froese, Johannes Beckers, Céline Bürer, G. T. Bommer, Jan Rozman, Andres Kaech, M. Forny, Daniel Hoces, J. P. Dewulf, Samuel E. Wuest, Stefan Kölker, M. Lucienne, Patrick Forny, Martin Irmler, Sven W. Sauer, Helmut Fuchs, Juan Antonio Aguilar-Pimentel, Matthias R. Baumgartner, F. Traversi, Birgit Rathkolb, Raffaele Gerlini, V. Gailus-Durner, M Hrabe de Angelis |
| Přispěvatelé: |
University of Zurich |
| Jazyk: |
němčina |
| Rok vydání: |
2021 |
| Předmět: |
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| Popis: |
Inherited disorders of mitochondrial metabolism, including isolated methylmalonic aciduria (MMAuria), present unique challenges to energetic homeostasis by disrupting energy producing pathways. To better understand global responses to energy shortage, we investigated a hemizygous mouse model of methylmalonyl-CoA mutase (Mmut) type MMAuria. We found Mmut mutant mice to have reduced appetite, energy expenditure and body mass compared to littermate controls, along with a relative reduction in lean mass but increase in fat mass. Brown adipose tissue showed a process of whitening, in line with lower body surface temperature and lesser ability to cope with cold challenge. Mutant mice had dysregulated plasma glucose, delayed glucose clearance and a lesser ability to regulate energy sources when switching from the fed to fasted state, while liver investigations indicated metabolite accumulation and altered expression of peroxisome proliferator-activated receptor and Fgf21-controlled pathways. Together, these indicate hypometabolism, energetic inflexibility and increased stores at the expense of active tissue as energy shortage consequences. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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