Essential role of UCP1 modulating the central effects of thyroid hormones on energy balance
Autor: | Miguel López, Barbara Cannon, Carlos Dieguez, Noelia Martínez-Sánchez, Jan Nedergaard, Robert I. Csikasz, Mayte Alvarez-Crespo |
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Přispěvatelé: | Universidade de Santiago de Compostela. Centro de Investigación en Medicina Molecular e Enfermidades Crónicas |
Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
AMPK lcsh:Internal medicine endocrine system medicine.medical_specialty UCP1 endocrine system diseases Thyroid hormones Hypothalamus 030209 endocrinology & metabolism Brown adipose tissue 03 medical and health sciences 0302 clinical medicine Internal medicine medicine lcsh:RC31-1245 Molecular Biology Biological sciences business.industry Cell Biology 030104 developmental biology Endocrinology medicine.anatomical_structure Metabolic effects Original Article business |
Zdroj: | Molecular Metabolism Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela instname Molecular Metabolism, Vol 5, Iss 4, Pp 271-282 (2016) |
ISSN: | 2212-8778 |
DOI: | 10.1016/j.molmet.2016.01.008 |
Popis: | Objective Classically, metabolic effects of thyroid hormones (THs) have been considered to be peripherally mediated, i.e. different tissues in the body respond directly to thyroid hormones with an increased metabolism. An alternative view is that the metabolic effects are centrally regulated. We have examined here the degree to which prolonged, centrally infused triiodothyronine (T3) could in itself induce total body metabolic effects and the degree to which brown adipose tissue (BAT) thermogenesis was essential for such effects, by examining uncoupling protein 1 (UCP1) KO mice. Methods Wildtype and UPC1 KO mice were centrally-treated with T3 by using minipumps. Metabolic measurements were analyzed by indirect calorimetry and expression analysis by RT-PCR or western blot. BAT morphology and histology were studied by immunohistochemistry. Results We found that central T3-treatment led to reduced levels of hypothalamic AMP-activated protein kinase (AMPK) and elevated body temperature (0.7 °C). UCP1 was essential for the T3-induced increased rate of energy expenditure, which was only observable at thermoneutrality and notably only during the active phase, for the increased body weight loss, for the increased hypothalamic levels of neuropeptide Y (NPY) and agouti-related peptide (AgRP) and for the increased food intake induced by central T3-treatment. Prolonged central T3-treatment also led to recruitment of BAT and britening/beiging (“browning”) of inguinal white adipose tissue (iWAT). Conclusions We conclude that UCP1 is essential for mediation of the central effects of thyroid hormones on energy balance, and we suggest that similar UCP1-dependent effects may underlie central energy balance effects of other agents. Highlights • Central thyroid hormone (TH) increases brown adipose tissue (BAT) thermogenesis. • Central TH increases oxygen consumption and energy expenditure. • Central TH increases food intake. • Central TH promotes britening/beiging of white adipose tissue (WAT). • All these metabolic effects of central TH are lost in UCP1 knockout mice. |
Databáze: | OpenAIRE |
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