JCI Insight · 2017 · 34 citations · 26 references
Life SciencesBiochemistryNutritional SciencesMetabolic PhysiologyMetabolic RegulationMetabolismAdipose TissueFatty Acid MetabolismLipid MetabolismMetabolic DiseaseMetabolic DisordersMetabolic SignalingAdipose Tissue BrowningAdipose Tissue Gene Expression ResponsesBrown Adipose Tissue ActivationBrown Adipose Tissue MetabolismGene Knockdown MechanismsObesity MetabolismVisceral Fat AccumulationWhite Adipose Tissue Biology
Visceral fat is considered the genuine and harmful white adipose tissue (WAT) that is associated to development of metabolic disorders, cardiovascular disease, and cancer. Here, we present a new concept to turn the harmful visceral fat into a beneficial energy consumption depot, which is beneficial for improvement of metabolic dysfunctions in obese mice. We show that low temperature–dependent browning of visceral fat caused decreased adipose weight, total body weight, and body mass index, despite increased food intake. In high-fat diet–fed mice, low temperature exposure improved browning of visceral fat, global metabolism via nonshivering thermogenesis, insulin sensitivity, and hepatic steatosis. Genome-wide expression profiling showed upregulation of WAT browning–related genes including Cidea and Dio2 . Conversely, Prdm16 was unchanged in healthy mice or was downregulated in obese mice. Surgical removal of visceral fat and genetic knockdown of UCP1 in epididymal fat largely ablated low temperature–increased global thermogenesis and resulted in the death of most mice. Thus, browning of visceral fat may be a compensatory heating mechanism that could provide a novel therapeutic strategy for treating visceral fat–associated obesity and diabetes.
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Beige Adipocytes Are a Distinct Type of Thermogenic Fat Cell in Mouse and Human
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PRDM16 controls a brown fat/skeletal muscle switch
Patrick Seale, Bryan C. Bjork, Wenli Yang et al. · Nature · 2008 · 2.3K citations · Full text
General and Abdominal Adiposity and Risk of Death in Europe
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