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Nat Commun ; 11(1): 1730, 2020 04 07.
Article in English | MEDLINE | ID: mdl-32265443

ABSTRACT

Cold stimuli and the subsequent activation of ß-adrenergic receptor (ß-AR) potently stimulate adipose tissue thermogenesis and increase whole-body energy expenditure. However, systemic activation of the ß3-AR pathway inevitably increases blood pressure, a significant risk factor for cardiovascular disease, and, thus, limits its application for the treatment of obesity. To activate fat thermogenesis under tight spatiotemporal control without external stimuli, here, we report an implantable wireless optogenetic device that bypasses the ß-AR pathway and triggers Ca2+ cycling selectively in adipocytes. The wireless optogenetics stimulation in the subcutaneous adipose tissue potently activates Ca2+ cycling fat thermogenesis and increases whole-body energy expenditure without cold stimuli. Significantly, the light-induced fat thermogenesis was sufficient to protect mice from diet-induced body-weight gain. The present study provides the first proof-of-concept that fat-specific cold mimetics via activating non-canonical thermogenesis protect against obesity.


Subject(s)
Adipocytes/metabolism , Adipose Tissue/metabolism , Channelrhodopsins/metabolism , Obesity/therapy , Optogenetics/instrumentation , Sarcoplasmic Reticulum Calcium-Transporting ATPases/metabolism , Thermogenesis/radiation effects , Adipocytes/radiation effects , Adipose Tissue/radiation effects , Animals , Body Weight/physiology , Body Weight/radiation effects , Calcium/metabolism , Cells, Cultured , Channelrhodopsins/radiation effects , Channelrhodopsins/therapeutic use , Diet , Energy Metabolism/radiation effects , Locomotion , Male , Mice , Mice, Knockout , Obesity/metabolism , Optogenetics/methods , Oxygen Consumption , Receptors, Adrenergic, beta/metabolism , Sarcoplasmic Reticulum Calcium-Transporting ATPases/genetics , Thermogenesis/physiology
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