| Literature DB >> 28683287 |
Celine E Riera1, Eva Tsaousidou2, Jonathan Halloran3, Patricia Follett4, Oliver Hahn5, Mafalda M A Pereira6, Linda Engström Ruud6, Jens Alber6, Kevin Tharp7, Courtney M Anderson7, Hella Brönneke6, Brigitte Hampel6, Carlos Daniel de Magalhaes Filho4, Andreas Stahl7, Jens C Brüning8, Andrew Dillin9.
Abstract
Olfactory inputs help coordinate food appreciation and selection, but their role in systemic physiology and energy balance is poorly understood. Here we demonstrate that mice upon conditional ablation of mature olfactory sensory neurons (OSNs) are resistant to diet-induced obesity accompanied by increased thermogenesis in brown and inguinal fat depots. Acute loss of smell perception after obesity onset not only abrogated further weight gain but also improved fat mass and insulin resistance. Reduced olfactory input stimulates sympathetic nerve activity, resulting in activation of β-adrenergic receptors on white and brown adipocytes to promote lipolysis. Conversely, conditional ablation of the IGF1 receptor in OSNs enhances olfactory performance in mice and leads to increased adiposity and insulin resistance. These findings unravel a new bidirectional function for the olfactory system in controlling energy homeostasis in response to sensory and hormonal signals.Entities:
Keywords: diet-induced obesity; energy balance; hyperosmia; hyposmia; insulin resistance; insulin-like growth factor 1 receptor; lipolysis; olfactory sensory neuron; thermogenesis
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Year: 2017 PMID: 28683287 DOI: 10.1016/j.cmet.2017.06.015
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287