Hameed Saira, Patterson Michael, Dhillo Waljit S, Rahman Sofia A, Ma Yue, Holton Christopher, Gogakos Apostolos, Yeo Giles S H, Lam Brian Y H, Polex-Wolf Joseph, Fenske Wiebke, Bell Jimmy, Anastasovska Jelena, Samarut Jacques, Bloom Stephen R, Bassett J H Duncan, Williams Graham R, Gardiner James V
Section of Investigative Medicine, Division of Diabetes, Endocrinology and Metabolism, Imperial College London, London W12 0NN, UK.
Section of Investigative Medicine, Division of Diabetes, Endocrinology and Metabolism, Imperial College London, London W12 0NN, UK; Department of Life Sciences, University of Roehampton, London SW15 4JD, UK.
Cell Rep. 2017 Jun 13;19(11):2202-2209. doi: 10.1016/j.celrep.2017.05.066.
The obesity epidemic is a significant global health issue. Improved understanding of the mechanisms that regulate appetite and body weight will provide the rationale for the design of anti-obesity therapies. Thyroid hormones play a key role in metabolic homeostasis through their interaction with thyroid hormone receptors (TRs), which function as ligand-inducible transcription factors. The TR-beta isoform (TRβ) is expressed in the ventromedial hypothalamus (VMH), a brain area important for control of energy homeostasis. Here, we report that selective knockdown of TRβ in the VMH of adult mice results in severe obesity due to hyperphagia and reduced energy expenditure. The observed increase in body weight is of a similar magnitude to murine models of the most extreme forms of monogenic obesity. These data identify TRβ in the VMH as a major physiological regulator of food intake and energy homeostasis.
肥胖流行是一个重大的全球健康问题。对调节食欲和体重的机制有更深入的了解将为抗肥胖疗法的设计提供理论依据。甲状腺激素通过与甲状腺激素受体(TRs)相互作用在代谢稳态中发挥关键作用,TRs作为配体诱导型转录因子发挥作用。TR-β亚型(TRβ)在下丘脑腹内侧核(VMH)中表达,VMH是控制能量稳态的重要脑区。在此,我们报告成年小鼠VMH中TRβ的选择性敲低会导致由于摄食过多和能量消耗减少而出现严重肥胖。观察到的体重增加幅度与最极端形式的单基因肥胖小鼠模型相似。这些数据表明VMH中的TRβ是食物摄入和能量稳态的主要生理调节因子。