Diabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
Mouse Metabolism Core, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
Nat Neurosci. 2018 Nov;21(11):1530-1540. doi: 10.1038/s41593-018-0249-3. Epub 2018 Oct 22.
Bombesin-like receptor 3 (BRS3) is an orphan G-protein-coupled receptor that regulates energy homeostasis and heart rate. We report that acute activation of Brs3-expressing neurons in the dorsomedial hypothalamus (DMH) increased body temperature (Tb), brown adipose tissue temperature, energy expenditure, heart rate, and blood pressure, with no effect on food intake or physical activity. Conversely, activation of Brs3 neurons in the paraventricular nucleus of the hypothalamus had no effect on Tb or energy expenditure, but suppressed food intake. Inhibition of DMH neurons decreased Tb and energy expenditure, suggesting a necessary role in Tb regulation. We found that the preoptic area provides major input (excitatory and inhibitory) to DMH neurons. Optogenetic stimulation of DMH projections to the raphe pallidus increased Tb. Thus, DMH→raphe pallidus neurons regulate Tb, energy expenditure, and heart rate, and Brs3 neurons in the paraventricular nucleus of the hypothalamus regulate food intake. Brs3 expression is a useful marker for delineating energy metabolism regulatory circuitry.
Bombesin 样受体 3(BRS3)是一种孤儿 G 蛋白偶联受体,它可以调节能量平衡和心率。我们的研究表明,急性激活下丘脑背内侧核(DMH)中表达 BRS3 的神经元可以升高体温(Tb)、棕色脂肪组织温度、能量消耗、心率和血压,而对食物摄入或体力活动没有影响。相反,激活下丘脑室旁核中的 BRS3 神经元对 Tb 或能量消耗没有影响,但会抑制食物摄入。DMH 神经元的抑制会降低 Tb 和能量消耗,这表明其在 Tb 调节中起必要作用。我们发现,视前区为 DMH 神经元提供了主要的输入(兴奋性和抑制性)。DMH 投射到苍白球的光遗传学刺激增加了 Tb。因此,DMH→苍白球神经元调节 Tb、能量消耗和心率,而下丘脑室旁核中的 BRS3 神经元调节食物摄入。BRS3 的表达是描绘能量代谢调节回路的有用标志物。