食欲
热量理论
下丘脑
肥胖
肽YY
人口
胰高血糖素样肽-1
生物
神经科学
内分泌学
内科学
医学
受体
神经肽
神经肽Y受体
糖尿病
环境卫生
2型糖尿病
作者
Chia Li,Jovana Navarrete,Jing Liang-Guallpa,Chunxia Lü,Samuel C Funderburk,Rui B. Chang,Stephen D. Liberles,David P. Olson,Michael J. Krashes
出处
期刊:Cell Metabolism
[Cell Press]
日期:2018-11-21
卷期号:29 (3): 681-694.e5
被引量:123
标识
DOI:10.1016/j.cmet.2018.10.016
摘要
Summary Understanding the neural framework behind appetite control is fundamental to developing effective therapies to combat the obesity epidemic. The paraventricular hypothalamus (PVH) is critical for appetite regulation, yet, the real-time, physiological response properties of PVH neurons to nutrients are unknown. Using a combination of fiber photometry, electrophysiology, immunohistochemistry, and neural manipulation strategies, we determined the population dynamics of four molecularly delineated PVH subsets implicated in feeding behavior: glucagon-like peptide 1 receptor (PVHGlp1r), melanocortin-4 receptor (PVHMc4r), oxytocin (PVHOxt), and corticotropin-releasing hormone (PVHCrh). We identified both calorie- and state-dependent sustained activity increases and decreases in PVHGlp1r and PVHCrh populations, respectively, while observing transient bulk changes of PVHMc4r, but no response in PVHOxt, neurons to food. Furthermore, we highlight the role of PVHGlp1r neurons in orchestrating acute feeding behavior, independent of the anti-obesity drug liraglutide, and demonstrate the indispensability of PVHGlp1r and PVHMc4r, but not PVHOxt or PVHCrh neurons, in body weight maintenance.
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