Dorsomedial Hypothalamic Signaling Pathways and Energy Balance

下丘脑背内侧信号通路和能量平衡

• 批准号: 9187010
• 负责人: SHENG BI
• 金额: $ 36.45万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-12-01 至 2019-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9187010
• 关键词: Adipose tissue; Adolescent; Adult; Affect; Agonist; Appetite Stimulants; Area; Body Temperature; Body Weight; Body Weight decreased; Brain; Brain Stem; Brown Fat; Calories; Cardiovascular Diseases; Cell Nucleus; Child; Cholecystokinin; Cholera; Comorbidity; Corticotropin-Releasing Hormone; Data; Dependovirus; Development; Diet; Disease; Eating; Energy Intake; Energy Metabolism; Epidemic; FOS gene; Fatty acid glycerol esters; Food Energy; Gene Proteins; Goals; Green Fluorescent Proteins; High Fat Diet; Homeostasis; Hyperphagia; Hypothalamic structure; Intervention; Lateral Hypothalamic Area; Lesion; Life; Link; Lipids; Mediating; Microinjections; Neural Pathways; Neurons; Non-Insulin-Dependent Diabetes Mellitus; Nucleus solitarius; Obesity; Overweight; Oxytocin; Pathway interactions; Peripheral; Pharmacology; Physiologic Thermoregulation; Physiological; Pilot Projects; Play; Prevention; Public Health; Rattus; Regulation; Renilla; Research Project Grants; Role; Satiation; Signal Pathway; Signal Transduction; Site; Structure of nucleus infundibularis hypothalami; System; Temperature; Thermogenesis; Tracer; United States; Weight; adeno-associated viral vector; adipocyte differentiation; aged; base; combat; energy balance; experimental study; feeding; gastrointestinal; insight; knock-down; neuromechanism; neuropeptide Y; neuroregulation; neurotransmission; novel; novel strategies; obesity treatment; overexpression; paraventricular nucleus; public health relevance; receptor; relating to nervous system; response; success

 DESCRIPTION (provided by applicant): Obesity has become a worldwide epidemic and causes serious public health problems. Now about one third of adults and approximately 17% of children and adolescents aged 2-19 years are obese in the United States. Obesity has been linked to life-threatening diseases such as type 2 diabetes and cardiovascular disease. Our strategies for tackling obesity epidemic are largely inadequate. Theoretically, obesity could be controlled by increasing energy expenditure and controlling diet, but the success rates with these approaches remain poor. A better understanding of the control of energy balance will facilitate our capability for overcoming this problem. Growing data from this and other labs have underscored specific roles for the dorsomedial hypothalamus (DMH) in the controls of both food intake and energy expenditure. The overall goal of this research project is to more comprehensively unravel the neural bases of these actions. We have found that overexpression of orexigenic neuropeptide Y (NPY) in the DMH causes hyperphagia and obesity, whereas DMH NPY knockdown results in decreased food intake, brown adipocyte development in white fat, increases in brown fat thermogenesis and body energy expenditure, and weight loss. These findings establish critical roles for DMH NPY in the controls of food intake and energy expenditure, but the underlying neural pathways remain undetermined. This project is aimed at elaborating such pathways by the following two Specific Aims. In Aim 1, we propose experiments to characterize the neural pathways underlying the feeding effects of DMH NPY by assessing whether: (1) DMH NPY descending signals modulate the activity of brainstem neurons innervated by vagal afferents to control food intake, and (2), DMH NPY innervates anorexigenic neurons (such as oxytocin) in the paraventricular nucleus to modulate food intake. Experiments proposed in Aim 2 are to ascertain the neural mechanisms underlying the thermogenic effects of DMH NPY. We will first determine the importance of DMH NPY in thermoregulation and characterize the underlying neuronal signaling. Given the presence of corticotrophin-releasing factor (CRF)-expressing neurons in the thermogenic area of the DMH, the second part of Aim 2 is to assess whether DMH CRF mediates DMH NPY modulation of thermogenesis and to evaluate a potential thermogenic function of DMH CRF. We will apply multiple approaches including an adeno-associated virus system to alter NPY and CRF expression in the DMH, pharmacological and physiological interventions of gastrointestinal signaling, neuroanatomical analyses using c-Fos as a neuronal activation marker and green fluorescent protein and cholera nontoxic B subunit for tracing neuronal projections, interfering neural signaling with central microinjections of receptor-specific antagonists or agonists, diet or cold challenges, and evaluating neural signaling at both gene and protein levels, to achieve these Aims. Overall, the results from this project will not only significantly advance our understanding of the central control of energy balance, but also provide the neural bases for the development of novel strategies for combatting obesity and its comorbidities.

 描述（由申请人提供）：肥胖已成为一种世界性的流行病，并导致严重的公共卫生问题。现在，在美国，大约三分之一的成年人和大约17%的2-19岁的儿童和青少年肥胖。肥胖与危及生命的疾病有关，如2型糖尿病和心血管疾病。我们应对肥胖流行病的策略在很大程度上是不够的。从理论上讲，肥胖可以通过增加能量消耗和控制饮食来控制，但这些方法的成功率仍然很低。更好地理解能量平衡的控制将有助于我们克服这个问题的能力。来自这个实验室和其他实验室的越来越多的数据强调了背内侧下丘脑（DMH）在控制食物摄入和能量消耗方面的特定作用。这个研究项目的总体目标是更全面地揭示这些行为的神经基础。我们已经发现，在DMH中的食欲神经肽Y（NPY）的过表达引起食欲过盛和肥胖，而DMH NPY敲低导致食物摄入减少、白色脂肪中的棕色脂肪细胞发育、棕色脂肪产热和身体能量消耗增加以及体重减轻。这些发现确立了DMH NPY在控制食物摄入和能量消耗中的关键作用，但潜在的神经通路仍不确定。该项目旨在通过以下两个具体目标详细阐述这些途径。在目的1中，我们提出实验来表征DMH NPY的摄食效应的神经通路，通过评估是否：（1）DMH NPY下行信号调节由迷走神经传入支配的脑干神经元的活动以控制食物摄入，以及（2）DMH NPY支配室旁核中的催产素神经元（如催产素）以调节食物摄入。目的2中提出的实验是为了确定DMH NPY产热作用的神经机制。我们将首先确定DMH NPY在体温调节中的重要性，并表征潜在的神经元信号传导。鉴于促肾上腺皮质激素释放因子（CRF）的存在下，表达神经元的产热区的DMH，第二部分的目的2是评估是否DMH CRF介导DMH神经肽Y调节产热和评估潜在的产热功能DMH CRF。我们将应用多种方法，包括腺相关病毒系统改变DMH中NPY和CRF的表达，胃肠信号的药理学和生理学干预，使用c-Fos作为神经元活化标记物和绿色荧光蛋白和霍乱无毒B亚基追踪神经元投射的神经解剖学分析，通过中枢显微注射受体特异性拮抗剂或激动剂干扰神经信号，饮食或 冷挑战，并在基因和蛋白质水平上评估神经信号，以实现这些目标。总的来说，该项目的结果不仅将显着提高我们对能量平衡的中央控制的理解，而且还为开发对抗肥胖及其合并症的新策略提供了神经基础。