Gastric bypass surgery alters the regulation of food reward

胃绕道手术改变了食物奖励的调节

• 批准号: 7651742
• 负责人: ANDRAS HAJNAL
• 金额: $ 37.02万
• 依托单位: PENNSYLVANIA STATE UNIV HERSHEY MED CTR
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-04-01 至 2013-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7651742
• 关键词: Acetylcholine; Acute; Address; Animal Model; Appetite Regulation; Area; Basal Ganglia; Behavior; Behavioral; Biological Assay; Body Weight; Body Weight decreased; Brain; Caloric Restriction; Cessation of life; Chronic; Clinical; DRD2 gene; Data; Dependence; Desire for food; Development; Diet; Dopamine; Dopamine Antagonists; Dopamine Receptor; Eating; Ensure; Ensure Plus; Epidemic; Fatty acid glycerol esters; Feeding behaviors; Food; Food Preferences; Health; Incentives; Ingestion; Intake; Laboratories; Malabsorption Syndromes; Measures; Medial; Medical; Methods; Microdialysis; Modeling; Morbid Obesity; Morbidity - disease rate; Non-Insulin-Dependent Diabetes Mellitus; Nucleus Accumbens; Obesity; Operative Surgical Procedures; Patient Care; Patients; Peptide Signal Sequences; Peptide YY; Peptides; Phenotype; Positioning Attribute; Psychological reinforcement; Quantitative Autoradiography; Rattus; Regulation; Research; Resistance; Rewards; Role; Sampling; Satiation; Savory; Signal Transduction; Solutions; Structure; Sucrose; Synapses; System; Taste Perception; Techniques; Testing; United States; bariatric surgery; base; density; dopamine system; extracellular; feeding; glucagon-like peptide 1; hedonic; improved; increased appetite; motivated behavior; multidisciplinary; neurochemistry; neuromechanism; neuroregulation; novel; obesity treatment; preference; relating to nervous system; research study; response; success; weight maintenance

DESCRIPTION (provided by applicant): Gastric bypass surgery (GBS) is an exceptionally successful therapy for morbid obesity and type 2 diabetes. GBS patients typically lose 25-35% of total body weight, demonstrate improvements in medical co- morbidities, and sustained weight loss over fifteen years. Given the epidemic of obesity in the United States, an improved understanding of the mechanisms by which GBS causes and maintains weight loss represents an important area of research. Although GBS mechanically restricts food intake, it also appears to reduce appetite and the appeal of savory meals. However, it is unclear why the motivational system fails to drive patients to compensate for this massive weight loss with increased food intake and preference for palatable, calorie-dense foods - the normal homeostatic response. Elucidating this paradox would substantially improve our understanding of the regulatory mechanisms for eating and body weight. We are in a unique position to address this question based on an animal model of GBS demonstrating alterations in the central neural mechanisms regulating food reward functions developed in our laboratory. The current study proposes behavioral, pharmacological, neurochemical and histological studies in high energy/high fat diet- induced obesity rat models to test the hypothesis that GBS alters appetite and food preference functions resulting in changes to the food reward system. The experiments target the nucleus accumbens, a critical structure for reward, with focus on two major transmitters: dopamine and acetylcholine. We propose four specific aims to test different components of this hypothesis. The first aim will establish the behavioral effects addressing specific aspects of food reward (i.e., incentive, reinforcement and hedonic value), and compare dopamine involvement in these behaviors across weight reduction methods (i.e. caloric restriction vs. GBS). The second and third aims will mechanistically address the underlying dynamic and static (i.e. neuroadaptive) signaling mechanisms, respectively. Aim 4 will investigate if increased gut-brain peptide signaling contributes to improved food reward functions following GBS. We believe the proposed research has significant potential to impact patient care as it will improve our understanding of factors that could positively or negatively contribute to long-term weight maintenance and could elucidate new targets for developing less invasive treatments for obesity. Preliminary data suggest GBS beneficially impacts the regulation of appetite and food choice resulting in more dramatic, sustained weight loss than dieting. The current study examines how GBS, in contrast to dieting, influences the rewarding effects of palatable food in the brains of dietary obese rats. Information concerning essential changes in motivated behavior and underlying neural substrates produced by GBS could assist in the development of effective non-surgical approaches to obesity treatment.

描述（由申请人提供）：胃旁路手术（GBS）是病态肥胖和2型糖尿病的一种非常成功的治疗方法。GBS患者通常减轻总体重的25-35%，表现出医学共病的改善，并且在十五年内持续减轻体重。鉴于肥胖症在美国的流行，对GBS引起和维持体重减轻的机制的进一步理解代表了一个重要的研究领域。虽然GBS机械地限制了食物的摄入，但它似乎也会降低食欲和美味佳肴的吸引力。然而，目前还不清楚为什么激励系统不能驱使患者通过增加食物摄入和偏好可口的、热量密集的食物来补偿这种巨大的体重减轻--这是正常的自我平衡反应。阐明这一悖论将大大提高我们对饮食和体重调节机制的理解。我们在一个独特的位置，以解决这个问题的基础上，GBS的动物模型证明在我们的实验室开发的调节食物奖励功能的中枢神经机制的改变。目前的研究提出了在高能量/高脂肪饮食诱导的肥胖大鼠模型中进行行为学、药理学、神经化学和组织学研究，以检验GBS改变食欲和食物偏好功能从而导致食物奖励系统改变的假设。实验的目标是丘脑核，这是奖励的关键结构，重点是两个主要的递质：多巴胺和乙酰胆碱。我们提出了四个具体的目标来测试这个假设的不同组成部分。第一个目标将建立针对食物奖励的特定方面的行为效应（即，激励，强化和享乐价值），并比较多巴胺参与这些行为的减肥方法（即热量限制与GBS）。第二个和第三个目标将分别机械地解决潜在的动态和静态（即神经适应性）信号机制。目的4将研究肠脑肽信号的增加是否有助于改善GBS后的食物奖励功能。我们相信，这项拟议中的研究具有影响患者护理的巨大潜力，因为它将提高我们对可能对长期体重维持产生积极或消极影响的因素的理解，并可能阐明开发微创肥胖治疗方法的新目标。初步数据表明，GBS有益地影响食欲和食物选择的调节，导致比节食更显著，持续的体重减轻。目前的研究探讨了GBS如何与节食形成对比，影响饮食性肥胖大鼠大脑中可口食物的奖励效应。有关GBS产生的动机行为和潜在神经基质的基本变化的信息可以帮助开发有效的非手术治疗肥胖的方法。