The role of hypothalamic-sympathoneural-adipocyte axis in healthy aging

下丘脑-交感神经-脂肪细胞轴在健康衰老中的作用

• 批准号: 8669898
• 负责人: Lei Cao
• 金额: $ 31.56万
• 依托单位: OHIO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-06-15 至 2018-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8669898
• 关键词: Adipocytes; Adipose tissue; Age; Aging; Aging-Related Process; American; Animal Model; Animals; Biochemical; Biological Markers; Body Composition; Body Weight; Brain; Brain-Derived Neurotrophic Factor; Brown Fat; Caloric Restriction; Cardiovascular Diseases; Cause of Death; Cognitive; Complex; Data; Development; Diabetes Mellitus; Diagnosis; Diet; Disease; Eating; Energy Metabolism; Environment; Environmental Impact; Environmental Risk Factor; Face; Fatty acid glycerol esters; Gene Mutation; Gene Transfer; Genes; Genetic; Goals; Growth; Growth Factor; Health; Hormonal; Housing; Human; Hypothalamic structure; Immune; Incidence; Individual; Insulin; Insulin Receptor; Insulin-Like Growth Factor I; Internet; Intervention; Knockout Mice; Knowledge; Leptin; Life; Life Expectancy; Long-Term Effects; Longevity; Longitudinal Studies; Malignant Neoplasms; Malnutrition; Mediating; Mental Health; Metabolism; MicroRNAs; Modeling; Monkeys; Mus; Nerve Degeneration; Nutrient; Obesity; Organ; Organism; Phenotype; Physiological; Play; Prevention; Process; Production; Quality of life; Research; Resistance; Rest; Role; Signal Pathway; Testing; Therapeutic Intervention; Transgenic Mice; Treatment Efficacy; United States; Work; Yeasts; adiponectin; age related; body system; combat; db/db mouse; disability; environmental enrichment for laboratory animals; environmental intervention; food shortage; gene therapy; healthy aging; immune function; improved; inflammatory marker; insight; insulin sensitivity; interdisciplinary approach; lifestyle factors; middle age; novel; overexpression; pre-clinical; prevent; public health relevance; research study; senescence; social; tumor growth

DESCRIPTION (provided by applicant): The face of aging in the United States is changing dramatically with the projection of 70 million Americans age 65 or older in the next 25 years. As life expectancy increases, the incidence of diseases such as cancer, cardiovascular disorders and neurodegeneration rises. It is vital, therefore, that we understand more about the dynamics of aging, how they interact with various environmental and lifestyle factors, and the connections between disease processes and aging in order to develop more effective ways to prevent, diagnose and treat age-related diseases. Our recent work on environmental enrichment, a housing environment boosting mental health, has revealed a novel phenotype characterized by a robust reduction in adiposity, resistance to diet-induced obesity, enhanced insulin sensitivity, enhanced immune function, and inhibition in cancer growth. Moreover the anti-cancer and anti-obesity phenotypes are mediated by the activation of a brain-fat axis, the hypothalamic-sympathoneural-adipocyte (HSA) axis. In this regulatory network, the key component in the brain is BDNF, which is highly responsive to activity and the environment, and it controls the HSA activity and thereby regulates fat. Fat, as the principal responsive organ in the periphery, subsequently influences multiple organ systems. The key features of activation of the HSA axis are shared by those environmental and genetic factors known to increase lifespan such as calorie restriction and fat-specific insulin receptor knockout mice. However the role of the HSA axis in the aging process has not been investigated. The long-term goal of this study is to understand how a physically, mentally, and socially active environment may influence healthspan and lifespan and to define the underlying mechanisms. Specifically, we propose to utilize a multidisciplinary approach to characterize the role of HSA axis in healthy aging. We plan to investigate the effects of short-term activation of the HSA axis via environmental intervention or gene transfer of BDNF on aging markers (adiposity, metabolism, hormonal and growth factor alteration, insulin sensitivity, and immune function), as well as the effects of long term HSA axis activation on healthspan and lifespan in both normal animals and obesity and diabetes models. Accomplishing the proposed experiments will assess the role of this newly characterized brain-fat axis in healthy aging and the effects of manipulating a single gene in the brain to regulate healthspan, and furthermore may reveal potential targets for the prevention and treatment of age-related diseases.

描述（由申请人提供）：在未来25年内，美国衰老面孔正在发生巨大变化，有7000万美国人65岁以上。随着预期寿命的增加，癌症，心血管疾病和神经退行性疾病等疾病的发生率会增加。因此，至关重要的是，我们更多地了解衰老动态，它们如何与各种环境和生活方式因素相互作用以及疾病过程与衰老之间的联系，以开发更有效的方法来预防，诊断和治疗与年龄相关的疾病。我们最近在环境富集方面的工作是一种增强心理健康的住房环境，揭示了一种新型的表型，其特征是肥胖，对饮食诱导的肥胖症的耐药性，增强的胰岛素敏感性，增强的免疫功能和抑制癌症生长。此外，抗癌和抗肥胖表型是由脑脂肪轴激活，下丘脑 - 同情 - 同情辅助细胞（HSA）轴介导的。在这个监管网络中，大脑中的关键组成部分是BDNF，它对活动和环境反应很高，它控制了HSA活性并因此调节脂肪。作为外围的主要反应器官，脂肪随后会影响多器官系统。 HSA轴激活的关键特征是由已知增加寿命（例如卡路里限制和脂肪特异性胰岛素受体敲除小鼠）的环境和遗传因素共享的。但是，尚未研究HSA轴在衰老过程中的作用。这项研究的长期目标是了解身体，精神和社会活动环境如何影响健康范围和寿命并定义基本机制。具体而言，我们建议利用一种多学科方法来表征HSA轴在健康衰老中的作用。我们计划通过环境干预或BDNF的基因转移对HSA轴的短期激活对衰老标记的影响（肥胖，代谢，激素和生长因子改变，胰岛素敏感性和免疫功能）以及长期的影响 正常动物和肥胖和糖尿病模型中的HSA轴术语HSA轴激活。完成提出的实验将评估这种新表征的脑脂肪轴在健康衰老中的作用，以及在大脑中操纵单个基因以调节健康范围的影响，此外，可能揭示了预防和治疗与年龄相关疾病的潜在目标。