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DESCRIPTION (provided by applicant): Obesity and overweight affects most Americans, but there are some who resist obesity, just as some animals resist obesity. Animal and human studies indicate that spontaneous physical activity (SPA), which generates nonexercise activity thermogenesis (NEAT), is an important defense against weight gain. Brain mechanisms control the level SPA, and the NEAT so generated, but the specifics are undefined. We propose that hypothalamic orexin A (OxA) is an important part of the SPA regulatory pathway, and that sensitivity to OxA signals enhancing SPA and NEAT helps determine propensity for obesity. The objectives of this application are to test the following hypotheses: (1) elevated OxA mediated SPA protects against weight gain and (2) increased OxA-mediated SPA in obesity resistant (OR) rats results from increased orexin receptor expression. Our long-range goal is to use knowledge of SPA and NEAT regulatory pathways to guide therapeutic interventions on these mechanisms among obese humans. We plan 3 aims: Aim 1) Characterize orexin neuron subpopulations important to SPA. A) Are there strain differences in orexin message and peptide in subpopulations of orexin neurons? B) Does destruction of subpopulations of orexin neurons affect SPA? Aim 2) Determine importance of OxA-mediated SPA to weight gain. A) Does reduced OxA action in rLH of OR rats reduce resistance to weight gain? B) Does SPA induced by high dose OxA stimulation of rLH reduce weight gain in OP rats? Aim 3) Verify that increased orexin sensitivity in OR rats is due to increased orexin receptor expression. A) Is orexin receptor number increased in OR compared to OP rats? B) Is c-fos activation in rLH orexin receptor bearing neurons higher in OR than OP rats? C) Does reducing orexin receptor bearing neurons in rLH of OR rats enhance weight gain? A greater understanding of brain orexin and its relationship to SPA in obesity will fill a large gap in knowledge of centrally mediated SPA and NEAT, and its importance to obesity resistance. PUBLIC HEALTH RELEVANCE The current proposal is aimed at understanding the role of a specific brain pathway that controls physical activity, which is important to body weight regulation. Obesity is a major health problem affecting at least one third of the U.S. population, and is a risk factor for several diseases, including heart disease, diabetes and several types of cancer. Underlying part of the problem is disordered regulation of physical activity, and a better understanding of the brain pathways important to this is necessary in developing treatments for obesity.
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Effect of acute and chronic caloric restriction and metabolic glucoprivation on spontaneous physical activity in obesity-prone and obesity-resistant rats.
急性和慢性热量限制和代谢性葡萄糖缺乏对肥胖倾向和肥胖抵抗大鼠自发体力活动的影响。
DOI: 10.1152/ajpregu.90866.2008
发表时间: 2009
期刊: American journal of physiology. Regulatory, integrative and comparative physiology
影响因子: --
作者: [Teske,JA, Kotz,CM]
通讯作者: Kotz,CM
Role of spontaneous physical activity in prediction of susceptibility to activity based anorexia in male and female rats.
自发体力活动在预测雄性和雌性大鼠对活动性厌食症易感性中的作用。
DOI: 10.1016/j.physbeh.2014.06.001
发表时间: 2014
期刊: Physiology & behavior
影响因子: 2.9
作者: [Perez-Leighton,ClaudioE, Grace,Martha, Billington,CharlesJ, Kotz,CatherineM]
通讯作者: Kotz,CatherineM
DOI: 10.1007/s11154-013-9259-3
发表时间: 2013-12
期刊: Reviews in endocrine & metabolic disorders
影响因子: 8.2
作者: [Butterick TA, Billington CJ, Kotz CM, Nixon JP]
通讯作者: Nixon JP
Reducing the post weight-loss energy expenditure gap with orexin agonists
  • 批准号:
    10745184
  • 项目类别:
  • 资助金额:
    $73.1万
  • 财政年份:
    2023
  • 负责人:
    CATHERINE M KOTZ
  • 依托单位:
Orexin agonists as novel obesity therapeutics
  • 批准号:
    10655285
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2022
  • 负责人:
    CATHERINE M KOTZ
  • 依托单位:
Fisetin as a treatment for community-acquired pathogen susceptibility during aging, obesity and neurodegenerative diseases
  • 批准号:
    10610378
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2022
  • 负责人:
    CATHERINE M KOTZ
  • 依托单位:
Fisetin as a treatment for community-acquired pathogen susceptibility during aging, obesity and neurodegenerative diseases
  • 批准号:
    10425193
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2022
  • 负责人:
    CATHERINE M KOTZ
  • 依托单位:
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