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Defining the role of BPA in promoting obesity and associated metabolic complicati

Defining the role of BPA in promoting obesity and associated metabolic complicati
定义 BPA 在促进肥胖和相关代谢并发症中的作用
批准号:
7942904
负责人:
ANDREW S GREENBERG
金额:
$81.42万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2012-12-31

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DESCRIPTION (provided by applicant): Obesity and its complications are a major health concern in the US and other industrialized nations. Based on the coincident increase in industrial chemical production and the meteoric rise in body weight in recent decades, a mechanistic connection between increased chemical exposure and the obesity 'epidemic' in industrialized nations has been postulated. Bisphenol A (BPA) is a ubiquitous estrogenic endocrine-disrupting chemical used in polycarbonate plastics and epoxy resins commonly found in food and beverage containers, and it is also present in countless other items that we come into contact with daily. BPA has been detected in the urine of 93% of the US population examined with the highest levels detected in the youngest cohort studied, children between 6 and 12 years of age. Data from our laboratory reveal a dose-dependent effect of perinatal BPA exposure on body weight and adiposity in CD-1 mice. However, neither the cause of BPA- associated weight gain nor the pathologic metabolic sequelae of this weight gain are currently elucidated. This proposal seeks funds to test the hypothesis that early life exposure to BPA promotes adult-onset obesity and hallmarks of the Metabolic Syndrome in CD-1 mice by altering energy metabolism in key metabolic tissues. Goals of the proposed research are to 1) determine the internal dose associated with BPA exposure levels that promote adult onset obesity and its complications, 2) determine the relative impact of perinatal vs. combined perinatal and prepubertal BPA exposure on risk for adult-onset obesity, 3) test the hypothesis that early BPA exposure exacerbates the obesitogenic and metabolic impacts of eating a 'western" diet (i.e., high in saturated fats), 4) test the hypothesis that BPA promotes obesity by altering relevant metabolic pathways in adipose tissue and skeletal muscle, and 5) identify BPA-associated transcriptional and epigenetic changes that underlie altered metabolic rate and/ or promote obesity-associated pathology in BPA-exposed mice. The proposed studies are highly collaborative, involving the integrated efforts of five investigators with distinct but complementary expertise in BPA, obesity and metabolism, diabetes, gene profiling, and epigenetics. Successful completion of the studies in this grant application will provide the first comprehensive and integrated study of how early life BPA exposure promotes adult obesity and its associated complications. These studies will identify the molecular, cell biological, and physiological mechanisms involved in the action of BPA on body weight and in so doing, these studies are likely to contribute to public health policy decisions concerning BPA. PUBLIC HEALTH RELEVANCE: Bisphenol A (BPA), is a ubiquitous chemical used in plastics and commonly found in food and beverage containers. Preliminary studies in our lab have revealed a dose- dependent increase in body weight in rodents exposed to BPA early in life. This proposal will further investigate the potential for BPA to promote obesity in adulthood.
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Research Training Program in Nutrition, Obesity and Metabolic Disorders
  • 批准号:
    10612728
  • 项目类别:
  • 资助金额:
    $16.53万
  • 财政年份:
    2020
  • 负责人:
    ANDREW S GREENBERG
  • 依托单位:
Research Training Program in Nutrition, Obesity and Metabolic Disorders
  • 批准号:
    10363666
  • 项目类别:
  • 资助金额:
    $16.73万
  • 财政年份:
    2020
  • 负责人:
    ANDREW S GREENBERG
  • 依托单位:
Role of ACSL5 in Intestinal and Liver Triacylglycerol Metabolism
  • 批准号:
    8697913
  • 项目类别:
  • 资助金额:
    $32.31万
  • 财政年份:
    2014
  • 负责人:
    ANDREW S GREENBERG
  • 依托单位:
Role of ACSL5 in Intestinal and Liver Triacylglycerol Metabolism
  • 批准号:
    9061681
  • 项目类别:
  • 资助金额:
    $30.29万
  • 财政年份:
    2014
  • 负责人:
    ANDREW S GREENBERG
  • 依托单位:
国内基金
海外基金
支链氨基酸代谢紊乱调控“Adipocytes - Macrophages Crosstalk”诱发2型糖尿病脂肪组织功能和结构障碍的作用及机制