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Vitamin E Requirements in Women,Obese Women and Diabetic Obese Women

女性、肥胖女性和糖尿病肥胖女性的维生素 E 需求量

基本信息

批准号：
8667425
负责人：
MARET G TRABER
金额：
$ 31.48万
依托单位：
OREGON STATE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2010
资助国家：
美国
起止时间：
2010-06-01 至 2017-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8667425
关键词：
Address Age American Antioxidants Ascorbic Acid Biological Availability Biological Markers Body Size Body fat Chronic Disease Clinical Research Collaborations Data Deuterium Diabetes Mellitus Diet Dose Drug Formulations Drug Kinetics Epidemiologic Studies Equipment Extramural Activities Fatty acid glycerol esters Food Funding Heart Diseases Human Human body Inflammation Intake Intravenous Kinetics Label Laboratories Lipid Peroxidation Lipids Measurement Measures Methods Modeling Normal tissue morphology Obesity Oral Oxidative Stress Pilot Projects Plasma Postmenopause Research Personnel Sampling Sampling Studies Solubility Stable Isotope Labeling Study Subject Techniques Tissues Tocopherols United States National Institutes of Health Vitamin E Weight Woman Work absorption adverse outcome alpha Tocopherol base cardiovascular disorder risk diabetic disorder risk evidence base experience high risk insight intravenous administration mathematical model men nutrition oxidation peroxidation response

项目摘要

DESCRIPTION (provided by applicant): Epidemiologic studies suggest that chronic disease risk can be reduced by a lifetime of consuming higher dietary vitamin E intakes. However, more than 90% of Americans consume less than 40% of the 15 mg (22 IU) 1-tocopherol recommended daily by the Food and Nutrition Board. Is the usual 6 mg consumed sufficient? The necessary evidence-based data are currently unavailable to answer this question; the proposed study seeks to fill this gap. Our previous studies show that oxidative stress in humans more rapidly depletes plasma vitamin E and sufficient vitamin C intake counters the accelerated vitamin E depletion. The proposed studies will use optimized methods for pharmacokinetic measurements to address how much vitamin E is needed by the body in response to either or both oxidative stress or depleted vitamin C status. This study is unique in that it is a collaboration between NIH intra- and extramural investigators. The proposed studies will be carried out with Dr. Mark Levine and his group at the NIH in the Clinical Research Center, who have extensive experience in measuring vitamin C pharmacokinetics and bioavailability. Our laboratory has the necessary expertise, experience and equipment to measure the low concentrations of stable isotope labeled vitamin E, its metabolites, and peroxidation biomarkers. This proposal seeks funding for the Traber group for the analysis of deuterium-labeled alpha-tocopherol samples and lipid peroxidation biomarkers. Specific Aim 1. Determine alpha-tocopherol pharmacokinetics in normal weight women. Vitamin E kinetic studies will allow determination of key measures of vitamin E status including fractional absorption, rates of delivery to tissues, and whole body efflux. Pilot Study 1: Determine the optimal fat content in the accompanying meal necessary to optimize alpha-tocopherol absorption. Pilot Study 2: Determine the optimal alpha-tocopherol dose for turnover kinetics. Specific Aims 2 & 3. Determine alpha-tocopherol pharmacokinetics before and after vitamin C depletion in normal-weight women, obese women and obese women with diabetes. Our working hypothesis is that alpha-tocopherol concentrations are maintained by adequate vitamin C (ascorbic acid) concentrations. Thus, the delivery of alpha-tocopherol to the target tissues will be increased if ascorbic acid is limiting. Furthermore to maintain tissue alpha-tocopherol concentrations, rates of delivery of alpha-tocopherol increase due to increased turnover resulting from oxidative stress caused by obesity and from obesity with diabetes. The successful completion of these studies will provide essential key measures of alpha-tocopherol status, including fractional absorption, rates of delivery to tissues, and whole body efflux, for formulation of recommended daily intakes in healthy women, as well as women with conditions associated with increased oxidative stress.

描述（由申请人提供）：流行病学研究表明，终生摄入较高的膳食维生素E可降低慢性疾病的风险。然而，超过90%的美国人每天摄入的1-生育酚还不到食品和营养委员会建议的15毫克（22国际单位）的40%。通常的6毫克摄入量足够吗？目前还没有必要的循证数据来回答这个问题；拟议的研究试图填补这一空白。我们之前的研究表明，人体的氧化应激会更快地消耗血浆中的维生素E，而摄入足够的维生素C可以抵消维生素E的加速消耗。拟议的研究将使用优化的药代动力学测量方法，以确定身体在应对氧化应激或维生素C耗尽状态时需要多少维生素E。这项研究的独特之处在于它是NIH内部和外部研究人员之间的合作。拟议的研究将由美国国立卫生研究院临床研究中心的Mark Levine博士和他的团队进行，他们在测量维生素C的药代动力学和生物利用度方面拥有丰富的经验。我们的实验室拥有必要的专业知识、经验和设备来测量低浓度的稳定同位素标记的维生素E、其代谢物和过氧化生物标志物。该提案为Traber小组寻求资金，用于分析氘标记的α -生育酚样品和脂质过氧化生物标志物。具体目标测定正常体重妇女α -生育酚的药代动力学。维生素E动力学研究将有助于确定维生素E状态的关键指标，包括部分吸收、组织输送率和全身外排。初步研究1：确定随餐中优化α -生育酚吸收所需的最佳脂肪含量。初步研究2：确定周转动力学的最佳α -生育酚剂量。具体目标2和3。测定正常体重妇女、肥胖妇女和肥胖妇女糖尿病患者维生素C消耗前后α -生育酚药代动力学。我们的工作假设是，α -生育酚浓度由足够的维生素C（抗坏血酸）浓度维持。因此，如果抗坏血酸受到限制，α -生育酚向靶组织的输送将会增加。此外，为了维持组织α -生育酚浓度，由于肥胖和肥胖合并糖尿病引起的氧化应激引起的新陈代谢增加，α -生育酚的递送率增加。这些研究的成功完成将提供α -生育酚状态的基本关键指标，包括部分吸收、输送到组织的速率和全身外排，为健康妇女以及与氧化应激增加有关的妇女制定推荐的每日摄入量。