THE ROLE OF DIETARY CARBOHYDRATE ON MATERNAL FAT MOBILIZATION AND OXIDATION D

膳食碳水化合物对母体脂肪动员和氧化的作用 D

基本信息

  • 批准号:
    8166688
  • 负责人:
  • 金额:
    $ 0.92万
  • 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
  • 起止时间:
    2009-12-01 至 2010-11-30
  • 项目状态:
    已结题

项目摘要

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Due to the increasing obesity risks, many lactating women are concerned about losing weight gained during pregnancy without adversely affecting their milk production. We have demonstrated previously that oral galactose which has low glycemic index compared to glucose, may provide a nutrient substrate that is converted to glucose, thus providing a substrate for lactose synthesis but not inhibit fat mobilization by increasing plasma glucose and insulin. The objective of this study is to determine the impact of a high (glucose) versus low (galactose) insulin stimulating oral carbohydrate meal on mobilization and oxidation of fat in post-partum and control women. We hypothesize that an isocaloric carbohydrate drink which does not stimulate insulin secretion, when compared to one which stimulates significant insulin secretion will promote fat mobilization and oxidation and will not affect on milk production in healthy lactating women. Should we demonstrate that the nature of the oral carbohydrate affects fatty acid mobilization and fat oxidation with no impact on lactose synthesis and milk production, we would have the scientific evidence to design a wider clinical trial of breast-feeding mothers who are desirous of losing weight while sustaining successful breast feeding. Hypothesis: Over a three day period, an isocaloric carbohydrate drink which does not stimulate insulin secretion (low glycemic index), when compared to one which stimulates significant insulin secretion (high glycemic index) will: i. Promote fat mobilization and oxidation. ii. Have no effect on milk production in healthy lactating women. This hypothesis will be tested in two different protocols. In protocol (1) the drink will be either just glucose or just galactose providing 55% of the subject''s daily basal metabolic needs. Protocol (2) will be the same as protocol (1) with the exception that the drink will be supplemented with extra 15% protein, essential fatty acids, minerals and vitamins. Thus, this drink will have exactly the same carbohydrate content as that used in protocol (1) but will provide 70% of the basal metabolic rate. The objective of this study is to determine whether low(galactose) versus high (glucose) glycemic index dietary carbohydrate content in a diet with reduced calories will facilitate fat mobilization and oxidation without adversely affecting milk production, or milk composition. Understanding the metabolic consequences of lactation on maternal metabolism and the regulation of lactose synthesis will give new insights into the regulation of human milk production, providing new strategies to improve the number of successfully breastfeeding women and to allow women to lose unwanted weight while maintaining adequate milk production. Many lactating women are concerned about losing weight gained during pregnancy. A large number of dietary approaches to achieve weight loss are available. Many high-carbohydrate foods common to Western diets produce a high glycemic response (high-glycemic index). These diets induce a rapid increase in blood glucose, resulting in insulin release which leads to inhibition of fat mobilization. Thus high-glycemic index diets may result in altering fuel partitioning in a way that may lead to body fat gain. On the other hand, diets that produce a low glycemic response (low-glycemic index diets) may enhance weight control because they promote satiety and minimize postprandial insulin secretion. Although regaining pre-pregnancy weight should be the goal, extreme dietary behaviors could impair milk production. It is postulated that the primary determinant of milk volume is lactose production. We have recently demonstrated that oral galactose, which has a low-glycemic index, provides a nutrient substrate that is converted to glucose and only minimally increases plasma glucose and insulin concentrations. Thus galactose is a potential substrate for lactose synthesis that might also promote fat mobilization.
这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者(PI)可能从另一个NIH来源获得了主要资金, 因此可在其他CRISP条目中表示。所列机构为 研究中心,而研究中心不一定是研究者所在的机构。 由于肥胖风险的增加,许多哺乳期妇女担心在怀孕期间体重增加而不会对产奶量产生不利影响。我们以前已经证明,口服半乳糖(与葡萄糖相比,其血糖指数较低)可以提供转化为葡萄糖的营养底物,从而提供乳糖合成的底物,但不会通过增加血糖和胰岛素抑制脂肪动员。 本研究的目的是确定高(葡萄糖)与低(半乳糖)胰岛素刺激口服碳水化合物餐对产后和对照女性脂肪动员和氧化的影响。我们假设,与刺激显著胰岛素分泌的饮料相比,不刺激胰岛素分泌的等热量碳水化合物饮料将促进脂肪动员和氧化,并且不会影响健康哺乳期妇女的产奶量。如果我们证明口服碳水化合物的性质会影响脂肪酸动员和脂肪氧化,而不会影响乳糖合成和产奶,我们将有科学证据设计一个更广泛的临床试验,母乳喂养的母亲谁是渴望减肥,同时保持成功的母乳喂养。 假设:在三天的时间内,不刺激胰岛素分泌(低血糖指数)的等热量碳水化合物饮料与刺激显著胰岛素分泌(高血糖指数)的碳水化合物饮料相比: I.促进脂肪动员和氧化。 二.对健康哺乳期妇女的产奶量没有影响。 该假设将在两个不同的方案中进行检验。在方案(1)中,饮料将仅为葡萄糖或仅为半乳糖,提供受试者每日基础代谢需求的55%。方案(2)将与方案(1)相同,不同之处在于饮料将补充额外的15%蛋白质、必需脂肪酸、矿物质和维生素。因此,这种饮料将具有与方案(1)中使用的完全相同的碳水化合物含量,但将提供基础代谢率的70%。 本研究的目的是确定低血糖指数(半乳糖)与高血糖指数(葡萄糖)饮食中碳水化合物含量在卡路里减少的饮食中是否会促进脂肪动员和氧化,而不会对产奶量或牛奶成分产生不利影响。 了解哺乳对母体代谢和乳糖合成调节的代谢后果将为母乳生产的调节提供新的见解,提供新的策略来提高成功母乳喂养妇女的数量,并使妇女在保持足够的牛奶产量的同时减轻不必要的体重。 许多哺乳期妇女担心减肥在怀孕期间增加。大量的饮食方法来实现减肥是可用的。西方饮食中常见的许多高碳水化合物食物会产生高血糖反应(高血糖指数)。这些饮食诱导血糖快速增加,导致胰岛素释放,从而抑制脂肪动员。因此,高血糖指数饮食可能会导致改变燃料分配的方式,可能会导致体脂增加。另一方面,产生低血糖反应的饮食(低血糖指数饮食)可能会增强体重控制,因为它们会促进饱腹感并最大限度地减少餐后胰岛素分泌。 虽然恢复怀孕前的体重应该是目标,但极端的饮食行为可能会损害牛奶产量。据推测,乳量的主要决定因素是乳糖产量。我们最近证明,口服半乳糖,具有低血糖指数,提供了一种营养底物,转化为葡萄糖,只有最低限度地增加血糖和胰岛素浓度。因此,半乳糖是乳糖合成的潜在底物,也可能促进脂肪动员。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

MOREY W HAYMOND其他文献

MOREY W HAYMOND的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('MOREY W HAYMOND', 18)}}的其他基金

Glucagon Mini-Dosing Pen for Treatment of Hypoglycemia
用于治疗低血糖的胰高血糖素小剂量笔
  • 批准号:
    8781802
  • 财政年份:
    2013
  • 资助金额:
    $ 0.92万
  • 项目类别:
Glucagon Mini-Dosing Pen for Treatment of Hypoglycemia
用于治疗低血糖的胰高血糖素小剂量笔
  • 批准号:
    8521920
  • 财政年份:
    2013
  • 资助金额:
    $ 0.92万
  • 项目类别:
The Childrens Nutrition Research Center Training Program
儿童营养研究中心培训计划
  • 批准号:
    8547086
  • 财政年份:
    2012
  • 资助金额:
    $ 0.92万
  • 项目类别:
The Childrens Nutrition Research Center Training Program
儿童营养研究中心培训计划
  • 批准号:
    8267142
  • 财政年份:
    2012
  • 资助金额:
    $ 0.92万
  • 项目类别:
The Childrens Nutrition Research Center Training Program
儿童营养研究中心培训计划
  • 批准号:
    8658130
  • 财政年份:
    2012
  • 资助金额:
    $ 0.92万
  • 项目类别:
A NOVEL THERAPEUTIC MODALITY FOR CONGENITAL ADRENAL HYPERPLASIA
先天性肾上腺增生症的新治疗方式
  • 批准号:
    8166690
  • 财政年份:
    2009
  • 资助金额:
    $ 0.92万
  • 项目类别:
A NOVEL THERAPEUTIC MODALITY FOR CONGENITAL ADRENAL HYPERPLASIA
先天性肾上腺增生症的新治疗方式
  • 批准号:
    7950638
  • 财政年份:
    2008
  • 资助金额:
    $ 0.92万
  • 项目类别:
THE ROLE OF DIETARY CARBOHYDRATE ON MATERNAL FAT MOBILIZATION AND OXIDATION D
膳食碳水化合物对母体脂肪动员和氧化的作用 D
  • 批准号:
    7950636
  • 财政年份:
    2008
  • 资助金额:
    $ 0.92万
  • 项目类别:
EFFECTS OF DIFFERENT BREAST PUMPING PROTOCOLS ON ALPHA LACTALBUMIN MRNA CONCE
不同吸奶方案对 α 乳清蛋白 mRNA 浓度的影响
  • 批准号:
    7605888
  • 财政年份:
    2007
  • 资助金额:
    $ 0.92万
  • 项目类别:
EFFECTS OF GROWTH HORMONE THERAPY ON GLUCOSE AND PROTEIN METABOLISM IN CHILDR
生长激素治疗对儿童葡萄糖和蛋白质代谢的影响
  • 批准号:
    7605861
  • 财政年份:
    2007
  • 资助金额:
    $ 0.92万
  • 项目类别:

相似海外基金

Fundamental study on estimation of body mass and basal metabolic rate of Jomon period people
绳文时代人体重和基础代谢率估算的基础研究
  • 批准号:
    20K06837
  • 财政年份:
    2020
  • 资助金额:
    $ 0.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Does individual variability of basal metabolic rate can be explained by sports-specific characteristics?
基础代谢率的个体差异是否可以通过运动特定特征来解释?
  • 批准号:
    24500801
  • 财政年份:
    2012
  • 资助金额:
    $ 0.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
BASAL METABOLIC RATE IN SCHIZOPHRENIA
精神分裂症的基础代谢率
  • 批准号:
    7205826
  • 财政年份:
    2005
  • 资助金额:
    $ 0.92万
  • 项目类别:
Basal Metabolic Rate in Schizophrenia
精神分裂症的基础代谢率
  • 批准号:
    7045223
  • 财政年份:
    2003
  • 资助金额:
    $ 0.92万
  • 项目类别:
The effect of colour, posture, and basal metabolic rate on animal energetics
颜色、姿势和基础代谢率对动物能量的影响
  • 批准号:
    93083-1997
  • 财政年份:
    2000
  • 资助金额:
    $ 0.92万
  • 项目类别:
    Discovery Grants Program - Individual
The effect of colour, posture, and basal metabolic rate on animal energetics
颜色、姿势和基础代谢率对动物能量的影响
  • 批准号:
    93083-1997
  • 财政年份:
    1999
  • 资助金额:
    $ 0.92万
  • 项目类别:
    Discovery Grants Program - Individual
The effect of colour, posture, and basal metabolic rate on animal energetics
颜色、姿势和基础代谢率对动物能量的影响
  • 批准号:
    93083-1997
  • 财政年份:
    1998
  • 资助金额:
    $ 0.92万
  • 项目类别:
    Discovery Grants Program - Individual
Dissertation Research: Basal Metabolic Rate of Mongolian Pastoral Nomads
论文研究:蒙古牧民基础代谢率
  • 批准号:
    9615749
  • 财政年份:
    1997
  • 资助金额:
    $ 0.92万
  • 项目类别:
    Standard Grant
PLASMA TESTOSTERONE CONCENTRATIONS ON GH SECRETION AND BASAL METABOLIC RATE
血浆睾酮浓度对 GH 分泌和基础代谢率的影响
  • 批准号:
    6249308
  • 财政年份:
    1997
  • 资助金额:
    $ 0.92万
  • 项目类别:
The effect of colour, posture, and basal metabolic rate on animal energetics
颜色、姿势和基础代谢率对动物能量的影响
  • 批准号:
    93083-1997
  • 财政年份:
    1997
  • 资助金额:
    $ 0.92万
  • 项目类别:
    Discovery Grants Program - Individual
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了