DETERMINATION OF METFORMIN AND INSULIN EFFECT ON HEPATIC TRIGLYCERIDE CONTENT

二甲双胍和胰岛素对肝甘油三酯含量影响的测定

基本信息

  • 批准号:
    7606339
  • 负责人:
  • 金额:
    $ 0.07万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2007
  • 资助国家:
    美国
  • 起止时间:
    2007-04-01 至 2007-09-16
  • 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. Fatty infiltration of the liver can occur by four distinct mechanisms: 1) increased flux of fatty acids to the liver; 2) increased synthesis of fatty acids in hepatocytes; 3) decreased hepatocyte secretion of fatty acids in the form of very-low-density-lipoprotein and; 4) decreased oxidation of fatty acids by hepatocytes. Animal models suggest that de novo synthesis of fatty acids plays a significant role in the accumulation of liver fat in the setting of insulin resistance. Importantly, the level of fatty acid synthesis in the liver is a function of circulating insulin levels, even in the setting of hepatocyte insulin resistance. One would expect that as insulin resistance worsens and insulin levels rise (either as a result of increased pancreatic islet cell output or supplementation with exogenous insulin), so to would the rate of hepatocyte fatty acid synthesis. This could potentially increase the liver fat content. Investigators in the study propose to examine the effect of two current standard care therapies for type 2 diabetes mellitus on liver fat content: metformin and insulin. Liver fat content will be assessed using proton magnetic resonance spectroscopy before and after 4 months of therapy. Subjects will be randomly assigned to one of the two medication to be studied and closely monitored for any drug-specific toxicities associated with their use.
这个子项目是众多研究子项目之一

项目成果

期刊论文数量(0)
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专利数量(0)

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JEFFREY D BROWNING其他文献

JEFFREY D BROWNING的其他文献

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{{ truncateString('JEFFREY D BROWNING', 18)}}的其他基金

Origin of Excess Acid in Uric Acid Urolithiasis
尿酸尿石症中酸过多的根源
  • 批准号:
    10442425
  • 财政年份:
    2019
  • 资助金额:
    $ 0.07万
  • 项目类别:
Origin of Excess Acid in Uric Acid Urolithiasis
尿酸尿石症中酸过多的根源
  • 批准号:
    10198912
  • 财政年份:
    2019
  • 资助金额:
    $ 0.07万
  • 项目类别:
The Role of Mitochondrial Dysfunction in Non-Alcoholic Fatty Liver Disease
线粒体功能障碍在非酒精性脂肪肝中的作用
  • 批准号:
    8039689
  • 财政年份:
    2011
  • 资助金额:
    $ 0.07万
  • 项目类别:
The Role of Mitochondrial Dysfunction in Non-Alcoholic Fatty Liver Disease
线粒体功能障碍在非酒精性脂肪肝中的作用
  • 批准号:
    8401182
  • 财政年份:
    2011
  • 资助金额:
    $ 0.07万
  • 项目类别:
The Role of Mitochondrial Dysfunction in Non-Alcoholic Fatty Liver Disease
线粒体功能障碍在非酒精性脂肪肝中的作用
  • 批准号:
    8600673
  • 财政年份:
    2011
  • 资助金额:
    $ 0.07万
  • 项目类别:
The Role of Mitochondrial Dysfunction in Non-Alcoholic Fatty Liver Disease
线粒体功能障碍在非酒精性脂肪肝中的作用
  • 批准号:
    8231420
  • 财政年份:
    2011
  • 资助金额:
    $ 0.07万
  • 项目类别:
EXTREME DIETARY CARBOHYDRATE RESTRICTION EFFECT ON HEPATIC GLUCOSE PRODUCTION
膳食碳水化合物的极端限制对肝葡萄糖产生的影响
  • 批准号:
    7606336
  • 财政年份:
    2007
  • 资助金额:
    $ 0.07万
  • 项目类别:
HEPATIC CARBOHYDRATE METABOLISM IN THE YOUNG AND ELDERLY
年轻人和老年人的肝脏碳水化合物代谢
  • 批准号:
    7606325
  • 财政年份:
    2007
  • 资助金额:
    $ 0.07万
  • 项目类别:
Human Biology Core, Project 10 of 10
人类生物学核心,项目 10(共 10 个)
  • 批准号:
    8106124
  • 财政年份:
    2007
  • 资助金额:
    $ 0.07万
  • 项目类别:
Non-Alcoholic Fatty Liver Disease Ethnicity and Hepatic Metabolism
非酒精性脂肪肝的种族和肝脏代谢
  • 批准号:
    7448557
  • 财政年份:
    2006
  • 资助金额:
    $ 0.07万
  • 项目类别:

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