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Argininosuccinate Lyase is an essential regulator of systemic nitric oxide produc

Argininosuccinate Lyase is an essential regulator of systemic nitric oxide produc
精氨基琥珀酸裂解酶是全身一氧化氮生成的重要调节剂
批准号:
8136577
负责人:
Brendan Lee
金额:
$37.27万
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 2014-08-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Nitric Oxide (NO) is an essential signaling molecule for diverse physiological and disease processes. While the regulation of NO flux has focused primarily on the study of the three NO synthases (NOS), their respective genetic deficiencies exhibit relatively modest phenotypes. This has led to difficulties in dissecting the specific cellular contributions to NO in different disease processes. In contrast, the hypothesized intracellular compartmentalized availability of arginine substrate in specifying NO flux may explain the "arginine paradox." In humans, the natural history of urea cycle disorders and specifically of argininosuccinic aciduria (ASA) caused by deficiency of argininosuccinic acid lyase (ASL) shows systemic and chronic features that may reflect global dysregulation of NO homeostasis. We propose that ASL is in fact the central regulator of NO homeostasis because it is essential for both the intracellular production of arginine and the utilization of extracellular arginine. In preliminary data, we identify a distinct subcellular and biochemical compartment where local cellular arginine production and channeling by ASL regulates systemic NO production. We have generated a conditional genetic model of Asl deficiency that will allow us to study the consequences of cell autonomous loss of NO in brain (neurons vs. glial cells), the cardiovascular system (endothelial vs. smooth muscle cells), and the pancreatic beta cell with broad implications on understanding the contribution of NO to models of neurodegeneration, cardiovascular disease, and metabolic syndrome. On a biochemical level, we will assess how ASL controls arginine availability for NO production. Our studies may identify novel and more effective strategies for manipulation NO in multi-system disease. PUBLIC HEALTH RELEVANCE: Nitric oxide (NO) is an important molecule in the cause of almost all human diseases. We propose to study a new way on how NO is produced in the body. A chemical called argininosuccinate lyase (ASL) is used to produce arginine which is required for NO production. We will determine whether inhibiting ASL may be the most effective way for controlling NO production in diseases affecting the brain, heart, and pancreas.
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会议论文
Targeting TGFb In Osteogenesis Imperfecta
  • 批准号:
    10736736
  • 项目类别:
  • 资助金额:
    $62.59万
  • 财政年份:
    2023
  • 负责人:
    Brendan Lee
  • 依托单位:
Regulation of Skeletal progenitor cells in Osteogenesis Imperfecta
  • 批准号:
    10528208
  • 项目类别:
  • 资助金额:
    $66.24万
  • 财政年份:
    2022
  • 负责人:
    Brendan Lee
  • 依托单位:
Regulation of Skeletal progenitor cells in Osteogenesis Imperfecta
  • 批准号:
    10665057
  • 项目类别:
  • 资助金额:
    $66.24万
  • 财政年份:
    2022
  • 负责人:
    Brendan Lee
  • 依托单位:
ALL OF US EVENINGS WITH GENETICS RESEARCH EDUCATION PROGRAM
  • 批准号:
    10307410
  • 项目类别:
  • 资助金额:
    $108.91万
  • 财政年份:
    2021
  • 负责人:
    Brendan Lee
  • 依托单位:
国内基金
海外基金
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
  • 批准号:
    81973577
  • 项目类别:
    面上项目
  • 资助金额:
    55.0万元
  • 批准年份:
    2019
  • 负责人:
    辛贵忠
  • 依托单位: