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Vasopeptidases and Beta Amyloid Accumulation

Vasopeptidases and Beta Amyloid Accumulation
血管肽酶和β淀粉样蛋白积累
批准号:
6770801
负责人:
CHRISTOPHER B ECKMAN
金额:
$28.49万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-04-01 至 2009-02-28

项目摘要

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CHRISTOPHER B ECKMAN的其他基金

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中文摘要
翻译
描述(由申请人提供):血管肽酶是负责生成或灭活血管活性肽的酶。因此,血管肽酶抑制是治疗心血管疾病的重要途径。例如,血管紧张素转换酶(ACE)抑制剂被FDA批准并广泛用于治疗高血压和心力衰竭。此外,另外两种血管肽酶的抑制剂,neprilysin (NEP)和内皮素转换酶(ECE),以及这些酶的联合抑制剂目前正处于临床前和临床开发阶段。最近,大量的数据表明血管肽酶ECE和NEP,可能还有ACE,在阿尔茨海默病淀粉样β肽(ABeta)的降解中起作用。由于ABeta的异常积累在AD的发病机制中起着关键作用,因此对这些血管肽酶的药理抑制引起了相当大的关注,因为它们可能以增加ABeta水平的方式增加患阿尔茨海默病的风险。在本申请中,我们建议直接评估ECE、NEP和ACE的慢性减少会导致ABeta积累增强和ad样病理的假设,方法是检查基因缺乏这些酶的小鼠和临床相关血管肽酶抑制剂治疗的小鼠的影响。这些研究的结果将进一步加深我们对NEP, ECE和ACE在确定大脑中ABeta浓度中的作用的理解,同时有助于评估临床使用血管肽酶抑制剂的潜在风险。
英文摘要
DESCRIPTION (provided by applicant): Vasopeptidases are enzymes responsible for the generation or inactivation of vasoactive peptides. As such, vasopeptidase inhibition represents a significant approach for the treatment of cardiovascular disease. For example, angiotensin-converting enzyme (ACE) inhibitors are FDA approved and widely used to treat hypertension and heart failure. In addition, inhibitors of two other vasopeptidases, neprilysin (NEP) and endothelin-converting enzyme (ECE), are currently in preclinical and clinical development as are combined inhibitors of these enzymes. Recently, considerable data has emerged indicating a role for the vasopeptidases ECE and NEP, and perhaps also ACE, in the degradation of the Alzheimer's amyloid beta-peptide (ABeta). As the abnormal accumulation of ABeta plays a pivotal role in AD pathogenesis, pharmacological inhibition of these vasopeptidases is of considerable concern as they may increase ABeta levels in a manner that increases risk of developing Alzheimer's disease. In this application we propose to directly evaluate the hypothesis that chronic reductions in ECE, NEP, and ACE will result in enhanced ABeta accumulation and AD-like pathology by examining the effects of mice genetically deficient in these enzymes and mice treated with clinically relevant vasopeptidase inhibitors. The results of these studies will further our understanding of the role of NEP, ECE, and ACE in determining ABeta concentration in the brain, while helping to assess the potential risk of the clinical use of vasopeptidase inhibitors.
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Protein Misprocessing in Krabbe Disease
  • 批准号:
    7268116
  • 项目类别:
  • 资助金额:
    $22.14万
  • 财政年份:
    2006
  • 负责人:
    CHRISTOPHER B ECKMAN
  • 依托单位:
Protein Misprocessing in Krabbe Disease
  • 批准号:
    7124133
  • 项目类别:
  • 资助金额:
    $19.0万
  • 财政年份:
    2006
  • 负责人:
    CHRISTOPHER B ECKMAN
  • 依托单位:
Vasopeptidases and Beta Amyloid Accumulation
  • 批准号:
    7209058
  • 项目类别:
  • 资助金额:
    $27.01万
  • 财政年份:
    2004
  • 负责人:
    CHRISTOPHER B ECKMAN
  • 依托单位:
Vasopeptidases and Beta Amyloid Accumulation
  • 批准号:
    7051392
  • 项目类别:
  • 资助金额:
    $27.82万
  • 财政年份:
    2004
  • 负责人:
    CHRISTOPHER B ECKMAN
  • 依托单位: