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Role of Cyclooxygenase-2-derived Prostanoids in Polymicrobial Sepsis

Role of Cyclooxygenase-2-derived Prostanoids in Polymicrobial Sepsis
环氧合酶 2 衍生的前列腺素在多种微生物脓毒症中的作用
批准号:
7741197
负责人:
LAURA ELIZABETH FREDENBURGH
金额:
$13.1万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-12-11 至 2012-11-30

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): DESCRIPTION: Sepsis is a disease process characterized by a systemic inflammatory response to an underlying infection. In the United States, 750,000 people develop severe sepsis annually and despite recent advances in critical care, over 210,000 people die each year. Polymicrobial sepsis due to intra-abdominal infection accounts for a significant and growing percentage of cases of severe sepsis and is often associated with substantial mortality. Cyclooxygenase-2 (COX-2), the inducible isoform of cyclooxygenase, plays a pivotal role in modulating both the inflammatory and anti-inflammatory innate immune responses and COX-2-derived prostanoids may be vital to gastrointestinal barrier defense during polymicrobial sepsis. Our overall hypothesis is that COX-2 plays a protective role during the host response to intra-abdominal polymicrobial sepsis. Our preliminary data demonstrate that COX-2 deficiency is detrimental in a murine model of peritonitis-induced polymicrobial sepsis. COX-2 deficient mice exhibit exaggerated mortality, severe ileal mucosal damage, increased bacteremia, and enhanced seeding of vital organs following cecal ligation and puncture (CLP). The Specific Aims of this proposal are: 1) to investigate the role of COX-2-derived prostanoids in a murine model of peritonitis-induced polymicrobial sepsis; 2) to elucidate the cell type(s) responsible for mediating the protective effects of COX-2 during peritonitis-induced polymicrobial sepsis; and 3) to determine the mechanisms by which COX-2 affords protection during sepsis. In addition to our scientific goals, the candidate seeks a formal, mentored training program to develop the skills necessary to become a successful physician-scientist. The candidate is an intensivist with a long-standing interest in the pathophysiology of sepsis. Her proposed career development plan includes: 1) mentorship and collaboration with successful leaders in the field of critical care research; 2) fundamental training in a wide range of techniques necessary to study clinically relevant models of sepsis; and 3) acquiring the intellectual skills to develop into an independent investigator in academic critical care medicine. SUMMARY: Sepsis is a disease associated with severe infections that afflicts three quarters of a million people each year. There is no specific treatment for sepsis and over 200,000 people die annually of this devastating illness. The main goal of this proposal is to determine how the COX-2 enzyme is protective during sepsis with the hope that this research will eventually lead to new therapies for this frequently fatal disease. PERFORMANCE SITE(S): Brigham and Women's Hospital, Boston, MA. PI: Fredenburgh, Laura Elizabeth.
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Mechanotransduction and YAP/TAZ Signaling in Pulmonary Arterial Hypertension
  • 批准号:
    9456950
  • 项目类别:
  • 资助金额:
    $66.99万
  • 财政年份:
    2018
  • 负责人:
    LAURA ELIZABETH FREDENBURGH
  • 依托单位:
Mechanobiology of Vascular Remodeling in Pulmonary Arterial Hypertension
  • 批准号:
    8690140
  • 项目类别:
  • 资助金额:
    $40.07万
  • 财政年份:
    2012
  • 负责人:
    LAURA ELIZABETH FREDENBURGH
  • 依托单位:
Mechanobiology of Vascular Remodeling in Pulmonary Arterial Hypertension
  • 批准号:
    9100847
  • 项目类别:
  • 资助金额:
    $41.79万
  • 财政年份:
    2012
  • 负责人:
    LAURA ELIZABETH FREDENBURGH
  • 依托单位:
Arterial Stiffness in the Pathogenesis of Human Pulmonary Arterial Hypertension
  • 批准号:
    8516592
  • 项目类别:
  • 资助金额:
    $8.5万
  • 财政年份:
    2012
  • 负责人:
    LAURA ELIZABETH FREDENBURGH
  • 依托单位:
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