Vulnerability to sepsis in old age
Vulnerability to sepsis in old age
批准号:
6903654
负责人:
Hiroshi Saito
金额:
$22.26万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-05-15 至 2010-04-30
关键词:
age differenceaginganimal mortalityanimal old ageanticoagulantsantiinflammatory agentsantioxidantsblood coagulationdisease /disorder modeldisease /disorder proneness /riskgene expressiongenetically modified animalsheartimmature animalimmunocytochemistryinflammationlaboratory mouselungmature animalmicroarray technologynonhuman therapy evaluationoxidative stresspathologic processseptic shocksepticemia
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant):
Sepsis is an infection-initiated manifestation of the systemic inflammatory response syndrome that often progresses to septic shock, multiple organ failure with high risks of death. Sepsis is a particularly serious problem in the geriatric population, as the elderly patients with sepsis suffer much higher morbidity and mortality than younger patients. In fact, sepsis is a major cause of death in elderly patients at intensive care units in the US. Although this problem is increasingly recognized, the underlying mechanism(s) responsible for this age-associated vulnerability remain largely unknown. The long-term goal of our research is to determine the mechanisms responsible for the increased septic vulnerability in the aged, and to use this information to develop new treatment strategies for sepsis. The age-associated vulnerability to sepsis is also seen in animal models. We have shown that aged mice suffer significantly higher mortality than young mice in two commonly used models for sepsis; endotoxemia induced by bacterial lipopolysaccharide injection, and an intra-abdominal sepsis induced by cecal ligation and puncture. We have also found that the elevated mortality in aged mice is associated with altered inflammatory and coagulation responses, and increased oxidative damages. Our central hypothesis is that loss of homeostasis in old age leads to excessive inflammation, oxidative damage, and coagulation, contributing to the age-associated vulnerability to sepsis. Our objective in this project is to define the age-associated alterations in pathophysiology and gene expression in the mouse model of sepsis, and to develop strategies to improve the survival of the old mice with sepsis. To achieve these goals, we pursue the following three specific aims: (1) To determine the effects of aging on the pathophysiology of sepsis, (2) To identify the age-associated alterations in gene expression that affects mortality in sepsis, and (3) To test likely strategies for their ability to decrease age-associated mortality in sepsis. The information obtained from this project should provide the basis for new therapeutic strategies to substantially decrease the mortality in elderly patients with sepsis.
期刊论文(0)
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科研奖励(0)
会议论文
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The Role of Adipose Tissue in Age-dependent Sensitivity to Critical Illness
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The Role of Adipose Tissue in Age-dependent Sensitivity to Critical Illness
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批准号:8706748
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财政年份:2011
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The Role of Adipose Tissue in Age-dependent Sensitivity to Critical Illness
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财政年份:2011
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The Role of Adipose Tissue in Age-dependent Sensitivity to Critical Illness
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批准号:8187763
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财政年份:2011
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The Role of Adipose Tissue in Age-dependent Sensitivity to Critical Illness
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批准号:8852028
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项目类别:
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资助金额:$29.53万
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财政年份:2011
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Vulnerability to sepsis in old age
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批准号:7415043
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资助金额:$21.05万
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财政年份:2005
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负责人:Hiroshi Saito
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依托单位:
Vulnerability to sepsis in old age
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批准号:7227082
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资助金额:$21.48万
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Vulnerability to sepsis in old age
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批准号:7065611
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资助金额:$22.12万
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负责人:Hiroshi Saito
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依托单位:
Vulnerability to sepsis in old age
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批准号:7617681
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项目类别:
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资助金额:$11.33万
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财政年份:2005
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负责人:Hiroshi Saito
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依托单位:
Vulnerability to sepsis in old age
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批准号:7932373
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项目类别:
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资助金额:$9.72万
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财政年份:2005
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负责人:Hiroshi Saito
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依托单位:
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