Role of Cyclooxygenase-2-derived Prostanoids in Polymicrobial Sepsis
Role of Cyclooxygenase-2-derived Prostanoids in Polymicrobial Sepsis
批准号:
8197378
负责人:
LAURA ELIZABETH FREDENBURGH
金额:
$12.01万
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 2013-05-30
关键词:
Abdominal InfectionAccountingAdrenal Cortex HormonesAdrenal gland hypofunctionAnimalsAnti-Inflammatory AgentsAnti-inflammatoryArachidonic AcidsBacteremiaBiological AssayBone MarrowBone Marrow TransplantationCellsCessation of lifeCoagulation ProcessCollaborationsCritical CareDataDevelopment PlansDiseaseEicosanoidsEndotoxemiaEnterocytesEnzymesEpithelial CellsExhibitsFibrinFunctional disorderGoalsGram-Negative BacteriaHMGB1 ProteinHematogenousHypotensionHypoxiaImmune responseImmune systemIn VitroIndividualInfectionInflammationInflammation MediatorsInflammatoryInflammatory ResponseInjuryIntestinesIntra-abdominalInvadedLeadLigationLipopolysaccharidesLungMediatingMediator of activation proteinMedicalMedicineMentorsMentorshipMicrobeModelingMorbidity - disease rateMucous MembraneMusOrganPeptidoglycanPeritonitisPhagocytosisPhysiciansPlayProcessProstaglandin-Endoperoxide SynthaseProstaglandinsProtein IsoformsPuncture procedureRefractoryRelative (related person)ResearchResearch PersonnelResolutionRoleScientistSepsisSeptic ShockSeriesStimulusTechniquesTissuesTrainingTraining ProgramsUnited StatesVentilatorWild Type Mouseactivated Protein Cbasecareer developmentcell typeclinically relevantcostcyclooxygenase 1cyclooxygenase 2cytokinegastrointestinalglycemic controlhemodynamicsimprovedinterestkillingsmicrobialmortalitypathogenprogramsprotective effectreceptorresponseskills
中文摘要
脓毒症是一种以对潜在感染的全身炎症反应为特征的疾病过程。
英文摘要
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.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1097/aln.0000000000000742
发表时间:
2015-08
期刊:
Anesthesiology
影响因子:
8.8
作者:
[Englert JA, Macias AA, Amador-Munoz D, Pinilla Vera M, Isabelle C, Guan J, Magaoay B, Suarez Velandia M, Coronata A, Lee A, Fredenburgh LE, Culley DJ, Crosby G, Baron RM]
通讯作者:
Baron RM
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:
Mechanobiology of Vascular Remodeling in Pulmonary Arterial Hypertension
-
批准号:8340773
-
项目类别:
-
资助金额:$43.13万
-
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:8887377
-
项目类别:
-
资助金额:$41.3万
-
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:8531343
-
项目类别:
-
资助金额:$39.05万
-
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:8355939
-
项目类别:
-
资助金额:$8.93万
-
财政年份:2012
-
负责人:LAURA ELIZABETH FREDENBURGH
-
依托单位:
Role of Cyclooxygenase-2-derived Prostanoids in Polymicrobial Sepsis
-
批准号:7922806
-
项目类别:
-
资助金额:$10.8万
-
财政年份:2009
-
负责人:LAURA ELIZABETH FREDENBURGH
-
依托单位:
Role of Cyclooxygenase-2-derived Prostanoids in Polymicrobial Sepsis
-
批准号:7540366
-
项目类别:
-
资助金额:$13.1万
-
财政年份:2007
-
负责人:LAURA ELIZABETH FREDENBURGH
-
依托单位:
Role of Cyclooxygenase-2-derived Prostanoids in Polymicrobial Sepsis
-
批准号:7741197
-
项目类别:
-
资助金额:$13.1万
-
财政年份:2007
-
负责人:LAURA ELIZABETH FREDENBURGH
-
依托单位:
Role of Cyclooxygenase-2-derived Prostanoids in Polymicrobial Sepsis
-
批准号:7360491
-
项目类别:
-
资助金额:$13.1万
-
财政年份:2007
-
负责人:LAURA ELIZABETH FREDENBURGH
-
依托单位:
Role of Cyclooxygenase-2-derived Prostanoids in Polymicrobial Sepsis
-
批准号:7993531
-
项目类别:
-
资助金额:$13.1万
-
财政年份:2007
-
负责人:LAURA ELIZABETH FREDENBURGH
-
依托单位:
海外基金