Vascular Function in SOD2-deficient Mice
Vascular Function in SOD2-deficient Mice
批准号:
6620219
负责人:
JON J ANDRESEN
金额:
$1.91万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-05-01 至 2003-12-31
关键词:
acetylcholine aorta atherosclerosis carotid artery disease /disorder model enzyme activity enzyme inhibitors free radical oxygen gender difference gene targeting genetically modified animals histochemistry /cytochemistry hypertension inflammation laboratory mouse lipopolysaccharides menadione nitric oxide synthase oxidative stress papaverine predoctoral investigator septic shock superoxide dismutase tissue /cell preparation vasomotion
中文摘要
描述(由申请人提供):本提案的主要目标是
英文摘要
DESCRIPTION (provided by the applicant): The major goal of this proposal is to
characterize vasomotor function in SOD2+/-mice. Studies are planned in the
aortae and carotid arteries of wild-type control and SOD2+/- mice because
diseases such as hypertension and atherosclerosis, which affect these vessels,
are risk factors for stroke and are associated with elevated levels of reactive
oxygen species in the vascular wall. Under normal conditions, and after
experimentally inducing oxidant stress using menadione in vitro and
lipopolysaccharide in vivo, vessels from both wild-type control and SOD2+/-mice
will be studied to determine vascular responses to acetylcholine and
papaverine. In some experiments, SOD1&3 will be inhibited using DETCA to
further unmask the function of SOD2. The superoxide dependency of any observed
vascular dysfunction will be determined by using tiron to scavenge superoxide.
In addition, the levels and location of superoxide and other reactive oxygen
species will be determined in vessels from both wild-type control and SOD2+I-mice
under normal conditions and after experimentally inducing oxidant stress.
Levels of superoxide will be measured using lucigenin chemiluminescence and
superoxide will be localized using hydroethidine staining. The location and
relative levels of other reactive oxygen species (ROS) will be estimated using
dichlorofluorescin (DCF) fluorescence.
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会议论文
Role of CO in Cerebrovascular EDHF-mediated Dilation
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批准号:6938767
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项目类别:
-
资助金额:$4.4万
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财政年份:2005
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负责人:JON J ANDRESEN
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依托单位:
Role of CO in Cerebrovascular EDHF-mediated Dilation
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批准号:7119598
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项目类别:
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资助金额:$4.88万
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财政年份:2005
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负责人:JON J ANDRESEN
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依托单位:
Vascular Function in SOD2-deficient Mice
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批准号:6406040
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项目类别:
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资助金额:$2.39万
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财政年份:2002
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负责人:JON J ANDRESEN
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依托单位:
海外基金