REDUCTION OF INFARCT SIZE AFTER SURGICAL REPURFUSION
REDUCTION OF INFARCT SIZE AFTER SURGICAL REPURFUSION
批准号:
3345398
负责人:
Lawrence H Cohn
金额:
$18.33万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1987
资助国家:
美国
项目状态:
已结题
起止时间:
1987-07-01 至 1990-12-31
关键词:
angiography calcium channel blockers cardiotonic agents coronary occlusion /thrombosis coronary vasodilator diltiazem disease /disorder model dyes enzyme inhibitors fluorocarbon polymers fluoroscopy heart /lung bypass heart catheterization heart circulation heart disorder chemotherapy heart function heart pharmacology heart preservation heart revascularization histochemistry /cytochemistry hydroxyl group myocardial infarct sizing myocardial infarction myocardial ischemia /hypoxia necrosis particle potassium radionuclide diagnosis radiotracer respiratory gas analyzer sheep thromboxanes tissue /cell preparation ultrasound blood flow measurement
中文摘要
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英文摘要
Reperfusion of the acutely ischemic and infarcted human myocardium
by Streptokinase/thrombolysis, by PTCA, by acute coronary artery
surgery or a combination of all these methods has become
increasingly utilized. Therefore, intraoperative myocardial
protection of the ischemic myocardium to reduce the magnitude of
the myocardial injury after coronary occlusion and reperfusion
continues to be of the highest priority. Based on our work
beginning in 1981, and continuing through the RO1 grant period, we
have established more sophisticated techniques to evaluate local
and global myocardial function after acute coronary occlusion and
have begun to evaluate agents to either increase delivery of oxygen
to ischemic myocardium or to interfere with the pathophysiologic
effects of ischemia and reperfusion.
In this grant period we will continue to pursue the concept of
preparation of the ischemic area prior to reperfusion as well as
treatment of the pathophysiologic effects of acute myocardial
ischemia concurrently. We will evaluate 1) free oxygen radicals
in both the acute and chronic ischemia models as well as the ex
vivo preserved heart to define more precisely the mechanisms of
their action, 2) thromboxane synthetase inhibitors in both the
acute and chronic model, 3) calcium channel blockers and 4) agents
that increase oxygen delivery to the ischemic myocardium,
oxygenated crystalloid cardioplegia, blood cardioplegia and
fluocarbons. In addition we intend to explore the use of other
protective agents, particularly the oxygenated cardioplegic
compounds applied distal to the site of coronary artery occlusion
in our closed chest model simulating PTCA treatment of coronary
occlusion. These studies will impact positively on the pre-
hospital, invasive and operative treatment of acute MI, the leading
cause of death in America. By reducing the total amount of
infarcted muscle and improving regional myocardial function by
these experimental approaches, the early and late mortality after
myocardial infarction should be improved.
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REDUCTION OF INFARCT SIZE AFTER SURGICAL REPURFUSION
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批准号:3345399
-
项目类别:
-
资助金额:$16.1万
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财政年份:1987
-
负责人:Lawrence H Cohn
-
依托单位:
REDUCTION OF INFARCT SIZE AFTER SURGICAL REPURFUSION
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批准号:3345394
-
项目类别:
-
资助金额:$20.48万
-
财政年份:1987
-
负责人:Lawrence H Cohn
-
依托单位:
REDUCTION OF INFARCT SIZE AFTER SURGICAL REPERFUSION
-
批准号:3345397
-
项目类别:
-
资助金额:$26.5万
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财政年份:1984
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负责人:Lawrence H Cohn
-
依托单位:
REDUCTION OF INFARCT SIZE AFTER SURGICAL REPERFUSION
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批准号:3345392
-
项目类别:
-
资助金额:$25.21万
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财政年份:1984
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负责人:Lawrence H Cohn
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依托单位:
海外基金