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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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Controlled reperfusion of the regionally ischemic myocardium with leukocyte-depleted blood reduces stunning, the no-reflow phenomenon, and infarct size.
用去白细胞的血液对局部缺血的心肌进行受控再灌注可减少击晕、无复流现象和梗塞面积。
DOI: --
发表时间: 1992
期刊: The Journal of thoracic and cardiovascular surgery
影响因子: --
作者: [Byrne,JG, Appleyard,RF, Lee,CC, Couper,GS, Scholl,FG, Laurence,RG, Cohn,LH]
通讯作者: Cohn,LH
The effect of superoxide dismutase and catalase on the extended preservation of the ex vivo heart for transplantation.
超氧化物歧化酶和过氧化氢酶对移植用离体心脏的长期保存的影响。
DOI: --
发表时间: 1988
期刊: The Journal of thoracic and cardiovascular surgery
影响因子: --
作者: [Gharagozloo,F, Melendez,FJ, Hein,RA, Shemin,RJ, DiSesa,VJ, Cohn,LH]
通讯作者: Cohn,LH
Measurement of coronary blood flow: a critical review.
冠状动脉血流量的测量:严格审查。
DOI: 10.1016/0022-4804(87)90149-1
发表时间: 1987
期刊: The Journal of surgical research
影响因子: --
作者: [Gharagozloo,F, Cohn,LH]
通讯作者: Cohn,LH
Effects of diltiazem cardioplegia on global function, segmental contractility, and the area of necrosis after acute coronary artery occlusion and surgical reperfusion.
地尔硫卓停搏液对急性冠状动脉闭塞和手术再灌注后整体功能、节段收缩力和坏死面积的影响。
DOI: --
发表时间: 1988
期刊: The Journal of thoracic and cardiovascular surgery
影响因子: --
作者: [Melendez,FJ, Gharagozloo,F, Sun,SC, Benfell,K, Austin,RE, Shemin,RJ, Cohn,LH]
通讯作者: Cohn,LH
10
    REDUCTION OF INFARCT SIZE AFTER SURGICAL REPURFUSION
    • 批准号:
      3345398
    • 项目类别:
    • 资助金额:
      $18.33万
    • 财政年份:
      1987
    • 负责人:
      Lawrence H Cohn
    • 依托单位:
    REDUCTION OF INFARCT SIZE AFTER SURGICAL REPURFUSION
    • 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
    • 财政年份:
      1984
    • 负责人:
      Lawrence H Cohn
    • 依托单位:
    REDUCTION OF INFARCT SIZE AFTER SURGICAL REPERFUSION
    • 批准号:
      3345392
    • 项目类别:
    • 资助金额:
      $25.21万
    • 财政年份:
      1984
    • 负责人:
      Lawrence H Cohn
    • 依托单位:
    海外基金