首页> 外文期刊>Journal of thrombosis and haemostasis: JTH >Cardiac fibrinolytic capacity is markedly increased after brief periods of local myocardial ischemia, but declines following successive periods in anesthetized pigs.
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Cardiac fibrinolytic capacity is markedly increased after brief periods of local myocardial ischemia, but declines following successive periods in anesthetized pigs.

机译:短暂的局部心肌缺血后,心脏的纤溶能力显着增加,但是在连续的麻醉过程中,心脏的纤溶能力却下降。

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BACKGROUND: Fibrinolysis in blood is mainly reflected by the activities of tissue plasminogen activator (tPA) and of plasminogen activator inhibitor-1 (PAI-1). The effect of myocardial ischemia on their activities in the coronary circulation is, however, not established. OBJECTIVES: With an improved experimental model, we therefore examined the effect of a brief period of myocardial ischemia on their activities. Furthermore, the consequences of repeated periods of ischemia, mimicking the situations in patients with unstable angina, were investigated. METHODS: In six anesthetized pigs, we occluded the distal left anterior descending coronary artery (LAD) four times for 10 min with 40 min intervals and determined the activities of tPA and PAI-1 in arterial and coronary venous blood. By simultaneously recording LAD flow, we could estimate cardiac release of these factors at baseline conditions and during reperfusion. RESULTS: Neither net cardiac release of PAI-1 nor alterations in plasma PAI-1 levels were demonstrated during the experiment. However, a significant net release of tPA activity of 10.4 +/- 3.2 IU mL(-1) (P < 0.005) was recorded during baseline conditions. During reperfusion following the first period of ischemia, the cardiac release of tPA activity increased to a peak of 103 +/- 30-fold baseline release, but declined progressively after repeated periods of ischemia. After the fourth period, tPA release did not exceed an estimated baseline accumulation during ischemia and early reperfusion. CONCLUSIONS: In this porcine model, a substantial local increase in fibrinolytic capacity was observed after brief periods of ischemia, but declined subsequently by repeated periods of ischemia.
机译:背景:血液中的纤维蛋白溶解主要通过组织纤溶酶原激活物(tPA)和纤溶酶原激活物抑制剂1(PAI-1)的活性来反映。但是,心肌缺血对其在冠状动脉循环中的活性的影响尚未确定。目的:通过改进的实验模型,我们因此研究了短暂的心肌缺血对其活动的影响。此外,还研究了反复缺血的结果,模仿不稳定型心绞痛患者的情况。方法:在六只麻醉的猪中,我们以40分钟的间隔四次阻塞远端左冠状动脉前降支(LAD)10次,每次10分钟,并测定动脉和冠状静脉血中tPA和PAI-1的活性。通过同时记录LAD流量,我们可以估计基线条件下和再灌注期间这些因素的心脏释放。结果:在实验期间,既没有显示出PAI-1的心脏净释放量,也没有显示血浆PAI-1水平的变化。但是,在基线条件下记录到的tPA活性的显着净释放为10.4 +/- 3.2 IU mL(-1)(P <0.005)。在第一段缺血后的再灌注期间,tPA活性的心脏释放增加至基线释放的103 +/- 30倍的峰值,但在反复缺血后逐渐下降。在第四阶段之后,tPA释放在缺血和早期再灌注期间未超过估计的基线累积。结论:在这种猪模型中,短暂缺血后观察到了局部纤溶能力的显着增加,但随后反复缺血却下降了。

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