Massarelli G, Muscari A, Giulioni A, Bastagli L, Poggiopollini G, Tomassetti V, Puddu G M, Puddu P
Dipartimento di Medicina Interna, Cardioangiologia, Epatologia, Università degli Studi, Bologna.
G Ital Cardiol. 1998 Mar;28(3):242-8.
During acute myocardial infarction, the ascending branch of creatine kinase curves has a sigmoidal course whose inflection point marks the maximum rate of enzymatic increase in serum. This study was performed to assess the relationship between these morphologic characteristics of creatine kinase curves and the progression of myocardial necrosis.
In isolated rat hearts exposed to different degrees of ischemia (coronary flow of 0.6 or 0.2 ml/g/min), the total quantity of creatine kinase released in the effluent had a sigmoidal course similar to the ascending branch of the curves from patients with acute myocardial infarction. Other rat hearts were frozen (which causes maximum damage to cell structures), thawed and then perfused. The resulting enzymatic curves had a downward concave ascending trend, similar to the portion beyond the inflection point of sigmoidal curves (the rate of creatine kinase release was maximum at the onset of perfusion and then decreased progressively). Finally, in some experiments ischemic rat hearts were further damaged by the perfusion, at different times, with highly concentrated catecholamines and without oxygen and substrates. This damaging perfusate was able to increase the rate of creatine kinase release (p = 0.0001) only when it was started before the inflection point of enzymatic curves. In 25 creatine kinase curves from patients with acute myocardial infarction (19 men and 6 women, age range 42 to 68 years), who were not treated with thrombolysis, the time of inflection varied from 1 to 12 hours from the onset of symptoms, with a maximum frequency between the 7th and the 8th hour.
Based on these data, a biological model with 3 compartments has been suggested to explain the shape of creatine kinase curves, according to which the inflection point would occur after the completion of myocardial necrosis. The variability of the time of inflection might account for the cases of beneficial late thrombolysis reported in literature.
在急性心肌梗死期间,肌酸激酶曲线的上升支呈S形,其拐点标志着血清中酶增加的最大速率。本研究旨在评估肌酸激酶曲线的这些形态学特征与心肌坏死进展之间的关系。
在暴露于不同程度缺血(冠状动脉血流量为0.6或0.2 ml/g/min)的离体大鼠心脏中,流出液中释放的肌酸激酶总量呈S形,类似于急性心肌梗死患者曲线的上升支。其他大鼠心脏被冷冻(这会对细胞结构造成最大损伤),解冻后再进行灌注。由此产生的酶曲线呈向下凹的上升趋势,类似于S形曲线拐点之后的部分(肌酸激酶释放速率在灌注开始时最大,然后逐渐下降)。最后,在一些实验中,缺血大鼠心脏在不同时间用高浓度儿茶酚胺且无氧和底物的灌注液进一步损伤。这种损伤性灌注液仅在酶曲线拐点之前开始时才能增加肌酸激酶释放速率(p = 0.0001)。在25例未接受溶栓治疗的急性心肌梗死患者(19名男性和6名女性,年龄范围42至68岁)的肌酸激酶曲线中,拐点时间在症状发作后1至12小时之间变化,最大频率出现在第7至8小时之间。
基于这些数据,提出了一个三室生物模型来解释肌酸激酶曲线的形状,根据该模型,拐点将在心肌坏死完成后出现。拐点时间的变异性可能解释了文献中报道的有益的晚期溶栓病例。