Panteghini M, Cuccia C, Malchiodi A, Calarco M, Pagnoni N
Clin Chim Acta. 1986 Feb 28;155(1):1-9. doi: 10.1016/0009-8981(86)90093-8.
Serum creatine kinase (CK, EC 2.7.3.2) isoenzymes MM and MB were resolved, respectively, into three (MM1, MM2, MM3) and two (MB1, MB2) isoforms (subforms derived from the same isoenzyme) by electrophoresis and the isoform patterns were determined in multiple sequential serum samples, timed from the onset of chest pain, from 58 patients with acute myocardial infarction (AMI). During the first 3 h after the onset of chest pain, the serum isoform activity resembled the pattern seen in normal volunteers. Specimens obtained 6 h after AMI showed predominantly MM3 and MB2 (45% and 11% of the total CK activity, respectively). Between 10 and 72 h, there was a gradual shift in which MM3, MM2 and MB2 decreased, while MM1 and MB1 increased. MB2 and MB1 disappeared from the pattern for samples collected after 24-48 h, while MM1 was always the most prominent band at the end of the observation period (66%, range 41-77%, at 48 h). These data suggest that a single determination of CK isoform pattern, drawn between 6 and 48 h after AMI, may provide an effective means of predicting the time of onset of necrosis. There were no significant differences in the CK isoform patterns according to infarct location and functional status of patients.
通过电泳分别将血清肌酸激酶(CK,EC 2.7.3.2)同工酶MM和MB解析为三种(MM1、MM2、MM3)和两种(MB1、MB2)亚型(源自同一同工酶的亚形式),并在58例急性心肌梗死(AMI)患者自胸痛发作开始计时的多个连续血清样本中测定亚型模式。在胸痛发作后的最初3小时内,血清亚型活性类似于正常志愿者中观察到的模式。AMI后6小时采集的样本主要显示MM3和MB2(分别占总CK活性的45%和11%)。在10至72小时之间,出现逐渐变化,其中MM3、MM2和MB2减少,而MM1和MB1增加。对于24 - 48小时后采集的样本,MB2和MB1从模式中消失,而在观察期结束时MM1始终是最突出的条带(48小时时为66%,范围41 - 77%)。这些数据表明,在AMI后6至48小时之间进行一次CK亚型模式测定,可能提供一种预测坏死发作时间的有效方法。根据梗死部位和患者功能状态,CK亚型模式无显著差异。