Radenković Sandra, Brajović Milan, Konjević Gordana, Gopcević Kristina
Institut za onkologiju i radiologiju Srbije, Odeljenje za eksperimentalnu onkologiju, Beograd, Srbija.
Vojnosanit Pregl. 2010 Oct;67(10):825-30. doi: 10.2298/vsp1010825r.
BACKGROUND/AIM: The main characteristic of matrix metalloproteinases (MMPs) is the degradation of extracellular matrix. Synthesis of MMPs has been reported in coronary atherosclerotic lesions in patients with coronary disease (CD) suggesting a pathogenic role of MMPs in its development. Recently there is increasing evidence that gelatinase A (pro MMP-2) and gelatinase B (proMMP-9) play a pathogenic role in the development of the atherosclerotic plaques. The aim of the study was to determine, by the use of a gel image system, a possible presence of active gelatinases in the serum of the patients with CD, as well as if their activity is higher in these patients than in healthy people.
By gelatin zymography we analyzed the activity of proMMP-2 and proMMP-9 in the serum of 50 patients with various coronary artery disease stages and in the serum of 15 healthy controls. The activity was measured by using a gel image system (Kodak Image 1D 3.6.).
ProMMP-2 and proMMP-9 activity was significantly higher in the serum of patients with CD compared to controls. There was higher activity of MMP-2 and MMP-9 in the serum of patients with acute myocardial infarction (AMI) compared to patients with stable angina pectoris, as well as higher proMMP-9 activity in patients with unstable angina pectoris compared to patients with stable angina pectoris.
ProMMP-2 and proMMP-9 participate in processes associated with destabilizing plaques and understanding the processes of MMPs activation and regulation may have significant benefits in clinical interpretation. The reported higher proMMP-2 and proMMP-9 activity in the serum of patients with CD suggests a role of proMMP-2 and proMMP-9 in prognostic stratification of these patients and in designing new drugs.
背景/目的:基质金属蛋白酶(MMPs)的主要特征是降解细胞外基质。已有报道称,在冠心病(CD)患者的冠状动脉粥样硬化病变中存在MMPs的合成,这表明MMPs在其发病过程中具有致病作用。最近,越来越多的证据表明,明胶酶A(前MMP-2)和明胶酶B(前MMP-9)在动脉粥样硬化斑块的形成过程中起致病作用。本研究的目的是通过使用凝胶图像系统,确定CD患者血清中是否可能存在活性明胶酶,以及这些患者中其活性是否高于健康人。
通过明胶酶谱法,我们分析了50例不同冠状动脉疾病阶段患者血清和15例健康对照者血清中前MMP-2和前MMP-9的活性。使用凝胶图像系统(柯达Image 1D 3.6.)测量活性。
与对照组相比,CD患者血清中前MMP-2和前MMP-9的活性显著更高。与稳定型心绞痛患者相比,急性心肌梗死(AMI)患者血清中MMP-2和MMP-9的活性更高,与稳定型心绞痛患者相比,不稳定型心绞痛患者血清中前MMP-9的活性更高。
前MMP-2和前MMP-9参与了与斑块不稳定相关的过程,了解MMPs的激活和调节过程可能对临床解释有显著益处。报道的CD患者血清中较高的前MMP-2和前MMP-9活性表明,前MMP-2和前MMP-9在这些患者的预后分层和新药设计中发挥作用。