Frass O, Sharma H S, Knöll R, Duncker D J, McFalls E O, Verdouw P D, Schaper W
Max Planck Institute of Physiological and Clinical Research, Department of Experimental Cardiology, Bad Nauheim, Germany.
Cardiovasc Res. 1993 Nov;27(11):2037-43. doi: 10.1093/cvr/27.11.2037.
Increasing evidence points to a molecular disturbance of Ca2+ homeostasis in stunned myocardium. The aim of this study was therefore to investigate the expression of mRNAs for Ca2+ binding proteins related to the sarcoplasmic reticulum in a porcine model of myocardial stunning.
In 22 anaesthetised pigs, stunning was achieved by one or two cycles of 10 min left anterior descending coronary artery occlusion and reperfusion. Hearts were excised at various timepoints of the protocol. Total RNA was extracted from stunned (experimental) as well as normally perfused (control) myocardium.
Northern blot analysis using radioactive cDNA probes revealed that the Ca(2+)-ATPase mRNA levels increased 1.6-fold compared to the control value at 90 min of the second reperfusion. The steady state level of phospholamban mRNA rose 2.5-fold at 180 min of reperfusion. A 2.3-fold increase in calsequestrin mRNAs was observed after 90 min of the second reperfusion. The calmodulin and alpha, beta myosin heavy chain mRNA levels were unchanged. A glyceraldehyde-3-phosphate dehydrogenase cDNA probe served as a reference system. Nuclear run-on assays showed increased transcription for Ca(2+)-ATPase and calsequestrin at 90 min of reperfusion, supporting the view that increased mRNA levels seen with northern hybridisation were due to increased transcription of the respective gene.
The results suggest specific repair mechanisms of stunned myocardium and point to the involvement of calcium regulatory proteins related to the sarcoplasmic reticulum in the pathogenesis of myocardial stunning.
越来越多的证据表明,顿抑心肌中存在钙稳态的分子紊乱。因此,本研究的目的是在猪心肌顿抑模型中,研究与肌浆网相关的钙结合蛋白的mRNA表达。
在22只麻醉猪中,通过1或2个周期的10分钟左前降支冠状动脉闭塞和再灌注实现心肌顿抑。在实验方案的不同时间点切除心脏。从顿抑(实验)心肌以及正常灌注(对照)心肌中提取总RNA。
使用放射性cDNA探针的Northern印迹分析显示,在第二次再灌注90分钟时,钙(2+)-ATP酶mRNA水平比对照值增加了1.6倍。在再灌注180分钟时,受磷蛋白mRNA的稳态水平上升了2.5倍。在第二次再灌注90分钟后,观察到肌集钙蛋白mRNA增加了2.3倍。钙调蛋白和α、β肌球蛋白重链mRNA水平未改变。甘油醛-3-磷酸脱氢酶cDNA探针用作参考系统。核转录分析显示,在再灌注90分钟时,钙(2+)-ATP酶和肌集钙蛋白的转录增加,支持了Northern杂交中观察到的mRNA水平增加是由于各自基因转录增加的观点。
结果提示了顿抑心肌的特异性修复机制,并表明与肌浆网相关的钙调节蛋白参与了心肌顿抑的发病机制。