摘要
为探讨急性心肌损害对心肌肌球蛋白磷酸化系统的影响,选择对于心肌有特异性损害作用的异丙基肾上腺素(ISP),造成大鼠实验性心肌损害的动物模型,动态观察心肌损害时肌球蛋白磷酸化系统的变化规律。研究结果表明,低剂量ISP导致心肌匀浆中肌球蛋白轻链激酶(MLCK)和肌动球蛋白ATP酶的活性下降,但心肌组织病理切片基本正常;高剂量注射ISP,MLCK和ATP酶活性显著下降,与正常对照组和低剂量组相比,差异十分显著(P<0.01)。在病理形态学上大鼠心肌组织有多处较大的坏死灶。提示,在未发生明显的病理性变化前,心肌细胞内就已发生了一系列的代谢紊乱,如酶活性下降,心肌细胞的收缩功能发生改变;当心肌组织出现病理形态学改变时,细胞内酶活性显著下降,表明已由可逆性损害发展到不可逆的心肌坏死。
Studies on the dynamic changes of MLCK and actinmyosin ATPase in myocardium injury were made.The activities of MLCK and ATPase in myocardium injured by ISP decreased,the pathological sections of myocardium were almost normal under light microscope.With the aggravation of the injury,the activies of MLCK and ATPase were much lower than those of the control and low dose groups and there were many greater necroticareas.The results suggested that before occurrence of pathological changes there was a series of metabolic disorders in cardiac cells.After changes of pathological morphology,the activities of enzymes in cells decreased significantly and the reversible damage developed irreversible myocardium necrosis.
出处
《白求恩医科大学学报》
CSCD
1997年第6期597-599,共3页
Journal of Norman Bethune University of Medical Science
关键词
心肌损害
心肌球蛋白
轻链磷酸化
MLCK
Myosin Light chain phosphorylation Myosin light chain kinase (MLCK)