Khlystov V V, Pavlenko V S, Usynin A F, Slepushkin V D
Arkh Patol. 1988;50(3):72-6.
The effect of opiate peptides (leu-enkephalin, met-enkephalin and beta-endorphin) as well as of enkephalin synthetic analogs (two tetrapeptides and dalargin hexapeptide) on the activity of blood enzymes CPK and LDG1, the scope of myocardial infarction and ultrastructure of periinfarction cardiomyocytes has been studied on 200 white outbred rats with simulated myocardial infarction. The endogenous opiate peptides and dalargin hexapeptide were found to significantly decrease CPK and LDG1 activity and to diminish the size of the infarction. The effect is related to the drugs influence on the survival of periinfarction cardiomyocytes that can be proved electron-microscopically and using colloid lanthanum test.
在200只模拟心肌梗死的白化远交大鼠身上,研究了阿片肽(亮氨酸脑啡肽、甲硫氨酸脑啡肽和β-内啡肽)以及脑啡肽合成类似物(两种四肽和六肽达乐argin)对血液中肌酸磷酸激酶(CPK)和乳酸脱氢酶1(LDG1)活性、心肌梗死范围以及梗死周围心肌细胞超微结构的影响。发现内源性阿片肽和六肽达乐argin能显著降低CPK和LDG1活性,并减小梗死面积。这种作用与药物对梗死周围心肌细胞存活的影响有关,这可以通过电子显微镜检查和使用胶体镧试验得到证实。