Mel'nikova N P, Timoshin S S, Murzina N B, Sazonova E N, Kuznetsov A V, Yarova E P
Central Research Laboratory, Far-Eastern State Medical University, Khabarovsk.
Bull Exp Biol Med. 2000 Dec;130(12):1206-8.
Effect of intraperitoneal injection of tetrapeptide A10 (H-Tyr-D-Orn-Phe-Gly-OH), selective mu-opiate receptor agonist, synthetic analog of dermorphine, in a dose of 100 microg/kg on DNA synthesis and protein content in the myocardium was studied in albino rats. Five injections of tetrapeptide on days 2-6 after birth caused no changes in DNA synthesis 17 days after the last injection, i. e. in 24-day rats. The number of nucleoli and their area increased. In adult males long-term (3-week) treatment with tetrapeptide A10 increased the number of nucleoli and the mean and integral optical density of isolated cardiomyocytes stained with amido black B, which probably attested to activation of protein synthesis in the myocardium. Simultaneously, the content of catecholamines in the heart increased. These data are comparable with delayed effects of kappa-opiate receptor agonist dinorphine A1-13 and indicate that morphogenetic properties of opioid peptides in rat myocardium are realized via the same routes.
研究了腹腔注射剂量为100微克/千克的四肽A10(H-Tyr-D-Orn-Phe-Gly-OH),一种选择性μ-阿片受体激动剂、地吗啡的合成类似物,对白化大鼠心肌中DNA合成和蛋白质含量的影响。在出生后第2至6天进行五次四肽注射,在最后一次注射17天后,即24日龄大鼠中,DNA合成未发生变化。核仁数量及其面积增加。在成年雄性大鼠中,长期(3周)用四肽A10治疗增加了核仁数量以及用酰胺黑B染色的分离心肌细胞的平均和积分光密度,这可能证明心肌中蛋白质合成被激活。同时,心脏中儿茶酚胺的含量增加。这些数据与κ-阿片受体激动剂地诺啡A1-13的延迟效应相当,表明阿片肽在大鼠心肌中的形态发生特性是通过相同途径实现的。