Xin H B, Zhang B H, Shen H J
Department of Pharmacology, School of Basic Medical Sciences, Beijing Medical University.
Yao Xue Xue Bao. 1992;27(11):806-11.
The protective effects of cyproheptadine, an antiserotonin-antihistaminic agent with calcium channel blocker activity, on calcium paradox in isolated Langendorff's heart in rats were studied. After a 5 min of calcium-free perfusion [standard Krebs-Henseleit (K-H) buffer without calcium, gassed with 95% O2 and 5% CO2] followed by a 20 min of normal K-H buffer (Ca2+ 2.5 mmol/L) perfusion, extensive and rapid myocardial injury was observed: release of massive cellular enzymes such as lactic dehydrogenase (LDH) and creatine phosphokinase (CPK), significant decrease of myocardial anti-oxygen free radical enzymes such as superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities but no obvious change of myocardial lipid peroxides such as malondialdehyde (MDA) content was observed. The loss of normal colour and mechanical activity, even contracture, was also observed in the injured hearts. Cyproheptadine (2.5-5 mumol/L) was shown to effectively antagonize the damage. The results suggest that the protective effects of cyproheptadine on the calcium paradox may be related to its actions of blocking calcium channel, protecting anti-oxygen free radical enzymes and scavenging oxygen free radicals in the myocardial tissues.
研究了具有钙通道阻滞剂活性的抗血清素 - 抗组胺药赛庚啶对大鼠离体Langendorff心脏钙反常的保护作用。在无钙灌注5分钟(不含钙的标准Krebs - Henseleit(K - H)缓冲液,用95% O₂和5% CO₂通气)后,再用正常K - H缓冲液(Ca²⁺ 2.5 mmol/L)灌注20分钟,观察到广泛而迅速的心肌损伤:大量细胞酶如乳酸脱氢酶(LDH)和肌酸磷酸激酶(CPK)释放,心肌抗氧自由基酶如超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH - Px)活性显著降低,但未观察到心肌脂质过氧化物如丙二醛(MDA)含量有明显变化。在受损心脏中还观察到正常颜色和机械活性丧失,甚至出现挛缩。结果表明,赛庚啶对钙反常的保护作用可能与其阻断钙通道、保护抗氧自由基酶以及清除心肌组织中的氧自由基的作用有关。