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缺血性离体大鼠心脏再灌注期间铜蓝蛋白的抗心律失常作用

Antiarrhythmic effects of ceruloplasmin during reperfusion in the ischemic isolated rat heart.

作者信息

Atanasiu R, Dumoulin M J, Chahine R, Mateescu M A, Nadeau R

机构信息

Department of Physiology, Université de Montréal, Hôpital du Sacré-Coeur de Montréal, Canada.

出版信息

Can J Physiol Pharmacol. 1995 Sep;73(9):1253-61. doi: 10.1139/y95-177.

Abstract

The ability of ceruloplasmin, an important serum antioxidant, to reduce the vulnerability of the isolated rat heart to reperfusion arrhythmias has been investigated. Bovine plasma ceruloplasmin was purified by chromatography on aminoethyl-agarose. Isolated rat hearts were submitted to 15 min of regional ischemia and 10 min of reperfusion. The dose-effect relationship and the role of ceruloplasmin conformational integrity in cardioprotection were established by treatment of ischemic hearts with ceruloplasmin at various concentrations (0.25, 0.5, 1, and 2 microM) and at different degrees of conformational integrity (A610/A280 = 0.02, 0.04, and 0.06), 5 min before reperfusion. Deferoxamine (20-500 microM) was used as a positive control. As negative controls we used chemically inactivated ceruloplasmin (1 microM), heat-denatured ceruloplasmin (1 microM), and albumin (1-4 microM). In the control group during the first 5 min of reperfusion, the incidence of total ventricular fibrillation was 100% and of irreversible ventricular fibrillation was 83%. The incidence of reversible and irreversible ventricular fibrillation was significantly decreased in the ceruloplasmin-treated groups in both a dose and molecular integrity dependent manner. Ceruloplasmin had no effect on the incidence of ventricular tachycardia. Deferoxamine reduced the incidence of ventricular fibrillation to the same degree as ceruloplasmin but at concentrations much higher than those of ceruloplasmin. Chemically inactivated ceruloplasmin, heat-denatured ceruloplasmin, and albumin had no protective effects on reperfusion-induced arrhythmias.

摘要

人们研究了一种重要的血清抗氧化剂——铜蓝蛋白降低离体大鼠心脏对再灌注心律失常易感性的能力。通过在氨乙基琼脂糖上进行层析,纯化了牛血浆铜蓝蛋白。将离体大鼠心脏进行15分钟的局部缺血和10分钟的再灌注。在再灌注前5分钟,用不同浓度(0.25、0.5、1和2微摩尔)和不同构象完整性程度(A610/A280 = 0.02、0.04和0.06)的铜蓝蛋白处理缺血心脏,从而确定铜蓝蛋白的剂量效应关系及其构象完整性在心脏保护中的作用。去铁胺(20 - 500微摩尔)用作阳性对照。作为阴性对照,我们使用化学灭活的铜蓝蛋白(1微摩尔)、热变性的铜蓝蛋白(1微摩尔)和白蛋白(1 - 4微摩尔)。在对照组再灌注的前5分钟,室颤总发生率为100%,不可逆室颤发生率为83%。在铜蓝蛋白处理组中,可逆性和不可逆性室颤的发生率均以剂量和分子完整性依赖的方式显著降低。铜蓝蛋白对室性心动过速的发生率没有影响。去铁胺将室颤发生率降低到与铜蓝蛋白相同的程度,但所需浓度远高于铜蓝蛋白。化学灭活的铜蓝蛋白、热变性的铜蓝蛋白和白蛋白对再灌注诱导的心律失常没有保护作用。

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