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羟苯磺酸钙(CLS 2210)在急性心肌梗死早期对心肌具有保护作用:一项关于其对生化标志物影响的初步随机、双盲、安慰剂对照研究

Calcium dobesilate (CLS 2210) protects the myocardium in early acute myocardial infarction: a preliminary randomized, double-blind, placebo-controlled study of its effects on biochemical markers.

作者信息

Szlavy L, Repa I, Lengyel I, Lamboy L

机构信息

Department of Diagnostic Radiology, National Institute for Vascular Surgery, Budapest, Hungary.

出版信息

J Cardiovasc Pharmacol. 1990 Jan;15(1):89-95. doi: 10.1097/00005344-199001000-00014.

Abstract

To determine the effect of calcium dobesilate (CLS 2210) on biochemical markers of acute myocardial infarction, and thereby assess its action in limiting myocardial necrosis, this compound was administered intravenously by a randomized, double-blind technique to 23 of 41 patients suffering their first infarction. The remaining 18 patients received a placebo. Administration was begun within 3 h of onset of symptoms and continued for 72 h. Before and during treatment, blood samples were taken for measurement of the serum activity of creatine kinase and its isoenzyme MB, and the serum and urinary concentrations of myoglobin and glycosaminoglycans. Serum creatine kinase and serum and urinary myoglobin were significantly lower in the CLS 2210-treated patients than in the placebo patients throughout the 72 h (p = 0.01, 0.005, and 0.004, respectively). Serum creatine kinase MB and serum glycosaminoglycan in the CLS 2210 patients were initially higher than in the controls, but fell below the control levels between the 40th and 55th hours (p = 0.89 and 0.02, respectively). The glycosaminoglycan urinary concentrations alone were higher in the CLS 2210 group than in the placebo group throughout (p = 0.0005). These findings suggest that CLS 2210 reduces myocardial infarct size in human subjects, as it is already known to do in animals.

摘要

为了确定羟苯磺酸钙(CLS 2210)对急性心肌梗死生化标志物的影响,从而评估其在限制心肌坏死方面的作用,采用随机双盲技术对41例首次发生心肌梗死的患者中的23例静脉注射了该化合物。其余18例患者接受安慰剂治疗。在症状出现后3小时内开始给药,并持续72小时。在治疗前和治疗期间,采集血样以测定肌酸激酶及其同工酶MB的血清活性,以及肌红蛋白和糖胺聚糖的血清及尿液浓度。在整个72小时内,接受CLS 2210治疗的患者的血清肌酸激酶、血清及尿液肌红蛋白均显著低于接受安慰剂治疗的患者(p分别为0.01、0.005和0.004)。CLS 2210组患者的血清肌酸激酶MB和血清糖胺聚糖最初高于对照组,但在第40至55小时之间降至对照水平以下(p分别为0.89和0.02)。整个过程中,仅CLS 2210组的糖胺聚糖尿液浓度高于安慰剂组(p = 0.0005)。这些发现表明,CLS 2210可减小人类受试者的心肌梗死面积,正如已知其在动物中具有此作用一样。

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