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CLS 2210对犬缺血心肌的挽救作用:一项初步双盲研究。

Salvage of ischemic myocardium by CLS 2210 in the dog: a preliminary double-blind study.

作者信息

Szlavy L, Repa I, Szabo Z, de Courten A, Hachen H J

出版信息

Angiology. 1987 Jan;38(1 Pt 2):85-91. doi: 10.1177/000331978703800112.

Abstract

To assess whether a cardiac lymphagogue, CLS 2210, would reduce myocardial infarct size after coronary artery ligation, studies were performed in 14 dogs. The left anterior descending coronary artery was ligated in each dog, and the dogs were randomized to either placebo or CLS 2210 treatment, which was carried on for seven days. After seven days the animals were sacrificed and the volume of infarcted myocardium was determined macroscopically on a double-blind basis, supported by histologic examination. CLS 2210 treatment resulted in a highly significant reduction in the volume of infarcted myocardium (p less than 0.001). Since CLS 2210 is chemically and pharmacologically unrelated to hyaluronidase but shares an action with hyaluronidase as a cardiac lymphagogue, the results offer further support for a role of myocardial lymphatics in the evolution of myocardial necrosis following coronary artery occlusion and provide an explanation for the mechanism by which these agents reduce myocardial infarction size.

摘要

为评估一种心脏促淋巴剂CLS 2210能否减小冠状动脉结扎后的心肌梗死面积,对14只犬进行了研究。每只犬均结扎左冠状动脉前降支,并随机分为安慰剂组或CLS 2210治疗组,持续治疗7天。7天后处死动物,在双盲条件下宏观测定梗死心肌体积,并辅以组织学检查。CLS 2210治疗使梗死心肌体积显著减小(p<0.001)。由于CLS 2210在化学和药理上与透明质酸酶无关,但作为一种心脏促淋巴剂与透明质酸酶有共同作用,这些结果进一步支持了心肌淋巴管在冠状动脉闭塞后心肌坏死演变中的作用,并为这些药物减小心肌梗死面积的机制提供了解释。

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