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美托洛尔在闭胸犬冠状动脉栓塞24小时后无法实现对梗死面积的持续限制。

Inability of metoprolol to achieve a sustained limitation of infarct size 24 h after coronary artery embolization in the closed chest dog.

作者信息

Kudoh Y, Maxwell M P, Hearse D J, Downey J M, Yellon D M

出版信息

J Cardiovasc Pharmacol. 1984 Nov-Dec;6(6):1201-9.

PMID:6084780
Abstract

Studies were undertaken to ascertain whether metoprolol, a beta 1-selective adrenergic blocking agent, could offer a limitation of myocardial injury throughout a 24-h period of coronary embolization in the dog. Regional myocardial ischaemia was induced through the use of a bead embolization technique which did not require thoracotomy. In order to delineate the zone at risk of infarction (hypoperfused area), radioactive microspheres (141Ce) were administered intraventricularly immediately after embolization. In the drug-treated group (n = 8) metoprolol administration was initiated by an intravenous bolus injection (0.3 mg X kg-1). This was followed by a continuous infusion (0.003 mg X kg-1 X min-1) during the 24-h experimental period. In the control group (n = 8) saline was administered throughout the 24-h period. Electrocardiographic activity was monitored throughout the experiment and this confirmed the negative chronotropic and antiarrhythmic properties of metoprolol. After 24 h, the hearts were excised and transverse myocardial sections (3 mm) prepared. Areas of necrosis were visualized by tetrazolium staining and risk zones were defined by microsphere autoradiography. In the control and metoprolol-treated groups, 73.3 +/- 7.7% and 68.2 +/- 6.1% of the risk zone became necrotic, respectively. There was no significant difference between these groups.

摘要

开展了多项研究,以确定β1选择性肾上腺素能阻滞剂美托洛尔是否能在犬冠状动脉栓塞24小时期间限制心肌损伤。通过使用无需开胸的微珠栓塞技术诱导局部心肌缺血。为了描绘梗死风险区域(灌注不足区域),在栓塞后立即经心室内注射放射性微球(141Ce)。在药物治疗组(n = 8)中,通过静脉推注(0.3 mg·kg-1)开始给予美托洛尔。随后在24小时实验期间持续输注(0.003 mg·kg-1·min-1)。在对照组(n = 8)中,在整个24小时期间给予生理盐水。在整个实验过程中监测心电图活动,这证实了美托洛尔的负性变时性和抗心律失常特性。24小时后,取出心脏并制备横向心肌切片(3 mm)。通过四氮唑染色观察坏死区域,并通过微球放射自显影确定风险区域。在对照组和接受美托洛尔治疗的组中,分别有73.3±7.7%和68.2±6.1%的风险区域发生坏死。这些组之间没有显著差异。

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