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茶碱和硝酸异山梨酯对稳定型心绞痛运动能力的比较作用及其作用机制。

Comparative effects of theophylline and isosorbide dinitrate on exercise capacity in stable angina pectoris, and their mechanisms of action.

作者信息

Crea F, Pupita G, Galassi A R, el-Tamimi H, Kaski J C, Davies G J, Maseri A

机构信息

Cardiovascular Unit, Royal Postgraduate Medical School, Hammersmith Hospital, London, England.

出版信息

Am J Cardiol. 1989 Nov 15;64(18):1098-102. doi: 10.1016/0002-9149(89)90859-x.

Abstract

While the role of nitrates in the prevention and treatment of myocardial ischemia is well established, the use of theophylline, proposed almost a century ago, is still controversial. Also controversial is its mechanism of action, initially thought to be coronary dilation. In this randomized, single-blind study, the acute effects on exercise capacity of sublingual isosorbide dinitrate (10 mg) and of intravenous theophylline ethylenediamine (7 mg/kg) were assessed in 10 patients with chronic stable angina and positive exercise test. After the administration of theophylline, the time to onset of angina, the heart rate-blood pressure product at 1-mm ST-segment depression and the exercise duration were similar to that after isosorbide dinitrate administration (9.8 +/- 2.3 vs 9.3 +/- 1.7 minutes, 207 +/- 41 vs 207 +/- 48 beats/min.mm Hg.10(-2) and 10.8 +/- 2 vs 10.4 +/- 2 minutes, respectively). Both drugs significantly (p less than 0.001) improved all these parameters compared to the baseline exercise test. The effect of the 2 drugs on the diameters of angiographically normal segments of large epicardial coronary arteries was then assessed using computerized quantitative angiography in 10 other patients with stable angina. Whereas theophylline failed to increase the coronary diameters compared to that in the baseline angiogram (2.9 +/- 0.6 vs 2.9 +/- 0.6 mm, respectively), the subsequent administration of isosorbide dinitrate resulted in an increase up to 3.2 +/- 0.7 mm (p less than 0.02). Thus, in patients with stable angina, theophylline delays the onset of angina, increases the ischemic threshold and prolongs the exercise duration to the same degree as isosorbide dinitrate.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

虽然硝酸盐在心肌缺血预防和治疗中的作用已得到充分证实,但近一个世纪前就已提出使用的茶碱,其应用仍存在争议。其作用机制也存在争议,最初认为是冠状动脉扩张。在这项随机、单盲研究中,对10例慢性稳定型心绞痛且运动试验阳性的患者,评估了舌下含服硝酸异山梨酯(10毫克)和静脉注射氨茶碱乙二胺(7毫克/千克)对运动能力的急性影响。给予茶碱后,心绞痛发作时间、ST段压低1毫米时的心率 - 血压乘积以及运动持续时间与给予硝酸异山梨酯后相似(分别为9.8±2.3分钟与9.3±1.7分钟、207±41与207±48次/分钟·毫米汞柱·10⁻²、10.8±2分钟与10.4±2分钟)。与基线运动试验相比,两种药物均显著(p<0.001)改善了所有这些参数。然后,在另外10例稳定型心绞痛患者中,使用计算机定量血管造影评估了这两种药物对心外膜大冠状动脉造影正常节段直径的影响。与基线血管造影相比,茶碱未能增加冠状动脉直径(分别为2.9±0.6毫米与2.9±0.6毫米),而随后给予硝酸异山梨酯则使直径增加至3.2±0.7毫米(p<0.02)。因此,在稳定型心绞痛患者中,茶碱延迟心绞痛发作、提高缺血阈值并延长运动持续时间的程度与硝酸异山梨酯相同。(摘要截短于250字)

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