Kumagae H, Koiwaya Y, Tanaka K
First Department of Internal Medicine, Miyazaki Medical College, Japan.
Clin Ther. 1990 Jan-Feb;12(1):31-43.
To determine whether hemodynamic effects of isosorbide dinitrate (ISDN) diminish and disappear during sustained administration, nine patients with recent myocardial infarction received 10 mg of ISDN intravenously before and 1, 4, 12, 24, and 48 weeks after sustained oral administration of 20 mg of the slow-release form of ISDN four times daily. Blood pressure always decreased after intravenous ISDN; the decrease tended to be diminished when preceded by oral ISDN, but no further attenuation in blood pressure was noted. The decrease in blood pressure was associated with consistent and nonsignificant increases in heart rate after intravenous ISDN. Plasma ISDN levels were not affected by prior oral ISDN. Plasma isosorbide 2-mononitrate and isosorbide 5-mononitrate levels were consistently higher when preceded by oral ISDN. The results suggest that the hemodynamic and metabolic properties of ISDN are preserved even after sustained therapy.
为了确定持续给药期间硝酸异山梨酯(ISDN)的血流动力学效应是否会减弱并消失,9例近期心肌梗死患者在每日4次持续口服20mg缓释型ISDN之前以及之后1、4、12、24和48周,静脉注射10mg ISDN。静脉注射ISDN后血压总是下降;口服ISDN后再静脉注射ISDN,血压下降趋势有所减弱,但未观察到血压进一步降低。静脉注射ISDN后血压下降与心率持续且不显著增加有关。血浆ISDN水平不受先前口服ISDN的影响。口服ISDN后,血浆5-单硝酸异山梨酯和2-单硝酸异山梨酯水平始终较高。结果表明,即使经过持续治疗,ISDN的血流动力学和代谢特性仍得以保留。