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β受体阻滞剂联合用药对单硝酸异山梨酯和二硝酸异山梨酯动力学的影响。

Influence of beta-blocker coadministration on the kinetics of isosorbide mononitrate and dinitrate.

作者信息

Ochs H R, Neugebauer G, Greenblatt D J, Labedzki L

出版信息

Klin Wochenschr. 1986 Dec 1;64(23):1213-6. doi: 10.1007/BF01734458.

Abstract

The influence of beta-blocker coadministration on the kinetics of oral isosorbide-5-mononitrate (ISMN) and isosorbide dinitrate (ISDN) was studied in healthy volunteers. In the first study, 12 subjects ingested 20 mg ISMN on three occasions: in the control state, during coadministration of metipranolol (20 mg 3 times daily), or during metoprolol (100 mg twice daily). There were no significant differences among the three phases in peak serum ISMN concentration (470 ng/ml), the time of peak (0.6 h after dose), elimination half-life (4.5 h), or oral clearance (142 ml/min). In the second study, 10 subjects received 20 mg ISDN in the control state and again during coadministration of propranolol (80 mg 3 times daily). There were no differences between the two phases in peak serum ISDN concentration (20 ng/ml) or the time of peak (0.6 h). Propranolol increased, although not significantly, ISDN clearance (16.5 vs 12.3 L/min, P less than 0.1), and had no effect on total area under the curve for ISMN, the major metabolite of ISDN. Thus, therapeutic doses of these beta-blockers have a minimal influence on the kinetics of single doses of ISMN or ISDN in healthy individuals.

摘要

在健康志愿者中研究了联合使用β受体阻滞剂对口服5-单硝酸异山梨酯(ISMN)和异山梨酯二硝酸酯(ISDN)动力学的影响。在第一项研究中,12名受试者分三次服用20mg ISMN:在对照状态下、在联合使用美替洛尔(每日3次,每次20mg)期间或在美托洛尔(每日2次,每次100mg)期间。在三个阶段之间,血清ISMN峰值浓度(470ng/ml)、峰值时间(给药后0.6小时)、消除半衰期(4.5小时)或口服清除率(142ml/min)均无显著差异。在第二项研究中,10名受试者在对照状态下接受20mg ISDN,并在联合使用普萘洛尔(每日3次,每次80mg)期间再次接受该剂量。两个阶段之间在血清ISDN峰值浓度(20ng/ml)或峰值时间(0.6小时)方面没有差异。普萘洛尔增加了ISDN的清除率(16.5对12.3L/min,P<0.1),尽管差异不显著,并且对ISDN的主要代谢产物ISMN的曲线下总面积没有影响。因此,这些β受体阻滞剂的治疗剂量对健康个体单次剂量的ISMN或ISDN的动力学影响极小。

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