Suppr超能文献

稳定型心绞痛患者对硝苯地平耐受性的发展

Development of tolerance to nifedipine in patients with stable angina pectoris.

作者信息

Martsevich S Y, Metelitsa V I, Rumiantsev D O, Piotrovskii V K, Slastnikova I D, Egorov L V, Vygodin V A

机构信息

USSR Research Center for Preventive Medicine, Moscow.

出版信息

Br J Clin Pharmacol. 1990 Mar;29(3):339-46. doi: 10.1111/j.1365-2125.1990.tb03645.x.

Abstract
  1. The possibility of development of tolerance to the anti-ischaemic and anti-anginal effects of nifedipine during sustained administration for 2 months was studied in 15 patients with stable angina pectoris by means of repeated exercise tests on a treadmill. 2. After acute administration of nifedipine (20-30 mg) substantial anti-ischaemic and anti-anginal effects lasted for at least 4 h in all patients. 3. During sustained nifedipine treatment with a dose schedule which provided continuous anti-ischaemic effect during a day (mean daily dose 82.7 +/- 6.0 mg, range 60-120 mg) a substantial attenuation of this effect was registered. The duration of the anti-ischaemic effect was 5.4 +/- 0.3 h after acute administration, decreasing significantly to 3.6 +/- 0.4 h during sustained administration. 4. The attenuation of the nifedipine effect was not associated with worsening of the patients' condition. 5. Plasma concentrations of nifedipine and its metabolite were similar after acute administration and during sustained treatment. Protein binding of nifedipine also remained constant during the study. 6. There was marked interindividual variation in the degree of attenuation of the nifedipine effect during sustained administration. In five patients nearly complete loss of nifedipine efficacy was registered. Eight to ten days after stopping regular administration of nifedipine only partial restoration of nifedipine effect was observed. 7. We conclude that during sustained nifedipine administration tolerance to its anti-ischaemic, anti-anginal and circulatory effects develops in a substantial number of patients with stable angina pectoris.
摘要
  1. 通过对15例稳定型心绞痛患者进行跑步机上的重复运动试验,研究了持续服用硝苯地平2个月期间对其抗缺血和抗心绞痛作用产生耐受性的可能性。2. 急性给予硝苯地平(20 - 30毫克)后,所有患者的显著抗缺血和抗心绞痛作用至少持续4小时。3. 在持续硝苯地平治疗期间,采用能在一天内提供持续抗缺血作用的剂量方案(平均日剂量82.7±6.0毫克,范围60 - 120毫克),观察到这种作用有显著减弱。急性给药后抗缺血作用持续时间为5.4±0.3小时,持续给药期间显著缩短至3.6±0.4小时。4. 硝苯地平作用的减弱与患者病情恶化无关。5. 急性给药后和持续治疗期间,硝苯地平及其代谢产物的血浆浓度相似。研究期间硝苯地平的蛋白结合也保持恒定。6. 在持续给药期间,硝苯地平作用减弱的程度存在明显的个体差异。在5例患者中,观察到硝苯地平疗效几乎完全丧失。停止常规服用硝苯地平8至10天后,仅观察到硝苯地平作用部分恢复。7. 我们得出结论,在持续服用硝苯地平期间,大量稳定型心绞痛患者会对其抗缺血、抗心绞痛和循环作用产生耐受性。

相似文献

本文引用的文献

10
Comparison of nitroglycerin patches and nifedipine.硝酸甘油贴片与硝苯地平的比较。
J Cardiovasc Pharmacol. 1987 Sep;10(3):315-9. doi: 10.1097/00005344-198709000-00010.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验