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硝苯地平和吲哚美辛对血管紧张素转换酶抑制剂所致咳嗽的影响:一项双盲、随机、交叉研究。

Effects of nifedipine and indomethacin on cough induced by angiotensin-converting enzyme inhibitors: a double-blind, randomized, cross-over study.

作者信息

Fogari R, Zoppi A, Tettamanti F, Malamani G D, Tinelli C, Salvetti A

机构信息

Department of Internal Medicine and Therapeutics, University of Pavia, Italy.

出版信息

J Cardiovasc Pharmacol. 1992 May;19(5):670-3.

PMID:1381763
Abstract

Prostaglandins (PG) have been suggested to play a role in the genesis of cough induced by angiotensin-converting enzyme inhibitors (ACE-I) and that inhibition of PG synthesis can reduce or abolish the incidence of this side effect. Moreover, experimental and clinical data suggest that nifedipine, a dihydropyridine Ca antagonist, can inhibit PG synthesis. Therefore, we wished to determine whether nifedipine can reduce cough induced by ACE-I as compared with indomethacin, a known inhibitor of PG synthesis. Fourteen hypertensive patients who developed cough during captopril chronic therapy randomly received slow-release nifedipine 20 mg twice daily (b.i.d.), indomethacin 50 mg b.i.d., and placebo b.i.d. for 1 week in a double-blind, cross-over design. At the end of each treatment phase, cough was evaluated by a self-administered questionnaire containing an ordinal scale for daily cough intensity and frequency. Indomethacin abolished or markedly reduced cough induced by ACE-I, whereas nifedipine reduced it but to a lesser degree. These findings suggest that PG can play a role in cough caused by ACE-I, and a dihydropyridine Ca antagonist can reduce the occurrence of this side effect.

摘要

前列腺素(PG)被认为在血管紧张素转换酶抑制剂(ACE-I)诱发的咳嗽发生中起作用,并且抑制PG合成可降低或消除这种副作用的发生率。此外,实验和临床数据表明,二氢吡啶类钙拮抗剂硝苯地平可抑制PG合成。因此,我们希望确定与已知的PG合成抑制剂吲哚美辛相比,硝苯地平是否能减轻ACE-I诱发的咳嗽。14名在卡托普利长期治疗期间出现咳嗽的高血压患者,采用双盲交叉设计,随机接受硝苯地平缓释片20mg每日两次(bid)、吲哚美辛50mg bid和安慰剂bid治疗1周。在每个治疗阶段结束时,通过一份包含每日咳嗽强度和频率序数量表的自填问卷对咳嗽进行评估。吲哚美辛消除或显著减轻了ACE-I诱发的咳嗽,而硝苯地平虽能减轻咳嗽,但程度较轻。这些发现表明,PG在ACE-I引起的咳嗽中起作用,并且二氢吡啶类钙拮抗剂可减少这种副作用的发生。

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