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在健康志愿者进行的乙酰甲胆碱激发试验中,对同工酶选择性磷酸二酯酶抑制剂AH 21-132的支气管扩张活性进行的试验。

Trials of the bronchodilator activity of the isoenzyme-selective phosphodiesterase inhibitor AH 21-132 in healthy volunteers during a methacholine challenge test.

作者信息

Foster R W, Rakshi K, Carpenter J R, Small R C

机构信息

Department of Physiological Sciences, Medical School, University of Manchester, UK.

出版信息

Br J Clin Pharmacol. 1992 Dec;34(6):527-34. doi: 10.1111/j.1365-2125.1992.tb05658.x.

DOI:10.1111/j.1365-2125.1992.tb05658.x
PMID:1493085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1381455/
Abstract
  1. An approximately steady-state reduction of specific airway conductance was induced in normal human subjects by means of a methacholine individualized loading+maintenance dose regime. Tested against this background bronchoconstriction, the mixed type III/IV phosphodiesterase inhibitor AH 21-132, ingested in doses up to 90 mg, had no detectable bronchodilator activity. 2. AH 21-132, infused intravenously over 15 min, evoked short-lived bronchodilatation at doses of 20 and 40 mg, without affecting blood pressure or heart rate. 3. AH 21-132, mixed 1:18.5 by weight with sucrose, dissolved in saline, nebulized and inhaled in doses between 2 and 24 mg of AH 21-132, produced dose-dependent bronchodilation. The ED50 was estimated as 9.2 mg AH 21-132. The peak relief of imposed bronchoconstriction was 80% and the apparent half-time of removal of AH 21-132 from its site of action was 25 min. 4. Inhaled, nebulized, hypertonic sucrose had a minor bronchodilator action. 5. AH 21-132, by intravenous and inhaled routes of administration, provides relief of methacholine-induced bronchoconstriction.
摘要
  1. 通过甲胆碱个体化负荷+维持剂量方案,在正常人类受试者中诱导出特定气道传导率的近似稳态降低。在这种背景性支气管收缩的测试中,口服剂量高达90毫克的III/IV型混合磷酸二酯酶抑制剂AH 21-132没有可检测到的支气管扩张活性。2. 将AH 21-132在15分钟内静脉输注,剂量为20毫克和40毫克时可引起短暂的支气管扩张,且不影响血压或心率。3. 将AH 21-132与蔗糖按重量比1:18.5混合,溶解于盐水中,雾化并吸入剂量为2至24毫克的AH 21-132,可产生剂量依赖性支气管扩张。估计ED50为9.2毫克AH 21-132。施加的支气管收缩的最大缓解率为80%,AH 21-132从其作用部位清除的表观半衰期为25分钟。4. 雾化吸入的高渗蔗糖有轻微的支气管扩张作用。5. 通过静脉内和吸入给药途径,AH 21-132可缓解甲胆碱诱导的支气管收缩。

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