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沙美特罗的非肺部效应是否会出现快速耐受性?

Does tachyphylaxis occur to the non-pulmonary effects of salmeterol?

作者信息

Maconochie J G, Minton N A, Chilton J E, Keene O N

机构信息

Clinical Pharmacology Division, Glaxo Group Research Ltd, Greenford, Middlesex.

出版信息

Br J Clin Pharmacol. 1994 Feb;37(2):199-204. doi: 10.1111/j.1365-2125.1994.tb04261.x.

Abstract
  1. The potential for tachyphylaxis to the non-pulmonary effects of salmeterol, a long-acting selective beta 2-adrenoceptor agonist was investigated in 12 healthy male subjects in a double-blind two period crossover study design. 2. Subjects received cumulative doses of up to 400 micrograms (50 + 50 + 100 + 100 + 100 micrograms at 45 min intervals) inhaled salmeterol prior to a 13 day dosing schedule of twice-daily inhaled salmeterol 100 micrograms or placebo. Twelve hours after the last dose of salmeterol or placebo, subjects again received cumulative doses of up to 400 micrograms inhaled salmeterol. 3. Pulse rate, blood pressure, 12-lead ECG, physiological tremor and peak expiratory flow rate (PEFR) were measured before administration of cumulative doses of salmeterol, at 10, 20, 30 and 40 min after each incremental dose of salmeterol and at 4, 6 and 8 h after the first dose. Blood samples were taken for plasma potassium, magnesium, non-esterified fatty acids (NEFA) and blood glucose concentrations at 20 and 40 min after each dose and at 4, 6 and 8 h after the first dose. 4. Eleven subjects completed the study. One subject withdrew due to beta 2-adrenoceptor related adverse events. All other adverse events reported were mild in nature. 5. Dose-related changes to the effects of salmeterol on pulse rate, QTc interval, tremor, PEFR, blood glucose and plasma potassium were seen, but there was no dose-related effect of salmeterol on blood pressure, plasma magnesium and NEFA. 6. Tachyphylaxis occurred to the effects of salmeterol on tremor, QTc and blood glucose.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 在一项双盲两阶段交叉研究设计中,对12名健康男性受试者研究了长效选择性β2肾上腺素能受体激动剂沙美特罗非肺部效应快速减敏的可能性。2. 在每日两次吸入100微克沙美特罗或安慰剂的13天给药方案之前,受试者接受累积剂量高达400微克(每隔45分钟吸入50 + 50 + 100 + 100 + 100微克)的吸入沙美特罗。在最后一剂沙美特罗或安慰剂12小时后,受试者再次接受累积剂量高达400微克的吸入沙美特罗。3. 在给予沙美特罗累积剂量之前、每次递增剂量的沙美特罗后10、20、30和40分钟以及首次给药后4、6和8小时测量脉搏率、血压、12导联心电图、生理性震颤和呼气峰值流速(PEFR)。在每次给药后20和40分钟以及首次给药后4、6和8小时采集血样,检测血浆钾、镁、非酯化脂肪酸(NEFA)和血糖浓度。4. 11名受试者完成了研究。一名受试者因β2肾上腺素能受体相关不良事件退出。报告的所有其他不良事件性质均较轻。5. 观察到沙美特罗对脉搏率、QTc间期、震颤、PEFR、血糖和血浆钾的影响存在剂量相关变化,但沙美特罗对血压、血浆镁和NEFA没有剂量相关影响。6. 沙美特罗对震颤、QTc和血糖的作用出现了快速减敏。(摘要截短至250字)

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