Bennett J A, Tattersfield A E
Division of Respiratory Medicine, City Hospital, Nottingham, UK.
Thorax. 1997 May;52(5):458-64. doi: 10.1136/thx.52.5.458.
The main adverse effects of beta 1 agonists relate to their systemic activity. The time course and dose response relations of the systemic effects of salmeterol compared with salbutamol were investigated.
A double blind, randomised, crossover study was carried out in 14 healthy subjects who attended on seven days. Heart rate, QTc interval, blood pressure, plasma potassium and glucose concentrations were measured for four hours following inhaled placebo, salmeterol 100, 200 and 400 micrograms and salbutamol 600, 1200 and 2400 micrograms given by metered dose inhaler. Maximum changes from baseline and maximum absolute values following each dose of treatment were used to construct log dose response curves and calculate relative dose potency.
Both salmeterol and salbutamol caused dose dependent changes in heart rate, QTc interval, and plasma potassium and glucose concentrations. The onset of cardiac effects was rapid following both drugs, whereas changes in glucose and potassium concentrations occurred more gradually with salmeterol. The increase in heart rate and fall in potassium level were sustained over the four hours whereas glucose levels gradually returned towards baseline. The relative dose potency of salmeterol compared with salbutamol for changes from baseline was 7.1 (95% CI 3.9 to 14.4) for the QTc interval and 8.2 (95% CI 5.7 to 12.6) for plasma potassium concentration. Salmeterol caused steeper dose response curves for heart rate and plasma glucose concentration than salbutamol so relative dose potency values could not be calculated.
These findings support previous data that salmeterol 100 micrograms is broadly equivalent to salbutamol 800 micrograms for systemic effects. The greater systemic effects of salmeterol are most likely to be due to greater potency relative to dose, although it may also have greater systemic bioavailability. The steeper dose response curve for heart rate with salmeterol indicates that it has a narrower therapeutic window than salbutamol and thus should be prescribed at the lowest effective dose.
β1 激动剂的主要不良反应与其全身活性有关。研究了沙美特罗与沙丁胺醇全身效应的时间过程和剂量反应关系。
对 14 名健康受试者进行了一项双盲、随机、交叉研究,受试者连续七天参与研究。通过定量吸入器分别给予吸入安慰剂、100、200 和 400 微克沙美特罗以及 600、1200 和 2400 微克沙丁胺醇后,测量四小时内心率、QTc 间期、血压、血浆钾和葡萄糖浓度。使用每次治疗剂量后相对于基线的最大变化和最大绝对值来构建对数剂量反应曲线并计算相对剂量效价。
沙美特罗和沙丁胺醇均引起心率、QTc 间期、血浆钾和葡萄糖浓度的剂量依赖性变化。两种药物给药后心脏效应起效迅速,而沙美特罗使葡萄糖和钾浓度的变化更为缓慢。心率增加和钾水平下降在四小时内持续存在,而葡萄糖水平逐渐恢复至基线。沙美特罗相对于沙丁胺醇在 QTc 间期相对于基线变化的相对剂量效价为 7.1(95%可信区间 3.9 至 14.4),血浆钾浓度为 8.2(95%可信区间 5.7 至 12.6)。沙美特罗引起的心率和血浆葡萄糖浓度剂量反应曲线比沙丁胺醇更陡峭,因此无法计算相对剂量效价值。
这些发现支持先前的数据,即 100 微克沙美特罗的全身效应大致相当于 800 微克沙丁胺醇。沙美特罗更大的全身效应最可能是由于相对于剂量的更大效价,尽管它也可能具有更高的全身生物利用度。沙美特罗心率的剂量反应曲线更陡峭,表明其治疗窗比沙丁胺醇更窄,因此应以最低有效剂量开具处方。