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在β2肾上腺素能受体阻滞定量分析中,评估气道、震颤及变时性对吸入沙丁胺醇的反应。

Assessment of airways, tremor and chronotropic responses to inhaled salbutamol in the quantification of beta 2-adrenoceptor blockade.

作者信息

Lipworth B J, Brown R A, McDevitt D G

机构信息

Department of Clinical Pharmacology, Ninewells Hospital, Medical School, Dundee.

出版信息

Br J Clin Pharmacol. 1989 Jul;28(1):95-102. doi: 10.1111/j.1365-2125.1989.tb03510.x.

Abstract
  1. The purpose of the study was to assess and compare the effects of inhaled salbutamol on heart rate (HR), finger tremor (Tr) and specific airways conductance (sGaw) in the measurement of beta 2-adrenoceptor blockade in normal subjects. 2. Five healthy volunteers were given oral doses of atenolol 50 mg, 100 mg, 200 mg (A50, A100, A200), propranolol 40 mg (P40) or identical placebo (P1) in a single-blind crossover design. 3. Three hours after drug ingestion, dose-response curves were constructed using cumulative doses of inhaled salbutamol: 200 micrograms, 700 micrograms, 1700 micrograms, 3200 micrograms, 6200 micrograms. HR, Tr and sGaw were measured at each dose increment, made every 20 min. 4. Increasing doses of atenolol were associated with progressive reduction in salbutamol induced beta-adrenoceptor responses. The greatest attenuation occurred with propranolol. These effects on beta-adrenoceptor responses were similar for HR, Tr and sGaw. Geometric mean dose ratios (compared with placebo) for A50, A100, A200 and P40 were as follows HR: 1.98, 2.75, 4.29; Tr: 1.60, 3.78, 6.34, 80.50; sGaw: 1.08, 4.35, 12.30, 66.0 (no dose ratio was obtained for HR with P40). 5. These results showed that atenolol and propranolol attenuated the effects of salbutamol on HR to a similar degree as Tr and sGaw. Furthermore, the variability was least in the measurement of chronotropic responses, suggesting that this may be used to quantify beta 2-adrenoceptor antagonism. The beta 1-adrenoceptor selectivity of atenolol was a dose-dependent phenomenon, although the beta 2-adrenoceptor blockade of A200 was much less than with P40.
摘要
  1. 本研究的目的是评估并比较吸入沙丁胺醇对正常受试者β2肾上腺素能受体阻滞测量中心率(HR)、手指震颤(Tr)和比气道传导率(sGaw)的影响。2. 采用单盲交叉设计,给5名健康志愿者口服剂量分别为50mg、100mg、200mg的阿替洛尔(A50、A100、A200)、40mg的普萘洛尔(P40)或相同的安慰剂(P1)。3. 服药3小时后,使用累积剂量的吸入沙丁胺醇构建剂量反应曲线:200微克、700微克、1700微克、3200微克、6200微克。每20分钟增加一次剂量,并在每次剂量增加时测量HR、Tr和sGaw。4. 阿替洛尔剂量增加与沙丁胺醇诱导的β肾上腺素能受体反应逐渐降低相关。普萘洛尔引起的衰减最大。HR、Tr和sGaw对β肾上腺素能受体反应的这些影响相似。A50、A100、A200和P40的几何平均剂量比(与安慰剂相比)如下:HR:1.98、2.75、4.29;Tr:1.60、3.78、6.34、80.50;sGaw:1.08、4.35、12.30、66.0(P40的HR未获得剂量比)。5. 这些结果表明,阿替洛尔和普萘洛尔减弱沙丁胺醇对HR的影响程度与对Tr和sGaw的影响相似。此外,变时反应测量中的变异性最小,表明这可用于量化β2肾上腺素能受体拮抗作用。阿替洛尔的β1肾上腺素能受体选择性是一种剂量依赖性现象,尽管A200对β2肾上腺素能受体的阻滞远小于P40。

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