Anna Bergendal , Åke Johansson , Björn Bake , Jan Lötvall , Bengt-Eric Skoogh , Claes-Göran Löfdahl
{"title":"Airway effects of salmeterol in healthy individuals","authors":"Anna Bergendal , Åke Johansson , Björn Bake , Jan Lötvall , Bengt-Eric Skoogh , Claes-Göran Löfdahl","doi":"10.1006/pulp.1995.1038","DOIUrl":null,"url":null,"abstract":"<div><p>The long-acting <em>β</em><sub>2</sub>-agonist salmeterol has been shown in several in vitro studies to produce non-β-mediated relaxant effects. The aim of the present study was to investigate whether these effects have any relevance in humans in vivo. Thirteen healthy individuals were studied in a randomized, double-blind, cross-over study on five separate days. The subjects were pre-treated orally with either propranolol 400 mg in order to block <em>β</em>-adrenoceptor mediated effects or placebo. Two hours after drug intake, three increasing doses of salmeterol (25 + 50 + 100 μg), salbutamol (100 + 200 + 400 μg) or placebo were given from matched meter dose inhalers at 1-h intervals between doses. Specific airway conductance (<em>sG</em>Aw) was measured in a body plethysmograph at the beginning of the experiment and 30 and 60 min after each inhaled dose of the <em>β</em>-agonists. Salmeterol and salbutamol produced the same maximal increase in <em>sG</em>Aw and had the same area under the dose-response curves. Pre-treatment with propranolol totally inhibited the effect of both drugs. In conclusion, salmeterol at clinically used doses did not produce any non-<em>β</em>-mediated bronchodilating effect in normal individuals, measured as <em>sG</em>Aw. Salmeterol and salbutamol showed the same efficacy but salmeterol was four times more potent than salbutamol.</p></div>","PeriodicalId":74618,"journal":{"name":"Pulmonary pharmacology","volume":"8 6","pages":"Pages 283-288"},"PeriodicalIF":0.0000,"publicationDate":"1995-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/pulp.1995.1038","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pulmonary pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0952060085710381","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
The long-acting β2-agonist salmeterol has been shown in several in vitro studies to produce non-β-mediated relaxant effects. The aim of the present study was to investigate whether these effects have any relevance in humans in vivo. Thirteen healthy individuals were studied in a randomized, double-blind, cross-over study on five separate days. The subjects were pre-treated orally with either propranolol 400 mg in order to block β-adrenoceptor mediated effects or placebo. Two hours after drug intake, three increasing doses of salmeterol (25 + 50 + 100 μg), salbutamol (100 + 200 + 400 μg) or placebo were given from matched meter dose inhalers at 1-h intervals between doses. Specific airway conductance (sGAw) was measured in a body plethysmograph at the beginning of the experiment and 30 and 60 min after each inhaled dose of the β-agonists. Salmeterol and salbutamol produced the same maximal increase in sGAw and had the same area under the dose-response curves. Pre-treatment with propranolol totally inhibited the effect of both drugs. In conclusion, salmeterol at clinically used doses did not produce any non-β-mediated bronchodilating effect in normal individuals, measured as sGAw. Salmeterol and salbutamol showed the same efficacy but salmeterol was four times more potent than salbutamol.