Effect of prenalterol in asthmatic patients
- PMID: 6129142
- DOI: 10.1007/BF00613609
Effect of prenalterol in asthmatic patients
Abstract
The bronchial effects of prenalterol, a selective inotropic beta-adrenoceptor agonist, were examined to see whether beta 1-adrenoceptor stimulation would produce bronchodilatation, or whether beta 2-adrenoceptor blockade could be demonstrated. In a first investigation 8 asthmatic patients were studied under standardized conditions in a double-blind, randomized, crossover comparison between i.v. doses of prenalterol and saline infusions. After the fourth dose of prenalterol/saline, 4 intravenous doses of terbutaline were given. All medication was given at 30 min intervals. In a second study in 7 of the previously studied patients, 5 increasing doses of prenalterol or saline were inhaled from a bird ventilator, and after the last dose 4 i.v. doses of terbutaline were given as before. Prenalterol and saline caused no change in FEV1 during the intravenous study. Terbutaline infusion produced a dose dependent increase in FEV1 which was not significantly altered after prenalterol treatment. In the inhalation study, in which a much larger dose was applied to the bronchial tree, there was no significant difference in FEV1, between the saline and prenalterol inhalations. However, prenalterol did show beta 2-blocking property, as the dose response curve of terbutaline was shifted to the right. The heart rate increased significantly and to the same degree during both the i.v. and inhaled prenalterol treatments. Thus, this study revealed no significant beta 2-blocking effect of therapeutic doses of i.v. prenalterol. However, when the drug was inhaled in a much higher dose, a beta 2-blocking effect on FEV1 was recorded. No significant beta 1-adrenoceptor-mediated bronchodilator effect of prenalterol could be demonstrated.
Similar articles
-
Ventilatory and haemodynamic effects of prenalterol and terbutaline in asthmatic patients.Eur J Clin Pharmacol. 1983;24(2):173-8. doi: 10.1007/BF00613813. Eur J Clin Pharmacol. 1983. PMID: 6132819 Clinical Trial.
-
Failure of beta-adrenergic stimulation to affect cholecystokinin-stimulated sigmoid motility in man.Scand J Gastroenterol. 1985 Dec;20(10):1169-74. doi: 10.3109/00365528509089271. Scand J Gastroenterol. 1985. PMID: 2869574 Clinical Trial.
-
Effects of beta-adrenoceptor stimulation on rectosigmoid motility in man.Dig Dis Sci. 1985 Jun;30(6):536-40. doi: 10.1007/BF01320259. Dig Dis Sci. 1985. PMID: 2859970 Clinical Trial.
-
Rectosigmoid motility response to beta-adrenoceptor stimulation in patients with the irritable bowel syndrome.Scand J Gastroenterol. 1985 Dec;20(10):1163-8. doi: 10.3109/00365528509089270. Scand J Gastroenterol. 1985. PMID: 2869573 Clinical Trial.
-
Beta adrenergic influence on oesophageal peristalsis in man.Gut. 1986 Mar;27(3):260-6. doi: 10.1136/gut.27.3.260. Gut. 1986. PMID: 2870956 Free PMC article. Clinical Trial.
Cited by
-
Airway receptors.Postgrad Med J. 1989 Aug;65(766):532-42. doi: 10.1136/pgmj.65.766.532. Postgrad Med J. 1989. PMID: 2557601 Free PMC article. Review. No abstract available.
-
Influence of circulating alpha adrenoceptor agonists on lung function in patients with exercise induced asthma and healthy subjects.Thorax. 1986 Jul;41(7):552-8. doi: 10.1136/thx.41.7.552. Thorax. 1986. PMID: 3787535 Free PMC article.
-
Transforming Growth Factor-β1 Decreases β2-Agonist-induced Relaxation in Human Airway Smooth Muscle.Am J Respir Cell Mol Biol. 2019 Aug;61(2):209-218. doi: 10.1165/rcmb.2018-0301OC. Am J Respir Cell Mol Biol. 2019. PMID: 30742476 Free PMC article.
-
A comparative study on the ventilatory and haemodynamic effects of xamoterol and atenolol in asthmatic patients.Br J Clin Pharmacol. 1986 Nov;22(5):595-602. doi: 10.1111/j.1365-2125.1986.tb02940.x. Br J Clin Pharmacol. 1986. PMID: 2878680 Free PMC article. Clinical Trial.
-
Beta-Adrenergic Agonists.Pharmaceuticals (Basel). 2010 Mar 30;3(4):1016-1044. doi: 10.3390/ph3041016. Pharmaceuticals (Basel). 2010. PMID: 27713285 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical