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Effects of sustained‐release tulobuterol on asthma control and β‐adrenoceptor function
Author(s) -
Kume Hiroaki,
Kondo Masashi,
Ito Yasushi,
Suzuki Ryujiro,
Yamaki Kenichi,
Takagi Kenzo
Publication year - 2002
Publication title -
clinical and experimental pharmacology and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 103
eISSN - 1440-1681
pISSN - 0305-1870
DOI - 10.1046/j.1440-1681.2002.03777.x
Subject(s) - medicine , pharmacology , methacholine , anesthesia , endocrinology , respiratory disease , lung
Summary 1. Recently, a patch formulation of tulobuterol, a β‐adrenoceptor (AR) agonist, has been developed using a transdermal delivery system. The present study was designed to determine whether β‐AR function and asthma control were affected by the sustained‐released β‐AR agonist. 2. Tulobuterol (2 mg) was applied daily for 8 weeks to seven patients with bronchial asthma in whom the morning dip in the peak expiratory flow (PEF) rate developed even though inhaled glucocorticoids were being taken. After treatment with tulobuterol, the early morning reduction in PEF was suppressed and PEF values were increased from 367 ± 35 to 439 ± 38 L/min ( P < 0.05). The rescue use of inhaled β‐AR agonists was decreased from 6.9 ± 2.0 to 1.0 ± 0.7 puffs/week ( P < 0.01). Symptom scores also decreased from 8.3 ± 3.4 to 2.1 ± 1.4 score/week ( P < 0.01). 3. Next, we sought to examine the effects of exposure to tulobuterol on β‐AR function in guinea‐pig tracheal smooth muscle. After exposure of tissues to tulobuterol (0.01–10 µmol/L) for 45 min, the inhibitory effects of tulobuterol on methacholine‐induced contractions were attenuated in a concentration‐dependent manner. However, the inhibitory effects of tulobuterol were not affected after exposure to 0.01 µmol/L tulobuterol (a concentration greater than serum levels in clinical use). In contrast, the inhibitory effects of procaterol were not affected after exposure to tulobuterol under the same experimental conditions. 4. These results indicate that the combination of sustained‐released tulobuterol with inhaled glucocorticoid therapy is beneficial to patients with bronchial asthma who suffer from symptoms induced by the morning dip in PEF. Moreover, chronic exposure to lower concentrations of tulobuterol does not lead to desensitization of β‐AR in airway smooth muscle.