Downregulation of the cough reflex by aclidinium and tiotropium in awake and anesthetized rabbits

被引:12
|
作者
Mutolo, Donatella [1 ]
Cinelli, Elenia [1 ]
Iovino, Ludovica [1 ]
Pantaleo, Tito [1 ]
Bongianni, Fulvia [1 ]
机构
[1] Univ Florence, Dipartimento Med Sperimentale & Clin, Sez Sci Fisiol, Viale GB Morgagni 63, I-50134 Florence, Italy
关键词
Tiotropium; Aclidinium; The cough reflex; Long-acting muscarinic receptor antagonists; ASICs; Airway mechanoreceptors; NUCLEUS-TRACTUS-SOLITARII; ACTING MUSCARINIC ANTAGONIST; FIBER RECEPTOR ACTIVATION; EXCITATORY AMINO-ACIDS; TRACHEOBRONCHIAL COUGH; CAPSAICIN RECEPTOR; ANTITUSSIVE AGENTS; EXPIRATION REFLEX; CITRIC-ACID; BROMIDE;
D O I
10.1016/j.pupt.2016.04.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Long-acting muscarinic receptor antagonists (LAMAS) have been reported to attenuate cough in pre-clinical and clinical studies. The present study was performed on rabbits to compare aclidinium and tiotropium efficacy in the downregulation of the cough reflex. This reflex was evoked by citric acid inhalation in unanesthetized animals and by both citric acid inhalation and mechanical stimulation of the tracheobronchial tree in anesthetized animals 90 min following the inhalation of each drug (nebulizer output always at 1 mL/min). Aclidinium 4 mg/mL and tiotropium 200 g/mL inhaled in 1 min proved to have similar protective effect on methacholine-induced bronchoconstriction in anesthetized animals. The total dosage employed for aclidinium and tiotropium was 4 mg and 200 mu g, respectively. In awake animals, similar reductions in the cough number were observed following 10-min inhalation of each drug with a slight, not significant tendency to higher antitussive effects for aclidinium. In anesthetized animals, 1-min inhalation of each drug caused similar depressant effects on cough responses induced by both mechanical and chemical stimulation. A complete suppression of cough responses to mechanical stimuli was seen in some preparations. The results strongly suggest that the LAMA-induced downregulation of cough may be mediated not only by transient receptor potential vanilloid type 1 channels, as already reported, but also by acid-sensing ion channels and mechanoreceptors. The route of administration along with the more rapid hydrolysis of aclidinium into inactive metabolites minimize potential systemic side effects and give to this drug a very favorable safety profile. (C) 2016 Elsevier Ltd. All rights reserved.
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页码:1 / 9
页数:9
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