Phosphodiesterase 4 inhibitors for the treatment of chronic obstructive pulmonary disease: a review of current and developing drugs

被引:28
作者
Mulhall, Aaron M. [1 ,2 ]
Droege, Christopher A. [3 ]
Ernst, Neil E. [3 ]
Panos, Ralph J. [1 ,2 ]
Zafar, Muhammad A. [1 ,2 ]
机构
[1] Univ Cincinnati, Med Ctr, Div Pulm & Crit Care Med, Cincinnati, OH 45267 USA
[2] Vet Affairs Med Ctr, Div Pulm & Crit Care Med, Cincinnati, OH 45267 USA
[3] Univ Cincinnati, Med Ctr, Dept Pharm Serv, Cincinnati, OH 45267 USA
基金
美国国家卫生研究院;
关键词
chf6001; chronic obstructive pulmonary disease; gsk256066; phosphodiesterase inhibitor; phosphodiesterase IV; roflumilast; rpl554; tetomilast; PDE4; INHIBITOR; ALLOSTERIC MODULATORS; MURINE MODEL; ROFLUMILAST; THEOPHYLLINE; PHARMACOLOGY; INFLAMMATION; EFFICACY; COPD; EXACERBATIONS;
D O I
10.1517/13543784.2015.1094054
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Phosphodiesterase (PDE) inhibitors modulate lung inflammation and cause bronchodilation by increasing intracellular cyclic adenosine 3', 5'-monophosphate in airway smooth muscle and inflammatory cells. Roflumilast is the only approved PDE-4 inhibitor (PDE4I) for use in chronic obstructive pulmonary disease (COPD). Its beneficial clinical effects occur preferentially in patients with chronic bronchitis and frequent COPD exacerbations. Use of roflumilast as adjunctive or alternate therapy to other COPD medications reduces exacerbations and modestly improves lung function.Areas covered: This article reviews the current role of PDE4I in COPD treatment emphasizing roflumilast's clinical efficacy and adverse effects. This article also reviews developing PDE4Is in early clinical trials and in preclinical studies.Expert opinion: After decades of research in drug development, PDE4Is are a welcomed addition to the COPD therapeutic armamentarium. In its current clinical role, the salubrious clinical effects of PDE4I in reducing exacerbations and stabilizing the frequent exacerbator phenotype have to be cautiously balanced with numerous adverse effects. Developing drugs may provide similar or better clinical benefits while minimizing adverse effects by changing the mode of drug delivery to inhaled formulations, combining dual PDE isoenzyme inhibitors (PDE1/4I and PDE3/4I) and by forming hybrid molecules with other bronchodilators (muscarinic receptor antagonist/PDE4I and 2-agonist/PDE4I).
引用
收藏
页码:1597 / 1611
页数:15
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