PDE4 inhibitors: current status

被引:275
作者
Spina, D. [1 ]
机构
[1] Kings Coll London, Sch Biomed & Hlth Sci, Pharmaceut Sci Res Div, Sackler Inst Pulm Pharmacol, London SE1 1UL, England
关键词
asthma; COPD; cilomilast; roflumilast; PDE4; inflammation; emesis;
D O I
10.1038/bjp.2008.307
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Phosphodiesterase4 inhibitors are currently under development for the treatment of respiratory diseases including asthma and chronic obstructive pulmonary disease. The rationale for the development of this drug class stems from our understanding of the role of PDE4 in suppressing the function of a range of inflammatory and resident cells thought to contribute toward the pathogenesis of these diseases. Similarly, numerous preclinical in vivo studies have shown that PDE4 inhibitors suppress characteristic features of these diseases, namely, cell recruitment, activation of inflammatory cells and physiological changes in lung function in response to a range of insults to the airways. These potentially beneficial actions of PDE4 inhibitors have been successfully translated in phase II and III clinical trials with roflumilast and cilomilast. However, dose limiting side effects of nausea, diarrhoea and headache have tempered the enthusiasm of this drug class for the treatment of these respiratory diseases. A number of strategies are currently being pursued in attempts to improve clinical efficacy and reduce side effects, including delivery via the inhaled route, and/or development of non-emetic PDE4 inhibitors and mixed PDE inhibitors.
引用
收藏
页码:308 / 315
页数:8
相关论文
共 88 条
[1]
Aoki M, 2000, J PHARMACOL EXP THER, V295, P255
[2]
Aoki M, 2001, J PHARMACOL EXP THER, V298, P1142
[3]
Nonredundant function of phosphodiesterases 4D and 4B in neutrophil recruitment to the site of inflammation [J].
Ariga, M ;
Neitzert, B ;
Nakae, S ;
Mottin, G ;
Bertrand, C ;
Pruniaux, MP ;
Jin, SLC ;
Conti, M .
JOURNAL OF IMMUNOLOGY, 2004, 173 (12) :7531-7538
[4]
Differential expression of PDE4 cAMP phosphodiesterase isoforms in inflammatory cells of smokers with COPD, smokers without COPD, and nonsmokers [J].
Barber, R ;
Baillie, GS ;
Bergmann, R ;
Shepherd, MC ;
Sepper, R ;
Houslay, MD ;
Van Heeke, G .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2004, 287 (02) :L332-L343
[7]
COPD: current therapeutic interventions and future approaches [J].
Barnes, PJ ;
Stockley, RA .
EUROPEAN RESPIRATORY JOURNAL, 2005, 25 (06) :1084-1106
[8]
Cyclic nucleotide phosphodiesterases: Molecular regulation to clinical use [J].
Bender, Andrew T. ;
Beavo, Joseph A. .
PHARMACOLOGICAL REVIEWS, 2006, 58 (03) :488-520
[9]
Sildenafil, a novel effective oral therapy for male erectile dysfunction [J].
Boolell, M ;
GepiAttee, S ;
Gingell, JC ;
Allen, MJ .
BRITISH JOURNAL OF UROLOGY, 1996, 78 (02) :257-261
[10]
Are phosphodiesterase 4 inhibitors just more theophylline? [J].
Boswell-Smith, Victoria ;
Cazzola, Mario ;
Page, Clive P. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 117 (06) :1237-1243