Phosphodiesterases as therapeutic targets for respiratory diseases

被引:89
作者
Zuo, Haoxiao [1 ,4 ]
Cattani-Cavalieri, Isabella [1 ,2 ,3 ,5 ]
Musheshe, Nshunge [1 ]
Nikolaev, Viacheslav O. [4 ,6 ]
Schmidt, Martina [1 ,2 ,3 ]
机构
[1] Univ Groningen, Dept Mol Pharmacol, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, GRIAC, Groningen Res Inst Asthma, Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, GRIAC, COPD, Groningen, Netherlands
[4] Univ Med Ctr Hamburg Eppendorf, Inst Expt Cardiovasc Res, D-20246 Hamburg, Germany
[5] Univ Fed Rio de Janeiro, Inst Biomed Sci, Rio De Janeiro, Brazil
[6] German Ctr Cardiovasc Res DZHK, D-20246 Hamburg, Germany
关键词
phosphodiesterases; cAMP; cGMP; COPD; asthma; CAMP-SPECIFIC PHOSPHODIESTERASE; OBSTRUCTIVE PULMONARY-DISEASE; CYCLIC-NUCLEOTIDE PHOSPHODIESTERASE; ROFLUMILAST N-OXIDE; BRONCHIAL EPITHELIAL-CELLS; TRACHEAL SMOOTH-MUSCLE; NECROSIS-FACTOR-ALPHA; INDUCED AIRWAY HYPERRESPONSIVENESS; INDUCED EOSINOPHIL INFILTRATION; PDE4 INHIBITOR ROFLUMILAST;
D O I
10.1016/j.pharmthera.2019.02.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chronic respiratory diseases, such as chronic obstructive pulmonary disease (COPD) and asthma, affect millions of people all over the world. Cyclic adenosine monophosphate (cAMP) which is one of the most important second messengers, plays a vital role in relaxing airway smooth muscles and suppressing inflammation. Given its vast role in regulating intracellular responses, cAMP provides an attractive pharmaceutical target in the treatment of chronic respiratory diseases. Phosphodiesterases (PDEs) are enzymes that hydrolyze cyclic nucleotides and help control cyclic nucleotide signals in a compartmentalized manner. Currently, the selective PDE4 inhibitor, roflumilast, is used as an add-on treatment for patients with severe COPD associated with bronchitis and a history of frequent exacerbations. In addition, other novel POE inhibitors are in different phases of clinical trials. The current review provides an overview of the regulation of various PDEs and the potential application of selective PDE inhibitors in the treatment of COPD and asthma. The possibility to combine various PDE inhibitors as a way to increase their therapeutic effectiveness is also emphasized. (C) 2019 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:225 / 242
页数:18
相关论文
共 275 条
[101]   Oxidative stress in asthma and COPD: Antioxidants as a therapeutic strategy [J].
Kirkham, Paul ;
Rahman, Irfan .
PHARMACOLOGY & THERAPEUTICS, 2006, 111 (02) :476-494
[102]   A low [Ca2+]i-induced enhancement of cAMP-activated ciliary beating by PDE1A inhibition in mouse airway cilia [J].
Kogiso, Haruka ;
Hosogi, Shigekuni ;
Ikeuchi, Yukiko ;
Tanaka, Saori ;
Shimamoto, Chikao ;
Matsumura, Hitoshi ;
Nakano, Takashi ;
Sano, Koh-ichi ;
Inui, Toshio ;
Marunaka, Yoshinori ;
Nakahari, Takashi .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2017, 469 (09) :1215-1227
[103]   Phosphodiesterase 4 inhibitor cilomilast inhibits fibroblast-mediated collagen gel degradation induced by tumor necrosis factor-α and neutrophil elastase [J].
Kohyama, T ;
Liu, XD ;
Zhu, YK ;
Wen, FQ ;
Wang, HJ ;
Fang, QH ;
Kobayashi, T ;
Rennard, SI .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2002, 27 (04) :487-494
[104]   PDE4 inhibitors attenuate fibroblast chemotaxis and contraction of native collagen gels [J].
Kohyama, T ;
Liu, XD ;
Wen, FQ ;
Zhu, YK ;
Wang, HJ ;
Kim, HJ ;
Takizawa, H ;
Cieslinski, LB ;
Barnette, MS ;
Rennard, SI .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2002, 26 (06) :694-701
[105]   Expression and Activity of Phosphodiesterase Isoforms during Epithelial Mesenchymal Transition: The Role of Phosphodiesterase 4 [J].
Kolosionek, Ewa ;
Savai, Rajkumar ;
Ghofrani, Hossein Ardeschir ;
Weissmann, Norbert ;
Guenther, Andreas ;
Grimminger, Friedrich ;
Seeger, Werner ;
Banat, Gamal Andre ;
Schermuly, Ralph Theo ;
Pullamsetti, Soni Savai .
MOLECULAR BIOLOGY OF THE CELL, 2009, 20 (22) :4751-4765
[106]   The Unrecognized Effects of Phosphodiesterase 4 on Epithelial Cells in Pulmonary Inflammation [J].
Konrad, Franziska M. ;
Bury, Annette ;
Schick, Martin A. ;
Ngamsri, Kristian-Christos ;
Reutershan, Joerg .
PLOS ONE, 2015, 10 (04)
[107]   Genomic origin and transcriptional regulation of two variants of cGMP-binding cGMP-specific phosphodiesterases [J].
Kotera, J ;
Fujishige, K ;
Imai, Y ;
Kawai, E ;
Michibata, H ;
Akatsuka, H ;
Yanaka, N ;
Omori, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 262 (03) :866-872
[108]   Anti-neutrophilic inflammatory activity of ASP3258, a novel phosphodiesterase type 4 inhibitor [J].
Kubo, Satoshi ;
Kobayashi, Miki ;
Iwata, Masahiro ;
Miyata, Keiji ;
Takahashi, Koichiro ;
Shimizu, Yasuaki .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2012, 12 (01) :59-63
[109]   Disease-modifying effect of ASP3258, a novel phosphodiesterase type 4 inhibitor, on subchronic cigarette smoke exposure-induced lung injury in guinea pigs [J].
Kubo, Satoshi ;
Kobayashi, Miki ;
Iwata, Masahiro ;
Takahashi, Koichiro ;
Miyata, Keiji ;
Shimizu, Yasuaki .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2011, 659 (01) :79-84
[110]   MODULATION OF CYTOKINE-INDUCED EOSINOPHIL INFILTRATION BY PHOSPHODIESTERASE INHIBITORS [J].
LAGENTE, V ;
PRUNIAUX, MP ;
JUNIEN, JL ;
MOODLEY, I .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 151 (06) :1720-1724