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
  • [1] Dual PDE3/4 and PDE4 Inhibitors: Novel Treatments For COPD and Other Inflammatory Airway Diseases
    Abbott-Banner, Katharine H.
    Page, Clive P.
    [J]. BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2014, 114 (05) : 365 - 376
  • [2] Characterisation of adhesion receptors mediating lymphocyte adhesion to bronchial endothelium provides evidence for a distinct lung homing pathway
    Ainslie, MP
    McNulty, CA
    Huynh, T
    Symon, FA
    Wardlaw, AJ
    [J]. THORAX, 2002, 57 (12) : 1054 - 1059
  • [3] Effects of L-arginine and phosphodiesterase-5 inhibitor, sildenafil, on inflammation and airway responsiveness of sensitized BP2 mice
    Al Qadi-Nassar, B.
    Bichon-Laurent, F.
    Portet, K.
    Tramini, P.
    Arnoux, B.
    Michel, A.
    [J]. FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2007, 21 (06) : 611 - 620
  • [4] New Classes of PDE7 Inhibitors Identified by a Fission Yeast-Based HTS
    Alaamery, Manal A.
    Wyman, Arlene R.
    Ivey, F. Douglas
    Allain, Christina
    Demirbas, Didem
    Wang, Lili
    Ceyhan, Ozge
    Hoffman, Charles S.
    [J]. JOURNAL OF BIOMOLECULAR SCREENING, 2010, 15 (04) : 359 - 367
  • [5] Phosphodiesterase type 5 and high altitude pulmonary hypertension
    Aldashev, AA
    Kojonazarov, BK
    Amatov, TA
    Sooronbaev, TM
    Mirrakhimov, MM
    Morrell, NW
    Wharton, J
    Wilkins, MR
    [J]. THORAX, 2005, 60 (08) : 683 - 687
  • [6] Aoki M, 2000, J PHARMACOL EXP THER, V295, P1149
  • [7] Novel Class of Benzoic Acid Ester Derivatives as Potent PDE4 Inhibitors for Inhaled Administration in the Treatment of Respiratory Diseases
    Armani, Elisabetta
    Amari, Gabriele
    Rizzi, Andrea
    De Fanti, Renato
    Ghidini, Eleonora
    Capaldi, Carmelida
    Carzaniga, Laura
    Caruso, Paola
    Guala, Matilde
    Peretto, Ilaria
    La Porta, Elena
    Bolzoni, Pier T.
    Facchinetti, Fabrizio
    Carnini, Chiara
    Moretto, Nadia
    Patacchini, Riccardo
    Bassani, Franco
    Cenacchi, Valentina
    Volta, Roberta
    Amadei, Francesco
    Capacchi, Silvia
    Delcanale, Maurizio
    Puccini, Paola
    Catinella, Silvia
    Civelli, Maurizio
    Villetti, Gino
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2014, 57 (03) : 793 - 816
  • [8] Regulation of T-cell activation by phosphodiesterase 4B2 requires its dynamic redistribution during immunological synapse formation
    Arp, J
    Kirchhof, MG
    Baroja, ML
    Nazarian, SH
    Chau, TA
    Strathdee, CA
    Ball, EH
    Madrenas, J
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (22) : 8042 - 8057
  • [9] Imidazopyridazinones as novel PDE7 inhibitors: SAR and in vivo studies in Parkinson's disease model
    Banerjee, Abhisek
    Patil, Sandip
    Pawar, Mahesh Y.
    Gullapalli, Srinivas
    Gupta, Praveen K.
    Gandhi, Maulik N.
    Bhateja, Deepak K.
    Bajpai, Malini
    Sangana, Ramachandra Rao
    Gudi, Girish S.
    Khairatkar-Joshi, Neelima
    Gharat, Laxmikant A.
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2012, 22 (19) : 6286 - 6291
  • [10] Differential expression of PDE4 cAMP phosphodiesterase isoforms in inflammatory cells of smokers with COPD, smokers without COPD, and nonsmokers
    Barber, R
    Baillie, GS
    Bergmann, R
    Shepherd, MC
    Sepper, R
    Houslay, MD
    Van Heeke, G
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2004, 287 (02) : L332 - L343