Adenosine receptors as promising therapeutic targets for drug development in chronic airway inflammation

被引:39
作者
Polosa, Riccardo
Holgate, Stephen T.
机构
[1] Univ Catania, Dipartimento Med Interna & Specialist, Ascoli Tomaselli Hosp, I-95125 Catania, Italy
[2] Southampton Gen Hosp, AIR Div, Southampton SO16 6YD, Hants, England
基金
英国医学研究理事会;
关键词
adenosine; adenosine receptors; inflammation; asthma; COPD;
D O I
10.2174/138945006777435236
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A growing body of evidence has emerged in support of a pro-inflammatory role for adenosine in the pathogenic mechanisms of chronic inflammatory disorders of the airways such as asthma and COPD. The demonstration that adenosine enhances mast cell allergen-dependent activation, the notion that elevated levels of adenosine are present in chronically inflamed airways, and the results from exposure studies of nebulised adenosine showing dose-dependent bronchoconstriction in subjects with asthma and COPD, emphasise the importance of adenosine in the initiation, persistence and progression in these common inflammatory disorders of the airways. Adenosine exerts its manifold biological activities by interacting with at least four adenosine receptor subtypes. Selective activation or blockade of these sites is being exploited by the pharmaceutical industry in an attempt to generate novel therapies for asthma and COPD. This review article intends to address the potential role of adenosine in asthma and to put forward the idea that drugs that have been developed to selectively activate or downregulate adenosine receptor subtypes may constitute a considerable advance in the management of chronic airway inflammation.
引用
收藏
页码:699 / 706
页数:8
相关论文
共 106 条
[11]  
Busse William W., 2000, Journal of Allergy and Clinical Immunology, V106, P1033
[12]   Advances in immunology - Asthma [J].
Busse, WW ;
Lemanske, RF .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (05) :350-362
[13]  
Chung KF, 1999, EUR RESPIR J, V13, P1198
[14]   Adenosine and its nucleotides activate wild-type and R117H CFTR through an A2B receptor-coupled pathway [J].
Clancy, JP ;
Ruiz, FE ;
Sorscher, EJ .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 276 (02) :C361-C369
[15]  
CRIMI N, 1995, EUR RESPIR J, V8, P905
[16]   ADENOSINE, AN ENDOGENOUS ANTIINFLAMMATORY AGENT [J].
CRONSTEIN, BN .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 76 (01) :5-13
[17]  
CRONSTEIN BN, 1992, J IMMUNOL, V148, P2201
[18]   INHALED ADENOSINE AND GUANOSINE ON AIRWAY-RESISTANCE IN NORMAL AND ASTHMATIC SUBJECTS [J].
CUSHLEY, MJ ;
TATTERSFIELD, AE ;
HOLGATE, ST .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1983, 15 (02) :161-165
[19]  
Dent G, 2000, LUNG BIOL HEALTH DIS, V145, P77
[20]   ADENOSINE IN BRONCHOALVEOLAR LAVAGE FLUID IN ASTHMA [J].
DRIVER, AG ;
KUKOLY, CA ;
ALI, S ;
MUSTAFA, SJ .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 148 (01) :91-97