Modeling asthma and COPD in animals: a pointless exercise?

被引:39
作者
Canning, BJ [1 ]
机构
[1] Johns Hopkins Asthma & Allergy Ctr, Baltimore, MD 21224 USA
关键词
D O I
10.1016/S1471-4892(03)00045-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Animal modeling has been essential to the development of every drug used to treat asthma and chronic obstructive pulmonary disease (COPD). Determining the safety and efficacy of new therapeutics will also depend upon animal experimentation, and future targets for therapeutic intervention will probably be identified during careful experimentation using animals. Animal modeling of chronic diseases is made possible by the fact that the processes associated with the regulation of breathing, gas exchange, airway smooth-muscle contraction and relaxation, blood flow through the pulmonary and bronchial vasculature, inflammatory cell recruitment, mucus secretion, mucociliary clearance and airway surface liquid composition are highly conserved in mammals. This conservation is apparent at the whole-organ level and also at the level of the cell and the genome. The subtleties of how the airways and lungs are regulated and experimentally measured in different species make the more complex processes associated with asthma and COPD difficult to faithfully model or duplicate in mammals, particularly in mammals such as rodents that are only distantly related to humans.
引用
收藏
页码:244 / 250
页数:7
相关论文
共 53 条
[1]  
[Anonymous], 1998, EXPERT PANEL REPORT
[2]   Efficacy of soluble IL-4 receptor for the treatment of adults with asthma [J].
Borish, LC ;
Nelson, HS ;
Corren, J ;
Bensch, G ;
Busse, WW ;
Whitmore, JB ;
Agosti, JM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2001, 107 (06) :963-970
[3]  
BOULET LP, 1995, EUR RESPIR J, V8, P913
[4]   HUMAN NEUTROPHIL ELASTASE CAUSES GLYCOCONJUGATE RELEASE FROM THE EPITHELIAL-CELL SURFACE OF HAMSTER TRACHEA IN ORGAN-CULTURE [J].
BREUER, R ;
CHRISTENSEN, TG ;
NILES, RM ;
STONE, PJ ;
SNIDER, GL .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 139 (03) :779-782
[5]   Effects of recombinant human interleukin-12 on eosinophils, airway hyper-responsiveness, and the late asthmatic response [J].
Bryan, SA ;
O'Connor, BJ ;
Matti, S ;
Leckie, MJ ;
Kanabar, V ;
Khan, J ;
Warrington, SJ ;
Renzetti, L ;
Rames, A ;
Bock, JA ;
Boyce, MJ ;
Hansel, TT ;
Holgate, ST ;
Barnes, PJ .
LANCET, 2000, 356 (9248) :2149-2153
[6]   Neural regulation of airway smooth muscle tone [J].
Canning, BJ ;
Fischer, A .
RESPIRATION PHYSIOLOGY, 2001, 125 (1-2) :113-127
[7]  
CANNING BJ, 2002, CURRENT PROTOCOLS PH
[8]   HUMAN ISOLATED BRONCHIAL MUSCLE PREPARATIONS FROM ASTHMATIC-PATIENTS - EFFECTS OF INDOMETHACIN AND CONTRACTILE AGONISTS [J].
CERRINA, J ;
LABAT, C ;
HAYELEGRANDE, I ;
RAFFESTIN, B ;
BENVENISTE, J ;
BRINK, C .
PROSTAGLANDINS, 1989, 37 (04) :457-469
[9]   IRREVERSIBLE BRONCHIAL GOBLET CELL METAPLASIA IN HAMSTERS WITH ELASTASE-INDUCED PANACINAR EMPHYSEMA [J].
CHRISTENSEN, TG ;
KORTHY, AL ;
SNIDER, GL ;
HAYES, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1977, 59 (03) :397-404
[10]   Tumor necrosis factor-α is central to acute cigarette smoke-induced inflammation and connective tissue breakdown [J].
Churg, A ;
Dai, J ;
Tai, H ;
Xie, CS ;
Wright, JL .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (06) :849-854