Mouse models of asthma: what physiological evidence are they based on?

G. Zosky, P. Sly, D. Turner
{"title":"Mouse models of asthma: what physiological evidence are they based on?","authors":"G. Zosky, P. Sly, D. Turner","doi":"10.1027/0838-1925.18.2.76","DOIUrl":null,"url":null,"abstract":"Background: Asthma is a chronic inflammatory disease of the lungs that is characterized by airway hyperresponsiveness (AHR) to bronchoconstricting stimuli. The physiological response of the asthmatic lung to inhaled allergen is often characterized by two distinct phases: An early-phase response (EPR) within the first hour following exposure which subsides, and a late-phase response (LPR) that is more prolonged and may occur several hours later. Ideally, a mouse model of asthma should be able to mimic all phases of the lung dysfunction associated with asthma. Methods/Data base: A review of the literature. Results/Conclusions: To date, a majority of the studies using mouse models of asthma have focussed on AHR as a physiological outcome measure. The few studies that have examined the EPR and LPR have been limited by the use of inappropriate and inaccurate measures of lung mechanics. On the basis of current evidence, it would appear that LPR is not correlated with presence of AHR in mice. Future studies should be aimed at determining the presence of a physiological late-phase response in mouse models of asthma and whether or not it is correlated with AHR as seen in human asthmatics.","PeriodicalId":55539,"journal":{"name":"Allergy & Clinical Immunology International","volume":"13 1","pages":"76-79"},"PeriodicalIF":0.0000,"publicationDate":"2006-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Allergy & Clinical Immunology International","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1027/0838-1925.18.2.76","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

Abstract

Background: Asthma is a chronic inflammatory disease of the lungs that is characterized by airway hyperresponsiveness (AHR) to bronchoconstricting stimuli. The physiological response of the asthmatic lung to inhaled allergen is often characterized by two distinct phases: An early-phase response (EPR) within the first hour following exposure which subsides, and a late-phase response (LPR) that is more prolonged and may occur several hours later. Ideally, a mouse model of asthma should be able to mimic all phases of the lung dysfunction associated with asthma. Methods/Data base: A review of the literature. Results/Conclusions: To date, a majority of the studies using mouse models of asthma have focussed on AHR as a physiological outcome measure. The few studies that have examined the EPR and LPR have been limited by the use of inappropriate and inaccurate measures of lung mechanics. On the basis of current evidence, it would appear that LPR is not correlated with presence of AHR in mice. Future studies should be aimed at determining the presence of a physiological late-phase response in mouse models of asthma and whether or not it is correlated with AHR as seen in human asthmatics.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
小鼠哮喘模型:基于什么生理证据?
背景:哮喘是一种肺部慢性炎症性疾病,其特征是气道对支气管收缩刺激的高反应性(AHR)。哮喘肺对吸入过敏原的生理反应通常表现为两个不同的阶段:早期反应(EPR)在接触过敏原后的第一个小时内消退,而晚期反应(LPR)则更长,可能在几个小时后发生。理想情况下,哮喘小鼠模型应该能够模拟与哮喘相关的肺功能障碍的所有阶段。方法/数据基础:查阅相关文献。结果/结论:迄今为止,大多数使用小鼠哮喘模型的研究都将AHR作为一种生理结果测量。少数检查EPR和LPR的研究由于使用不适当和不准确的肺力学测量而受到限制。根据目前的证据,在小鼠中,LPR似乎与AHR的存在无关。未来的研究应旨在确定哮喘小鼠模型中是否存在一种生理晚期反应,以及它是否与人类哮喘患者的AHR相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
The rising tide of novel allergens and allergic crosssensitizations Genetic polymorphisms in aspirin-intolerant chronic urticaria Breathe Right Strips® for nasal congestion associated with positive airway pressure therapy for sleep apnea Is allergy a result or a modifier of viral infections? An incoordination hypothesis Siglec-8 and siglec-F: Inhibitory receptors on eosinophils, basophils, and mast cells
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1