Muscarinic Receptor Antagonism and Allergen Induced Airway Responses in Allergic Asthma: A Scoping Review.

IF 1.2 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Beth E Davis, Kayla J Cropper, Donald W Cockcroft Cockcroft
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引用次数: 1

Abstract

Purpose: The purpose of this scoping review was to identify existing clinical and basic science knowledge surrounding the effect of muscarinic receptor antagonism on allergen-induced airway responses to inform future clinical research in this area.

Methods: Multiple advanced searches were performed using the National Library of Medicine PubMed search engine. Each search began with two terms; for example, "atropine and asthma" or "tiotropium and airway inflammation". Results were then further refined to include terms such as "allergen" or "ovalbumin (OVA)". Abstracts of refined searches were reviewed for relevance to allergic asthma and allergen-induced airway responses including the early and late asthmatic responses, airway inflammation and tissue remodelling. There was no restriction regarding publication date. Reference lists of selected papers were also reviewed for relevant publications.

Results: Nine human clinical trial publications and fourteen animal model publications were identified. In humans, single dose atropine (n=4), ipratropium (n=4) or oxitropium (n=1) administered pre-challenge produced equivocal effects on allergen-induced early asthmatic responses as reported but favored inhibition in eight of nine studies after re-analyses. Animal model investigations (n=14) showed mostly favorable results, especially with respect to airway inflammation and tissue remodelling, although two studies were negative, and one study showed a worsening in allergen induced airway inflammation following muscarinic receptor antagonism.

Conclusion: Existing human and animal model data suggest muscarinic receptor antagonism may be beneficial in preventing allergen induced airway responses in those with allergic asthma. Additional human research utilizing current standardized methodologies is required.

毒蕈碱受体拮抗剂和过敏原诱导的过敏性哮喘气道反应:范围综述。
目的:本综述的目的是确定现有的临床和基础科学知识,围绕毒蕈碱受体拮抗剂对过敏原诱导的气道反应的影响,为该领域未来的临床研究提供信息。方法:使用国家医学图书馆PubMed搜索引擎进行多次高级搜索。每次搜索都以两个词开始;例如,“阿托品和哮喘”或“噻托溴铵和气道炎症”。结果进一步细化,包括“过敏原”或“卵白蛋白(OVA)”等术语。摘要综述了精细化搜索与过敏性哮喘和过敏原诱导的气道反应的相关性,包括早期和晚期哮喘反应、气道炎症和组织重构。对出版日期没有限制。还审查了选定论文的参考文献清单,以供有关出版物参考。结果:确定了9篇人类临床试验出版物和14篇动物模型出版物。在人类中,单剂量阿托品(n=4)、异丙托品(n=4)或奥氧托品(n=1)预激发对过敏原诱导的早期哮喘反应产生模棱两可的影响,但在重新分析后的9项研究中有8项有利于抑制。动物模型研究(n=14)显示了大多数有利的结果,特别是在气道炎症和组织重塑方面,尽管有两项研究是阴性的,一项研究显示在毒蕈碱受体拮抗剂后过敏原诱导的气道炎症恶化。结论:现有的人和动物模型数据表明,毒蕈碱受体拮抗剂可能有助于预防变应性哮喘患者的过敏原诱导的气道反应。需要利用目前的标准化方法进行更多的人体研究。
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来源期刊
Clinical and Investigative Medicine
Clinical and Investigative Medicine 医学-医学:研究与实验
CiteScore
1.50
自引率
12.50%
发文量
18
审稿时长
>12 weeks
期刊介绍: Clinical and Investigative Medicine (CIM), publishes original work in the field of Clinical Investigation. Original work includes clinical or laboratory investigations and clinical reports. Reviews include information for Continuing Medical Education (CME), narrative review articles, systematic reviews, and meta-analyses.
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