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慢性阻塞性肺疾病模型

Models of chronic obstructive pulmonary disease.

作者信息

Groneberg David A, Chung K Fan

机构信息

Pneumology and Immunology, Otto-Heubner-Centre, Charité School of Medicine, Free University and Humboldt-University, Berlin, Germany.

出版信息

Respir Res. 2004 Nov 2;5(1):18. doi: 10.1186/1465-9921-5-18.

DOI:10.1186/1465-9921-5-18
PMID:15522115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC533858/
Abstract

Chronic obstructive pulmonary disease (COPD) is a major global health problem and is predicted to become the third most common cause of death by 2020. Apart from the important preventive steps of smoking cessation, there are no other specific treatments for COPD that are as effective in reversing the condition, and therefore there is a need to understand the pathophysiological mechanisms that could lead to new therapeutic strategies. The development of experimental models will help to dissect these mechanisms at the cellular and molecular level. COPD is a disease characterized by progressive airflow obstruction of the peripheral airways, associated with lung inflammation, emphysema and mucus hypersecretion. Different approaches to mimic COPD have been developed but are limited in comparison to models of allergic asthma. COPD models usually do not mimic the major features of human COPD and are commonly based on the induction of COPD-like lesions in the lungs and airways using noxious inhalants such as tobacco smoke, nitrogen dioxide, or sulfur dioxide. Depending on the duration and intensity of exposure, these noxious stimuli induce signs of chronic inflammation and airway remodelling. Emphysema can be achieved by combining such exposure with instillation of tissue-degrading enzymes. Other approaches are based on genetically-targeted mice which develop COPD-like lesions with emphysema, and such mice provide deep insights into pathophysiological mechanisms. Future approaches should aim to mimic irreversible airflow obstruction, associated with cough and sputum production, with the possibility of inducing exacerbations.

摘要

慢性阻塞性肺疾病(COPD)是一个重大的全球健康问题,预计到2020年将成为第三大常见死因。除了戒烟这一重要的预防措施外,对于COPD没有其他能有效逆转病情的特异性治疗方法,因此有必要了解可能带来新治疗策略的病理生理机制。实验模型的开发将有助于在细胞和分子水平剖析这些机制。COPD是一种以周围气道进行性气流阻塞为特征的疾病,伴有肺部炎症、肺气肿和黏液高分泌。已开发出不同的方法来模拟COPD,但与过敏性哮喘模型相比存在局限性。COPD模型通常无法模拟人类COPD的主要特征,通常基于使用烟草烟雾、二氧化氮或二氧化硫等有害吸入剂在肺部和气道诱导出类似COPD的病变。根据暴露的持续时间和强度,这些有害刺激会诱发慢性炎症和气道重塑的迹象。通过将这种暴露与注入组织降解酶相结合可实现肺气肿。其他方法基于基因靶向小鼠,这些小鼠会出现伴有肺气肿的类似COPD的病变,此类小鼠能深入洞察病理生理机制。未来的方法应旨在模拟与咳嗽和咳痰相关的不可逆气流阻塞,并有可能诱发病情加重。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e21/533858/88bb2e1432b1/1465-9921-5-18-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e21/533858/8fe048aa8ff9/1465-9921-5-18-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e21/533858/88bb2e1432b1/1465-9921-5-18-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e21/533858/8fe048aa8ff9/1465-9921-5-18-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e21/533858/88bb2e1432b1/1465-9921-5-18-2.jpg

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本文引用的文献

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Inflammatory cells as source of tachykinin-induced mucus secretion in chronic bronchitis.炎症细胞作为慢性支气管炎中速激肽诱导黏液分泌的来源。
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Airway obstruction in chronic obstructive pulmonary disease.慢性阻塞性肺疾病中的气道阻塞
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Oxidative stress and cigarette smoke alter chromatin remodeling but differentially regulate NF-kappaB activation and proinflammatory cytokine release in alveolar epithelial cells.
动物模型与烟草烟雾导致慢性阻塞性肺疾病(COPD)的机制。
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Effect of Herbal Medicine Formulation (Compound Honey Syrup) on Quality of Life in Patients With COPD: A Randomized Clinical Trial.草药配方(复方蜂蜜糖浆)对慢性阻塞性肺疾病患者生活质量的影响:一项随机临床试验。
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The Involvement of PDE4 in the Protective Effects of Melatonin on Cigarette-Smoke-Induced Chronic Obstructive Pulmonary Disease.PDE4 在褪黑素对香烟烟雾诱导的慢性阻塞性肺疾病的保护作用中的参与。
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