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气态甲醛对卵清蛋白致敏的哮喘小鼠模型高反应性和炎症的辅助作用。

Adjuvant effects of gaseous formaldehyde on the hyper-responsiveness and inflammation in a mouse asthma model immunized by ovalbumin.

机构信息

Laboratory of Environmental Sciences, Huazhong Normal University, Wuhan City, China.

出版信息

J Immunotoxicol. 2011 Oct-Dec;8(4):305-14. doi: 10.3109/1547691X.2011.600738. Epub 2011 Aug 19.

DOI:10.3109/1547691X.2011.600738
PMID:21854218
Abstract

Asthma is a complex pulmonary inflammatory disease, which is characterized by airway hyper-responsiveness, airflow obstruction, and airway inflammation. Exposure to a number of chemicals including formaldehyde (FA) can lead to asthma. This study aimed to explore the underlying role of FA exposure in occupational asthma, especially when it is combined with allergen exposure. Balb/c mice were randomly divided into six groups (n = 6/group): (1) saline control; (2) ovalbumin (OVA)-immunized (OVA(imm)) only; (3) 0.5 mg FA/m(3) exposure; (4) OVA(imm) + 0.5 mg FA/m(3); (5) 3.0 mg FA/m(3) FA exposure; and, (6) OVA(imm) + 3.0 mg FA/m(3). These low and high exposure FA levels were adopted from current (0.5 mg/m(3)) and original (3.0 mg/m(3)) Chinese Occupational Threshold Limit Values. Experiments were conducted after 3 week of combined exposure and a 1-week challenge with aerosolized OVA. Airway hyper-responsiveness, pulmonary tissue damage, eosinophil infiltration, and increased interleukin (IL)-4 and IL-6 levels in lung tissues were found in the OVA + 3.0 mg FA/m(3) hosts as compared to values seen in the OVA-immunized only mice. The results here suggest to us that FA exposure can induce and aggravate asthma in Balb/c mice when it is combined with OVA immunization.

摘要

哮喘是一种复杂的肺部炎症性疾病,其特征是气道高反应性、气流阻塞和气道炎症。接触包括甲醛(FA)在内的许多化学物质可导致哮喘。本研究旨在探讨 FA 暴露在职业性哮喘中的潜在作用,特别是当它与过敏原暴露结合时。Balb/c 小鼠被随机分为六组(n = 6/组):(1)生理盐水对照;(2)卵清蛋白(OVA)免疫(OVA(imm));(3)0.5mg FA/m(3) 暴露;(4)OVA(imm) + 0.5mg FA/m(3);(5)3.0mg FA/m(3) FA 暴露;(6)OVA(imm) + 3.0mg FA/m(3)。这些低和高 FA 暴露水平分别取自当前(0.5mg/m(3)) 和原始(3.0mg/m(3)) 中国职业阈限值。在联合暴露 3 周后进行实验,并在第 1 周用雾化 OVA 进行挑战。与仅接受 OVA 免疫的小鼠相比,OVA + 3.0mg FA/m(3) 组的气道高反应性、肺组织损伤、嗜酸性粒细胞浸润以及肺组织中白细胞介素(IL)-4 和 IL-6 水平增加。这些结果表明,FA 暴露与 OVA 免疫结合后可诱导和加重 Balb/c 小鼠的哮喘。

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