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经皮肤暴露于干燥偏苯三酸酐粉末致敏的棕色挪威大鼠中的哮喘样双相气道反应。

Asthmalike biphasic airway responses in Brown Norway rats sensitized by dermal exposure to dry trimellitic anhydride powder.

作者信息

Zhang Xing-Dong, Fedan Jeffrey S, Lewis Daniel M, Siegel Paul D

机构信息

Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention. Morgantown, WV, USA.

出版信息

J Allergy Clin Immunol. 2004 Feb;113(2):320-6. doi: 10.1016/j.jaci.2003.11.047.

Abstract

BACKGROUND

Trimellitic anhydride (TMA) can induce specific IgE and occupational asthma. The significance of dermal exposure to TMA in immunologic sensitization and on subsequent airway responses is not clearly known. An animal model displaying both an early-phase airway response (EAR) and a late-phase airway response (LAR) after sensitization and subsequent inhalation challenge to a low-molecular-weight chemical has not been previously reported.

OBJECTIVE

The present study investigated EAR and LAR after TMA inhalation challenge in Brown Norway rats sensitized by skin exposure to TMA dry powder.

METHODS

Twenty milligrams of dry TMA powder was applied to the skin of each clipped rat's dorsum on days 0, 7, 14, and 21 and occluded overnight with surgical tape. Rats were challenged for 10 minutes with 0.2 to 40 mg/m(3) of TMA aerosol after day 35. Enhanced pause (an index of airway resistance) was recorded overnight in a whole-body plethysmography system. Specific IgE and pulmonary eosinophilia were also measured.

RESULTS

Concentration-dependent responses to TMA were observed: provocation with 0.2 mg/m(3) produced no response; 1 mg/m(3) induced only EAR; and 5 mg/m(3) and 40 mg/m(3) induced both EAR and LAR. Specific IgE was positive; airway eosinophilic inflammation was observed.

CONCLUSION

TMA powder applied to the skin can lead to both immunologic sensitization and subsequent dose-dependent biphasic airway responses after TMA aerosol challenge.

摘要

背景

偏苯三酸酐(TMA)可诱导特异性IgE和职业性哮喘。皮肤接触TMA在免疫致敏及随后气道反应中的意义尚不清楚。此前尚未报道过一种在对低分子量化学物质致敏并随后进行吸入激发后,能同时显示早期气道反应(EAR)和晚期气道反应(LAR)的动物模型。

目的

本研究调查了经皮肤暴露于TMA干粉致敏的棕色挪威大鼠在吸入TMA激发后的EAR和LAR。

方法

在第0、7、14和21天,将20毫克TMA干粉涂抹于每只剃毛大鼠的背部皮肤,并用手术胶带封闭过夜。在第35天后,用0.2至40毫克/立方米的TMA气雾剂对大鼠进行10分钟的激发。在全身体积描记系统中记录过夜的增强间歇(气道阻力指标)。还测量了特异性IgE和肺嗜酸性粒细胞增多情况。

结果

观察到对TMA的浓度依赖性反应:用0.2毫克/立方米激发无反应;1毫克/立方米仅诱导EAR;5毫克/立方米和40毫克/立方米诱导EAR和LAR。特异性IgE呈阳性;观察到气道嗜酸性粒细胞炎症。

结论

涂抹于皮肤的TMA粉末可导致免疫致敏,并在TMA气雾剂激发后产生随后的剂量依赖性双相气道反应。

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