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[甲苯二异氰酸酯在职业性肺病动物模型中诱发的支气管高反应性]

[Toluene diisocyanate-induced bronchial hyperreactivity in an animal model of occupationally-induced lung diseases].

作者信息

Marek W, Potthast J, Marczynski B, Baur X

机构信息

Berufsgenossenschaftliches Forschungsinstitut für Arbeitsmedizin, Institut an der Ruhr-Universität Bochum.

出版信息

Pneumologie. 1993 Mar;47(3):215-22.

PMID:8387192
Abstract

UNLABELLED

Diisocyanates, widely used in industry for the production of polyurethanes, paints and adhesives represent a growing problem in occupational medicine. Beside toxic responses, isocyanates induce sensitization of exposed workers and may cause asthmatic reactions. To study the pathomechanisms of acute isocyanate induced lung injury, we developed an animal model using anaesthetised rabbits. Inhalation of toluene diisocyanate (TDI) in the range of threshold limit value (TLV) of 10 ppb (as well as 5 and 30 ppb) four times for a period of one hour, performed in 3 groups of 8 rabbits, did not significantly alter airway resistance (R), dynamic elastance (Edyn), slope of inspiratory pressure generation (dPoes/TI), arterial pressure (Pa) or arterial blood-gas tensions (PaO2, Pa-CO2) within time of exposure. In these experiments, before and after each TDI inhalation, unspecific airway responsiveness to 2% Acetylcholine (ACH) aerosol, inhaled for 1 minute, was measured. After 4 hours of TDI-inhalation, the amplitude of the bronchoconstrictory responses to ACH rose significantly (p < 0.005) to 3.6 times of the control value. Similar changes in the amplitude of airway resistance were measured. After inhalation of 5 ppb TDI no significant changes in airway reactivity were noticed, whereas the responses were further enhanced with 30 ppb TDI. In a control group of 8 animals, not undergoing TDI inhalation, the responses of Edyn, R and delta Pöes/TI to ACH aerosol inhalation did not significantly alter from one challenge to another.

CONCLUSION

Diisocyanate atmospheres of threshold limit value of 10 ppb cause bronchial hyperreactivity within 4 hours of exposure in our rabbit model of occupational lung disease.

摘要

未标记

二异氰酸酯在工业上广泛用于生产聚氨酯、涂料和粘合剂,在职业医学中是一个日益严重的问题。除了毒性反应外,异氰酸酯还会使接触工人致敏,并可能引发哮喘反应。为了研究急性异氰酸酯诱导的肺损伤的发病机制,我们使用麻醉兔建立了一种动物模型。在3组每组8只兔子中,以10 ppb(以及5和30 ppb)的阈限值(TLV)吸入甲苯二异氰酸酯(TDI)4次,每次1小时,在暴露期间气道阻力(R)、动态弹性(Edyn)、吸气压力产生斜率(dPoes/TI)、动脉压(Pa)或动脉血气张力(PaO2、Pa - CO2)没有显著变化。在这些实验中,每次TDI吸入前后,测量对吸入1分钟的2%乙酰胆碱(ACH)气雾剂的非特异性气道反应性。TDI吸入4小时后,对ACH的支气管收缩反应幅度显著升高(p < 0.005),达到对照值的3.6倍。测量到气道阻力幅度有类似变化。吸入5 ppb TDI后,气道反应性没有显著变化,而吸入30 ppb TDI时反应进一步增强。在未进行TDI吸入的8只动物的对照组中,Edyn、R和δPöes/TI对ACH气雾剂吸入的反应在一次刺激到另一次刺激之间没有显著变化。

结论

在我们的职业性肺病兔模型中,阈限值为10 ppb的二异氰酸酯环境在暴露4小时内会导致支气管高反应性。

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Pneumologie. 1993 Mar;47(3):215-22.
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引用本文的文献

1
Toluene diisocyanate induction of airway hyperresponsiveness at the threshold limit value (10 ppb) in rabbits.甲苯二异氰酸酯在兔阈限值(10 ppb)下诱发气道高反应性。
Lung. 1995;173(6):333-46. doi: 10.1007/BF00172141.
2
Respiratory and other hazards of isocyanates.异氰酸酯的呼吸道及其他危害。
Int Arch Occup Environ Health. 1994;66(3):141-52. doi: 10.1007/BF00380772.