Hexamethylene diisocyanate induction of transient airway hyperresponsiveness in guinea pigs

被引:0
|
作者
Marek, W [1 ]
Mensing, T [1 ]
Riedel, F [1 ]
Viso, N [1 ]
Marczynski, B [1 ]
Baur, X [1 ]
机构
[1] RUHR UNIV BOCHUM,DEPT PEDIAT,D-4630 BOCHUM,GERMANY
关键词
acetylcholine aerosol; animal model; airway hyperresponsiveness; occupational lung disease; threshold limit value; hexamethylene diisocyanate; guinea pig challenge test;
D O I
暂无
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The induction of lung injury and the development of airway hyperresponsiveness (AHR) by exposure to hexamethylene diisocyanate (HDI) were studied in a guinea pig model of occupational lung diseases. In addition to an unexposed control group of 16 guinea pigs (A), two groups (B, C) of 8 animals inhaled HDI atmospheres in the range of the threshold limit value (TLV) of 10 ppb for 6 h/day on 5 days/week over a period of 8 weeks. Airway responses to aerosols of 0.125, 0.25, 0.5, 1.0 and 2.0% acetylcholine (AGH) were measured in exposed as well as in unexposed animals. Basal values of respiratory mechanical and cardiovascular parameters were not significantly altered after 8 weeks of HDI inhalation (group B). Furthermore, additional acute challenge by IO ppb HDI for a period of 60 min, performed under continuous registration of respiratory and cardiovascular parameters, did not cause any significant changes in functional parameters. After 8 weeks of HDI exposure, the amplitude of airway constriction as a response to 2.0% AGH, indicated by the changes in dynamic elastance (E(dyn)) rose significantly to almost 5 times the ACH response in group A (p < 0.0005). In group C of 8 guinea pigs, ACH response was evaluated after a latency period of 8 weeks. In this group, changes of airway responsiveness to ACH were significantly smaller than in group B without a latency period. They were comparable to those of group A. In summary, HDI-induced airway hyperresponsiveness to ACH in the guinea pig is reversible within 8 weeks of HDI avoidance. It is assumed that the augmented airway responsiveness indicates an increased risk of developing isocyanate-induced obstructive lung diseases.
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页码:35 / 44
页数:10
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