Utell M J, Frampton M W, Morrow P E, Cox C, Levy P C, Speers D M, Gibb F R
Department of Medicine, University of Rochester School of Medicine and Dentistry, NY 14642.
Res Rep Health Eff Inst. 1994 Nov(70):37-93, discussion 95-112.
These studies were undertaken to evaluate pulmonary responses of humans sequentially exposed to acidic aerosols and ozone at levels that could reasonably be encountered in actual environmental exposures. Subjects first were exposed to sulfuric acid (H2SO4) aerosol to sensitize the airways to ozone. The exposure protocols were designed to provide more quantitative information about the threshold levels of ozone that produce adverse biological effects and to provide exposure-response data on ozone. Two groups of 30 nonsmoking volunteers of both sexes, between the ages of 18 and 45 years, were recruited. The healthy study population comprised 16 men and 14 women with an average age of 28 years and no airway hyperreactivity. The second group comprised 10 men and 20 women comparable in age to the control group, but with allergic asthma and positive skin tests. The study examined an exposure-response relationship using three levels of ozone ranging from below the current standard to one and one-half times the ambient air quality standard (0.08, 0.12, and 0.18 ppm* [parts per million]) with preexposure 24 hours earlier to H2SO4 (100 micrograms/m3) or sodium chloride (NaCl) (control) aerosol in a 45-m3 environmental chamber. The study used an incomplete block design in which each subject was exposed to four of the six paired experimental atmospheres. Both the selection of paired exposures and the order in which they were presented were randomized. The exposure protocol required nine days: Day 1, training and baseline preexposure measurements; Day 2, the first of the three-hour particle (H2SO4 or NaCl) exposures; Day 3 (24 hours after Day 2), ozone exposure at 0.08, 0.12, or 0.18 ppm for three hours; Day 4 (two to four weeks later), exposure to the same ozone concentration as on Day 4. After at least another two weeks, Days 6, 7, 8, and 9 repeated Days 2, 3, 4, and 5 using a second ozone concentration. All three-hour exposures included several predetermined periods of exercise and pulmonary function measurements. To examine for delayed effects, pulmonary function tests were measured two and four hours after exposure on the ozone days. Data were analyzed over the time course of exposure and by exposure level of ozone at each time point to reveal dose-response relationships more closely. The main findings of the study are as follows. No significant symptomatic or physiologic effects of exposure to either aerosol or ozone on lung function were found for the healthy group.(ABSTRACT TRUNCATED AT 400 WORDS)
开展这些研究是为了评估人类在实际环境暴露中可能合理接触到的酸性气溶胶和臭氧水平下的肺部反应。受试者首先暴露于硫酸(H₂SO₄)气溶胶中,以使气道对臭氧敏感。暴露方案旨在提供更多关于产生不良生物学效应的臭氧阈值水平的定量信息,并提供有关臭氧的暴露 - 反应数据。招募了两组年龄在18至45岁之间的30名非吸烟志愿者,男女各半。健康研究人群包括16名男性和14名女性,平均年龄28岁,无气道高反应性。第二组包括10名男性和20名女性,年龄与对照组相当,但患有过敏性哮喘且皮肤试验呈阳性。该研究使用三种臭氧水平(从低于当前标准到环境空气质量标准的1.5倍,即0.08、0.12和0.18 ppm*[百万分率]),在暴露于硫酸(100微克/立方米)或氯化钠(NaCl)(对照组)气溶胶24小时之前,于45立方米的环境舱中研究暴露 - 反应关系。该研究采用不完全区组设计,其中每个受试者暴露于六对实验大气中的四对。配对暴露的选择及其呈现顺序均是随机的。暴露方案需要九天时间:第1天,培训和基线暴露前测量;第2天,进行三小时的颗粒物(H₂SO₄或NaCl)暴露中的第一次;第3天(第2天24小时后),以0.08、0.12或0.18 ppm的臭氧暴露三小时;第4天(两到四周后),暴露于与第3天相同的臭氧浓度。至少再过两周后,第6、7、8和9天使用第二种臭氧浓度重复第2、3、4和5天的过程。所有三小时的暴露都包括几个预定的运动时段和肺功能测量。为了检查延迟效应,在臭氧暴露日暴露后两小时和四小时测量肺功能测试。在暴露的时间过程中以及在每个时间点按臭氧暴露水平分析数据,以更密切地揭示剂量 - 反应关系。该研究的主要发现如下。对于健康组,未发现暴露于气溶胶或臭氧对肺功能有明显的症状或生理影响。(摘要截断于400字)