Pearson A C, Bhalla D K
Department of Community and Environmental Medicine, University of California, Irvine, USA.
J Toxicol Environ Health. 1997 Feb 7;50(2):143-57. doi: 10.1080/009841097160546.
Inhalation exposure to ozone (O3) is known to induce epithelial and inflammatory changes in the lungs, characterized by neutrophilia and changes in epithelial permeability. Several cell types and their soluble mediators, including interleukin-1 (IL-1) and tumor necrosis factor-alpha (TNF-alpha), are involved in the evolution of these responses. In this study, we have compared the effects of the combination of anti-IL-1 alpha and anti-TNF-alpha on in vitro and in vivo responses to inhaled O3. Male, Sprague-Dawley rats were exposed, nose-only, to 0.8 ppm O3 for 3 h and the in vitro and in vivo parameters were measured 8-12 h following exposure. The in vitro studies revealed that the adherence of inflammatory cells, primarily macrophages, harvested from the lungs of O3-exposed rats to cultured lung epithelial cells (ARL-14) was significantly greater than the adherence of macrophages from air-exposed controls. Furthermore, this adherence was significantly reduced in antibody-treated cells as compared to cells treated with preimmune rabbit serum. In vivo, elevations were found in the percentage of neutrophils in bronchoalveolar lavage fluid (BALF), transport of 99mTc-diethylenetriaminepentaacetate (DTPA) across the tracheal epithelium, and concentrations of total protein and albumin in BALF following O3 exposure. However, these effects were not significantly altered by treatment with the anti-IL-1 alpha/anti-TNF-alpha combination. Therefore, it was concluded that O3 affects the early stages of the inflammatory response, particularly with respect to macrophage activation and adherence to epithelial cells, and that this early response may be mediated by IL-1 alpha and/or TNF-alpha. The results also suggest that the in vivo effects of O3 are controlled by complex mechanisms involving factors other than IL-1 alpha and TNF-alpha, even though these cytokines are capable of modifying macrophage function as revealed by the in vitro adherence studies.
已知吸入臭氧(O₃)会引起肺部上皮和炎症变化,其特征为中性粒细胞增多和上皮通透性改变。几种细胞类型及其可溶性介质,包括白细胞介素-1(IL-1)和肿瘤坏死因子-α(TNF-α),参与了这些反应的演变。在本研究中,我们比较了抗IL-1α和抗TNF-α联合使用对吸入O₃的体外和体内反应的影响。将雄性Sprague-Dawley大鼠仅通过鼻腔暴露于0.8 ppm的O₃中3小时,并在暴露后8 - 12小时测量体外和体内参数。体外研究表明,从暴露于O₃的大鼠肺部收获的炎症细胞(主要是巨噬细胞)对培养的肺上皮细胞(ARL-14)的粘附明显大于空气暴露对照组巨噬细胞的粘附。此外,与用免疫前兔血清处理的细胞相比,抗体处理的细胞中这种粘附明显降低。在体内,臭氧暴露后支气管肺泡灌洗液(BALF)中中性粒细胞百分比、⁹⁹ᵐTc-二乙三胺五乙酸(DTPA)跨气管上皮的转运以及BALF中总蛋白和白蛋白浓度均升高。然而,抗IL-1α/抗TNF-α联合处理并未显著改变这些效应。因此,得出的结论是,O₃影响炎症反应的早期阶段,特别是在巨噬细胞活化和对上皮细胞的粘附方面,并且这种早期反应可能由IL-1α和/或TNF-α介导。结果还表明,O₃的体内效应受涉及IL-1α和TNF-α以外因素的复杂机制控制,尽管这些细胞因子能够如体外粘附研究所揭示的那样改变巨噬细胞功能。