Roemer E, Anton H J, Kindt R
INBIFO Institut für biologische Forschung, Köln, Germany.
J Appl Toxicol. 1993 Mar-Apr;13(2):103-7. doi: 10.1002/jat.2550130206.
Male Sprague Dawley rats were exposed by inhalation for 6 h per day on one or three successive days to 0, 2, 6 or 20 ppm formaldehyde or 0, 0.2 or 0.6 ppm acrolein. Nasal and tracheal epithelial and free lung cells were then analyzed for proliferative responses. The proliferative response was expressed as the proportion of DNA synthesizing cells determined by the 5-bromodeoxyuridine (BrdU) labeling technique. Single exposure to both irritants increased the DNA synthesizing (proliferating) cells by a factor of 3. After three exposures the increase was distinctly lower. All sites analyzed showed approximately the same concentration/response pattern. Significant changes in cell proliferation could be detected at 2 ppm formaldehyde and 0.2 ppm acrolein.
将雄性斯普拉格-道利大鼠每天吸入暴露6小时,连续1天或3天,使其暴露于浓度为0、2、6或20 ppm的甲醛或0、0.2或0.6 ppm的丙烯醛环境中。然后分析鼻和气管上皮细胞以及游离肺细胞的增殖反应。增殖反应通过5-溴脱氧尿苷(BrdU)标记技术测定的DNA合成细胞比例来表示。单次暴露于这两种刺激物均可使DNA合成(增殖)细胞增加3倍。三次暴露后,这种增加明显降低。所有分析部位均呈现大致相同的浓度/反应模式。在甲醛浓度为2 ppm和丙烯醛浓度为0.2 ppm时可检测到细胞增殖的显著变化。