吸入二乙烯基苯-55对B6C3F1小鼠的毒性研究

Daniel L. Morgan , Joel F. Mahler , Ralph E. Wilson , Michael P. Moorman , Herman C. Price Jr. , Robert W. O'connor
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摘要

二乙烯基苯(DVB)是一种交联单体,主要用于与苯乙烯共聚生产离子交换树脂。由于工人可能接触到DVB,并且其结构与苯乙烯(一种潜在的致癌物)相似,因此对吸入DVB的毒性进行了研究。雄性和雌性B6C3F1小鼠分别暴露于0、25、50或75 ppm的DVB中,每天6小时,每周5天,持续2周。暴露于3、5、10天后,6只/性别/剂量组小鼠死亡;暴露于10天后,75 ppm组6只/性别小鼠死亡。最严重的影响发生在鼻腔和肝脏,较轻的影响发生在肾脏。鼻腔嗅上皮早期出现急性坏死和炎症,最后一次暴露后7天出现再生、结构重组和局灶性呼吸道化生。嗅觉上皮的变化是浓度依赖性的,在75 ppm时广泛受累,在25 ppm时外周保留。嗅觉相关的鲍曼腺和侧鼻腺也有坏死和再生。仅在75 ppm剂量组观察到肝细胞小叶中心(CL)坏死,与苯乙烯引起的肝细胞小叶中心坏死相似。观察到一个时间依赖性的进展,其特征是1次暴露后CL变性,3次和5次暴露后坏死,10次暴露后慢性炎症伴CL核肿大,第10次暴露后7天。肝GSH水平呈剂量依赖性降低。在肾脏中,暴露于75ppm的一些雄性小鼠观察到短暂的肾小管损伤,这似乎是对dvb诱导的肾小管上皮损伤的反应。
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Toxicity of Divinylbenzene-55 for B6C3F1 Mice in a Two-Week Inhalation Study

Divinylbenzene (DVB) is a crosslinking monomer used primarily for copolymerization with styrene to produce ion-exchange resins. The toxicity of inhaled DVB was investigated because of the potential for worker exposure and the structural similarity of DVB to styrene, a potential carcinogen. Male and female B6C3F1 mice were exposed to 0, 25, 50, or 75 ppm DVB for 6 hr/day, 5 days/week for up to 2 weeks. Six mice/sex/dose group were killed after 3, 5, and 10 exposures and six mice/sex in the 75 ppm group were killed 7 days after 10 exposures. The most severe effects occurred in the nasal cavity and liver, with less severe effects occurring in the kidneys. In the nasal cavity olfactory epithelium acute necrosis and inflammation were present at early time points followed by regeneration, architectural reorganization, and focal respiratory metaplasia by 7 days after the last exposure. Olfactory epithelial changes were concentration-dependent with extensive involvement at 75 ppm and peripheral sparing at 25 ppm. There was also necrosis and regeneration of olfactory-associated Bowman's glands as well as the lateral nasal (Steno's) glands. Hepatocellular centrilobular (CL) necrosis was observed only in the 75 ppm dose group and was similar to that caused by styrene. A time-dependent progression was observed, characterized by CL degeneration after 1 exposure, necrosis after 3 and 5 exposures, and chronic inflammation with CL karyomegaly after 10 exposures and 7 days after the 10th exposure. Hepatic GSH levels were decreased in a dose-dependent manner. In the kidneys, transient tubular damage was observed in some male mice exposed to 75 ppm, and appeared to be a response to DVB-induced tubular epithelial injury.

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