Franzen Allison, Greene Tracy, Van Landingham Cynthia, Gentry Robinan
Ramboll Environ US Corporation, Monroe, LA, United States.
Ramboll Environ US Corporation, Monroe, LA, United States.
Toxicol Lett. 2017 Oct 20;279 Suppl 1:2-22. doi: 10.1016/j.toxlet.2017.06.007. Epub 2017 Jun 20.
Octamethylcyclotetrasiloxane (D) is a volatile cyclic siloxane used primarily as a monomer or intermediate in the production of some silicon-based polymers widely used in industrial and consumer applications and may be present as a residual impurity in a variety of consumer products. A robust toxicological data set exists for D Treatment-related results from a chronic inhalation study conducted in rats are limited to mild effects on the respiratory tract, increases in liver weight, increases in the incidence of uterine endometrial epithelial hyperplasia, and a dose-related trend in the incidence of endometrial adenomas. The observed increases in liver weight appear to be related to the induction of hepatic metabolizing enzymes, similar to those that are induced in the presence of phenobarbital. D is not mutagenic or genotoxic in standard in vitro and in vivo tests; therefore, the benign uterine tumors observed likely occur by a non-genotoxic mechanism. Results from mechanistic studies suggest that D has very weak estrogenic and antiestrogenic activity, as well as dopamine agonist-like activity. In rats, D exposure delays ovulation and hypothesized to prolong exposure of the uterine endometrium to endogenous estrogen. Though this mode of action may play a role in the development of benign uterine tumors in the rat, it is considered unlikely to occur in the human due to the marked differences in cycle regulatory mechanisms. Reproductive effects were observed following D exposure in female rats. These effects appear to be related to a delay of the luteinizing hormone (LH) surge, which fails to induce complete ovulation in the rat. However, based on differences in ovulatory control in rats and humans, it appears these effects may be species-specific with no risk or relevance to human health. Results from pharmacokinetic studies indicate that dermal absorption of D is limited, due to its high volatility and, if absorbed via dermal, oral or inhalation exposure, the majority of D is rapidly cleared from the body, indicating bioaccumulation is unlikely.
八甲基环四硅氧烷(D)是一种挥发性环状硅氧烷,主要用作单体或中间体,用于生产一些广泛应用于工业和消费领域的硅基聚合物,并且可能作为残留杂质存在于多种消费品中。关于D有大量可靠的毒理学数据。在大鼠中进行的慢性吸入研究中,与治疗相关的结果仅限于对呼吸道的轻微影响、肝脏重量增加、子宫内膜上皮增生发生率增加以及子宫内膜腺瘤发生率的剂量相关趋势。观察到的肝脏重量增加似乎与肝脏代谢酶的诱导有关,类似于在苯巴比妥存在时诱导的那些酶。在标准的体外和体内试验中,D没有致突变性或基因毒性;因此,观察到的良性子宫肿瘤可能通过非基因毒性机制发生。机制研究结果表明,D具有非常弱的雌激素和抗雌激素活性,以及多巴胺激动剂样活性。在大鼠中,D暴露会延迟排卵,并推测会延长子宫内膜对内源性雌激素的暴露时间。尽管这种作用模式可能在大鼠良性子宫肿瘤的发生中起作用,但由于周期调节机制存在明显差异,认为在人类中不太可能发生。在雌性大鼠中,D暴露后观察到了生殖效应。这些效应似乎与促黄体生成素(LH)高峰延迟有关,这未能在大鼠中诱导完全排卵。然而,基于大鼠和人类排卵控制的差异,这些效应似乎可能具有物种特异性,对人类健康没有风险或相关性。药代动力学研究结果表明,由于D挥发性高,其经皮吸收有限,并且如果通过皮肤、口服或吸入接触吸收,大部分D会迅速从体内清除,表明不太可能发生生物蓄积。