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钾全氟己烷磺酸盐在 CD-1 小鼠体内的生殖和发育毒性。

Reproductive and developmental toxicity of potassium perfluorohexanesulfonate in CD-1 mice.

机构信息

3M Company, Medical Department, St. Paul, MN 55144, United States.

Salutox, L.L.C., Lake Elmo, MN 55042, United States.

出版信息

Reprod Toxicol. 2018 Jun;78:150-168. doi: 10.1016/j.reprotox.2018.04.007. Epub 2018 Apr 22.

Abstract

Potassium perfluorohexanesulfonate (KPFHxS) was evaluated for reproductive/developmental toxicity in CD-1 mice. Up to 3 mg/kg-d KPFHxS was administered (n = 30/sex/group) before mating, for at least 42 days in F males, and for F females, through gestation and lactation. F pups were directly dosed with KPFHxS for 14 days after weaning. There was an equivocal decrease in live litter size at 1 and 3 mg/kg-d, but the pup-born-to-implant ratio was unaffected. Adaptive hepatocellular hypertrophy was observed, and in 3 mg/kg-d F males, it was accompanied by concomitant decreased serum cholesterol and increased alkaline phosphatase. There were no other toxicologically significant findings on reproductive parameters, hematology/clinical pathology/TSH, neurobehavioral effects, or histopathology. There were no treatment-related effects on postnatal survival, development, or onset of preputial separation or vaginal opening in F mice. Consistent with previous studies, our data suggest that the potency of PFHxS is much lower than PFOS in rodents.

摘要

全氟己基磺酸钾(KPFHxS)在 CD-1 小鼠中被评估为具有生殖/发育毒性。在交配前,雄性给予高达 3mg/kg-d 的 KPFHxS,至少 42 天;雌性则在妊娠和哺乳期给予 KPFHxS。F 代幼鼠在断奶后直接接受 KPFHxS 处理 14 天。在 1mg/kg-d 和 3mg/kg-d 剂量组,活仔数略有减少,但产仔数/着床数比不受影响。观察到适应性肝细胞肥大,在 3mg/kg-d 的雄性 F 代中,还伴随着血清胆固醇降低和碱性磷酸酶升高。在生殖参数、血液学/临床病理学/促甲状腺激素、神经行为效应或组织病理学方面没有其他具有毒理学意义的发现。在 F 代小鼠的产后生存、发育或包皮分离或阴道开口的出现方面,没有与处理相关的影响。与先前的研究一致,我们的数据表明,PFHxS 的效力在啮齿动物中远低于 PFOS。

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