大鼠皮肤应用合塔底的全身和发育毒性。

M. Feuston, C. E. Hamilton, C. Mackerer
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引用次数: 8

摘要

对Syntower bottoms (STB)进行了亚慢性和发育毒性评价。在亚慢性研究中,未稀释的STB以0、8、30、125和500 mg/kg的剂量水平应用于雄性和雌性大鼠剃光的背部,持续13周,每周5天。暴露地点没有包括在内。在发育毒性研究中,STB同样适用于怀孕大鼠,但在妊娠0-19天,剂量水平分别为0、8、30和125 mg/kg。此外,从妊娠第0天开始,每隔一天给药4mg /kg,每隔一天给药8mg /kg,妊娠第10-12天给药500mg /kg。在亚慢性研究中观察到的毒性证据包括死亡、体重下降、血清化学和血液学值异常、器官重量改变和各种器官的组织病理学改变。未观察到系统性毒性的不良反应水平无法确定。在发育研究中,在所有暴露水平下都观察到母体毒性的证据。无论暴露时间长短,STB对发育中的胎儿都是有毒的。观察到的发育毒性证据包括吸收增加,同时产仔数减少和胎儿体重减少。在妊娠10-12天,胎儿在子宫内暴露于500 mg/kg的STB中,观察到腭裂。当暴露期为整个妊娠期时,未观察到致畸性的证据。在子宫内暴露于STB剂量超过4 mg/kg的胎儿中观察到骨化延迟。没有观察到母体和发育毒性的不良反应水平无法确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systemic and developmental toxicity of dermally applied syntower bottoms in rats.
Syntower bottoms (STB) was evaluated for subchronic and developmental toxicity. In the subchronic study, undiluted STB was applied on the shaved backs of male and female rats at dose levels of 0, 8, 30, 125, and 500 mg/kg for 13 weeks, 5 days per week. Exposure sites were not covered. In the developmental toxicity study, STB was similarly applied, but to pregnant rats at dose levels of 0, 8, 30, and 125 mg/kg on Gestation Days 0-19. In addition, 4 mg/kg was dosed as 8 mg/kg every other day, starting on Gestation Day 0, and 500 mg/kg was dosed on Gestation Days 10-12. Evidence of toxicity observed in the subchronic study included death, decreased body weights, aberrant serum chemistry and hematology values, altered organ weights, and histopathologic changes in a variety of organs. A no observed adverse effect level for systemic toxicity could not be established. Evidence of maternal toxicity was observed at all exposure levels in the development study. Regardless of the length of the exposure period, STB was toxic to the developing conceptus. Evidence of developmental toxicity observed included increased resorptions with a concomitant decrease in litter size and reduced fetal body weights. Cleft palate was observed in fetuses exposed in utero to STB during Gestation Days 10-12 at 500 mg/kg. No evidence of teratogenicity was observed when the exposure period was throughout gestation. Ossification delays were observed in fetuses exposed in utero to STB at doses in excess of 4 mg/kg. A no observed adverse effect level for maternal and developmental toxicity could not be established.
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