The effect of maternal exposure to dioxolane on prenatal and postnatal development in rats.

K Sitarek, B Barański, B Berlińska
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Abstract

Female rats were given by gavage every other day from days 8-20 of gestation an aqueous solution of dioxolane at daily doses equal to 0.025, 0.1 and 0.2 LD50 (first series--prenatal development) or from days 2-20 of gestation at daily doses equal to 0.025, 0.075 and 0.15 LD50 (second series--postnatal development). At doses toxic or subtoxic to maternal rats (0.1 and 0.2 LD50) dioxolane did not cause increased embryo or fetus intrauterine death rates or congenital defects, it did cause, however, dose-related delays in fetal development. Dioxolane does not cause impairment of physical development or behavioral disturbances. Exposure to higher doses of the compound (0.2 LD50) leads to increased perinatal death rates in the offspring, without causing, however, disturbances in the maternal instinct. The exposure of pregnant rats to dioxolane decreased haemoglobin levels in 5-week-old offspring. At a dose 1.15 g/kg (0.2 LD50) the chemical significantly increased exploratory motor activity of female offspring at the age of 8 weeks, but did not affect significantly locomotor activity of males and the active avoidance acquisition of adult offspring.

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母体接触二恶唑烷对大鼠产前和产后发育的影响。
雌性大鼠从妊娠第8-20天开始,每隔一天灌胃一次日剂量为0.025、0.1和0.2 LD50的二恶唑烷水溶液(第一组——产前发育),或从妊娠第2-20天开始,日剂量为0.025、0.075和0.15 LD50的二恶唑烷水溶液(第二组——产后发育)。对母鼠有毒性或亚毒性剂量(0.1和0.2 LD50)的二恶唑烷不会导致胚胎或胎儿宫内死亡率增加或先天性缺陷,但确实会导致与剂量相关的胎儿发育延迟。二恶唑烷不会造成身体发育障碍或行为障碍。暴露于较高剂量的化合物(0.2 LD50)会导致后代围产期死亡率增加,但不会对母性本能造成干扰。怀孕大鼠暴露于二恶唑烷降低了5周大的后代血红蛋白水平。在1.15 g/kg (0.2 LD50)剂量下,该化学物质显著增加了8周龄雌性后代的探索性运动活动,但对雄性后代的运动活动和成年后代的主动回避习得没有显著影响。
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International Code of Ethics for occupational health professionals. International conference on peripheral nerve toxicity. (12-13 June, 1993, Kanazawa, Japan). Increased urinary excretion of the oxidative DNA adduct, 8-hydroxydeoxyguanosine, as a possible early indicator of occupational cancer hazards in the asbestos, rubber, and azo-dye industries. Computer-aided methods for evaluating cancer risk in miners due to radiation exposure. Mutagenicity of B(a)P in the presence of some hydralazine derivatives.
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