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Comparative developmental toxicity study of indium in rats and mice.

机译:铟对大鼠和小鼠的发育毒性比较研究。

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The developmental toxicity of indium was examined in both rats and mice using comparable experimental protocols. Pregnant rats received a single intravenous administration of indium trichloride (InCl(3)) at 0.4 mg In/kg, on day 9, 10, or 11 of pregnancy and their fetuses were examined on day 20. Pregnant mice were treated in the same manner at 0.8 or 1.6 mg In/kg on day 7, 8, or 9 of pregnancy and their fetuses were examined on day 18. In rats, indium caused fetal weight decrease and fetal gross malformations, such as brachyury, kinked tail, cleft palate, and oligodactyly, most severely by the administration on day 10. In mice, however, indium did not cause fetal gross malformations, although it caused fetal weight decrease at 0.8 mg In/kg or more and fetal death at 1.6 mg In/kg, most severely by the administration on day 8. It was concluded from these results that rats and mice were susceptible to the embryotoxicity of indium at similar developmental stages in the early organogenetic period, but mice were less susceptible to the teratogenicity of indium than rats in terms of gross malformation. Toxicokinetic factors may be involved in this different susceptibility. Teratogenesis Carcinog. Mutagen. 20:219-227, 2000. Copyright 2000 Wiley-Liss, Inc.
机译:使用可比较的实验方案在大鼠和小鼠中检查了铟的发育毒性。怀孕的大鼠在怀孕的第9、10或11天单次静脉内注射0.4 mg In / kg的三氯化铟(InCl(3)),并在第20天检查它们的胎儿。在怀孕的第7、8或9天以0.8或1.6 mg In / kg的剂量和18天的胎儿进行检查,在大鼠中,铟引起的胎儿体重减轻和胎儿总体畸形,例如短毛瘤,弯曲的尾巴,c裂,在第10天给药最严重;在铟中,铟不会引起胎儿总体畸形,尽管铟会导致胎儿体重减少0.8 mg In / kg或更多,而胎儿死亡则减少1.6 mg In / kg,大多数从第8天开始严重给药。从这些结果可以得出结论,在有机发育早期,大鼠和小鼠在相似的发育阶段对铟的胚胎毒性敏感,但是从老鼠的角度来看,小鼠对铟的致畸性的敏感性比大鼠低。严重畸形。毒代动力学因素可能与这种不同的敏感性有关。致癌作用。诱变剂。 20:219-227,2000。版权所有2000 Wiley-Liss,Inc.。

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