新型氟喹诺酮类抗菌药物DW-116对大鼠发育毒性评价。

Jong-Choon Kim, Dong-Ho Shin, Sung-Ho Kim, Tae-Ho Ahn, Seong-Soo Kang, Beom-Su Jang, Choong-Yong Kim, Moon-Koo Chung
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引用次数: 8

摘要

我们最近报道了氟喹诺酮类抗菌药物DW-116对大鼠具有显著的发育毒性。本研究旨在更好地了解DW-116在不同发育毒性剂量下对大鼠的致畸作用。DW-116分别以0、320、400和500 mg/kg/天的剂量给药于妊娠第6至16天妊娠大鼠。所有孕妇在妊娠第20天进行剖宫产,检查胎儿的外部、内脏和骨骼异常。当剂量超过400 mg/kg时,母体增重、食量、产仔数、胎儿体重和胎盘重量均显著降低,吸收率显著升高,胎儿形态发生改变。在320 mg/kg剂量下,产妇体重增加、食物消耗、胎儿体重和胎盘体重轻度下降,胎儿变异和发育迟缓轻度增加。以上结果表明,DW-116在320 mg/kg/d以上对妊娠大鼠具有胚胎毒性,在400 mg/kg以上对妊娠大鼠具有胚胎致毒和致畸作用,DW-116是大鼠妊娠期的选择性发育毒物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Developmental toxicity evaluation of the new fluoroquinolone antibacterial DW-116 in rats.

We have recently reported that the fluoroquinolone antibacterial DW-116 induces a significant developmental toxicity in rat. The present study was conducted to better understand the teratogenic effects of DW-116 at several developmental toxic doses in rats. DW-116 was orally administered to pregnant rats from gestational day (GD) 6 through 16 at dose levels of 0, 320, 400, and 500 mg/kg/day. All dams were subjected to caesarean section on GD 20 and their fetuses were examined for external, visceral, and skeletal abnormalities. At above 400 mg/kg, severe decreases in maternal body weight gain, food consumption, litter size, fetal weight and placental weight, and severe increases in resorption rate and fetal morphological alterations were observed. At 320 mg/kg, mild decreases in maternal body weight gain, food consumption, fetal weight and placental weight, and mild increases in fetal variations and retardations were observed. These results suggest that DW-116 is embryotoxic at above 320 mg/kg/day and is embryolethal and teratogenic at above 400 mg/kg in pregnant rats and that DW-116 is a selective developmental toxicant in rat conceptuses.

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