癌变·畸变·突变 ›› 2024, Vol. 36 ›› Issue (4): 294-297.doi: 10.3969/j.issn.1004-616x.2024.04.008

• 论著 • 上一篇    

异丙隆原药对大鼠的致畸作用

程秀荣, 王海华, 陈巍, 梁一帆, 谢广云   

  1. 中国疾病预防控制中心职业卫生与中毒控制所, 北京 100050
  • 收稿日期:2023-09-21 修回日期:2024-03-11 发布日期:2024-08-06
  • 通讯作者: 谢广云
  • 作者简介:程秀荣,E-mail:chengxiu_rong@126.com。

Teratogenicity of isoproturon in rats

CHENG Xiurong, WANG Haihua, CHEN Wei, LIANG Yifan, XIE Guangyun   

  1. National Institute of Occupational Health and Poison Control, Chinese Center for Disease Control and Prevention, Beijing 100050, China
  • Received:2023-09-21 Revised:2024-03-11 Published:2024-08-06

摘要: 目的:研究异丙隆原药对大鼠的致畸作用。方法:将受孕的雌性Wistar大鼠随机分为对照组(花生油)和低(36.9 mg/kg)、中(73.8 mg/kg)、高(369.0 mg/kg)3个异丙隆原药染毒剂量组,每组15只孕鼠。对照组和各染毒组于大鼠妊娠第6~15天灌胃给予受试物,每天1次,连续10 d。于妊娠第20天处死各组孕鼠,观察母鼠和胎鼠的生长、发育情况。结果:与对照组比较,低、中剂量组孕鼠各项观察指标差异均无统计学意义(P>0.05)。高剂量组孕鼠于受孕第9天出现萎靡不振、背毛蓬松、体质量下降(P<0.01);着床数、活胎数减少,死胎数增多,窝均体质量降低(P<0.5);部分胎鼠出现囟门大、枕骨及胸骨骨化不全、肋骨弯曲,骨骼畸形率为27.78%,与对照组相比,差异均具有统计学意义(P<0.05)。结论:在本实验条件下,369.0 mg/kg组异丙隆原药可引起Wistar大鼠的母体毒性和胚胎发育毒性。

关键词: 异丙隆原药, Wistar大鼠, 母体毒性, 胚胎发育毒性, 致畸作用

Abstract: OBJECTIVE:To investigate teratogenicity of isoproturon in rats. METHODS:Pregnant Wistar rats were divided into 4 groups of 15 rats per group. Control group (peanut oil) and isoproturon (36.9,73.8 and 369.0 mg/kg) were administered by gavage once per day from day 6th to 15th of gestation. Rats were killed at the 20th day of gestation,maternal and embryonic developmental indicators were examined. RESULTS:Compared to the control group,all observation indicators of 36.9 and 73.8 mg/kg of isoproturon group were no statistically significant difference (P>0.05). On the 9th day,the 369.0 mg/kg group showed signs of fatigue,fluffy back hair,and significantly lower body weight (P<0.01). The implantation counts and live fetus counts were lower (P<0.5),dead embryos were increased and the average body weight of the litters were significantly less than that in the control group (P<0.5,P<0.01). Abnormalities were observed such as widened fontanelle,occipital ossifications,and incomplete and rib bending. The skeleton malformation rate of 27.78% was increased compared to the control group (P<0.05). CONCLUSION:Under our conditions,369.0 mg/kg of isoproturon treatment induced maternal toxicity and embryonic developmental toxicity in Wistar rats.

Key words: isoproturon, Wistar rats, maternal toxicity, embryonic developmental toxicity, teratogenicity

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