癌变·畸变·突变 ›› 2024, Vol. 36 ›› Issue (2): 150-154,158.doi: 10.3969/j.issn.1004-616x.2024.02.012

• 检测研究 • 上一篇    

天冬对大鼠的亚慢性和致畸毒性研究

夏祺悦1, 蒋勇1, 王东霞2, 李彬3   

  1. 1. 四川省疾病预防控制中心, 四川 成都 610041;
    2. 绵阳市疾病预防控制中心, 四川绵阳 621000;
    3. 广西壮族自治区疾病预防控制中心, 广西 南宁 530028
  • 收稿日期:2023-09-28 修回日期:2024-02-28 发布日期:2024-04-11
  • 通讯作者: 李彬
  • 作者简介:夏祺悦,E-mail:15785159@qq.com

The subchronic toxicity and teratogenicity of Radix Asparagi in rats

XIA Qiyue1, JIANG Yong1, WANG Dongxia2, LI Bin3   

  1. 1. Sichuan Center for Disease Prevention and Control, Chengdu 610041, Sichuan;
    2. Mianyang Center for Disease Prevention and Control, Mianyang 621000, Sichuan;
    3. Guangxi Center for Disease Prevention and Control, Nanning 530028, Guangxi, China
  • Received:2023-09-28 Revised:2024-02-28 Published:2024-04-11

摘要: 目的:研究天冬对大鼠经口重复给药的亚慢性毒性和致畸毒性。方法:90天经口毒性试验采用SD大鼠80只,雌雄各半,体质量65.4~94.0 g,拌饲法设2 000、4 000、8 000 mg/kg共3个剂量组和1个阴性对照组,连续给予受试物90天,观察动物一般状况,记录动物体质量、摄食量,计算食物利用率,并进行血液学、血生化及病理学检测,从而评价其亚慢性毒性。传统致畸试验采用雌性 SD孕鼠,剂量为 1 000、2 000、4 000 mg/kg共 3个剂量组,另设阴性对照组(蒸馏水),每组 22只,经口灌胃给药,于孕第20天处死母体,检查受孕情况和胎仔发育,观察胎仔外观,检查骨骼及内脏,以评估致畸毒性。结果:90天经口毒性试验中大鼠未出现中毒症状及死亡,试验组大鼠组织病理学检查未见毒性损伤作用。致畸试验中低、中剂量组胎仔胸骨发育不全发生率分别为21.49%和26.32%,与对照组(6.25%)相比显著升高(P<0.01),未见其他异常。结论:在本试验条件下,90天经口毒性试验中天冬对大鼠的未观察到有害作用剂量(NOAEL)为 8 000 mg/kg;在致畸试验中,未观察到与染毒剂量相关的效应,天冬对SD大鼠无致畸性。

关键词: 天冬, 亚慢性毒性, 90天经口毒性试验, 致畸试验

Abstract: OBJECTIVE: To investigate the subchronic toxicity and teratogenicity of Radix Asparagi by repeated oral administration to rats orally. METHODS:The 90-day oral toxicity of the Radix Asparagi was detected by eighty Sprague-Dawley rats (half male and half female,65.4-94.0 g) and rats were administered with the doses of 2 000,4 000 and 8 000 mg/kg and negative control for consecutive 90 days to observe their general conditions, weight changes and food intake of animals, food utilization rates, and to conduct hematology,biochemical and pathological tests. In the traditional teratogenic test,22 pregnant female SD rats were used in each group,and the doses of 1 000,2 000 and 4 000 mg/kg body weight and negative control group (distilled water) were administered orally. The pregnant rats were sacrificed on the 20th day of pregnancy to examine the pregnancy status and fetal development, and to observe the appearance, the bone and the internal organs of the fetus for teratogenicity evaluation. RESULTS:No toxic symptoms and death occurred in the 90-day oral toxicity test,and no toxic damage was observed in the histopathological examination in the experimental group. In the teratogenicity test,the incidence of sternum hypoplasia was 21.49% and 26.32% in the low and medium dose group,respectively,which was significantly higher than that in the control group (6.25% ) (P<0.01), and no other abnormalities were found. CONCLUSION: The no observed adverse effect level (NOAEL) in 90-day oral toxicity test was 8 000 mg/kg bw. In the teratogenicity study,there were no treatment-related effects observed and Radix Asparagi did not show teratogenic effect on SD rats.

Key words: Radix Asparagi, subchronic toxicity, 90-day oral toxicity test, teratogenicity test

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