中国药物警戒 ›› 2017, Vol. 14 ›› Issue (6): 326-330.

• 基础与临床研究 • 上一篇    下一篇

牛蒡子苷元对大鼠生育力与早期胚胎发育毒性的研究

李春燕,姚景春,王会萍,刘奋,王恩力*   

  1. 鲁南制药集团股份有限公司新药安评中心,中药制药共性技术国家重点实验室,临沂市天然药物免疫毒理企业重点实验室,山东 临沂,273400
  • 收稿日期:2017-04-10 修回日期:2017-08-17 出版日期:2017-06-20 发布日期:2017-08-17
  • 通讯作者: 王恩力,男,硕士,工程师,药理毒理实验研究。E-mail:weli51@163.com。
  • 作者简介:李春燕,女,硕士,工程师,药理毒理实验研究。
  • 基金资助:
    2015山东省自主创新及成果转化专项(2015ZDQJ05004):牛蒡子苷元及其衍生物(IDO抑制剂)的研究与开发。

Fertility and Early Embryo Developmental Toxicity of Arctigenin in Rats

LI Chun-yan, YAO Jing-chun, WANG Hui-Ping, LIU Feng, WANG En-li*   

  1. Center For Drug Safety Evaluation of Lunan Pharmaceutical Group Corporation, State Key Laboratory of Generic Manufacture Technology of Chinese Traditional Medicine, Enterprise Key Laboratory of Immunotoxicity of Natural Drug, Shandong Linyi 273400, China
  • Received:2017-04-10 Revised:2017-08-17 Online:2017-06-20 Published:2017-08-17

摘要: 目的 以SD大鼠为实验系统评价牛蒡子苷元的生育力与早期胚胎发育毒性。方法 SD大鼠按照体重随机分为溶媒对照组和牛蒡子苷元4、16、64 mg?kg-1三个剂量组,每组50只,雌雄各半。全部动物皮下注射给予对应药物,每日1次,给药体积2 mL?kg-1。雌雄大鼠分别给药10 wk和2 wk后将动物按照1:1比例合笼交配。动物交配期间持续给药,交配成功雌鼠继续给药至妊娠第6天(GD 6),交配成功雄鼠持续给药直至处死。试验期间,每日观察动物一般体征,定期检测动物体重和摄食量;雄鼠于交配成功后1 wk处死,检查精子质量和称量生殖器官重量;雌鼠于GD 15处死,检查黄体数、着床数、活胎数、吸收胎数和死胎数,称量子宫和卵巢重量。结果 给药期间,各组均可见给药导致的给药部位刺激反应,牛蒡子苷元16、64 mg?kg-1剂量组各有1只动物因药物毒性死亡;与溶媒对照组相比较,牛蒡子苷元各剂量组体重和摄食量均未见异常变化,动物交配天数、交配率和雌鼠受孕率、雄鼠精子质量和雌鼠妊娠结局均未见异常改变。结论 在本实验条件下,牛蒡子苷元未见大鼠生育力与早期胚胎发育毒性,其未观察毒性剂量(NOAEL)为64 mg?kg-1。

关键词: 牛蒡子苷元, 生育力, 早期胚胎, 着床数

Abstract: Objective To observe the toxicity effect of arctigenin on rat fertility and early embryo development in SD rats. Methods SD rats were divided into solvent control group and arctigenin 4, 16, 64 mg?kg-1 three dose groups, 25 animals per sex per group. Prior to mating, male rats were treated 10 weeks and female rats were treated 2 weeks respectively by subcutaneous injection with volume 2 mL?kg-1 once a day. Within each treatment group, the male and female rats were co-housed (1:1) until evidence of mating was seen or for 2 consecutive weeks. During cohabitation period, total animals were continuously treated. After successful mating, female rats still were treated until day 6 of pregnancy and male rats were kept treating until euthanized. Clinical observations, body weights and food consumption were recorded routinely. Male rats were euthanized 1 week after successful mating, then sperm quality and reproductive organs were inspected; female rats were euthanized on day 15 of pregnancy, then the corpora luteum number, implantation number, viable fetuses number, absorbed fetuses number, dead fetuses number, uterus and ovary weight were inspected. Results During treating times, stimulation of drug delivery site were seen on all groups animals, arctigenin 16, 64 mg?kg-1 dose group caused 1 animal death respectively. Body weights and feed consumption in all arctigenin treatment groups were not significantly different when compared with the solvent group. There had no abnormal changes on animal precoital interval, mating index, gestation index, sperm quality of male rats and pregnancy outcome of female rats. Conclusion Under this experimental environment, arctigenin has no significant toxicity on rat fertility and early embryo development, and the no observed adverse effect level(NOAEL)is 64 mg?kg-1.

Key words: arctigenin, fertility, early embryo, implantation

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