...
首页> 外文期刊>Environmental toxicology >Cloperastine Rescues Impairment of Passive Avoidance Response in Mice Prenatally Exposed to Diethylstilbestrol
【24h】

Cloperastine Rescues Impairment of Passive Avoidance Response in Mice Prenatally Exposed to Diethylstilbestrol

机译:氯吡斯汀挽救出生前暴露于己烯雌酚的小鼠被动回避反应的障碍。

获取原文
获取原文并翻译 | 示例
           

摘要

We previously reported that prenatal exposure to diethylstilbestrol (DES) Impaired passive avoidance responses in mice. Apart from the above, we also found that cloperastine, a centrally acting antitussive, ameliorated depression-like and anxiety-like behaviors in rodents at antitussive-effective doses. In this study, we investigated whether or not cloperastine rescues impairment of passive avoidance responses in mice prenatally exposed to DES. Male DES-exposed mice were subcutaneously administered cloperastine at 10 or 30 mg/kg twice a day from 32 to 41 days after birth and subjected to behavioral testing 42 to 46 days after birth. Cloperastine at 10 and 30 mg/kg ameliorated DES-induced impairment of passive avoidance responses. In addition, cloperastine affected the levels of 5-HT_(1A) receptors, GIRK and BDNF in the hippocampus of DES-exposed mice. However, the number of BrdUpositive cells in the hippocampus of DES-exposed mice was not changed by chronic administration of cloperastine. These findings suggest that the action of endocrine disruptors in the brain may not always be irreversible, and that the symptoms caused by endocrine disruptors might be curable with drugs such as cloperastine.
机译:我们以前曾报道,产前暴露于己烯雌酚(DES)会损害小鼠的被动回避反应。除上述以外,我们还发现氯吡斯汀是一种具有镇咳作用的中枢镇咳药,在镇咳有效剂量下可减轻啮齿类动物的抑郁样和焦虑样行为。在这项研究中,我们调查了氯培斯汀是否能挽救出生前暴露于DES的小鼠的被动回避反应的损伤。雄性DES暴露小鼠从出生后32到41天每天两次以10或30 mg / kg皮下注射氯吡汀,并在出生后42到46天进行行为测试。氯吡斯汀10和30 mg / kg改善了DES引起的被动回避反应障碍。此外,氯吡斯汀影响暴露于DES的小鼠海马中5-HT_(1A)受体,GIRK和BDNF的水平。但是,暴露于DES的小鼠的海马中BrdU阳性细胞的数量并没有因氯吡汀的长期给药而改变。这些发现表明,内分泌干扰物在大脑中的作用可能并非始终是不可逆的,并且由内分泌干扰物引起的症状可以用氯吡斯汀等药物治愈。

著录项

  • 来源
    《Environmental toxicology》 |2014年第2期|216-225|共10页
  • 作者单位

    Department of Environmental and Molecular Health Sciences, Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan;

    Department of Environmental and Molecular Health Sciences, Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan;

    Department of Environmental and Molecular Health Sciences, Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan;

    Department of Environmental and Molecular Health Sciences, Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan;

    Department of Environmental and Molecular Health Sciences, Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    endocrine disruptor; learning and memory; BDNF; 5-HT_(1A) receptor; GIRK;

    机译:内分泌干​​扰物学习和记忆;BDNF;5-HT_(1A)受体;女孩;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号