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Pyrethroid Pesticides Inhibit Nerve Growth Factor and Laminin-1 Mediated Neurite Outgrowth.

机译:拟除虫菊酯类农药可抑制神经生长因子和Laminin-1介导的神经突增生。

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摘要

Insecticides inhibit or over-excite insect nerve impulses thereby killing these agricultural pests. Unfortunately these neurotoxins are also toxic to humans. Recently a new class of insecticides, the pyrethroids, have shown effective insecticidal activity with greatly reduced toxicity to human systems. Here we address the concern that at sub-lethal levels, the pyrethroids may exhibit developmental neurotoxicity in mammals. To assess this concern, studies were conducted with pyrethroid bifenthrin, showing inhibition of neurite outgrowth formation in NGF dependent PC12 cells. In order to further the investigation of pyrethroids as developmental neurotoxins, we investigated additional pyrethroids such as permethrin, cypermethrin, deltamethrin and esfenvalerate and extended these observations to laminin mediated neurite outgrowth in Neuro 2a cells. We found that the pyrethroid pesticides showed maximum inhibition of neurites at highest concentration of 10-5M in PC12 and Neuro 2a cells and almost no effect at 10-9 M concentration. Cypermethrin had the greatest inhibitory effect showing 2.0% neurites at 10-5 M concentration and permethrin showed the least inhibitory effect with 8.1% neurites in PC12 cells. Bifenthrin had the greatest inhibitory effect showing only 2.6% neurites at 10-5M concentration and permethrin showed the least inhibitory effect with 3.7% neurites in Neuro 2a cells. These inhibitions were observed in the absence of cell death as determined by the adherent ability of the cells and trypan blue exclusion assay. These data show that pyrethroid pesticides inhibit neurite outgrowth suggesting their generalized effect on neurite formation. This raised the possibility of these pyrethroid pesticides acting as developmental neurotoxins.
机译:杀虫剂抑制或过度激发昆虫神经冲动,从而杀死这些农业害虫。不幸的是,这些神经毒素也对人类有毒。最近,一类新型杀虫剂拟除虫菊酯显示了有效的杀虫活性,并且对人体系统的毒性大大降低。在这里,我们解决了在致死水平下拟除虫菊酯可能在哺乳动物中表现出发育性神经毒性的问题。为了评估这种担忧,对拟除虫菊酯联苯菊酯进行了研究,结果显示在依赖NGF的PC12细胞中神经突生长的形成受到抑制。为了进一步研究拟除虫菊酯作为发育性神经毒素,我们研究了其他拟除虫菊酯,例如氯菊酯,氯氰菊酯,溴氰菊酯和艾芬戊酸酯,并将这些观察结果扩展到层粘连蛋白介导的神经2a细胞神经突生长。我们发现,拟除虫菊酯类农药在PC12和Neuro 2a细胞中的最高浓度为10-5M时,对神经突的抑制作用最大,而在10-9 M浓度下几乎没有作用。氯氰菊酯在PC12细胞中具有最大的抑制作用,在10-5 M浓度下显示2.0%的神经突,而苄氯菊酯对PC12细胞的抑制作用最小,对8.1%的神经突。联苯菊酯在10-5M浓度下具有最大的抑制作用,仅显示2.6%的神经突,而苄氯菊酯在Neuro 2a细胞中显示的抑制作用最小,仅有3.7%的神经突。通过细胞的粘附能力和台盼蓝排除法测定,在没有细胞死亡的情况下观察到了这些抑制作用。这些数据表明拟除虫菊酯农药可抑制神经突生长,表明它们对神经突的形成具有普遍作用。这增加了这些拟除虫菊酯类农药充当发育神经毒素的可能性。

著录项

  • 作者

    Mannath, Thejus.;

  • 作者单位

    Adelphi University.;

  • 授予单位 Adelphi University.;
  • 学科 Biology Neuroscience.;Biology Neurobiology.;Biology Cell.
  • 学位 M.S.
  • 年度 2011
  • 页码 34 p.
  • 总页数 34
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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