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鱼藤酮农药对神经元极化的神经毒性:一种机制研究方法。

Neurotoxicity of the pesticide rotenone on neuronal polarization: a mechanistic approach.

作者信息

Bisbal Mariano, Sanchez Mónica

机构信息

Laboratory of Neurobiology, Instituto Mercedes y Martín Ferreyra (INIMEC-CONICET); Universidad Nacional de Córdoba; Instituto Universitario Ciencias Biomédicas Córdoba, Córdoba, Argentina.

出版信息

Neural Regen Res. 2019 May;14(5):762-766. doi: 10.4103/1673-5374.249847.

Abstract

Neurons are the most extensive and polarized cells that display a unique single long axon and multiple dendrites, which are compartments exhibiting structural and functional differences. Polarity occurs early in neuronal development and it is maintained by complex subcellular mechanisms throughout cell life. A well-defined and controlled spatio-temporal program of cellular and molecular events strictly regulates the formation of the axon and dendrites from a non-polarized cell. This event is critical for an adequate neuronal wiring and therefore for the normal functioning of the nervous system. Neuronal polarity is very sensitive to the harmful effects of different factors present in the environment. In this regard, rotenone is a crystalline, colorless and odorless isoflavone used as insecticide, piscicide and broad spectrum pesticide commonly used earlier in agriculture. In the present review we will summarize the toxicity mechanism caused by this pesticide in different neuronal cell types, focusing on a particular biological mechanism whereby rotenone could impair neuronal polarization in cultured hippocampal neurons. Recent advances suggest that the inhibition of axonogenesis produced by rotenone could be related with its effect on microtubule dynamics, the actin cytoskeleton and their regulatory pathways, particularly affecting the small RhoGTPase RhoA. Unveiling the mechanism by which rotenone produces neurotoxicity will be instrumental to understand the cellular mechanisms involved in neurodegenerative diseases influenced by this environmental pollutant, which may lead to research focused on the design of new therapeutic strategies.

摘要

神经元是最广泛且具有极性的细胞,具有独特的单一长轴突和多个树突,这些部分表现出结构和功能上的差异。极性在神经元发育早期就出现,并在细胞整个生命过程中由复杂的亚细胞机制维持。细胞和分子事件明确且受控制的时空程序严格调节非极性细胞轴突和树突的形成。这一事件对于适当的神经元布线至关重要,因此对于神经系统的正常功能也至关重要。神经元极性对环境中存在的不同因素的有害影响非常敏感。在这方面,鱼藤酮是一种结晶、无色无味的异黄酮,用作杀虫剂、鱼毒剂和广谱农药,早些时候在农业中普遍使用。在本综述中,我们将总结这种农药在不同神经元细胞类型中引起的毒性机制,重点关注鱼藤酮可能损害培养的海马神经元中神经元极性的特定生物学机制。最近的进展表明,鱼藤酮产生的轴突发生抑制可能与其对微管动力学、肌动蛋白细胞骨架及其调节途径的影响有关,尤其影响小RhoGTPase RhoA。揭示鱼藤酮产生神经毒性的机制将有助于理解受这种环境污染物影响的神经退行性疾病所涉及的细胞机制,这可能会引发针对新治疗策略设计的研究。

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