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首页> 外文期刊>Archives of Toxicology >Titanium dioxide nanoparticles via oral exposure leads to adverse disturbance of gut microecology and locomotor activity in adult mice
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Titanium dioxide nanoparticles via oral exposure leads to adverse disturbance of gut microecology and locomotor activity in adult mice

机译:通过口服暴露的二氧化钛纳米颗粒导致成人小鼠对肠道微生态学和运动活性的不利扰动

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摘要

Titanium dioxide nanoparticles (TiO(2)NPs) have been widely used as food additives in daily life. However, the impact of oral intake of TiO(2)NPs on the nervous system is largely unknown. In this study, 7-week-old mice were treated with either vehicle or TiO(2)NPs suspension solution at 150 mg/kg by intragastric administration for 30 days. Our results demonstrated that oral exposure to TiO(2)NPs resulted in aberrant excitement of enteric neurons, although unapparent pathological changes were observed in gut. We also found the richness and evenness of gut microbiota were remarkably decreased and the gut microbial community compositions were significantly changed in the TiO2NP-treated group as compared with vehicle controls. Interestingly, oral exposure to TiO(2)NPs was capable to induce the inhibitory effects on locomotor activity, but it did not lead to significant change on the spatial learning and memory ability. We further revealed the mechanism that TiO(2)NPs could specifically cause locomotor dysfunction by elevating the excitement of enteric neuron, which might spread to brain via gut-brain communication by vagal pathway. However, inflammation response, enteric neurotransmitter 5-HT and major gut peptides might not be involved in this pathological process. Together, these findings provide valuable insights into the novel mechanism of TiO2NP-induced neurotoxicity. Understanding the microbiota-gut-brain axis will provide the foundation for potential therapeutic or prevention approaches against TiO2NP-induced gut and brain-related disorders.
机译:二氧化钛纳米颗粒(TiO(2)NPS)已被广泛用作日常生活中的食品添加剂。然而,在神经系统上的TiO(2)NPS口服摄入的影响在很大程度上是未知的。在本研究中,通过胃内给药30天以150mg / kg用载体或TiO(2)NPS悬浮液处理7周龄小鼠。我们的研究结果表明,TiO(2)NPS的口腔暴露导致肠道神经元的异常兴奋,但在肠道中观察到不遵守的病理变化。我们还发现肠道微生物的丰富性和均匀性显着降低,与载体对照组相比,TiO2NP治疗组中的肠道微生物群落组合物显着变化。有趣的是,口服暴露于TiO(2)NPS能够诱导对运动活动的抑制作用,但它不会导致空间学习和记忆能力的重大变化。我们进一步揭示了TiO(2)NPS可以通过升高肠道神经元的兴奋来特异性地引起运动功能障碍的机制,这可能通过迷入途径通过肠道脑沟传播到大脑。然而,炎症反应,肠道神经递质5-HT和主要肠肽可能不会参与该病理过程。这些发现在一起,为TiO2NP诱导的神经毒性的新机制提供了有价值的见解。了解微生物肠肠轴将为潜在治疗或预防肠道诱导的肠道和脑相关疾病提供潜在治疗或预防方法的基础。

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