Laboratory of Histology and Cytogenetics (UR12ES10), Faculty of Medicine, 5019 Monastir, Tunisia.
Laboratory of Physics of Materials and Nanomaterials Applied at Environment (LaPhyMNE), Gabes University, Faculty of Sciences in Gabes, 6072, Tunisia; Imam Mohammad Ibn Saud Islamic University (IMISU), College of Sciences, Department of Physics, Riyadh 11623, Saudi Arabia.
Brain Res Bull. 2020 Feb;155:119-128. doi: 10.1016/j.brainresbull.2019.10.005. Epub 2019 Nov 9.
Titanium dioxide nanoparticles were widely used in food as dietary supplements, in drugs, in toothpaste, ect. Few numbers of studies were interested to the neurotoxicity of TiO NPs through oral pathway. The present study aims firstly to understand the connection between the physicochemical properties of TiO NPs and their associated toxicological oral pathway by evaluation the colloidal stability of TiO NPs over time in different media simulating physiological gastric, intestinal and serum conditions at 37 °C to be close to the oral administraton. Secondly, this study aims to evaluate the neurotoxicity of a subchronic intragastric administration of TiO NPs to rats. Different doses of anatase TiO NPs were administrated to Wistar rats every day for consecutives eight weeks. Titanium (Ti) content in brain, oxidative antioxidant biomarkers, lipid peroxidation, nitric oxide (NO) levels, tumor necrosis factor-alpha (TNF-α) levels, histophatological changes, degenerated and apoptosis neurons were investigated. Results suggested that TiO NPs can reach the brain and cross the brain blood barrier (BBB) to been accumulated in the brain of rats causing cerebral oxidative stress damage, increasing NO levels and histopathological injury. At higher dose, we observed the most cerebral injury by the highest accumulation of Ti and by the remarkable increase of TNF-α besides to the most increase of degenerated and apoptosis neurons in the brain of exposed rats. TiO NPs led to a neurotoxic damage accompanied by the increase of degenerated and apoptotic neurons in cerebral cortex.
二氧化钛纳米颗粒广泛应用于食品作为膳食补充剂、药物、牙膏等。很少有研究关注通过口服途径的 TiO NPs 的神经毒性。本研究旨在首先通过评估 TiO NPs 在不同模拟生理胃、肠和血清条件的介质中的胶体稳定性,了解 TiO NPs 的物理化学性质与其相关毒理学口服途径之间的联系,时间为 37°C 以接近口服给药。其次,本研究旨在评估 TiO NPs 亚慢性经口给予大鼠的神经毒性。每天给 Wistar 大鼠不同剂量的锐钛矿 TiO NPs 连续八周。研究了大脑中的钛 (Ti) 含量、氧化抗氧化生物标志物、脂质过氧化、一氧化氮 (NO) 水平、肿瘤坏死因子-α (TNF-α) 水平、组织病理学变化、变性和凋亡神经元。结果表明,TiO NPs 可以到达大脑并穿过血脑屏障 (BBB) 并在大鼠大脑中积累,导致大脑氧化应激损伤,增加 NO 水平和组织病理学损伤。在较高剂量下,我们观察到最高的大脑损伤是由于 Ti 的最高积累和 TNF-α 的显著增加,以及暴露大鼠大脑中变性和凋亡神经元的增加。TiO NPs 导致神经毒性损伤,伴随大脑皮质中变性和凋亡神经元的增加。