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吸入二氧化钛纳米气溶胶后衰老大鼠的脑炎症、血脑屏障功能障碍和神经元突触素减少。

Brain Inflammation, Blood Brain Barrier dysfunction and Neuronal Synaptophysin Decrease after Inhalation Exposure to Titanium Dioxide Nano-aerosol in Aging Rats.

机构信息

Service de Pharmacologie et d'Immunoanalyse, UMR 0496, CEA, Université Paris-Saclay, F-91191, Gif-sur-Yvette, France.

INRS, Département Toxicologie et Biométrologie, Rue du Morvan, CS 60027, 54519, Vandœuvre Cedex, France.

出版信息

Sci Rep. 2017 Sep 22;7(1):12196. doi: 10.1038/s41598-017-12404-5.

DOI:10.1038/s41598-017-12404-5
PMID:28939873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5610323/
Abstract

Notwithstanding potential neurotoxicity of inhaled titanium dioxide nanoparticles (TiO NPs), the toxicokinetics and consequences on blood-brain barrier (BBB) function remain poorly characterized. To improve risk assessment, we need to evaluate the impact on BBB under realistic environmental conditions and take into account vulnerability status such as age. 12-13 week and 19-month-old male rats were exposed by inhalation to 10 mg/m of TiO nano-aerosol (6 hrs/day, 5 day/week, for 4 weeks). We showed an age-dependent modulation of BBB integrity parameters suggesting increased BBB permeability in aging rats. This alteration was associated with a significant increase of cytokines/chemokines in the brain, including interleukin-1β, interferon-γ, and fractalkine as well as a decreased expression of synaptophysin, a neuronal activity marker. These observations, in absence of detectable titanium in the brain suggest that CNS-related effects are mediated by systemic-pathway. Moreover, observations in terms of BBB permeability and brain inflammation underline age susceptibility. Even if TiO NPs were not evidenced in the brain, we observed an association between the exposure to TiO NPs and the dysregulation of BBB physiology associated with neuroinflammation and decreased expression of neuronal activity marker, which was further exacerbated in the brain of aged animal's.

摘要

尽管吸入的二氧化钛纳米颗粒(TiO2 NPs)具有潜在的神经毒性,但它们的毒代动力学和对血脑屏障(BBB)功能的影响仍知之甚少。为了改善风险评估,我们需要在现实环境条件下评估对 BBB 的影响,并考虑到年龄等脆弱性状态。12-13 周龄和 19 月龄雄性大鼠通过吸入暴露于 10 mg/m 的 TiO2 纳米气溶胶中(6 小时/天,每周 5 天,持续 4 周)。我们显示 BBB 完整性参数随年龄的变化具有调节作用,提示衰老大鼠 BBB 通透性增加。这种改变与大脑中细胞因子/趋化因子的显著增加有关,包括白细胞介素-1β、干扰素-γ和 fractalkine,以及神经元活动标志物突触素的表达降低。这些观察结果在大脑中未检测到钛表明,中枢神经系统相关效应是通过全身途径介导的。此外,BBB 通透性和脑炎症的观察结果强调了年龄易感性。即使在大脑中未发现 TiO2 NPs,我们也观察到暴露于 TiO2 NPs 与 BBB 生理学的失调之间存在关联,这种失调与神经炎症和神经元活动标志物表达降低有关,在老年动物的大脑中进一步加剧。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/9bb6818adb2a/41598_2017_12404_Fig9_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/0eccf16181d6/41598_2017_12404_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/10f144254310/41598_2017_12404_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/9bb6818adb2a/41598_2017_12404_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/6e6963c51da4/41598_2017_12404_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/2fba3445ef4a/41598_2017_12404_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/5be9fc0221e2/41598_2017_12404_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/d56731a32d36/41598_2017_12404_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/bb3faf1a6ef4/41598_2017_12404_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/407ab62267c5/41598_2017_12404_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/0eccf16181d6/41598_2017_12404_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/10f144254310/41598_2017_12404_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90c/5610323/9bb6818adb2a/41598_2017_12404_Fig9_HTML.jpg

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