Department of Neurophysiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, Poland.
Division of Nutrition Physiology, Department of Dietetics, Faculty of Human Nutrition and Consumer Science, Warsaw University of Life Sciences - SGGW, Nowoursynowska 159C, 02-776 Warsaw, Poland.
Toxicol Lett. 2018 Jun 15;290:133-144. doi: 10.1016/j.toxlet.2018.03.019. Epub 2018 Mar 22.
Increasing use of silver nanoparticles (AgNPs) results in increased human exposure. AgNPs are able to cross brain-blood barrier and are a risk factor for the brain. Thus, we hypothesized that AgNPs exposure might affect hippocampal dependent memory, which required cognitive coordination processes. To verify the assumption, in this study we evaluated the effects of orally administered bovine serum albumin (BSA)-coated AgNPs on spatial memory, which engage cognitive coordination processes for on-going stimuli segregation. Rats following 28 days of oral administration with 1 mg/kg (n = 10) or 30 mg/kg (n = 10) BSA-AgNPs or saline, a control groups (n = 10, n = 8), were tested with an active place avoidance task in the Carousel Maze test. The study revealed significant impairment of long- and short-term memory, irrespectively of dose of AgNPs, whereas non-cognitive activity was on a similar level. We found significantly higher content of silver in the hippocampus in comparison to the lateral cortex. No silver was found in the cerebellum and the frontal cortex. The nanoSIMS analysis reveal a weak signal of silver in the hippocampus of AgNPs treated animals that should be attributed to the presence of silver in ionic form rather than AgNPs. Our findings indicate that oral exposure to a low dose AgNPs induces detrimental effect on memory and cognitive coordination processes. The presence of silver ions rather than AgNPs in different brain regions, in particular the hippocampus, suggests crucial role of silver ions in AgNPs-induced impairment of the higher brain functions.
越来越多的人接触到纳米银(AgNPs),这增加了人类的暴露风险。AgNPs 能够穿过血脑屏障,是大脑的一个风险因素。因此,我们假设 AgNPs 的暴露可能会影响海马体依赖的记忆,而海马体依赖的记忆需要认知协调过程。为了验证这一假设,在这项研究中,我们评估了口服牛血清白蛋白(BSA)包裹的 AgNPs 对空间记忆的影响,空间记忆涉及到对正在进行的刺激进行认知协调的过程。28 天后,1mg/kg(n=10)或 30mg/kg(n=10)BSA-AgNPs 或生理盐水(对照组,n=10,n=8)组的大鼠接受口服处理,然后在 Carousel Maze 测试中进行主动回避任务测试。研究表明,AgNPs 的剂量对长时和短时记忆都有显著的损害,而对非认知活动的影响则相似。与外侧皮质相比,我们在海马体中发现了明显更高含量的银。在小脑和额叶皮质中没有发现银。nanoSIMS 分析显示,AgNPs 处理动物的海马体中存在微弱的银信号,这归因于离子形式的银的存在,而不是 AgNPs。我们的研究结果表明,口服低剂量 AgNPs 会对记忆和认知协调过程产生不利影响。不同脑区,特别是海马体中存在银离子而非 AgNPs,表明银离子在 AgNPs 诱导的高级脑功能损伤中起着关键作用。