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Size-dependent impairment of cognition in mice caused by the injection of gold nanoparticles

机译:纳米金的注射引起的小鼠认知大小依赖性

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We explored the size-dependent impairment of cognition in mice caused by the injection of gold nanoparticles (GNPs). GNPs of 17 and 37 nm in diameter were injected intraperitoneally into BALB/c mice at doses ranging from 0.5 to 14.6 mg kg~(-1). ICP-MS was performed on brain tissue collected 1, 14 and 21 days after the injection. A passive-avoidance test was performed on day 21. Monoamine levels were determined on day 21. The microscopic distribution of GNPs in the hippocampus was examined using coherent anti-Stokes Raman scattering (CARS) microscopy and transmission electron microscopy (TEM). The results indicated that 17 nm GNPs passed through the blood-brain barrier more rapidly than 37 nm GNPs. Treatment with 17 nm GNPs decreased the latency time, which was comparable to the effect of scopolamine treatment, while 37 nm GNPs showed no significant effect. Dopamine levels and serotonin levels in the brain were significantly altered by the injection of 17 and 37 nm GNPs. GNPs affected dopaminergic and serotonergic neurons. CARS microscopy indicated that 17 nm GNPs entered the Cornu Ammonis (CA) region of the hippocampus, while 37 nm GNPs were excluded from the CA region. TEM verified the presence of 17 nm GNPs in the cytoplasm of pyramidal cells. In this study, we showed that the ability of GNPs to damage cognition in mice was size-dependent and associated with the ability of the particles to invade the hippocampus. The dosage and duration of the treatment should be taken into account if GNPs are used in the future as vehicles to carry therapeutic agents into the brain.
机译:我们探讨了由金纳米颗粒(GNPs)注射引起的小鼠认知能力的大小依赖性。腹膜内将直径分别为17和37 nm的GNP注射到BALB / c小鼠中,剂量范围为0.5至14.6 mg kg〜(-1)。注射后1、14和21天对收集的脑组织进行ICP-MS。在第21天进行被动回避测试。在第21天确定单胺水平。使用相干抗斯托克斯拉曼散射(CARS)显微镜和透射电子显微镜(TEM)检查海马中GNP的微观分布。结果表明,17 nm GNP比37 nm GNP通过血脑屏障的速度更快。用17 nm GNP进行治疗可减少潜伏时间,这与东pol碱治疗的效果相当,而37 nm GNP则无显着影响。通过注射17和37 nm GNP,大脑中的多巴胺水平和血清素水平显着改变。 GNP影响多巴胺能和5-羟色胺能神经元。 CARS显微镜检查表明,有17 nm GNP进入海马的Cornu Ammonis(CA)区,而从CA CA区排除了37 nm GNP。 TEM证实锥体细胞的细胞质中存在17 nm GNP。在这项研究中,我们表明GNP损害小鼠认知的能力与大小有关,并且与颗粒侵袭海马的能力有关。如果将来将GNP用作将治疗剂携带到大脑的媒介,则应考虑治疗的剂量和持续时间。

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