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Maternal administration of nanomaterials elicits hemoglobin upregulation in the neonatal brain of non-human primates

机译:母体给药纳米材料会引起非人类灵长类动物新生儿大脑中的血红蛋白上调

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To investigate the influence of nanomaterial exposure during fetal development, diesel exhaust particles (DEPs), carbon black (CB), or titanium dioxide (TiO2) was injected intradermally to pregnant rhesus macaques. The hippocampus and cerebellum of newborn infants were then examined. DNA microarray and quantitative real-time RT-PCR, western blot, and immunohistochemical analyses were used to measure the expression of the hemoglobin genes, HBA, HBB, and HBG. Of the nanomaterials tested, DEP elicited the greatest increase in mRNA and protein levels of hemoglobin genes in the brain tissues. Strong signal of HbA protein was detected in the pyramidal cell layer, the polymorphic cell layer and in the alveus of the hippocampi of the DEP-treated animals. The altered gene expression was likely due to responses to oxidative or nitrosative stress and/or hypoxia in the fetaleonatal brain. Since excessive hemoglobin is reportedly neurotoxic, the vulnerability of developing brains by long-term upregulation of hemoglobin should be considered. Maternal exposure to nanomaterials may increase the risk of brain dysfunction in offspring.
机译:为了研究胎儿发育过程中纳米材料暴露的影响,将柴油机排气颗粒(DEPs),炭黑(CB)或二氧化钛(TiO 2 )皮内注射到怀孕的恒河猴中。然后检查新生儿的海马和小脑。 DNA微阵列和定量实时RT-PCR,蛋白质印迹和免疫组化分析用于测量血红蛋白基因,HBA,HBB和HBG的表达。在所测试的纳米材料中,DEP引起脑组织中血红蛋白基因的mRNA和蛋白质水平的最大增加。在接受DEP处理的动物的锥体细胞层,多态性细胞层和海马肺泡中检测到HbA蛋白的强信号。基因表达的改变可能是由于对胎儿/新生儿大脑中的氧化或亚硝化应激和/或缺氧的反应。由于据报道过量的血红蛋白具有神经毒性,因此应考虑由于长期上调血红蛋白而使大脑发育的脆弱性。母体接触纳米材料可能会增加后代脑功能障碍的风险。

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