Department of Chemistry.
Department of Biology, CICECO - Aveiro Institute of Materials, University of Aveiro, 3810-193 Aveiro, Portugal.
Toxicol Sci. 2017 Oct 1;159(2):422-435. doi: 10.1093/toxsci/kfx142.
Although silver nanoparticles (AgNPs) are widely disseminated and show great potential in the biomedical field, there is a recognized need to better understand their action at the metabolic and functional levels. In this work, we have used NMR metabolomics, together with conventional clinical chemistry and histological examination, to characterize multi-organ and systemic metabolic responses to AgNPs intravenously administered to mice at 8 mg/kg body weight (a dose not eliciting overt toxicity). The major target organs of AgNPs accumulation, liver and spleen, showed the greatest metabolic changes, in a clear 2-stage response. In particular, the liver of dosed mice was found to switch from glycogenolysis and lipid storage, at 6 h postinjection, to glycogenesis and lipolysis, at subsequent times up to 48 h. Moreover, metabolites related to antioxidative defense, immunoregulation and detoxification seemed to play a crucial role in avoiding major hepatic damage. The spleen showed several early changes, including depletion of several amino acids, possibly reflecting impairment of hemoglobin recycling, while only a few differences remained at 48 h postinjection. In the heart, the metabolic shift towards TCA cycle intensification and increased ATP production possibly reflected a beneficial adaptation to the presence of AgNPs. On the other hand, the TCA cycle appeared to be down regulated in the lungs of injected mice, which showed signs of inflammation. Thekidneys showed the mildest metabolic response to AgNPs. Overall, this study has shown that NMR metabolomics is a powerful tool to monitor invivo metabolic responses to nanoparticles, revealing unforeseen effects.
尽管纳米银颗粒(AgNPs)在生物医学领域得到了广泛的应用,并显示出巨大的潜力,但人们认识到需要更好地了解它们在代谢和功能水平上的作用。在这项工作中,我们使用 NMR 代谢组学,结合常规临床化学和组织学检查,来描述静脉注射 8mg/kg 体重的 AgNPs 对小鼠多器官和全身代谢的影响(该剂量不会引起明显的毒性)。AgNPs 积累的主要靶器官肝脏和脾脏表现出最大的代谢变化,呈现出明显的 2 阶段反应。特别是,注射后 6 小时,给药小鼠的肝脏从糖原分解和脂质储存转变为糖异生和脂肪分解,直到随后的 48 小时。此外,与抗氧化防御、免疫调节和解毒相关的代谢物似乎在避免肝脏重大损伤方面发挥了关键作用。脾脏显示出几个早期变化,包括几种氨基酸的消耗,可能反映了血红蛋白再循环的损害,而在注射后 48 小时仅剩下少数差异。在心脏中,TCA 循环的代谢转变和 ATP 生成的增加可能反映了对 AgNPs 存在的有益适应。另一方面,在注射小鼠的肺部,TCA 循环似乎受到抑制,这表明存在炎症迹象。肾脏对 AgNPs 的代谢反应最温和。总的来说,这项研究表明,NMR 代谢组学是一种监测纳米颗粒体内代谢反应的强大工具,可以揭示意想不到的影响。