Department of Chemistry, Faculty of Science, Guilan University, Guilan, P. O. Box: 41335-1914, Rasht, Iran.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Shahid Beheshti University of Medical Sciences, P.O. Box 14155-6153, Tehran, Iran.
Biol Trace Elem Res. 2018 Aug;184(2):350-357. doi: 10.1007/s12011-017-1170-4. Epub 2017 Oct 24.
CuO nanoparticles (CuO-NPs) serve several important functions in human life, particularly in the fields of medicine, engineering, and technology. These nanoparticles have been utilized as catalysts, semiconductors, sensors, gaseous and solid ceramic pigments, and magnet rotatable devices. Further use for CuO-NPs has been employed in the pharmaceutical industry especially in the production of anti-microbial fabric treatments or prevention of infections caused by Escherichia coli and methicillin-resistant Staphylococcus aureus. Two key potential routes of exposure to CuO-NPs exist through inhalation and skin exposure. Toxicity of these nanoparticles has been reported in various studies; however, no study as of yet has investigated the complete cellular mechanisms involved in CuO-NPs toxicity on human cells. The aim of this study was to determine the cytotoxicity of CuO-NPs on human blood lymphocytes. Blood lymphocytes were obtained from healthy male subjects through the use of Ficoll polysaccharide subsequently by gradient centrifugation. The following parameters were assayed in blood lymphocytes after a 6-h incubation with different concentrations of CuO-NPs: cell viability, reactive oxygen species (ROS) formation, lipid peroxidation, cellular glutathione levels, and mitochondrial and lysosomal damage. Our results demonstrate that CuO-NPs, in particular, decreased cell viability in a concentration-dependent manner and the IC50 determined was 382 μM. CuO-NP cytotoxicity was associated with significant increase at intracellular ROS level and loss of mitochondrial membrane potential and lysosomal membrane leakiness. Hence, CuO-NPs are shown to effectively induce oxidative stress in addition to inflict damage on mitochondria and lysosomes in human blood lymphocytes.
氧化铜纳米颗粒(CuO-NPs)在人类生活中具有多种重要功能,特别是在医学、工程和技术领域。这些纳米颗粒已被用作催化剂、半导体、传感器、气态和固态陶瓷颜料以及磁旋转装置。氧化铜纳米颗粒在医药行业的进一步应用尤其在于生产抗菌织物处理剂或预防大肠杆菌和耐甲氧西林金黄色葡萄球菌引起的感染。人们主要通过吸入和皮肤接触这两种关键途径接触到 CuO-NPs。已有研究报道了这些纳米颗粒的毒性,但目前尚无研究调查 CuO-NPs 对人类细胞毒性的完整细胞机制。本研究旨在确定 CuO-NPs 对人血淋巴细胞的细胞毒性。通过使用菲可葡聚糖,随后通过梯度离心从健康男性受试者中获得血淋巴细胞。在与不同浓度的 CuO-NPs 孵育 6 小时后,对血淋巴细胞进行以下参数检测:细胞活力、活性氧(ROS)形成、脂质过氧化、细胞谷胱甘肽水平以及线粒体和溶酶体损伤。我们的研究结果表明,CuO-NPs 可显著降低细胞活力,且呈浓度依赖性,确定的 IC50 为 382 μM。CuO-NP 的细胞毒性与细胞内 ROS 水平的显著增加以及线粒体膜电位和溶酶体膜通透性丧失有关。因此,CuO-NPs 可有效诱导人血淋巴细胞发生氧化应激,并对线粒体和溶酶体造成损伤。