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Single-Walled Carbon Nanotubes Induces Oxidative Stress in Rat Lung Epithelial Cells

机译:单壁碳纳米管诱导大鼠肺上皮细胞氧化应激。

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摘要

Single-walled carbon nanotubes (SWCNT) show unique properties find applications in micro devices; electronics to biological systems specially drug delivery and gene therapy. However the manufacture and extensive use of nanotubes raises concern about its safe use and human health. Very few studies have been carried out on toxicity of carbon nanotubes in experimental animals and humans, thus resulted in limiting their use. The extensive toxicological studies using in vitro and in vivo models are necessary and are required to establish safe manufacturing guidelines and also the use of SWCNT. These studies also help the chemists to prepare derivative of SWCNT with less or no toxicity. The present study was undertaken to determine the toxicity exhibited by SWCNT in rat lung epithelial cells as a model system. Lung epithelial cells (LE cells) were cultured with or without SWCNT and reactive oxygen species (ROS) produced were measured by change in fluorescence using dichloro fluorescein (DCF). The results show increased ROS on exposure to SWCNT in a dose and time dependent manner. The decrease in glutathione content suggested the depletion and loss of protective mechanism against ROS in SWCNT treated cells. Use of rotenone, the inhibitor of mitochondrial function have no effect on ROS levels suggested that mitochondria is not involved in SWCNT induced ROS production. Studies carried out on the effect of SWCNT on superoxide dismutase (SOD-1 and SOD-2) levels in LE cells, indicates that these enzyme levels decreased by 24 hours. The increased ROS induced by SWCNT on LE cells decreased by treating the cells with 1 mM of glutathione, N-Acetyl Cysteine, and Vitamin C. These results further prove that SWCNT induces oxidative stress in LE cells and shows loss of antioxidants.
机译:单壁碳纳米管(SWCNT)具有独特的性能,可在微型设备中找到应用。电子系统到生物系统,尤其是药物输送和基因治疗。然而,纳米管的制造和广泛使用引起人们对其安全使用和人类健康的关注。关于碳纳米管在实验动物和人类中的毒性的研究很少,因此限制了它们的使用。使用体外和体内模型进行广泛的毒理学研究是必要的,也是建立安全生产准则以及使用SWCNT所必需的。这些研究还帮助化学家制备毒性较小或无毒性的SWCNT衍生物。进行本研究以确定SWCNT在大鼠肺上皮细胞中表现出的毒性作为模型系统。在有或没有SWCNT的情况下培养肺上皮细胞(LE细胞),并使用二氯荧光素(DCF)通过荧光变化来测量产生的活性氧(ROS)。结果表明,暴露于SWCNT的ROS呈剂量和时间依赖性增加。谷胱甘肽含量的减少表明SWCNT处理的细胞中ROS的消耗和失去了保护机制。鱼藤酮是线粒体功能的抑制剂,对ROS水平没有影响,提示线粒体不参与SWCNT诱导的ROS产生。对SWCNT对LE细胞中超氧化物歧化酶(SOD-1和SOD-2)水平的影响进行的研究表明,这些酶水平降低了24小时。通过用1 mM的谷胱甘肽,N-乙酰半胱氨酸和维生素C处理细胞,SWCNT诱导的LE细胞上的ROS增加而减少。这些结果进一步证明SWCNT诱导LE细胞中的氧化应激并显示抗氧化剂的损失。

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