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Silver ion-induced mitochondrial dysfunction via a nonspecific pathway

机译:银离子诱导的线粒体功能障碍通过非特异性途径

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Silver, once regarded as a safe noble metal for humans, has been widely used in industrial and commercial products, especially in nanometer biomaterials. It is now well known that Ag+ is biologically active and is able to interact with the cell membrane, proteins and DNA. However, very little is understood about the potential impacts of Ag+ at the sub-cellular level. Our work investigated the potential toxicity of Ag+ on mitochondria isolated from rat livers by examining the mitochondrial morphology, respiration, swelling, membrane fluidity and reactive oxygen species (ROS) generation. We observed that Ag+ significantly affects the mitochondrial structure and function, including mitochondrial swelling, collapse of the transmembrane potential, change of permeability and fluidity, decline of the respiratory rate, and acceleration of ROS, indicating that Ag+ should be seriously regarded as a potentially hazardous substance. Moreover, we conclude that Ag+ injures the mitochondrial structure and function by a nonspecific approach, in which the interaction is unregulated by inherent parts such as the mitochondria permeability transition pore (MPTP). These results help us learn more about the toxicity of Ag+ at the subcellular (mitochondrial) level and influence future biological and medical applications of Ag-based materials.
机译:银曾被认为是人类安全的贵金属,已被广泛用于工业和商业产品,尤其是纳米生物材料。众所周知,Ag+具有生物活性,能够与细胞膜、蛋白质和DNA相互作用。然而,人们对Ag+在亚细胞水平上的潜在影响知之甚少。我们的工作通过检测线粒体形态、呼吸、肿胀、膜流动性和活性氧(ROS)的产生来研究Ag+对从大鼠肝脏分离的线粒体的潜在毒性。我们观察到,Ag+显著影响线粒体结构和功能,包括线粒体肿胀、跨膜电位崩溃、通透性和流动性改变、呼吸频率下降和活性氧加速,表明Ag+应被视为一种潜在危险物质。此外,我们还得出结论,Ag+通过非特异性的方式损害线粒体的结构和功能,这种相互作用不受线粒体通透性转换孔(MPTP)等固有部分的调节。这些结果有助于我们在亚细胞(线粒体)水平上更多地了解Ag+的毒性,并影响Ag基材料未来的生物学和医学应用。

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    《Toxicology Research》 |2017年第5期|共10页
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  • 正文语种 eng
  • 中图分类 药学;
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