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首页> 外文期刊>International journal of toxicology >Synergistic Effects of Zinc Oxide Nanoparticles and Fatty Acids on Toxicity to Caco-2 Cells
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Synergistic Effects of Zinc Oxide Nanoparticles and Fatty Acids on Toxicity to Caco-2 Cells

机译:氧化锌纳米颗粒和脂肪酸对Caco-2细胞毒性的协同作用

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Fatty acids exposure may increase sensitivity of intestinal epithelial cells to cytotoxic effects of zinc oxide (ZnO) nanoparticles (NPs). This study evaluated the synergistic effects of ZnO NPs and palmitic acid (PA) or free fatty acids (FFAs) mixture (oleic/PA 2:1) on toxicity to human colon epithelial (Caco-2) cells. The ZnO NPs exposure concentration dependently induced cytotoxicity to Caco-2 cells showing as reduced proliferation and activity measured by 3 different assays. PA exposure induced cytotoxicity, and coexposure to ZnO NPs and PA showed the largest cytotoxic effects. The presence of FFAs mixture did not affect the ZnO NPs-induced cytotoxicity. Filtration of freshly prepared suspension of NPs through a 0.45-mu m pore size membrane significantly reduced the cytotoxicity, indicating a role of concentration or size of particles in cytotoxic effects. The ZnO NPs and PA coexposure induced production of mitochondrial reactive oxygen species (mROS) but not intracellular ROS production, whereas FFAs mixture exposure did not induce mROS and inhibited intracellular ROS. Both ZnO NPs and fatty acids (PA and FFAs mixture) promoted lysosomal destabilization, which was not correlated with cytotoxicity. These results indicated that PA can enhance ZnO NPs-induced cytotoxicity probably by the augmentation of mROS production, whereas FFAs mixture did not affect ROS production. Synergistic effects between ZnO NPs and fatty acids may be important when considering NPs toxicity via oral exposure.
机译:暴露于脂肪酸可能会增加肠上皮细胞对氧化锌(ZnO)纳米颗粒(NPs)的细胞毒性作用的敏感性。这项研究评估了ZnO NP和棕榈酸(PA)或游离脂肪酸(FFA)混合物(油酸/ PA 2:1)对人结肠上皮(Caco-2)细胞毒性的协同作用。 ZnO NPs暴露浓度依赖性地诱导了对Caco-2细胞的细胞毒性,显示通过3种不同的测定方法可以降低增殖和活性。 PA暴露引起细胞毒性,ZnO NP和PA的共同暴露显示出最大的细胞毒性作用。 FFAs混合物的存在不会影响ZnO NPs诱导的细胞毒性。通过0.45微米孔径的膜过滤新鲜制备的NPs悬浮液,可显着降低细胞毒性,表明颗粒浓度或大小在细胞毒性作用中具有重要作用。 ZnO NPs和PA共同暴露诱导了线粒体活性氧(mROS)的产生,但未引起细胞内ROS的产生,而FFAs混合物暴露并未诱导mROS并抑制了细胞内ROS。 ZnO NP和脂肪酸(PA和FFA的混合物)均可促进溶酶体去稳定作用,这与细胞毒性无关。这些结果表明PA可能通过增加mROS产生来增强ZnO NPs诱导的细胞毒性,而FFA混合物不影响ROS产生。当考虑通过口服接触引起的NPs毒性时,ZnO NPs与脂肪酸之间的协同作用可能很重要。

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