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The protective effect of nitronyl nitroxide radical on peroxidation of A549 cell damaged by iron overload

机译:亚硝酰基硝基氧自由基对铁超载损伤的A549细胞过氧化的保护作用

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Particulate pollution in the air has strong links with increased morbidity of cardiopulmonary diseases. Iron is one of the major carcinogens in air pollution and can produce hydroxyl radical which induce oxidative stress, lead to cell damage and even to cancer. In this work, a novel nitronyl nitroxide radical NITPh(OMe)(2) (2-(2,4-dimethoxyphenyl) 4,4,5,5- tetramethylimidazoline- 1- oxyl-3- oxide) was prepared and characterized by electron spin-resonance spectroscopy (ESR), X-ray crystal diffraction, Fourier transform infrared (IR), X-ray powder diffraction (XRD), elemental analysis, ultraviolet and visible spectra (UV Vis), and the electronic transition processes was also calculated by time-dependent density functional theory (TDDFT) to analysis UV-Vis spectrum. In vitro cell model of oxidative damage was established by ferric ammonium citrate (FAC) overload, and NITPh(OMe)(2) was studied as a free radical scavenger to protect peroxidation of A549 cells. Results showed that NITPh(OMe)(2) could significantly alleviate the damage of A549 cells by iron overload in cell morphology, cell viability, cell proliferation and cell apoptosis. The apoptotic signaling pathway of A549 cells induced by FAC and the protection mechanism of NITPh(OMe)(2) were all discussed through the expression of three relating proteins, Bcl-2, Bax and DDIT3. This work confirms that nitroxide radicals are effective antioxidants, and have potential application in clinical practice as therapeutic agents.
机译:空气中的微粒污染与心肺疾病的发病率增加有很强的联系。铁是空气污染中的主要致癌物之一,可产生羟自由基,从而诱发氧化应激,导致细胞损伤,甚至致癌。在这项工作中,制备了新型的硝酰基硝基氧自由基NITPh(OMe)(2)(2-(2,4-二甲氧基苯基)4,4,5,5-四甲基咪唑啉-1-氧化1-3氧化),并通过电子对其进行了表征。自旋共振光谱(ESR),X射线晶体衍射,傅立叶变换红外(IR),X射线粉末衍射(XRD),元素分析,紫外和可见光谱(UV Vis)以及电子跃迁过程也已计算出来通过时变密度泛函理论(TDDFT)来分析UV-Vis光谱。通过柠檬酸铁铵(FAC)过载建立了体外氧化损伤细胞模型,并研究了NITPh(OMe)(2)作为自由基清除剂来保护A549细胞的过氧化。结果表明,NITPh(OMe)(2)可以显着减轻铁超负荷对细胞形态,细胞活力,细胞增殖和细胞凋亡的损害。通过三种相关蛋白Bcl-2,Bax和DDIT3的表达,探讨了FAC诱导的A549细胞凋亡的信号通路和NITPh(OMe)(2)的保护机制。这项工作证实了氮氧化物自由基是有效的抗氧化剂,并且在临床实践中具有作为治疗剂的潜在应用。

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