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氧化锌纳米颗粒联合维生素C和酪蛋白磷酸肽对小鼠胃上皮细胞及肠道吸收的毒性作用

Toxic effects of zinc oxide nanoparticles combined with vitamin C and casein phosphopeptides on gastric epithelium cells and the intestinal absorption of mice.

作者信息

Gu Tianjiao, Yao Chenjie, Zhang Kangkang, Li Chenchen, Ding Lin, Huang Yanan, Wu Minghong, Wang Yanli

机构信息

Institute of Nanochemistry and Nanobiology, Shanghai University Shanghai China

School of Environmental and Chemical Engineering, Shanghai University Shanghai China

出版信息

RSC Adv. 2018 Jul 20;8(46):26078-26088. doi: 10.1039/c8ra03693d. eCollection 2018 Jul 19.

Abstract

Zinc oxide nanomaterials have become common food additives in recent years. Casein phosphopeptides (CPP) and vitamin C (VC) are used as functional food additives together with ZnO nanoparticles (ZnO NPs) in many commercial foods. Our previous studies showed that VC can increase the cytotoxicity induced by ZnO NPs both and , while CPP can have a cytoprotective effect against oxidative stress induced by ZnO NPs. However, the combined toxic effect of the three additives together in food is unknown. Herein, we have investigated the combined toxicity of ZnO NPs, CPP and VC by altering the sequence of their addition to clarify their toxic mechanisms in the composite systems. When the order of addition of the three materials changes, the cytotoxicity induced by the ZnO NPs changes due to the different concentrations of dissolved Zn ions in the different groups. We have also probed the intestinal absorption of Zn ions with an everted gut sac model. The amount of Zn absorbed in the intestine in different composite systems also responds differently to the sequence of addition of the additives. VC is more powerful at controlling the synergistic toxic effect induced by ZnO NPs compared to the protective role of CPP in the combined systems.

摘要

近年来,氧化锌纳米材料已成为常见的食品添加剂。酪蛋白磷酸肽(CPP)和维生素C(VC)在许多商业食品中与氧化锌纳米颗粒(ZnO NPs)一起用作功能性食品添加剂。我们之前的研究表明,VC在体内和体外均可增加ZnO NPs诱导的细胞毒性,而CPP对ZnO NPs诱导的氧化应激具有细胞保护作用。然而,这三种添加剂在食品中的联合毒性尚不清楚。在此,我们通过改变它们的添加顺序来研究ZnO NPs、CPP和VC的联合毒性,以阐明它们在复合体系中的毒性机制。当三种材料的添加顺序改变时,由于不同组中溶解的锌离子浓度不同,ZnO NPs诱导的细胞毒性也会发生变化。我们还使用外翻肠囊模型探究了锌离子的肠道吸收情况。在不同的复合体系中,肠道吸收的锌量对添加剂添加顺序的反应也不同。与CPP在联合体系中的保护作用相比,VC在控制ZnO NPs诱导的协同毒性作用方面更有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14c0/9082813/80e2177ad6f0/c8ra03693d-f1.jpg

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