• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

氧化铈纳米颗粒通过调节氧化应激来保护HepG2细胞免受丙烯酰胺诱导的毒性作用。

Cerium oxide nanoparticles protects against acrylamide induced toxicity in HepG2 cells through modulation of oxidative stress.

作者信息

Azari Aala, Shokrzadeh Mohammad, Zamani Ehsan, Amani Nahid, Shaki Fatemeh

机构信息

a Pharmaceutical Sciences Research Center , Mazandaran University of Medical Sciences , Sari , Iran.

b Department of Toxicology and Pharmacology, Faculty of Pharmacy , Mazandaran University of Medical Sciences , Sari , Iran.

出版信息

Drug Chem Toxicol. 2019 Jan;42(1):54-59. doi: 10.1080/01480545.2018.1477793. Epub 2018 Jun 6.

DOI:10.1080/01480545.2018.1477793
PMID:29871546
Abstract

Acrylamide (AA) is a toxic chemical compound found in cooked foods. Considerable evidences suggest that oxidative stress and mitochondrial dysfunction are contributed to AA toxicity. Ceric oxide (CeO) nanoparticles (nano-ceria) have the potential to be developed as a therapeutic for oxidative stress insults due to their catalytic antioxidant properties. In this study we investigated, whether nano-ceria exerted a protective effect against AA-induced cytotoxicity and oxidative damage. HepG2 human cancer cell lines were exposed to nano-ceria (50, 100, and 200 µM) and after 30 min, AA in the half maximal inhibitory concentration (IC50) concentration (200 µM) was added to the cells. Twenty four hours later, cellular viability, reactive oxygen species (ROS) generation, lipid peroxidation (LPO), and cellular levels of glutathione (GSH) were assayed. AA decreased cell viability and pretreatment with nano-ceria significantly decreased AA-induced cytotoxicity. In addition, nano-ceria alleviated AA-induced ROS generation and LPO and depressed GSH level. Our results suggested that nano-ceria prevented cellular and oxidative damage induced by AA.

摘要

丙烯酰胺(AA)是一种在熟食中发现的有毒化合物。大量证据表明,氧化应激和线粒体功能障碍与AA毒性有关。氧化铈(CeO)纳米颗粒(纳米氧化铈)因其催化抗氧化特性,有潜力被开发成为一种针对氧化应激损伤的治疗方法。在本研究中,我们调查了纳米氧化铈是否对AA诱导的细胞毒性和氧化损伤具有保护作用。将HepG2人癌细胞系暴露于纳米氧化铈(50、100和200μM)中,30分钟后,向细胞中加入半数最大抑制浓度(IC50)(200μM)的AA。24小时后,检测细胞活力、活性氧(ROS)生成、脂质过氧化(LPO)和细胞内谷胱甘肽(GSH)水平。AA降低了细胞活力,而纳米氧化铈预处理显著降低了AA诱导的细胞毒性。此外,纳米氧化铈减轻了AA诱导的ROS生成和LPO,并降低了GSH水平。我们的结果表明,纳米氧化铈可预防AA诱导的细胞和氧化损伤。

相似文献

1
Cerium oxide nanoparticles protects against acrylamide induced toxicity in HepG2 cells through modulation of oxidative stress.氧化铈纳米颗粒通过调节氧化应激来保护HepG2细胞免受丙烯酰胺诱导的毒性作用。
Drug Chem Toxicol. 2019 Jan;42(1):54-59. doi: 10.1080/01480545.2018.1477793. Epub 2018 Jun 6.
2
Restoration and stabilization of acrylamide-induced DNA, mitochondrial damages and oxidative stress by chrysin in human lymphocyte.白杨素对丙烯酰胺诱导的人淋巴细胞 DNA、线粒体损伤及氧化应激的修复和稳定作用。
Expert Opin Drug Metab Toxicol. 2021 Jul;17(7):857-865. doi: 10.1080/17425255.2021.1940951. Epub 2021 Jun 15.
3
Neuro-protective effects of cerium and yttrium oxide nanoparticles on high glucose-induced oxidative stress and apoptosis in undifferentiated PC12 cells.铈和氧化钇纳米颗粒对高糖诱导的未分化PC12细胞氧化应激和凋亡的神经保护作用。
Neurol Res. 2015 Jul;37(7):624-32. doi: 10.1179/1743132815Y.0000000037. Epub 2015 Mar 19.
4
ROS-responsive nano-drug delivery system combining mitochondria-targeting ceria nanoparticles with atorvastatin for acute kidney injury.ROS 响应型载药系统,将靶向线粒体的铈纳米颗粒与阿托伐他汀结合用于急性肾损伤。
Theranostics. 2020 Jan 16;10(5):2342-2357. doi: 10.7150/thno.40395. eCollection 2020.
5
Glutathione replenishing potential of CeO₂ nanoparticles in human breast and fibrosarcoma cells.二氧化铈纳米颗粒对人乳腺癌细胞和纤维肉瘤细胞的谷胱甘肽补充潜力
J Colloid Interface Sci. 2015 Sep 1;453:21-27. doi: 10.1016/j.jcis.2015.04.049. Epub 2015 Apr 30.
6
Antioxidant and anti-genotoxic properties of cerium oxide nanoparticles in a pulmonary-like cell system.氧化铈纳米颗粒在类肺细胞系统中的抗氧化和抗遗传毒性特性。
Arch Toxicol. 2016 Feb;90(2):269-78. doi: 10.1007/s00204-015-1468-y. Epub 2015 Jan 25.
7
Panthenol-stabilized cerium dioxide nanoparticles for cosmeceutic formulations against ROS-induced and UV-induced damage.潘婷醇稳定的二氧化铈纳米粒子,用于对抗 ROS 诱导和 UV 诱导损伤的化妆品制剂。
J Photochem Photobiol B. 2014 Jan 5;130:102-8. doi: 10.1016/j.jphotobiol.2013.10.015. Epub 2013 Nov 2.
8
In vivo ameliorative effect of cerium oxide nanoparticles in isoproterenol-induced cardiac toxicity.氧化铈纳米颗粒对异丙肾上腺素诱导的心脏毒性的体内改善作用。
Exp Toxicol Pathol. 2017 Sep 5;69(7):435-441. doi: 10.1016/j.etp.2017.03.001. Epub 2017 Apr 18.
9
Cerium Oxide Nanoparticles Protect against Oxidant Injury and Interfere with Oxidative Mediated Kinase Signaling in Human-Derived Hepatocytes.氧化铈纳米颗粒可防止氧化损伤并干扰人源性肝细胞中氧化应激介导的激酶信号通路。
Int J Mol Sci. 2019 Nov 27;20(23):5959. doi: 10.3390/ijms20235959.
10
Effects of Nano-CeO₂ with Different Nanocrystal Morphologies on Cytotoxicity in HepG2 Cells.不同纳米晶体形态的纳米二氧化铈对HepG2细胞毒性的影响
Int J Environ Res Public Health. 2015 Sep 2;12(9):10806-19. doi: 10.3390/ijerph120910806.

引用本文的文献

1
Acrylamide Neurotoxicity Studies in Model.模型中的丙烯酰胺神经毒性研究
Antioxidants (Basel). 2025 May 27;14(6):641. doi: 10.3390/antiox14060641.
2
The regulatory mechanisms of cerium oxide nanoparticles in oxidative stress and emerging applications in refractory wound care.氧化铈纳米颗粒在氧化应激中的调控机制及其在难愈合伤口护理中的新兴应用。
Front Pharmacol. 2024 Aug 2;15:1439960. doi: 10.3389/fphar.2024.1439960. eCollection 2024.
3
Isolation and structure elucidation of the compounds from Teucrium hyrcanicum L. and the investigation of cytotoxicity, antioxidant activity, and protective effect on hydrogen peroxide-induced oxidative stress.
从hyrcanicum 薰衣草中分离化合物的结构阐明及其细胞毒性、抗氧化活性和对过氧化氢诱导的氧化应激的保护作用的研究。
BMC Complement Med Ther. 2023 Dec 12;23(1):447. doi: 10.1186/s12906-023-04262-8.
4
Green synthesis of silver nanoparticles, graphene, and silver-graphene nanocomposite using ethanolic extract: Anticancer effect on MCF-7 cell line.使用乙醇提取物绿色合成银纳米颗粒、石墨烯及银-石墨烯纳米复合材料:对MCF-7细胞系的抗癌作用。
Iran J Basic Med Sci. 2023 Jan;26(1):57-68. doi: 10.22038/IJBMS.2022.65503.14410.
5
Effect of Acrylamide Treatment on Cyp2e1 Expression and Redox Status in Rat Hepatocytes.丙烯酰胺处理对大鼠肝细胞中 Cyp2e1 表达和氧化还原状态的影响。
Int J Mol Sci. 2022 May 28;23(11):6062. doi: 10.3390/ijms23116062.
6
Metallic Engineered Nanomaterials and Ocular Toxicity: A Current Perspective.金属工程纳米材料与眼毒性:当前观点
Pharmaceutics. 2022 May 3;14(5):981. doi: 10.3390/pharmaceutics14050981.
7
L. Protects against Diabetes-Induced Nephropathy by Attenuation of Mitochondrial Oxidative Damage in Mice.L通过减轻小鼠线粒体氧化损伤来预防糖尿病诱导的肾病。
Adv Pharmacol Pharm Sci. 2021 Dec 26;2021:4657514. doi: 10.1155/2021/4657514. eCollection 2021.
8
The Protective Agents Used against Acrylamide Toxicity: An Cell Culture Study-Based Review.用于对抗丙烯酰胺毒性的保护剂:基于细胞培养研究的综述。
Cell J. 2021 Sep;23(4):367-381. doi: 10.22074/cellj.2021.7286. Epub 2021 Aug 29.
9
The preparation temperature influences the physicochemical nature and activity of nanoceria.制备温度会影响纳米氧化铈的物理化学性质和活性。
Beilstein J Nanotechnol. 2021 Jun 4;12:525-540. doi: 10.3762/bjnano.12.43. eCollection 2021.
10
Investigation of therapeutic potential of cerium oxide nanoparticles in Alzheimer's disease using transgenic .使用转基因技术研究氧化铈纳米颗粒在阿尔茨海默病中的治疗潜力。
3 Biotech. 2021 Apr;11(4):159. doi: 10.1007/s13205-021-02706-x. Epub 2021 Mar 6.