• 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

氧化钇纳米粒子治疗暴发性肝衰竭的疗效。

Therapeutic effect of yttrium oxide nanoparticles for the treatment of fulminant hepatic failure.

机构信息

Institute of Health Service & Transfusion Medicine, Academy of Military Medical Sciences, Hebei 100850, PR China.

Department of Blood Transfusion, The 988 hospital of PLA, Henan 450042, PR China.

出版信息

Nanomedicine (Lond). 2019 Oct;14(19):2519-2533. doi: 10.2217/nnm-2019-0154. Epub 2019 Jul 18.

DOI:10.2217/nnm-2019-0154
PMID:31317822
Abstract

To explore the potential therapeutic effect of yttrium oxide nanoparticles (YO NPs) on fulminant hepatic failure. RAW264.7 cells and a lipopolysaccharide/D-galactosamine-induced hepatic failure murine model were used to assess the effects of YO NPs. YO NPs exhibited anti-inflammatory activity by scavenging cellular reactive oxygen species and dampening reactive oxygen species-mediated NF-κB activation . A single intraperitoneal administration of YO NPs (30 mg/kg) enhanced hepatic antioxidant status and reduced oxidative stress and inflammatory response in lipopolysaccharide/galactosamine-induced mice. YO NPs also attenuated hepatic NF-κB activation, cell apoptosis and liver injury. YO NP administration could be used as a novel therapeutic strategy for treating fulminant hepatic failure and oxidative stress-related diseases.

摘要

探讨氧化钇纳米粒子 (YO NPs) 对暴发性肝衰竭的潜在治疗作用。使用 RAW264.7 细胞和脂多糖/半乳糖胺诱导的肝衰竭小鼠模型来评估 YO NPs 的作用。YO NPs 通过清除细胞内活性氧物质和抑制活性氧介导的 NF-κB 激活来发挥抗炎作用。单次腹腔注射 YO NPs(30mg/kg)可增强肝抗氧化状态,减轻脂多糖/半乳糖胺诱导的小鼠的氧化应激和炎症反应。YO NPs 还可减轻肝 NF-κB 激活、细胞凋亡和肝损伤。YO NP 给药可作为治疗暴发性肝衰竭和氧化应激相关疾病的新治疗策略。

相似文献

1
Therapeutic effect of yttrium oxide nanoparticles for the treatment of fulminant hepatic failure.氧化钇纳米粒子治疗暴发性肝衰竭的疗效。
Nanomedicine (Lond). 2019 Oct;14(19):2519-2533. doi: 10.2217/nnm-2019-0154. Epub 2019 Jul 18.
2
Role of α-lipoic acid in LPS/d-GalN induced fulminant hepatic failure in mice: studies on oxidative stress, inflammation and apoptosis.α-硫辛酸在脂多糖/右旋半乳糖胺诱导的小鼠暴发性肝衰竭中的作用:关于氧化应激、炎症和细胞凋亡的研究
Int Immunopharmacol. 2014 Oct;22(2):293-302. doi: 10.1016/j.intimp.2014.07.008. Epub 2014 Jul 18.
3
Multi-organ Toxicity Attenuation by Cerium Oxide and Yttrium Oxide Nanoparticles: Comparing the Beneficial Effects on Tissues Oxidative Damage Induced by Sub-acute Exposure to Diazinon.氧化铈和氧化钇纳米粒子对多器官毒性的衰减作用:亚急性暴露于二嗪农诱导的组织氧化损伤的有益效果比较。
Pharm Nanotechnol. 2020;8(3):225-238. doi: 10.2174/2211738508666200808135226.
4
Hepatoprotective Effects of Kaempferol-3-O-α-l-Arabinopyranosyl-7-O-α-l-Rhamnopyranoside on d-Galactosamine and Lipopolysaccharide Caused Hepatic Failure in Mice.山奈酚-3-O-α-L-阿拉伯吡喃糖苷-7-O-α-L-鼠李吡喃糖苷对 D-半乳糖胺和脂多糖诱导的肝衰竭小鼠的肝保护作用。
Molecules. 2017 Oct 18;22(10):1755. doi: 10.3390/molecules22101755.
5
Cerium and yttrium oxide nanoparticles against lead-induced oxidative stress and apoptosis in rat hippocampus.铈和钇氧化物纳米颗粒对铅诱导的大鼠海马氧化应激和细胞凋亡的影响
Biol Trace Elem Res. 2015 Mar;164(1):80-9. doi: 10.1007/s12011-014-0197-z. Epub 2014 Dec 18.
6
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.
7
CQMUH-011, a novel adamantane sulfonamide compound, inhibits lipopolysaccharide- and D-galactosamine-induced fulminant hepatic failure in mice.CQMUH-011是一种新型金刚烷磺酰胺化合物,可抑制脂多糖和D-半乳糖胺诱导的小鼠暴发性肝衰竭。
Int Immunopharmacol. 2017 Jun;47:231-243. doi: 10.1016/j.intimp.2017.04.015. Epub 2017 Apr 25.
8
The antagonistic effect of tamoxifen against d-galactosamine/lipopolysaccharide-induced acute liver failure is associated with reactivation of hepatic nuclear factor-κB.他莫昔芬拮抗半乳糖胺/脂多糖诱导的急性肝衰竭的拮抗作用与肝核因子-κB 的再激活有关。
Immunopharmacol Immunotoxicol. 2019 Apr;41(2):192-198. doi: 10.1080/08923973.2019.1569044. Epub 2019 Feb 5.
9
Erythropoietin increases survival and attenuates fulminant hepatic failure injury induced by D-galactosamine/lipopolysaccharide in mice.促红细胞生成素可提高 D-半乳糖胺/脂多糖诱导的暴发性肝衰竭小鼠的存活率并减轻其损伤。
Transplantation. 2011 Jul 15;92(1):18-24. doi: 10.1097/TP.0b013e31821cdea5.
10
Obeticholic acid differentially regulates hepatic injury and inflammation at different stages of D-galactosamine/lipopolysaccharide-evoked acute liver failure.鹅去氧胆酸在半乳糖胺/脂多糖诱导的急性肝衰竭不同阶段对肝损伤和炎症有不同的调节作用。
Eur J Pharmacol. 2019 May 5;850:150-157. doi: 10.1016/j.ejphar.2019.02.011. Epub 2019 Feb 15.

引用本文的文献

1
Targeting oxidative damage in diabetic foot ulcers: integrative strategies involving antioxidant drugs and nanotechnologies.针对糖尿病足溃疡中的氧化损伤:涉及抗氧化药物和纳米技术的综合策略。
Burns Trauma. 2025 Mar 10;13:tkaf020. doi: 10.1093/burnst/tkaf020. eCollection 2025.
2
Potential Applications of Rare Earth Metal Nanoparticles in Biomedicine.稀土金属纳米粒子在生物医学中的潜在应用
Pharmaceuticals (Basel). 2025 Jan 24;18(2):154. doi: 10.3390/ph18020154.
3
Dietary Natural Melanin Nanozymes Delay Aging and Ameliorate Neurodegeneration via Improving Gut Microbiota and Redox Homeostasis.
膳食天然黑色素纳米酶通过改善肠道微生物群和氧化还原稳态来延缓衰老并改善神经退行性变。
ACS Omega. 2025 Jan 22;10(4):3610-3621. doi: 10.1021/acsomega.4c08419. eCollection 2025 Feb 4.
4
Systematic review of the osteogenic effect of rare earth nanomaterials and the underlying mechanisms.稀土纳米材料成骨作用及其机制的系统评价
J Nanobiotechnology. 2024 Apr 16;22(1):185. doi: 10.1186/s12951-024-02442-3.
5
Time-resolved single-cell transcriptomics reveals the landscape and dynamics of hepatic cells in sepsis-induced acute liver dysfunction.时间分辨单细胞转录组学揭示脓毒症诱导的急性肝功能障碍中肝细胞的格局和动态变化。
JHEP Rep. 2023 Mar 1;5(6):100718. doi: 10.1016/j.jhepr.2023.100718. eCollection 2023 Jun.
6
Yttrium Oxide Nanoparticles Moderate the Abnormal Cognitive Behaviors in Male Mice Induced by Silver Nanoparticles.氧化钇纳米颗粒可调节银纳米颗粒诱导的雄性小鼠异常认知行为。
Oxid Med Cell Longev. 2022 Apr 26;2022:9059371. doi: 10.1155/2022/9059371. eCollection 2022.
7
Neutrophil membrane-mimicking nanodecoys with intrinsic anti-inflammatory properties alleviate sepsis-induced acute liver injury and lethality in a mouse endotoxemia model.具有内在抗炎特性的中性粒细胞膜模拟纳米诱饵可减轻小鼠内毒素血症模型中败血症诱导的急性肝损伤和致死率。
Mater Today Bio. 2022 Mar 16;14:100244. doi: 10.1016/j.mtbio.2022.100244. eCollection 2022 Mar.
8
In vivo study of dose-dependent antioxidant efficacy of functionalized core-shell yttrium oxide nanoparticles.体内研究功能化核壳氧化钇纳米粒子的剂量依赖抗氧化功效。
Naunyn Schmiedebergs Arch Pharmacol. 2022 May;395(5):593-606. doi: 10.1007/s00210-022-02219-1. Epub 2022 Feb 24.
9
Alleviation of silver nanoparticle-induced sexual behavior and testicular parameters dysfunction in male mice by yttrium oxide nanoparticles.氧化钇纳米颗粒减轻银纳米颗粒诱导的雄性小鼠性行为和睾丸参数功能障碍
Toxicol Rep. 2021 Jun 1;8:1121-1130. doi: 10.1016/j.toxrep.2021.05.014. eCollection 2021.
10
High Surface Reactivity and Biocompatibility of YO NPs in Human MCF-7 Epithelial and HT-1080 FibroBlast Cells.YO 纳米颗粒在人 MCF-7 上皮细胞和 HT-1080 成纤维细胞中的高表面反应性和生物相容性。
Molecules. 2020 Mar 3;25(5):1137. doi: 10.3390/molecules25051137.