• 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

靶向肺泡上皮细胞的肿瘤坏死因子-α 小干扰 RNA 纳米颗粒减轻脓毒症 C57BL/6J 小鼠的肺损伤。

Tumor necrosis factor-α small interfering RNA alveolar epithelial cell-targeting nanoparticles reduce lung injury in C57BL/6J mice with sepsis.

机构信息

Department of Burn and Plastic Surgery, The Affiliated Zhangjiagang Hospital of Soochow University, Zhangjiagang, China.

Burn Institute of PLA, Department of Burn Surgery, The First Affiliated Hospital. Naval Medical University, Shanghai, China.

出版信息

J Int Med Res. 2021 Jan;49(1):300060520984652. doi: 10.1177/0300060520984652.

DOI:10.1177/0300060520984652
PMID:33435767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7809319/
Abstract

BACKGROUND

The role of tumor necrosis factor (TNF)-α small interfering (si)RNA alveolar epithelial cell (AEC)-targeting nanoparticles in lung injury is unclear.

METHODS

Sixty C57BL/6J mice with sepsis were divided into normal, control, sham, 25 mg/kg, 50 mg/kg, and 100 mg/kg siRNA AEC-targeting nanoparticles groups (n = 10 per group). The wet:dry lung weight ratio, and hematoxylin and eosin staining, western blotting, and enzyme-linked immunosorbent assays for inflammatory factors were conducted to compare differences among groups.

RESULTS

The wet:dry ratio was significantly lower in control and sham groups than other groups. TNF-α siRNA AEC-targeting nanoparticles significantly reduced the number of eosinophils, with significantly lower numbers in the 50 mg/kg group than in 25 mg/kg and 100 mg/kg groups. The nanoparticles also significantly reduced the expression of TNF-α, B-cell lymphoma-2, caspase 3, interleukin (IL)-1β, and IL-6, with TNF-α expression being significantly lower in the 50 mg/kg group than in 25 mg/kg and 100 mg/kg groups.

CONCLUSION

TNF-α siRNA AEC-targeting nanoparticles appear to be effective at improving lung injury-related sepsis, and 50 mg/kg may be a preferred dose option for administration.

摘要

背景

肿瘤坏死因子 (TNF)-α 小干扰 (si)RNA 肺泡上皮细胞 (AEC)靶向纳米颗粒在肺损伤中的作用尚不清楚。

方法

将 60 只脓毒症 C57BL/6J 小鼠分为正常组、对照组、假手术组、25mg/kg、50mg/kg 和 100mg/kg siRNA AEC 靶向纳米颗粒组(每组 10 只)。比较各组间的肺湿重/干重比、苏木精-伊红染色、Western blot 和酶联免疫吸附试验检测炎症因子的差异。

结果

对照组和假手术组的湿重/干重比明显低于其他组。TNF-α siRNA AEC 靶向纳米颗粒明显减少嗜酸性粒细胞数量,50mg/kg 组比 25mg/kg 和 100mg/kg 组明显减少。纳米颗粒还明显降低 TNF-α、B 细胞淋巴瘤-2、半胱氨酸天冬氨酸蛋白酶 3、白细胞介素 (IL)-1β 和 IL-6 的表达,50mg/kg 组 TNF-α 的表达明显低于 25mg/kg 和 100mg/kg 组。

结论

TNF-α siRNA AEC 靶向纳米颗粒似乎能有效改善与脓毒症相关的肺损伤,50mg/kg 可能是更优的给药剂量选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/61f26d664c64/10.1177_0300060520984652-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/02e43fb10d50/10.1177_0300060520984652-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/6c4c710eb93d/10.1177_0300060520984652-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/4736b9c85264/10.1177_0300060520984652-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/f6b942e3ab99/10.1177_0300060520984652-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/83086a9cce8f/10.1177_0300060520984652-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/61f26d664c64/10.1177_0300060520984652-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/02e43fb10d50/10.1177_0300060520984652-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/6c4c710eb93d/10.1177_0300060520984652-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/4736b9c85264/10.1177_0300060520984652-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/f6b942e3ab99/10.1177_0300060520984652-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/83086a9cce8f/10.1177_0300060520984652-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9379/7809319/61f26d664c64/10.1177_0300060520984652-fig6.jpg

相似文献

1
Tumor necrosis factor-α small interfering RNA alveolar epithelial cell-targeting nanoparticles reduce lung injury in C57BL/6J mice with sepsis.靶向肺泡上皮细胞的肿瘤坏死因子-α 小干扰 RNA 纳米颗粒减轻脓毒症 C57BL/6J 小鼠的肺损伤。
J Int Med Res. 2021 Jan;49(1):300060520984652. doi: 10.1177/0300060520984652.
2
Heat Shock Protein A12B Protects Vascular Endothelial Cells Against Sepsis-Induced Acute Lung Injury in Mice.热休克蛋白A12B保护小鼠血管内皮细胞免受脓毒症诱导的急性肺损伤。
Cell Physiol Biochem. 2017;42(1):156-168. doi: 10.1159/000477308. Epub 2017 May 25.
3
[The protective effect of bone marrow mesenchymal stem cell on lung injury induced by vibrio vulnificus sepsis].[骨髓间充质干细胞对创伤弧菌败血症所致肺损伤的保护作用]
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2014 Nov;26(11):821-6. doi: 10.3760/cma.j.issn.2095-4352.2014.11.011.
4
[Role of Rho/ROCK signaling pathway in the protective effects of hydrogen against acute lung injury in septic mice].[Rho/ROCK信号通路在氢气对脓毒症小鼠急性肺损伤保护作用中的作用]
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2016 May;28(5):401-6.
5
Amphiregulin inhibits TNF-α-induced alveolar epithelial cell death through EGFR signaling pathway. Amphiregulin 通过 EGFR 信号通路抑制 TNF-α 诱导的肺泡上皮细胞死亡。
Biomed Pharmacother. 2020 May;125:109995. doi: 10.1016/j.biopha.2020.109995. Epub 2020 Feb 27.
6
[Blockade of programmed death-ligand 1 attenuates indirect acute lung injury in mice through targeting endothelial cells but not epithelial cells].[程序性死亡配体1的阻断通过靶向内皮细胞而非上皮细胞减轻小鼠间接急性肺损伤]
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2019 Jan;31(1):37-43. doi: 10.3760/cma.j.issn.2095-4352.2019.01.009.
7
[Changes in circulating microparticles in mice with ventilator-induced lung injury].[呼吸机诱导性肺损伤小鼠循环微颗粒的变化]
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2018 Jan;30(1):8-12. doi: 10.3760/cma.j.issn.2095-4352.2018.01.002.
8
Macrophage tumor necrosis factor-alpha induces epithelial expression of granulocyte-macrophage colony-stimulating factor: impact on alveolar epithelial repair.巨噬细胞肿瘤坏死因子-α诱导粒细胞-巨噬细胞集落刺激因子的上皮表达:对肺泡上皮修复的影响。
Am J Respir Crit Care Med. 2009 Sep 15;180(6):521-32. doi: 10.1164/rccm.200812-1837OC. Epub 2009 Jul 9.
9
[Baicalein attenuates acute lung injury induced by intestinal ischemia/reperfusion via inhibition of nuclear factor-κB pathway in mice].[黄芩苷通过抑制小鼠核因子-κB通路减轻肠道缺血/再灌注诱导的急性肺损伤]
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2017 Mar;29(3):228-232. doi: 10.3760/cma.j.issn.2095-4352.2017.03.007.
10
[Inhibitory effect of kukoamine B on lung inflammatory responses in mice with sepsis].[库可胺B对脓毒症小鼠肺部炎症反应的抑制作用]
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2014 Jul;26(7):493-7. doi: 10.3760/cma.j.issn.2095-4352.2014.07.010.

引用本文的文献

1
Nucleic acid-based nanotherapeutics for treating sepsis and associated organ injuries.用于治疗脓毒症及相关器官损伤的核酸纳米疗法。
Theranostics. 2024 Jul 16;14(11):4411-4437. doi: 10.7150/thno.98487. eCollection 2024.
2
Attenuation of Chronic Inflammation in Intestinal Organoids with Graphene Oxide-Mediated Tumor Necrosis Factor-α_Small Interfering RNA Delivery.氧化石墨烯介导肿瘤坏死因子-α小干扰RNA递送减轻肠道类器官中的慢性炎症
Langmuir. 2024 Feb 7;40(7):3402-13. doi: 10.1021/acs.langmuir.3c02741.
3
Apoptotic cell death in disease-Current understanding of the NCCD 2023.

本文引用的文献

1
An Update on Sepsis Biomarkers.脓毒症生物标志物的最新进展
Infect Chemother. 2020 Mar;52(1):1-18. doi: 10.3947/ic.2020.52.1.1.
2
Sepsis trends: increasing incidence and decreasing mortality, or changing denominator?脓毒症趋势:发病率上升与死亡率下降,还是分母变化?
J Thorac Dis. 2020 Feb;12(Suppl 1):S89-S100. doi: 10.21037/jtd.2019.12.51.
3
Sepsis and septic shock: Guideline-based management.脓毒症与脓毒性休克:基于指南的管理。
疾病中的细胞凋亡性死亡——2023 年对 NCCD 的最新理解。
Cell Death Differ. 2023 May;30(5):1097-1154. doi: 10.1038/s41418-023-01153-w. Epub 2023 Apr 26.
Cleve Clin J Med. 2020 Jan;87(1):53-64. doi: 10.3949/ccjm.87a.18143. Epub 2020 Jan 2.
4
Global, regional, and national sepsis incidence and mortality, 1990-2017: analysis for the Global Burden of Disease Study.全球、地区和国家脓毒症发病率和死亡率,1990-2017 年:全球疾病负担研究分析。
Lancet. 2020 Jan 18;395(10219):200-211. doi: 10.1016/S0140-6736(19)32989-7.
5
Sepsis-associated encephalopathy: a vicious cycle of immunosuppression.脓毒症相关性脑病:免疫抑制的恶性循环。
J Neuroinflammation. 2020 Jan 10;17(1):14. doi: 10.1186/s12974-020-1701-3.
6
Light-Addressable Nanoclusters of Ultrasmall Iron Oxide Nanoparticles for Enhanced and Dynamic Magnetic Resonance Imaging of Arthritis.用于增强型和动态磁共振成像关节炎的超小氧化铁纳米颗粒的光寻址纳米团簇
Adv Sci (Weinh). 2019 Aug 8;6(19):1901800. doi: 10.1002/advs.201901800. eCollection 2019 Oct 2.
7
Prognostic and predictive enrichment in sepsis.脓毒症的预后和预测性富集。
Nat Rev Nephrol. 2020 Jan;16(1):20-31. doi: 10.1038/s41581-019-0199-3. Epub 2019 Sep 11.
8
Downregulation of TNF-/TNF-R1 Signals by AT-Lipoxin A4 May Be a Significant Mechanism of Attenuation in SAP-Associated Lung Injury.AT-脂氧素 A4 下调 TNF-/TNF-R1 信号可能是 SAP 相关肺损伤中衰减的重要机制。
Mediators Inflamm. 2019 Apr 11;2019:9019404. doi: 10.1155/2019/9019404. eCollection 2019.
9
Association between Tumor Necrosis Factor-α Promoter -308 G/A Polymorphism and Early Onset Sepsis in Preterm Infants.肿瘤坏死因子-α启动子-308 G/A 多态性与早产儿早发性败血症的关系。
Tohoku J Exp Med. 2019 Apr;247(4):259-264. doi: 10.1620/tjem.247.259.
10
Sepsis: evolving concepts and challenges.脓毒症:不断演变的概念与挑战
Braz J Med Biol Res. 2019;52(4):e8595. doi: 10.1590/1414-431X20198595. Epub 2019 Apr 15.