• 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

壳聚糖功能化 MnO 纳米颗粒通过调节细胞氧化还原状态来对抗小鼠溃疡性结肠炎。

Chitosan functionalized MnO nanoparticles counteracts ulcerative colitis in mice through modulation of cellular redox state.

机构信息

Department of Chemical, Biological Sciences, S. N. Bose National Centre for Basic Sciences, Block JD, Sector 3, Salt Lake, Kolkata, 700106, India.

Department of Zoology, Uluberia College, University of Calcutta, Uluberia, Howrah, 711315, India.

出版信息

Commun Biol. 2023 Jun 16;6(1):647. doi: 10.1038/s42003-023-05023-6.

DOI:10.1038/s42003-023-05023-6
PMID:37328528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10275949/
Abstract

Recent findings suggest a key role for reactive oxygen species (ROS) in the pathogenesis and progression of ulcerative colitis (UC). Several studies have also highlighted the efficacy of citrate functionalized MnO nanoparticles as redox medicine against a number of ROS-mediated disorders. Here we show that synthesized nanoparticles consisting of chitosan functionalized tri-manganese tetroxide (MnO) can restore redox balance in a mouse model of UC induced by dextran sulfate sodium (DSS). Our in-vitro characterization of the developed nanoparticle confirms critical electronic transitions in the nanoparticle to be important for the redox buffering activity in the animal model. A careful administration of the developed nanoparticle not only reduces inflammatory markers in the animals, but also reduces the mortality rate from the induced disease. This study provides a proof of concept for the use of nanomaterial with synergistic anti-inflammatory and redox buffering capacity to prevent and treat ulcerative colitis.

摘要

最近的研究结果表明,活性氧(ROS)在溃疡性结肠炎(UC)的发病机制和进展中起着关键作用。几项研究还强调了柠檬酸盐功能化 MnO 纳米粒子作为氧化还原医学在治疗多种 ROS 介导的疾病方面的疗效。在这里,我们展示了由壳聚糖功能化三氧化锰(MnO)组成的合成纳米粒子可以恢复葡聚糖硫酸钠(DSS)诱导的 UC 小鼠模型中的氧化还原平衡。我们对开发的纳米粒子的体外特性分析证实,纳米粒子中的关键电子跃迁对于动物模型中的氧化还原缓冲活性很重要。谨慎地给予开发的纳米粒子不仅可以降低动物中的炎症标志物,还可以降低诱导疾病的死亡率。这项研究为使用具有协同抗炎和氧化还原缓冲能力的纳米材料来预防和治疗溃疡性结肠炎提供了概念验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/5c8ada60cf76/42003_2023_5023_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/751c1dccdbf8/42003_2023_5023_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/000f75272cb4/42003_2023_5023_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/a2511cd97b4f/42003_2023_5023_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/77c5563debe9/42003_2023_5023_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/866339bffbc2/42003_2023_5023_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/5c8ada60cf76/42003_2023_5023_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/751c1dccdbf8/42003_2023_5023_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/000f75272cb4/42003_2023_5023_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/a2511cd97b4f/42003_2023_5023_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/77c5563debe9/42003_2023_5023_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/866339bffbc2/42003_2023_5023_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3651/10275949/5c8ada60cf76/42003_2023_5023_Fig6_HTML.jpg

相似文献

1
Chitosan functionalized MnO nanoparticles counteracts ulcerative colitis in mice through modulation of cellular redox state.壳聚糖功能化 MnO 纳米颗粒通过调节细胞氧化还原状态来对抗小鼠溃疡性结肠炎。
Commun Biol. 2023 Jun 16;6(1):647. doi: 10.1038/s42003-023-05023-6.
2
Redox Buffering Capacity of Nanomaterials as an Index of ROS-Based Therapeutics and Toxicity: A Preclinical Animal Study.纳米材料的氧化还原缓冲能力作为基于 ROS 的治疗和毒性的指标:一项临床前动物研究。
ACS Biomater Sci Eng. 2021 Jun 14;7(6):2475-2484. doi: 10.1021/acsbiomaterials.1c00402. Epub 2021 Jun 1.
3
Specific accumulation of orally administered redox nanotherapeutics in the inflamed colon reducing inflammation with dose-response efficacy.经口服给予的氧化还原纳米治疗剂在炎症结肠中的特异性聚集,以剂量反应疗效减轻炎症。
J Control Release. 2015 Jul 28;210:19-25. doi: 10.1016/j.jconrel.2015.05.275. Epub 2015 May 19.
4
Oral nanotherapeutics: effect of redox nanoparticle on microflora in mice with dextran sodium sulfate-induced colitis.口服纳米疗法:氧化还原纳米颗粒对葡聚糖硫酸钠诱导的小鼠结肠炎模型肠道菌群的影响
J Gastroenterol. 2014 May;49(5):806-13. doi: 10.1007/s00535-013-0836-8. Epub 2013 May 29.
5
Oral Delivery of Nanoparticles Loaded With Ginger Active Compound, 6-Shogaol, Attenuates Ulcerative Colitis and Promotes Wound Healing in a Murine Model of Ulcerative Colitis.姜辣素 6-姜烯酚载药纳米粒子经口给药减轻溃疡性结肠炎小鼠模型的炎症并促进其创面愈合。
J Crohns Colitis. 2018 Jan 24;12(2):217-229. doi: 10.1093/ecco-jcc/jjx115.
6
Orally Targeted Delivery of Tripeptide KPV via Hyaluronic Acid-Functionalized Nanoparticles Efficiently Alleviates Ulcerative Colitis.通过透明质酸功能化纳米颗粒口服靶向递送三肽KPV可有效缓解溃疡性结肠炎。
Mol Ther. 2017 Jul 5;25(7):1628-1640. doi: 10.1016/j.ymthe.2016.11.020. Epub 2017 Jan 28.
7
Geniposide ameliorates dextran sulfate sodium-induced ulcerative colitis via KEAP1-Nrf2 signaling pathway.栀子苷通过 KEAP1-Nrf2 信号通路改善葡聚糖硫酸钠诱导的溃疡性结肠炎。
J Ethnopharmacol. 2023 Oct 5;314:116626. doi: 10.1016/j.jep.2023.116626. Epub 2023 May 13.
8
aqueous extracts ameliorate colonic mucosal damage and modulate gut microbiota disorder in mice with ulcerative colitis by inhibiting inflammation and oxidative stress.水提物通过抑制炎症和氧化应激改善溃疡性结肠炎小鼠的结肠黏膜损伤和调节肠道微生物失调。
J Zhejiang Univ Sci B. 2022 Jun 15;23(6):481-501. doi: 10.1631/jzus.B2100988.
9
Glycogen-based pH and redox sensitive nanoparticles with ginsenoside Rh for effective treatment of ulcerative colitis.基于糖原的 pH 值和氧化还原敏感纳米颗粒与人参皂苷 Rh 联合用于溃疡性结肠炎的有效治疗。
Biomaterials. 2022 Jan;280:121077. doi: 10.1016/j.biomaterials.2021.121077. Epub 2021 Aug 20.
10
Biomimetic MOF Nanoparticles Delivery of C-Dot Nanozyme and CRISPR/Cas9 System for Site-Specific Treatment of Ulcerative Colitis.仿生 MOF 纳米粒子递送 C-Dot 纳米酶和 CRISPR/Cas9 系统用于溃疡性结肠炎的靶向治疗。
ACS Appl Mater Interfaces. 2022 Feb 9;14(5):6358-6369. doi: 10.1021/acsami.1c21700. Epub 2022 Jan 31.

引用本文的文献

1
Phillygenin ameliorates tight junction proteins reduction, fibrosis, and apoptosis in mice with chronic colitis via TGR5-mediated PERK-eIF2α-Ca pathway.穿龙薯蓣皂苷元通过TGR5介导的PERK-eIF2α-Ca途径改善慢性结肠炎小鼠的紧密连接蛋白减少、纤维化和细胞凋亡。
J Pharm Anal. 2025 Jan;15(1):101042. doi: 10.1016/j.jpha.2024.101042. Epub 2024 Jul 14.
2
Locally Acting Budesonide-Loaded Solid Self-Microemulsifying Drug Delivery Systems (SMEDDS) for Distal Ulcerative Colitis.局部作用的布地奈德负载固体自微乳药物传递系统(SMEDDS)治疗远端溃疡性结肠炎。
Int J Nanomedicine. 2024 Nov 13;19:11819-11846. doi: 10.2147/IJN.S484277. eCollection 2024.
3

本文引用的文献

1
Chemoprevention of bilirubin encephalopathy with a nanoceutical agent.用纳米药物预防胆红素脑病。
Pediatr Res. 2023 Mar;93(4):827-837. doi: 10.1038/s41390-022-02179-5. Epub 2022 Jul 6.
2
Novel one pot synthesis and spectroscopic characterization of a folate-MnO nanohybrid for potential photodynamic therapeutic application.一种用于潜在光动力治疗应用的叶酸-MnO纳米杂化物的新型一锅法合成及光谱表征
RSC Adv. 2019 Sep 24;9(52):30216-30225. doi: 10.1039/c9ra06835j. eCollection 2019 Sep 23.
3
Advances in the colon-targeted chitosan based multiunit drug delivery systems for the treatment of inflammatory bowel disease.
Transforming Medicine with Nanobiotechnology: Nanocarriers and Their Biomedical Applications.
用纳米生物技术变革医学:纳米载体及其生物医学应用
Pharmaceutics. 2024 Aug 23;16(9):1114. doi: 10.3390/pharmaceutics16091114.
4
A spectroscopy based prototype for the noninvasive detection of diabetes from human saliva using nanohybrids acting as nanozyme.基于光谱学的原型,使用作为纳米酶的纳米杂化材料,从人唾液中进行非侵入性的糖尿病检测。
Sci Rep. 2023 Oct 12;13(1):17306. doi: 10.1038/s41598-023-44011-y.
用于治疗炎症性肠病的结肠靶向壳聚糖基多单位药物传递系统的研究进展。
Carbohydr Polym. 2022 Jul 15;288:119351. doi: 10.1016/j.carbpol.2022.119351. Epub 2022 Mar 14.
4
A narrative review of pyrolysis and its role in ulcerative colitis.热解及其在溃疡性结肠炎中的作用的叙述性综述。
Eur Rev Med Pharmacol Sci. 2022 Feb;26(4):1156-1163. doi: 10.26355/eurrev_202202_28107.
5
VX765 alleviates dextran sulfate sodium-induced colitis in mice by suppressing caspase-1-mediated pyroptosis.VX765 通过抑制半胱氨酸天冬氨酸蛋白酶-1 介导的细胞焦亡缓解葡聚糖硫酸钠诱导的小鼠结肠炎。
Int Immunopharmacol. 2022 Jan;102:108405. doi: 10.1016/j.intimp.2021.108405. Epub 2021 Dec 2.
6
Newer Biologic and Small-Molecule Therapies for Inflammatory Bowel Disease.用于炎症性肠病的新型生物制剂和小分子疗法。
N Engl J Med. 2021 Sep 30;385(14):1302-1315. doi: 10.1056/NEJMra1907607.
7
Ozanimod as Induction and Maintenance Therapy for Ulcerative Colitis.奥扎莫德用于溃疡性结肠炎的诱导缓解和维持治疗。
N Engl J Med. 2021 Sep 30;385(14):1280-1291. doi: 10.1056/NEJMoa2033617.
8
Redox nanomedicine ameliorates chronic kidney disease (CKD) by mitochondrial reconditioning in mice.氧化还原纳米医学通过线粒体修复改善小鼠慢性肾脏病(CKD)。
Commun Biol. 2021 Aug 26;4(1):1013. doi: 10.1038/s42003-021-02546-8.
9
The role of the mitochondrial protein VDAC1 in inflammatory bowel disease: a potential therapeutic target.线粒体蛋白 VDAC1 在炎症性肠病中的作用:一个潜在的治疗靶点。
Mol Ther. 2022 Feb 2;30(2):726-744. doi: 10.1016/j.ymthe.2021.06.024. Epub 2021 Jul 2.
10
Redox Buffering Capacity of Nanomaterials as an Index of ROS-Based Therapeutics and Toxicity: A Preclinical Animal Study.纳米材料的氧化还原缓冲能力作为基于 ROS 的治疗和毒性的指标:一项临床前动物研究。
ACS Biomater Sci Eng. 2021 Jun 14;7(6):2475-2484. doi: 10.1021/acsbiomaterials.1c00402. Epub 2021 Jun 1.