• 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

四面体框架核酸可减轻牛磺胆酸钠诱导的小鼠重症急性胰腺炎及其随后的多器官损伤。

Tetrahedral Framework Nucleic Acids Can Alleviate Taurocholate-Induced Severe Acute Pancreatitis and Its Subsequent Multiorgan Injury in Mice.

机构信息

State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan 610041, China.

Department of Orthopedic Surgery and Orthopedic Research Institute Rehabilitation Medicine Center, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China.

出版信息

Nano Lett. 2022 Feb 23;22(4):1759-1768. doi: 10.1021/acs.nanolett.1c05003. Epub 2022 Feb 9.

DOI:10.1021/acs.nanolett.1c05003
PMID:35138113
Abstract

Severe acute pancreatitis (SAP) is an inflammatory disease of the pancreas accompanied by tissue injury and necrosis. It not only affects the pancreas but also triggers a systemic inflammatory response that leads to multiorgan failure or even death. Moreover, there is no effective treatment currently that can reverse the disease progression. In this study, tetrahedral framework nucleic acids (tFNAs) were utilized to treat SAP in mice for the first time and proved to be effective in suppressing inflammation and preventing pathological cell death. Serum levels of pancreatitis-related biomarkers witnessed significant changes after tFNAs treatment. Reduction in the expression of certain cytokines involved in local and systemic inflammatory response were observed, together with alteration in proteins related to cell death and apoptosis. Collectively, our results demonstrate that tFNAs could both alleviate SAP and its subsequent multiorgan injury in mice, thus offering a novel and effective option to deal with SAP in the future.

摘要

重症急性胰腺炎(SAP)是一种胰腺炎症性疾病,伴有组织损伤和坏死。它不仅影响胰腺,还会引发全身性炎症反应,导致多器官衰竭甚至死亡。此外,目前尚无有效的治疗方法可以逆转疾病进展。在这项研究中,首次利用四面体框架核酸(tFNAs)治疗 SAP,结果证明其在抑制炎症和防止病理性细胞死亡方面非常有效。tFNAs 治疗后,与胰腺炎相关的生物标志物的血清水平发生了显著变化。观察到与局部和全身炎症反应相关的某些细胞因子的表达减少,以及与细胞死亡和凋亡相关的蛋白质的改变。总的来说,我们的结果表明,tFNAs 既能缓解 SAP,又能减轻 SAP 后继发的多器官损伤,为未来治疗 SAP 提供了一种新的有效选择。

相似文献

1
Tetrahedral Framework Nucleic Acids Can Alleviate Taurocholate-Induced Severe Acute Pancreatitis and Its Subsequent Multiorgan Injury in Mice.四面体框架核酸可减轻牛磺胆酸钠诱导的小鼠重症急性胰腺炎及其随后的多器官损伤。
Nano Lett. 2022 Feb 23;22(4):1759-1768. doi: 10.1021/acs.nanolett.1c05003. Epub 2022 Feb 9.
2
Protective effects of daphnetin on sodium taurocholate‑induced severe acute pancreatitis in rats.瑞香素对牛磺胆酸钠诱导的大鼠重症急性胰腺炎的保护作用
Mol Med Rep. 2014 May;9(5):1709-14. doi: 10.3892/mmr.2014.1995. Epub 2014 Feb 28.
3
Effects of sildenafil on inflammatory injury of the lung in sodium taurocholate-induced severe acute pancreatitis rats.西地那非对牛磺胆酸钠诱导的重症急性胰腺炎大鼠肺组织炎症损伤的影响。
Int Immunopharmacol. 2020 Mar;80:106151. doi: 10.1016/j.intimp.2019.106151. Epub 2020 Jan 10.
4
Protective effects of heme oxygenase-1 against severe acute pancreatitis via inhibition of tumor necrosis factor-α and augmentation of interleukin-10.血红素加氧酶-1通过抑制肿瘤坏死因子-α和增强白细胞介素-10对重症急性胰腺炎的保护作用。
BMC Gastroenterol. 2017 Aug 24;17(1):100. doi: 10.1186/s12876-017-0651-4.
5
Effect of percutaneous catheter drainage on pancreatic injury in rats with severe acute pancreatitis induced by sodium taurocholate.经皮导管引流对牛磺胆酸钠诱导的大鼠重症急性胰腺炎胰腺损伤的影响。
Pancreatology. 2015 Jan-Feb;15(1):71-7. doi: 10.1016/j.pan.2014.10.005. Epub 2014 Oct 27.
6
Establishment of a Mouse Severe Acute Pancreatitis Model using Retrograde Injection of Sodium Taurocholate into the Biliopancreatic Duct.经胆胰管逆行注射牛磺胆酸钠建立小鼠重症急性胰腺炎模型。
J Vis Exp. 2022 Apr 1(182). doi: 10.3791/63129.
7
Activation of TLR4 induces severe acute pancreatitis-associated spleen injury via ROS-disrupted mitophagy pathway.TLR4 的激活通过 ROS 破坏的线粒体自噬途径诱导严重急性胰腺炎相关的脾损伤。
Mol Immunol. 2022 Feb;142:63-75. doi: 10.1016/j.molimm.2021.12.012. Epub 2021 Dec 26.
8
SRT1720 ameliorates sodium taurocholate-induced severe acute pancreatitis in rats by suppressing NF-κB signalling.SRT1720通过抑制NF-κB信号通路改善牛磺胆酸钠诱导的大鼠重症急性胰腺炎。
Biomed Pharmacother. 2018 Dec;108:50-57. doi: 10.1016/j.biopha.2018.09.035. Epub 2018 Sep 11.
9
Pioglitazone attenuates the severity of sodium taurocholate-induced severe acute pancreatitis.吡格列酮可减轻牛磺胆酸钠诱导的重症急性胰腺炎的严重程度。
World J Gastroenterol. 2007 Apr 7;13(13):1983-8. doi: 10.3748/wjg.v13.i13.1983.
10
Emodin alleviates intestinal mucosal injury in rats with severe acute pancreatitis via the caspase-1 inhibition.大黄素通过抑制半胱氨酸天冬氨酸蛋白酶-1缓解重症急性胰腺炎大鼠的肠道黏膜损伤。
Hepatobiliary Pancreat Dis Int. 2017 Aug 15;16(4):431-436. doi: 10.1016/S1499-3872(17)60041-9.

引用本文的文献

1
Liquid Crystal Microcavity Biosensors for Real-Time Liver Injury Monitoring via Whispering Gallery Mode Laser.用于通过回音壁模式激光实时监测肝损伤的液晶微腔生物传感器。
Research (Wash D C). 2025 Aug 5;8:0824. doi: 10.34133/research.0824. eCollection 2025.
2
Tetrahedron DNA Nanostructures as microRNA Inhibitors to Alleviate Acute Pancreatitis.四面体DNA纳米结构作为微小RNA抑制剂减轻急性胰腺炎
JACS Au. 2025 Jun 20;5(7):3521-3532. doi: 10.1021/jacsau.5c00549. eCollection 2025 Jul 28.
3
Natural product-based nano-antioxidant for the treatment of acute pancreatitis.
用于治疗急性胰腺炎的天然产物基纳米抗氧化剂。
Regen Biomater. 2025 Apr 21;12:rbaf012. doi: 10.1093/rb/rbaf012. eCollection 2025.
4
Current Understanding and Translational Prospects of Tetrahedral Framework Nucleic Acids.四面体骨架核酸的当前理解与转化前景
JACS Au. 2025 Feb 10;5(2):486-520. doi: 10.1021/jacsau.4c01170. eCollection 2025 Feb 24.
5
Hypophosphatemia as a Predictor of Pancreatic Necrosis in Acute Alcohol-induced Pancreatitis.低磷血症作为急性酒精性胰腺炎中胰腺坏死的预测指标
Pancreas. 2025 May 1;54(5):e460-e465. doi: 10.1097/MPA.0000000000002459.
6
From micro to macro, nanotechnology demystifies acute pancreatitis: a new generation of treatment options emerges.从微观到宏观,纳米技术揭开了急性胰腺炎的神秘面纱:新一代治疗方案应运而生。
J Nanobiotechnology. 2025 Jan 29;23(1):57. doi: 10.1186/s12951-025-03106-6.
7
Tetrahedral Framework Nucleic Acid Relieves Sepsis-Induced Intestinal Injury by Regulating M2 Macrophages.四面体框架核酸通过调节M2巨噬细胞减轻脓毒症诱导的肠道损伤。
Cell Prolif. 2025 May;58(5):e13803. doi: 10.1111/cpr.13803. Epub 2025 Jan 22.
8
Tetrahedral framework nucleic acids-based delivery of microRNA-155 alleviates intervertebral disc degeneration through targeting Bcl-2/Bax apoptosis pathway.基于四面体型核酸框架的 microRNA-155 递送来通过靶向 Bcl-2/Bax 凋亡途径缓解椎间盘退变。
Cell Prolif. 2024 Nov;57(11):e13689. doi: 10.1111/cpr.13689. Epub 2024 Jun 20.
9
Tetrahedral framework nucleic acids/hyaluronic acid-methacrylic anhydride hybrid hydrogel with antimicrobial and anti-inflammatory properties for infected wound healing.具有抗菌和抗炎特性的四面体框架核酸/透明质酸-甲基丙烯酰酐杂化水凝胶用于感染性伤口愈合。
Int J Oral Sci. 2024 Apr 16;16(1):30. doi: 10.1038/s41368-024-00290-3.
10
Framework Nucleic Acids-Based VEGF Signaling Activating System for Angiogenesis: A Dual Stimulation Strategy.基于框架核酸的血管内皮生长因子信号激活系统用于血管生成:一种双重刺激策略。
Adv Sci (Weinh). 2024 Jun;11(21):e2308701. doi: 10.1002/advs.202308701. Epub 2024 Mar 9.