• 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

乌司他丁抑制实验性腹主动脉瘤的形成和进展。

Ulinastatin Inhibits the Formation and Progression of Experimental Abdominal Aortic Aneurysms.

作者信息

Li Gang, Zhou Hua, He Yuxiang, Sun Shunji, Wu Xuejun, Yuan Hai

机构信息

Department of Vascular Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.

Vascular Intervention Department, Hospital Affiliated to Weifang Medical University, Weifang, China.

出版信息

J Vasc Res. 2020;57(2):58-64. doi: 10.1159/000504848. Epub 2020 Jan 21.

DOI:10.1159/000504848
PMID:31962313
Abstract

AIMS

Aortic mural inflammatory damage takes a vital part in abdominal aortic aneurysm (AAA). Recently, ulinastatin (UTI) has attracted attention for its anti-inflammatory function. Our study aimed to evaluate potential influences of UTI on experimental AAA.

METHODS

A mouse model of AAA was induced by infusion of porcine pancreatic elastase (PPE) into the abdominal aorta. Mice were treated with UTI (50,000 U/kg/day i.p.) beginning either immediately or on the 4th day after PPE infusion, with treatment being continued until the 14th day. UTI effects were assessed by aortic diameter measurements and aortic histopathological analysis.

RESULTS

Significant and time-dependent aortic diameter enlargement persisted in the control mice from day 0. In the UTI group, aortic diameter increased, and depletion of aortic mural smooth muscle cells and elastin was significantly -attenuated. Simultaneously, mural CD68+ macrophages, CD8+ T-cell and B220+ B-cell density, as well as neoangiogenesis were suppressed by UTI. In addition, delayed UTI treatment could still effectively limit aneurysm expansion.

CONCLUSIONS

UTI treatment limits the formation and growth of experimental AAA, and UTI may be a potential treatment for early AAA disease.

摘要

目的

主动脉壁炎症损伤在腹主动脉瘤(AAA)中起关键作用。近来,乌司他丁(UTI)因其抗炎功能而受到关注。我们的研究旨在评估UTI对实验性AAA的潜在影响。

方法

通过向腹主动脉内注入猪胰弹性蛋白酶(PPE)诱导建立AAA小鼠模型。小鼠在PPE注入后立即或第4天开始接受UTI治疗(腹腔注射,50,000 U/kg/天),持续治疗至第14天。通过测量主动脉直径和进行主动脉组织病理学分析来评估UTI的作用。

结果

从第0天起,对照小鼠的主动脉直径持续显著且随时间增大。在UTI组中,主动脉直径增加,主动脉壁平滑肌细胞和弹性蛋白的损耗明显减轻。同时,UTI抑制了壁内CD68+巨噬细胞、CD8+ T细胞和B220+ B细胞密度以及新生血管形成。此外,延迟的UTI治疗仍可有效限制动脉瘤扩张。

结论

UTI治疗可限制实验性AAA的形成和生长,UTI可能是早期AAA疾病的一种潜在治疗方法。

相似文献

1
Ulinastatin Inhibits the Formation and Progression of Experimental Abdominal Aortic Aneurysms.乌司他丁抑制实验性腹主动脉瘤的形成和进展。
J Vasc Res. 2020;57(2):58-64. doi: 10.1159/000504848. Epub 2020 Jan 21.
2
Hypoxia-inducible factor 1 in clinical and experimental aortic aneurysm disease.临床和实验性主动脉瘤疾病中的缺氧诱导因子1
J Vasc Surg. 2018 Nov;68(5):1538-1550.e2. doi: 10.1016/j.jvs.2017.09.030. Epub 2017 Dec 11.
3
Inhibition of Receptor-Interacting Protein Kinase 1 with Necrostatin-1s ameliorates disease progression in elastase-induced mouse abdominal aortic aneurysm model.使用 Necrostatin-1s 抑制受体相互作用蛋白激酶 1 可改善弹性蛋白酶诱导的小鼠腹主动脉瘤模型的疾病进展。
Sci Rep. 2017 Feb 10;7:42159. doi: 10.1038/srep42159.
4
Continuous periaortic infusion improves doxycycline efficacy in experimental aortic aneurysms.主动脉周围持续输注可提高多西环素在实验性主动脉瘤中的疗效。
J Vasc Surg. 2004 Jun;39(6):1312-21. doi: 10.1016/j.jvs.2004.01.036.
5
Temporal and Quantitative Analysis of Aortic Immunopathologies in Elastase-Induced Mouse Abdominal Aortic Aneurysms.弹性蛋白酶诱导的小鼠腹主动脉瘤主动脉免疫病理学的时相和定量分析。
J Immunol Res. 2021 Nov 16;2021:6297332. doi: 10.1155/2021/6297332. eCollection 2021.
6
Inhibition of miR-188-5p Suppresses Progression of Experimental Abdominal Aortic Aneurysms.抑制 miR-188-5p 可抑制实验性腹主动脉瘤的进展。
J Cardiovasc Pharmacol. 2021 Jan 1;77(1):107-114. doi: 10.1097/FJC.0000000000000915.
7
Inhibition or deletion of angiotensin II type 1 receptor suppresses elastase-induced experimental abdominal aortic aneurysms.血管紧张素 II 型 1 型受体的抑制或缺失可抑制弹性蛋白酶诱导的实验性腹主动脉瘤。
J Vasc Surg. 2018 Feb;67(2):573-584.e2. doi: 10.1016/j.jvs.2016.12.110. Epub 2017 Apr 20.
8
Daphnetin suppresses experimental abdominal aortic aneurysms in mice via inhibition of aortic mural inflammation.瑞香素通过抑制主动脉壁炎症来抑制小鼠实验性腹主动脉瘤。
Exp Ther Med. 2020 Dec;20(6):221. doi: 10.3892/etm.2020.9351. Epub 2020 Oct 15.
9
No Effect of Hypercholesterolemia on Elastase-Induced Experimental Abdominal Aortic Aneurysm Progression.高胆固醇血症对弹性蛋白酶诱导的实验性腹主动脉瘤进展无影响。
Biomolecules. 2021 Sep 30;11(10):1434. doi: 10.3390/biom11101434.
10
Kunming mouse strain is less susceptible to elastase-induced abdominal aortic aneurysms.昆明小鼠对弹性蛋白酶诱导的腹主动脉瘤的易感性较低。
Animal Model Exp Med. 2022 Feb;5(1):72-80. doi: 10.1002/ame2.12197. Epub 2021 Dec 7.

引用本文的文献

1
Application and challenges of TCR and BCR sequencing to investigate T- and B-cell clonality in elastase-induced experimental murine abdominal aortic aneurysm.TCR和BCR测序在研究弹性蛋白酶诱导的实验性小鼠腹主动脉瘤中T细胞和B细胞克隆性方面的应用及挑战
Front Cardiovasc Med. 2023 Nov 14;10:1221620. doi: 10.3389/fcvm.2023.1221620. eCollection 2023.
2
T cells in abdominal aortic aneurysm: immunomodulation and clinical application.腹主动脉瘤中的 T 细胞:免疫调节与临床应用。
Front Immunol. 2023 Aug 18;14:1240132. doi: 10.3389/fimmu.2023.1240132. eCollection 2023.
3
Isolation and primary culture of human abdominal aorta smooth muscle cells from brain-dead donors: an experimental model for vascular diseases.
从脑死亡供体中分离和原代培养人腹主动脉平滑肌细胞:血管疾病的实验模型。
Cell Tissue Bank. 2024 Mar;25(1):187-194. doi: 10.1007/s10561-023-10091-3. Epub 2023 May 5.
4
Identification of potential novel biomarkers for abdominal aortic aneurysm based on comprehensive analysis of circRNA-miRNA-mRNA networks.基于环状RNA-微小RNA-信使核糖核酸网络综合分析鉴定腹主动脉瘤潜在的新型生物标志物
Exp Ther Med. 2021 Dec;22(6):1468. doi: 10.3892/etm.2021.10903. Epub 2021 Oct 21.
5
Urinary Trypsin Inhibitor Protects Tight Junctions of Septic Pulmonary Capillary Endothelial Cells by Regulating the Functions of Macrophages.尿胰蛋白酶抑制剂通过调节巨噬细胞功能保护脓毒症肺毛细血管内皮细胞紧密连接
J Inflamm Res. 2021 May 17;14:1973-1989. doi: 10.2147/JIR.S303577. eCollection 2021.