• 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

用于皮肤新生血管形成的血管生成基因软膏的研究。

Study of angiogenic gene ointments designed for skin neovascularization.

作者信息

Hajdukiewicz Karolina, Stachurska Anna, Proczka Robert, Małecki Maciej

机构信息

Department of Molecular Biology, Medical University of Warsaw, Warsaw, Poland.

出版信息

Med Wieku Rozwoj. 2013 Jan-Mar;17(1):31-6.

PMID:23749693
Abstract

AIM

In this study attention was focused on gene preparations that stimulate angiogenesis in the skin. Angiogenesis was stimulated by gene preparations encoding angiogenic factors introduced into the skin by injection, and applied as ointments.

MATERIAL AND METHODS

The appropriate angiogenic formulations containing angiogenic nonviral vectors (pVEGF, pFGF, pSDF, pVIF), or viral vectors (rAAV/VEGF, rAAV/SDF) were prepared for the test. Cholesterol ointment was used as the vehicle for viral and non-viral vectors. The new vessels in the mouse skin were counted according to the criteria suggested by Sidky and Auerbach.

RESULTS

Studies indicate that all non-viral (pVEGF, pFGF, pSDF, pVIF) and viral (rAAV/VEGF, rAAV/SDF) vectors strongly stimulate new vessel formation when administered into mouse skin as injections. The impact of angiogenic gene ointments for skin angiogenesis was about 3-4 times weaker than that observed for injection preparations.

CONCLUSIONS

Angiogenic injection gene preparations strongly stimulate skin neovascularization. The clinical usefulness of gene ointments should stimulate further laboratory studies in the field of experimental skin gene therapy.

摘要

目的

本研究聚焦于刺激皮肤血管生成的基因制剂。通过注射将编码血管生成因子的基因制剂引入皮肤,并制成软膏应用,以此刺激血管生成。

材料与方法

制备含血管生成非病毒载体(pVEGF、pFGF、pSDF、pVIF)或病毒载体(rAAV/VEGF、rAAV/SDF)的合适血管生成制剂用于试验。胆固醇软膏用作病毒和非病毒载体的载体。根据Sidky和Auerbach建议的标准对小鼠皮肤中的新血管进行计数。

结果

研究表明,所有非病毒载体(pVEGF、pFGF、pSDF、pVIF)和病毒载体(rAAV/VEGF、rAAV/SDF)经注射施用于小鼠皮肤时,均强烈刺激新血管形成。血管生成基因软膏对皮肤血管生成的影响比注射制剂弱约3 - 4倍。

结论

血管生成注射基因制剂强烈刺激皮肤新血管形成。基因软膏的临床实用性应推动实验性皮肤基因治疗领域的进一步实验室研究。

相似文献

1
Study of angiogenic gene ointments designed for skin neovascularization.用于皮肤新生血管形成的血管生成基因软膏的研究。
Med Wieku Rozwoj. 2013 Jan-Mar;17(1):31-6.
2
Advances in growth factor delivery for therapeutic angiogenesis.用于治疗性血管生成的生长因子递送进展。
J Vasc Res. 2013;50(1):35-51. doi: 10.1159/000345108. Epub 2012 Nov 15.
3
Therapeutic angiogenesis: controlled delivery of angiogenic factors.治疗性血管生成:血管生成因子的可控递送
Ther Deliv. 2012 Jun;3(6):693-714. doi: 10.4155/tde.12.50.
4
In vivo study of angiogenic plasmid preparations--the bicistronic plasmid as a new type of drug for vascular diseases.
Acta Pol Pharm. 2004 Jul-Aug;61(4):289-95.
5
Therapeutic angiogenesis: a biologic bypass.治疗性血管生成:一种生物搭桥术。
Cardiology. 2004;101(1-3):131-43. doi: 10.1159/000075994.
6
Vascular endothelial growth factor and soluble FLT-1 receptor interactions and biological implications.血管内皮生长因子与可溶性FLT-1受体的相互作用及其生物学意义。
Oncol Rep. 2005 Dec;14(6):1565-9.
7
Assessment of the VEGF, bFGF, aFGF and IL8 angiogenic activity in urinary bladder carcinoma, using the mice cutaneous angiogenesis test.利用小鼠皮肤血管生成试验评估膀胱癌中血管内皮生长因子(VEGF)、碱性成纤维细胞生长因子(bFGF)、酸性成纤维细胞生长因子(aFGF)和白细胞介素8(IL8)的血管生成活性。
Anticancer Res. 2001 Nov-Dec;21(6B):4259-63.
8
Erythropoietin and growth factors exhibit differential angiogenic potential in mouse heart.促红细胞生成素和生长因子在小鼠心脏中表现出不同的血管生成潜力。
In Vivo. 2008 Sep-Oct;22(5):587-91.
9
Calcium alginate beads as a slow-release system for delivering angiogenic molecules in vivo and in vitro.海藻酸钙珠作为一种在体内和体外递送血管生成分子的缓释系统。
J Cell Physiol. 1992 Aug;152(2):422-9. doi: 10.1002/jcp.1041520225.
10
A novel way of therapeutic angiogenesis using an adeno-associated virus-mediated angiogenin gene transfer.一种使用腺相关病毒介导的血管生成素基因转移进行治疗性血管生成的新方法。
Exp Mol Med. 2007 Jun 30;39(3):412-8. doi: 10.1038/emm.2007.46.