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生肌象皮膏对糖尿病溃疡大鼠Ang/Tie-2通路的影响

刘鹏 朱子昭 常柏 李巧芬

天津中医药2018,Vol.35Issue(2):127-130,4.
天津中医药2018,Vol.35Issue(2):127-130,4.DOI:10.11656/j.issn.1672-1519.2018.02.15

生肌象皮膏对糖尿病溃疡大鼠Ang/Tie-2通路的影响

Effect of Shengji Xiangpi mastic on diabetic ulcer rats Ang/Tie-2 pathway

刘鹏 1朱子昭 2常柏 2李巧芬1

作者信息

  • 1. 天津中医药大学,天津300193
  • 2. 天津医科大学代谢病医院,天津300050
  • 折叠

摘要

Abstract

[Objective]Through the dynamic observation of diabetic ulcers Tie-2,Ang-1 and Ang-2 transcriptional level,to investigate the effect of Shengji Xiangpi mastic on diabetic ulcer rats Ang/Tie-2 pathway. [Methods]The first step is having an injection of STZ at rats'tail vein and back drilling prepared ulcer refractory animal model of T2DM, according to blood glucose and body weight were randomly divided into diabetic group,saline group,Shengji Xiangpi mastic group and normal control group.Shengji Xiangpi mastic group used Shengji Xiangpi mastic gauze topical ulcer, vaseline group with vaseline gauze, control group, diabetic control group with saline gauze group,on the first day and in 3 days,7 days after trauma,14 days and 21 days respectively were part of rats.And take the ulcer tissue expression of Ang-1, Ang-2 and Tie-2 transcriptional level were detected by Western Blotting method in ulcer tissue. [Results] Shengji Xiangpi mastic group were higher than those of other groups of Ang-1 and Tie-2 transcriptional level at different time points in granulation tissue,the expression level of Ang-2 was lower than that of other groups(P<0.05).[Conclusion]Shengji Xiangpi mastic may through increase wound granulation tissue in Ang-1,the expression of Tie-2,inhibit the expression of Ang-2 in diabetic rats,and promote ulcer surface angiogenesis,accelerate the healing of diabetic ulcers.

关键词

生肌象皮膏/糖尿病溃疡/Ang/Tie-2通路

Key words

Shengji Xiangpi mastic/diabetic ulcer/Ang/Tie-2 pathway

分类

医药卫生

引用本文复制引用

刘鹏,朱子昭,常柏,李巧芬..生肌象皮膏对糖尿病溃疡大鼠Ang/Tie-2通路的影响[J].天津中医药,2018,35(2):127-130,4.

基金项目

国家自然科学基金项目(81373846) (81373846)

天津医科大学重点实验室开放项目(2016DX002). (2016DX002)

天津中医药

OACSTPCD

1672-1519

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