[1]邓祥丽,陈丽娟,邵 梅,等.益肺汤调控TGF-β1/Smad2通路抗肺纤维化机制研究[J].陕西中医杂志,2024,(4):435-439.[doi:DOI:10.3969/j.issn.1000-7369.2024.04.001]
 DENG Xiangli,CHEN Lijuan,SHAO Mei,et al.Mechanism of Yifei decoction regulating TGF-β1/Smad2 signaling pathway against pulmonary fibrosis[J].,2024,(4):435-439.[doi:DOI:10.3969/j.issn.1000-7369.2024.04.001]
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益肺汤调控TGF-β1/Smad2通路抗肺纤维化机制研究
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《陕西中医》杂志[ISSN:1000-7369/CN:61-1281/TN]

卷:
期数:
2024年4期
页码:
435-439
栏目:
基础研究
出版日期:
2024-04-05

文章信息/Info

Title:
Mechanism of Yifei decoction regulating TGF-β1/Smad2 signaling pathway against pulmonary fibrosis
作者:
邓祥丽1陈丽娟2邵 梅1吴 梅1杨 梅1吴海茵1马信文1黄 芬1
(1.云南中医药大学第一临床医学院,云南 昆明 650051; 2.云南中医药大学第一附属医院,云南 昆明 650021)
Author(s):
DENG XiangliCHEN LijuanSHAO MeiWU MeiYANG MeiWU HaiyinMA XinwenHUANG Fen
(The First Clinical Medical College of Yunnan University of Traditional Chinese Medicine,Kunming 650051,China)
关键词:
肺纤维化 益肺汤 TGF-β1/Smad2信号通路 血管紧张素Ⅱ 肺成纤维细胞 α-平滑肌肌动蛋白
Keywords:
Pulmonary fibrosis Yifei decoction TGF-β1/Smad2 signaling pathway Angiotensin Ⅱ NIH-3T3 α-SMA
分类号:
R 563
DOI:
DOI:10.3969/j.issn.1000-7369.2024.04.001
文献标志码:
A
摘要:
目的:研究益肺汤含药血清对血管紧张素Ⅱ(Ang Ⅱ)诱导的肺成纤维细胞(NIH-3T3)的影响,探讨其抑制肺纤维化的作用机制。方法:采用SPF级C57小鼠灌胃益肺汤,1次/d,连续给药3 d制备含药血清。实验分为正常对照组、模型组、模型+正常血清组、模型+含药血清组,给药48 h后0.1%FBS的培养基饥饿处理24 h,100 ng/μl的Ang Ⅱ诱导造模24 h。免疫组化检测α-平滑肌肌动蛋白(α-SMA); 免疫荧光检测Smad2; Western blot检测Ⅰ型胶原蛋白(Col Ⅰ)、α-SMA、纤维连接蛋白(FN)、Smad2; ELISA检测细胞上清转化生长因子-β1(TGF-β1)的表达情况。结果:Western blot和免疫荧光显示,造模后,α-SMA、FN、Col Ⅰ、Smad2的蛋白相对表达显著升高,差异具有统计学意义(均P<0.05)。益肺汤含药血清干预48 h后造模,α-SMA、FN、Smad2、Col Ⅰ的相对量较模型组下降(均P<0.05)。ELISA结果显示,造模后,TGF-β1的相对表达显著升高(P<0.05),益肺汤含药血清干预48 h后,TGF-β1相对量较模型组下降(P<0.05)。结论:益肺汤含药血清对Ang Ⅱ诱导的NIH-3T3有一定影响,可有效减轻肺纤维化,其作用机制可能与调控TGF-β1/Smad2信号通路,降低α-SMA、Col Ⅰ、FN的表达有关。
Abstract:
Objective:To study the effect of serum containing Yifei decoction on NIH-3T3 induced by angiotensin Ⅱ(Ang Ⅱ),and to explore its mechanism of inhibiting pulmonary fibrosis.Methods:SPF C57 mice were given Yifei decoction once a day for 3 days to prepare medicated serum.The experiment was divided into normal control group,model group,model+normal serum group and model+medicated serum group.After 48 hours of administration,0.1%FBS was starved for 24 hours,and 100 ng/μl Ang Ⅱ was used to induce the model for 24 hours.α-smooth muscle actin(α-SMA)was detected by immunohistochemistry.Smad2 was detected by immunofluorescence.Collagen Ⅰ(Col Ⅰ),α-SMA,fibronectin(FN)and Smad2 were detected by Western blot.The expression of transforming growth factor-β1(TGF-β1)in cell supernatant was detected by ELISA.Results:Western blot and immunofluorescence showed that the relative expression of α-SMA,FN,Col Ⅰ and Smad2 increased significantly after modeling,with statistical significance(all P<0.05).After 48 hours of intervention with medicated serum,the relative amounts of α-SMA,FN,Smad2 and Col Ⅰ decreased locally compared with the model group(all P<0.05).The results of ELISA showed that the relative expression of TGF-β1 increased significantly after modeling(P<0.05),the relative amount of TGF-β1 decreased locally compared with the model group after 48 hours of intervention with drug-containing serum(P<0.05).Conclusion:The serum containing Yifei decoction has certain effect on NIH-3T3 induced by Ang Ⅱ,which can effectively alleviate pulmonary fibrosis.This mechanism may be related to the regulation of TGF-β1/Smad2 signaling pathway and the reduction of α-SMA,Col Ⅰ and FN expression.

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备注/Memo

备注/Memo:
基金项目:国家自然科学基金地区基金资助项目(82360922); 云南省科技厅科技计划项目-中医联合面上项目[2019FF002(-034)]; 云南中医药大学第一临床医学院研究生科学研究基金资助项目(2022YS12)
更新日期/Last Update: 2024-04-10