|本期目录/Table of Contents|

[1]唐诗慧,张 丽,方步武.蒿鳖养阴软坚方对TGF-β1诱导的肝纤维化的作用[J].天津医科大学学报,2018,24(05):381-384.
 TANG Shi-hui,Zhang Li,FANG Bu-wu.Effect of HaoBieYangYinRuanJian on liver fibrosis induced by TGF-β1[J].Journal of Tianjin Medical University,2018,24(05):381-384.
点击复制

蒿鳖养阴软坚方对TGF-β1诱导的肝纤维化的作用(PDF)
分享到:

《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
24卷
期数:
2018年05期
页码:
381-384
栏目:
基础医学
出版日期:
2018-09-20

文章信息/Info

Title:
Effect of HaoBieYangYinRuanJian on liver fibrosis induced by TGF-β1
作者:
唐诗慧张 丽方步武
天津医科大学药理学系,天津300070
Author(s):
TANG Shi-huiZhang LiFANG Bu-wu
Department of Pharmacology,Tianjin Medical University,Tianjin 300070,China
关键词:
肝纤维化蒿鳖养阴软坚方TGF-β1collagen Ι α-SMA
Keywords:
hepatic fibrosis HaoBieYangYinRuanJian TGF-β1collagen Ι α-SMA
分类号:
R96
DOI:
-
文献标志码:
A
摘要:
目的:研究蒿鳖养阴软坚方在体外对LX-2细胞的影响,从而探讨蒿鳖养阴软坚方对TGF-β1诱导的肝纤维化的作用。方法:体外培养人肝星状细胞LX-2,实验分为正常对照组、TGF-β1刺激组和蒿鳖养阴软坚方低、中、高浓度给药组。MTT法检测LX-2细胞增殖情况;比色法检测细胞培养液中乳酸脱氢酶(LDH)的活性;酶消化法检测细胞上清羟脯氨酸(Hyp)的含量;Western blot法检测collagen Ι以及α-SMA蛋白表达量。结果:TGF-β1作用于LX-2能够明显促进细胞的增殖,collagen I、α-SMA的表达量显著升高。蒿鳖养阴软坚方能抑制LX-2细胞增殖并且能够降低collagen Ι和α-SMA的表达。结论:蒿鳖养阴软坚方能够显著抑制LX-2增殖,下调collagen Ι和α-SMA的表达,降低Hyp生成,从而发挥抗肝纤维化的作用。
Abstract:
Objective: To investigate the effect of HBYYRJ on hepatic stellate cells (HSCs, LX-2) in vitro, and explore the effect of HBYYRJ on liver fibrosis induced TGF-β1. Methods: LX-2 cells were cultured in vitro and divided into control group, TGF-β1 stimulation group and HBYYRJ low dose group, middle dose group and high dose group. The proliferation of LX-2 cells was detected by MTT assay; the activity of LDH was detected by colorimetric assay; and the content of Hyp was detected by enzyme digestion. Western blot was used to detect the protein expression of collagen Ι and α-SMA. Results: TGF-β1 significantly promoted the proliferation of LX-2, TGF-β1 significantly increased the level of collagen Ι and α-SMA. HBYYRJ significantly reduced the proliferation of LX-2, and significantly reduced the level of collagen Ι and α-SMA. Conclusion: HBYYRJ can significantly reduce the proliferation of LX-2, down-regulate the expression of collagen Ι and α-SMA, and decrease the synthesis of Hyp to attenuate hepatic fibrosis.

参考文献/References:


[1] Popov Y,Schuppan D. Targeting liver fibrosis: strategies for development and validation of antifibrotictherapies[J]. Hepatology,2009, 50(4):1294
[2] Yin C,Evason K J,Asahina K,et al. Hepatic stellate cells in liver development,regeneration,and cancer[J]. J Clin Invest,2013,123(5):1902
[3] Dooley S,Delvoux B,Streckert M,et al. Transforming growth factor beta signal transduction in hepatic stellate cells via Smad2/3 phosphorylation,a pathway that is abrogated during in vitro progression tomyofibroblasts. TGFbeta signal transduction during transdifferentiation of hepatic stellate cells[J]. FEBS Lett,2001,502(1-2):4
[4] Liu X,Hu H,Yin J Q. Therapeutic strategies against TGF-beta signaling pathway in hepatic fibrosis[J]. Liver Int,2006,26(1):8
[5] 率红莉,方步武,邢伟,等.蒿鳖养阴软坚方对四氯化碳复合因素所致肝纤维化的预防作用[J]. 中国实验方剂学杂志,2013(16):197
[6] Friedman S L. Mechanisms of hepatic fibrogenesis[J]. Gastroenterology,2008,134(6):1655
[7] Anthony B,Allen J T,Li Y S,et al. Hepatic stellate cells and parasite-induced liver fibrosis[J]. Parasit Vectors,2010,3(1):60
[8] Chen Y W,Li D G,Wu J X,et al. Tetrandrine inhibits activation of rat hepatic stellate cells stimulated by transforming growth factor-beta in vitro via up-regulation of Smad 7[J]. J Ethnopharmacol,2005, 100(3):299
[9] Oh C J,Kim J Y,Min A K,et al. Sulforaphane attenuates hepatic fibrosis via NF-E2-related factor 2-mediated inhibition of transforming growth factor-beta/Smadsignaling[J]. Free RadicBiol Med,2011,52(3):671
[10] Sancho-Bru P,Juez E,Moreno M,et al. Hepatocarcinoma cells stimulate the growth,migration and expression of pro-angiogenic genes in human hepatic stellate cells[J]. Liver Int,2010,30(1):31
[11] Cheng Y,Zheng H,Wang B,et al. Sorafenib and fluvastatin synergistically alleviate hepatic fibrosis via inhibiting the TGFbeta1/Smad3 pathway[J]. Dig Liver Dis,2018,50(4):381

相似文献/References:

[1]李杉杉,刘 悦,唐诗慧,等.蒿鳖养阴软坚方通过Nrf2/γ-GCS信号转导通路抑制酒精性肝纤维化作用及其机制[J].天津医科大学学报,2018,24(01):14.
 LI Shan-shan,LIU Yue,TANG Shi-hui,et al.Effects and mechanism of HaoBieYangYinRuanJian prescription on inhibition of alcoholic liver fibrosis through Nrf2/-GCS pathway[J].Journal of Tianjin Medical University,2018,24(05):14.
[2]刘 悦,李杉杉,唐诗慧,等.蒿鳖养阴软坚方通过激活Nrf2/NQO1信号通路抑制肝纤维化发生[J].天津医科大学学报,2018,24(01):19.
 LIU Yue,LI Shan-shan,TANG Shi-hui,et al.Effects of HaobieYangyinRuanjian on inhibition of hepatic fibroesis through upregulated Nrf2/NQO1 pathway[J].Journal of Tianjin Medical University,2018,24(05):19.
[3]卢娜,方步武.蒿鳖养阴软坚方对刀豆球蛋白A诱导的肝纤维化Nrf2/HO-1信号通路影响[J].天津医科大学学报,2018,24(02):112.
 LU Na,FANG Bu-wu.Effect of Haobie yangyin ruanjian prescription on Nrf2/HO-1 signaling pathway in ConA-induced hepatic fibrosis[J].Journal of Tianjin Medical University,2018,24(05):112.

备注/Memo

备注/Memo:
-
更新日期/Last Update: 2018-09-30