RETRACTED: Antifibrotic effects of protocatechuic aldehyde on experimental liver fibrosis (Retracted article. See vol. 51, pg. 675, 2013)

被引:36
作者
Li, Chunmei [1 ]
Jiang, Wanglin [1 ,2 ]
Zhu, Haibo [2 ]
Hou, Jian [2 ]
机构
[1] Yantai Univ, Sch Pharm, Laishan Dist 264003, Yantai, Peoples R China
[2] Luye Pharma Grp Ltd, State Key Lab Long acting & Targeting Drug Delive, Yantai, Peoples R China
关键词
Liver fibrosis; protocatechuic aldehyde; transforming growth factor-beta 1; connective transforming growth factor; TISSUE GROWTH-FACTOR; HEPATIC-FIBROSIS; IN-VITRO; EXPRESSION; RATS; CELLS; BETA; HYALURONAN; CIRRHOSIS; MARKERS;
D O I
10.3109/13880209.2011.608193
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Recent studies have demonstrated that transforming growth factor-beta 1 (TGF-beta 1) and connective transforming growth factor (CTGF) are associated with the pathophysiology of liver fibrosis. We isolated protocatechuic aldehyde, the major degradation of phenolic acids. Objective: This study was carried out to investigate the potential antifibrotic effect of Protocatechuic aldehyde (PA) on experimental liver fibrosis in vitro and in vivo, and to explore its possible mechanism. Materials and methods: Cell proliferation was determined. Type I collagen, type III collagen, transforming growth factor-beta 1 (TGF-beta 1) and connective transforming growth factor (CTGF) were measured by ELISA kits in TNF-alpha stimulated HSCs. In the carbon tetrachloride (CCL4)-induced rat liver fibrosis model, liver fibrosis grade and histopathological changes were evaluated, and biochemical indicators were determined. Furthermore, immunostaining and Western blot analysis were used to detect hepatic TGF-beta 1 and CTGF expression in liver tissue. Results: Overall, our results indicated that PA inhibits HSCs proliferation, inhibits the levels of TGF-beta 1, CTGF, type I collagen and type III collagen in TNF-alpha stimulated HSCs. Treatment of PA causes a significant reduction in fibrosis grade, ameliorates biochemical indicators and histopathological morphology, and reduces liver TGF-beta 1 and CTGF expression in rat model of CCL4 -induced liver fibrosis. Conclusion: These findings suggest that PA has potentially conferring antifibrogenic effects.
引用
收藏
页码:413 / 419
页数:7
相关论文
共 27 条
[1]   Liver fibrosis [J].
Bataller, R ;
Brenner, DA .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (02) :209-218
[2]   Gene regulation of connective tissue growth factor: new targets for antifibrotic therapy [J].
Blom, IE ;
Goldschmeding, R ;
Leask, A .
MATRIX BIOLOGY, 2002, 21 (06) :473-482
[3]   Worldwide mortality from cirrhosis: An update to 2002 [J].
Bosetti, Cristina ;
Levi, Fabio ;
Lucchini, Franca ;
Zatonski, Witold A. ;
Negri, Eva ;
La Vecchia, Carlo .
JOURNAL OF HEPATOLOGY, 2007, 46 (05) :827-839
[4]  
China Medical Association Infectious Branch, 1995, ZHONGHUA CHUANRANBIN, V13, P241
[5]   siRNA-mediated knockdown of connective tissue growth factor prevents N-nitrosodimethylamine-induced hepatic fibrosis in rats [J].
George, J. ;
Tsutsumi, M. .
GENE THERAPY, 2007, 14 (10) :790-803
[6]   The tightrope of therapeutic suppression of active transforming growth factor-β:: high enough to fall deeply? [J].
Gressner, AM ;
Weiskirchen, R .
JOURNAL OF HEPATOLOGY, 2003, 39 (05) :856-859
[7]   Roles of TGF-beta in hepatic fibrosis [J].
Gressner, AM ;
Weiskirchen, R ;
Breitkopf, K ;
Dooley, S .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2002, 7 :D793-D807
[8]   Pharmacological application of caffeine inhibits TGF-β-stimulated connective tissue growth factor expression in hepatocytes via PPARγ and SMAD2/3-dependent pathways [J].
Gressner, Olav A. ;
Lahme, Birgit ;
Rehbein, Katharina ;
Siluschek, Monika ;
Weiskirchen, Ralf ;
Gressner, Axel M. .
JOURNAL OF HEPATOLOGY, 2008, 49 (05) :758-767
[9]   Connective tissue growth factor: a fibrogenic master switch in fibrotic liver diseases [J].
Gressner, Olav A. ;
Gressner, Axel M. .
LIVER INTERNATIONAL, 2008, 28 (08) :1065-1079
[10]  
Griffiths Clare, 2005, Health Stat Q, P6