Gualou Xiebai Decoction prevents myocardial fibrosis by blocking TGF-beta/Smad signalling

被引:47
作者
Ding, Yong-fang [1 ,2 ]
Peng, Yun-ru [2 ]
Li, Juan [2 ]
Shen, Hong [2 ]
Shen, Ming-qin [2 ]
Fang, Tai-hui [1 ]
机构
[1] Nanjing Univ Tradit Chinese Med, Jiangsu Key Lab Pharmacol & Safety Evaluat Chines, Nanjing 210046, Jiangsu, Peoples R China
[2] Jiangsu Prov Inst Tradit Chinese Med, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Gualou Xiebai Decoction (GXD); myocardial fibrosis; myocardial infarction; transforming growth factor 1; BETA; AGGREGATION; DISEASE;
D O I
10.1111/jphp.12102
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objectives The present study is aimed to investigate the effect of Gualou Xiebai Decoction (GXD) ethanol extract on myocardial fibrosis and clarify the possible mechanism. Methods Rats with ligated left anterior descending coronary artery were treated with GXD ethanol extract (1.14g/kg, 2.27g/kg, 4.53g/kg) daily via gavage for 4 weeks. Histopathological changes and collagen distribution were evaluated by haematoxylin and eosin and Masson staining. The mRNA levels of Collagen I and Collagen III were detected by real-time PCR. The expressions of TGF-1, TGF receptor (TGFR)I, TGFRII, P-Smad2/3 and Smad7 were determined by Western blot. Results GXD treatment was significantly reduced the heart weight/body weight ratio (P<0.05) as well as the left ventricle weight/body weight ratio (P<0.05). It also significantly alleviated the degree of inflammation, decreased myocardial collagen volume fraction (P<0.05 approximate to 0.01), together with markedly prevented the upregulations of Collagen I and Collagen III (P<0.05 approximate to 0.01). Moreover, GXD downregulated expressions of TGF-1, TGFRI, TGFRII, Smad2/3 whereas improved Smad7 expression in the myocardial fibrosis rats. Conclusions GXD ameliorates myocardial fibrosis induced by cardiac infarction with ligated left anterior descending coronary artery, the mechanism maybe involve in inhibiting the TGF-1 signalling pathway.
引用
收藏
页码:1373 / 1381
页数:9
相关论文
共 25 条
[1]   Compensated cardiac hypertrophy: Arrhythmogenicity and the new myocardial phenotype .1. Fibrosis [J].
Assayag, P ;
Carre, F ;
Chevalier, B ;
Delcayre, C ;
Mansier, P ;
Swynghedauw, B .
CARDIOVASCULAR RESEARCH, 1997, 34 (03) :439-444
[2]   Cyclic GMP/protein kinase G phosphorylation of Smad3 blocks transforming growth factor-β-induced nuclear smad translocation -: A key antifibrogenic mechanism of atrial natriuretic peptide [J].
Buxton, Iain L. O. ;
Duan, Dayue .
CIRCULATION RESEARCH, 2008, 102 (02) :151-153
[3]  
Chen B, 1997, CHIN J INTEGR MED, V17, P1
[4]  
Ding YF, 2009, JIANGSU J TRADIT CHI, V41, P80
[5]   Natural Polypill Xuezhikang: Its Clinical Benefit and Potential Multicomponent Synergistic Mechanisms of Action in Cardiovascular Disease and Other Chronic Conditions [J].
Feng, Yan ;
Xu, Hao ;
Chen, Keji .
JOURNAL OF ALTERNATIVE AND COMPLEMENTARY MEDICINE, 2012, 18 (04) :318-328
[6]   Effects of Chinese herb medicine Radix Scrophulariae on ventricular remodeling [J].
Gu, Wei-Liang ;
Chen, Chang-Xun ;
Wu, Qi ;
Lue, Jian ;
Liu, Ying ;
Zhang, Shi-Jie .
PHARMAZIE, 2010, 65 (10) :770-775
[7]   Effects of Tribuli saponins on ventricular remodeling after myocardial infarction in hyperlipidemic rats [J].
Guo, Yan ;
Shi, Da-Zhuo ;
Yin, Hui-Jun ;
Chen, Ke-Ji .
AMERICAN JOURNAL OF CHINESE MEDICINE, 2007, 35 (02) :309-316
[8]   Matrix control of transforming growth factor-β function [J].
Horiguchi, Masahito ;
Ota, Mitsuhiko ;
Rifkin, Daniel B. .
JOURNAL OF BIOCHEMISTRY, 2012, 152 (04) :321-329
[9]   Green tea extract protects rats against myocardial infarction associated with left anterior descending coronary artery ligation [J].
Hsieh, Shih-Rong ;
Tsai, Dan-Chin ;
Chen, Jan-Yow ;
Tsai, Sen-Wei ;
Liou, Ying-Ming .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2009, 458 (04) :631-642
[10]   Effect of timosaponin E1 and E2 on superoxide generation induced by various stimuli in human neutrophils and on platelet aggregation in human blood [J].
Kaname, N ;
Zhang, JY ;
Meng, ZY ;
Xu, SX ;
Sugahara, K ;
Doi, Y ;
Kodama, H .
CLINICA CHIMICA ACTA, 2000, 295 (1-2) :129-140