RETRACTED: PASS-Predicted Hepatoprotective Activity of Caesalpinia sappan in Thioacetamide-Induced Liver Fibrosis in Rats (Retracted Article)

被引:27
作者
Kadir, Farkaad A. [1 ]
Kassim, Normadiah M. [1 ]
Abdulla, Mahmood Ameen [2 ]
Kamalidehghan, Behnam [3 ]
Ahmadipour, Fatemeh [3 ]
Yehye, Wageeh A. [4 ]
机构
[1] Univ Malaya, Fac Med, Dept Anat, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Fac Med, Dept Biomed Sci, Kuala Lumpur 50603, Malaysia
[3] Univ Malaya, Fac Med, Dept Pharm, Kuala Lumpur 50603, Malaysia
[4] Univ Malaya, Nanotechnol & Catalysis Res Ctr NANOCAT, Kuala Lumpur 50603, Malaysia
关键词
EXPRESSION; CIRRHOSIS; MECHANISM; BERBERINE; HEARTWOOD; DISEASE; DAMAGE;
D O I
10.1155/2014/301879
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The antifibrotic effects of traditional medicinal herb Caesalpinia sappan (CS) extract on liver fibrosis induced by thioacetamide (TAA) and the expression of transforming growth factor beta 1 (TGF-beta 1), alpha-smooth muscle actin (alpha SMA), and proliferating cell nuclear antigen (PCNA) in rats were studied. A computer-aided prediction of antioxidant and hepatoprotective activities was primarily performed with the Prediction Activity Spectra of the Substance (PASS) Program. Liver fibrosis was induced in male Sprague Dawley rats by TAA administration (0.03% w/v) in drinking water for a period of 12 weeks. Rats were divided into seven groups: control, TAA, Silymarin (SY), and CS 300 mg/kg body weight and 100 mg/kg groups. The effect of CS on liver fibrogenesis was determined by Masson's trichrome staining, immunohistochemical analysis, and western blotting. In vivo determination of hepatic antioxidant activities, cytochrome P450 2E1 (CYP2E1), and matrix metalloproteinases (MPPS) was employed. CS treatment had significantly increased hepatic antioxidant enzymes activity in the TAA-treated rats. Liver fibrosis was greatly alleviated in rats when treated with CS extract. CS treatment was noted to normalize the expression of TGF-beta 1, alpha SMA, PCNA, MMPs, and TIMP1 proteins. PASS-predicted plant activity could efficiently guide in selecting a promising pharmaceutical lead with high accuracy and required antioxidant and hepatoprotective properties.
引用
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页数:12
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共 50 条
[31]   Antifibrotic effects of a tissue inhibitor of metalloproteinase-1 antibody on established liver fibrosis in rats [J].
Parsons, CJ ;
Bradford, BU ;
Pan, CQ ;
Cheung, E ;
Schauer, M ;
Knorr, A ;
Krebs, B ;
Kraft, S ;
Zahn, S ;
Brocks, B ;
Feirt, N ;
Mei, BS ;
Cho, MS ;
Ramamoorthi, R ;
Roldan, G ;
Ng, P ;
Lum, P ;
Hirth-Dietrich, C ;
Tomkinson, A ;
Brenner, DA .
HEPATOLOGY, 2004, 40 (05) :1106-1115
[32]  
Poli Giuseppe, 2000, Molecular Aspects of Medicine, V21, P49, DOI 10.1016/S0098-2997(00)00004-2
[33]  
Pramely R, 2012, J BIOTECHNOL TECHNOL, V3, P375
[34]   Activation of hepatic stellate cells - A key issue in liver fibrosis [J].
Reeves, HL ;
Friedman, SL .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2002, 7 :D808-D826
[35]  
Salama S. M., 2013, BMC COMPLEMENTARY AL, V13
[36]   HEPATIC EXPRESSION OF MATURE TRANSFORMING GROWTH-FACTOR-BETA-1 IN TRANSGENIC MICE RESULTS IN MULTIPLE TISSUE LESIONS [J].
SANDERSON, N ;
FACTOR, V ;
NAGY, P ;
KOPP, J ;
KONDAIAH, P ;
WAKEFIELD, L ;
ROBERTS, AB ;
SPORN, MB ;
THORGEIRSSON, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :2572-2576
[37]  
Sarumathy K., 2011, INT J PHARM THERAPE, V1, P19
[38]   Liver cirrhosis [J].
Schuppan, Detlef ;
Afdhal, Nezam H. .
LANCET, 2008, 371 (9615) :838-851
[39]   Effects of oxymatrine on experimental hepatic fibrosis and its mechanism in vivo [J].
Shi, Guang-Feng ;
Li, Qian .
WORLD JOURNAL OF GASTROENTEROLOGY, 2005, 11 (02) :268-271
[40]  
Shrishailappa Badami Shrishailappa Badami, 2004, Natural Product Radiance, V3, P75