Influence of bear bile on rat hepatocarcinoma induced by diethylnitrosamine



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Acta Pharmaceutica Sinica 2012, 47 (11): 1483 1488 1483 1, 2, 1, 2, 3, 3, 1, 2, 1, 2, 4, 1, 2, 1, 2* (1., 361004; 2., 361004; 3., 361005; 4., 361004) : (diethylnitrosamine, DEN) (200 400 mg kg 1, 18, 5 ) DEN,,, HE, (PCNA) (α-sma) : 4 (P < 0.01), (P < 0.05);,, ;, ; PCNA α-sma,, α-sma : DEN, : ; ; : R963 : A : 0513-4870 (2012) 11-1483-06 Influence of bear bile on rat hepatocarcinoma induced by diethylnitrosamine ZHOU Jian-yin 1, 2, YIN Zhen-yu 1, 2, WANG Sheng-yu 3, YAN Jiang-hua 3, ZHAO Yi-lin 1, 2, WU Duan 1, 2, LIU Zheng-jin 4, ZHANG Sheng 1, 2 1, 2*, WANG Xiao-min (1. Department of Hepatobiliary Surgery, Zhongshan Hospital, Xiamen University, Xiamen 361004, China; 2. Digestive Disease Center of Xiamen, Xiamen 361004, China; 3. Cancer Research Center, Medical College, Xiamen University, Xiamen 361005, China; 4. Department of Pathology, Zhongshan Hospital, Xiamen University, Xiamen 361004, China) Abstract: To investigate the influence of bear bile on rat hepatocarcinoma induced by diethylnitrosamine (DEN), a total of 40 rats were randomly divided into 4 groups: normal control group, model group, and two bear bile treatment groups. The rat liver cancer model was induced by breeding with water containing 100 mg L 1 DEN for 14 weeks. The rats of the bear bile groups received bear bile powder (200 or 400 mg kg 1 ) orally 5 times per week for 18 weeks. The general condition and the body weight of rats were examined every day. After 18 weeks the activities of serum alanine transaminase (ALT), aspartate transaminase (AST) and total bilirubin (TBIL) were detected. Meanwhile, the pathological changes of liver tissues were observed after H&E staining. The expression of proliferative cell nuclear antigen (PCNA) and α-smooth muscle actin (α-sma) in liver tissue were detected by immunohistochemical method. After 4 weeks the body weights of rats in normal group were significantly more than that in other groups (P < 0.05); and that in the two bile groups was sig- : 2012-05-31; : 2012-07-27. : (2012ZX10002-011-005); (81171976); (wzy0904). * Tel: 86-592-2292203, Fax: 86-592-2212328, E-mail: wxm2203@xmu.edu.cn

1484 Acta Pharmaceutica Sinica 2012, 47 (11): 1483 1488 nificantly more than that in the model group. Compared with normal group, the level of serum glutamic- pyruvic transaminase and total bilirubin increased significantly in other groups; compared with model group, these two indexes decreased significantly in two bile groups. Hepatocellular carcinoma occurred in all rats except for normal group; there were classic cirrhosis and cancer in model group while there were mild cirrhosis and high differentiation in two bile groups. There were almost no expressions of PCNA and α-sma in normal group while there were high expressions in model group; the two bile groups had some expressions but were inferior to the model group, and α-sma reduced markedly. It indicated that bear bile restrained the development of liver cancer during DEN inducing rat hepatocarcinoma, which may be related to its depressing hepatic stellate cell activation and relieving hepatic lesion and cirrhosis. Key words: bear bile; diethylnitrosamine; hepatocarcinoma,,,,, [1],, [2, 3],, [4 7] (hepatic stellate cell, HSC), HSC, [8],, (diethylnitrosamine, DEN, > 0.99 g ml 1, Sigma ), 100 mg L 1 DEN,, ; ( : 20100809, ),,,,,, 44.2%; (ALT) (AST) (TBIL) ; (PCNA) ; (α-sma) DenmakDako ; SD 40,, (150 ± 19.8) g,, : SCXK ( ) 2008-0001, 3 d 10, ;, 10, 100 mg L 1 DEN,, DEN 2 mg, 14 [9], 200 mg kg 1 400 mg kg 1, 5, 18 ; ; 18, 4 ml, (3 000 r min 1, 2 min),, 20,, 3, 1 cm 1 cm 1 cm,, 10% ALT AST, TBIL MODULAR P800,,, 5 μm, HE, 4 μm,, SP, PCNA 1 200, α-sma 1 500 PBS, PCNA, α-sma,

: 1485, [10] : 0, 1, 2, 3 : < 5% 0 ; 6% 25% 1 ; 26% 50% 2 ; 51% 75% 3 ; > 75% 4, 0 1 ( ), 2 3 (+), 4 5 (++), > 5 (+++) x ± s,, SPSS 18.0, ALT TBIL, AST (P > 0.05);, ALT TBIL (P < 0.05), AST ;, (P > 0.05) 1 1,,, 4,, 4 (P < 0.01), (P < 0.05); (P > 0.05), 1 14, 2, 20%, 1, 1 ; 1, 10%, 2 18 :, ALT AST TBIL (P < 0.05); Figure 1 The animals body weight of the different groups 3, :,,, ;,, ;, ; HE :,, ( 2A);,,,, Table 1 Liver function indexes of rats at the end of 18 weeks ( x ± s). ALT: Alanine transaminase; AST: Aspartate transaminase; TBIL: Total bilirubin. (n): Death numbers of rats. * P < 0.05 vs control group; P < 0.05 vs model group Group n ALT/u L 1 AST/u L 1 TBIL/μmol L 1 Control 10 54.83 ± 5.70 199.37 ± 11.64 1.73 ± 0.38 Model 8 (2) 142.73 ± 15.59 * 299.17 ± 38.84 * 6.07 ± 1.86 * Low-dosage bear bile (200 mg kg 1 ) 9 (1) 101.70 ± 22.17 * 253.90 ± 35.31 3.86 ± 1.15 * High-dosage bear bile (400 mg kg 1 ) 10 95.47 ± 16.61 * 207.60 ± 35.31 2.75 ± 0.62 * Figure 2 HE staining micrographs of liver below ( 200). A: Control; B: Model; C: Low-dosage bear bile; D: High-dosage bear bile

1486 Acta Pharmaceutica Sinica 2012, 47 (11): 1483 1488 ( 2B);,,, ( 2C, D) 4 PCNA α-sma 4.1 PCNA PCNA ( 3A ), PCNA, ( 3B, ), PCNA ( 3C, D ), (P > 0.05) ( 2) 4.2 α-sma α-sma,, ( 3A ) (HSC, α-sma), ( 3B ) HSC, ( 3C, D ), α-sma (P < 0.05), (P > 0.05) ( 2) Table 2 Comparison of proliferative cell nuclear antigen (PCNA) or α-smooth muscle actin (α-sma) in different groups. (n): Death numbers of rats. Comparison of PCNA among these three groups, P > 0.05; Comparison of α-sma among these three groups, P < 0.05; Comparison of α-sma between two bile groups, P > 0.05 Group n PCNA α-sma + ++ +++ + ++ +++ Model 8 (2) 0 2 2 4 0 1 2 5 Low-dosage bear bile 9 (1) 0 3 3 3 1 4 3 1 High-dosage bear bile 10 0 3 4 3 2 4 3 1 DEN DEN,,,, [11] : DEN, ;, ;, ; 3,, DEN 14, 18,, [12],,,, DEN,, DEN,, ;, 1 2,,, ;,, Figure 3 Expression of PCNA above and α-sma below by immunocytochemistry staining in different groups ( 400). A: Control; B: Model; C: Low-dosage bear bile; D: High-dosage bear bile

: 1487,,,,, [13] PCNA,, DNA PCNA DNA,,, G 1, S, G 2 M [14],,,, PCNA [15, 16] PCNA : ;, ;,,,, [17] HSC,, HSC, (myofibroblast, MFB), α-sma [18] HSC, ;,, [18, 19] HSC, HSC, T, HSC, [8] HSC α-sma, α-sma,,, HSC, DEN,, DEN,,,, References [1] Sun HF, Hou HL, Lu P, et al. Isocorydine inhibits cell proliferation in hepatocellular carcinoma cell lines by inducing G2/M cell cycle arrest and apoptosis[j]. PLoS One, 2012, 7: e36808. doi:10.1371/journal.pone.0036808. [2] Ling J, Wang X. The synergistic antitumor effects of berberine α-hydroxy-β-decanoylethyl sulfonate with hydroxycamptothecine and its effect on topoisomerase [J]. Acta Pharm Sin ( ), 2012, 46: 390 394. [3] Huang XY, Wang L, Huang ZL, et al. Herbal compound extract Songyou Yin inhibits tumor growth and prolongs survival in nude mice bearing human hepatocellular carcinoma xenograft with high metastatic potential [J]. J Cancer Res Clin Oncol, 2009, 135: 1245 1255. [4] Jin Y, Moon YS, Choi IJ, et al. Effects of bears bile on the expression of tumor cell p53 protein [J]. Chin J Integr Tradit West Med ( ), 2006, 26: 86 88. [5] Kang JH, Zhang WQ, Song W, et al. Apoptosis mechanism of human cholangiocarcinoma cells induced by bile extract from crocodile [J]. Appl Biochem Biotechnol, 2012, 166: 942 951. [6] Alberts DS, Martinez ME, Hess LM, et al. Phase III trial of ursodeoxycholic acid to prevent colorectal adenoma recurrence [J]. J Nat Cancer Inst, 2005, 97: 846 853. [7] Choi YH, Im EO, Suh H, et al. Apoptosis and modulation of cell cycle control by synthetic derivatives of ursodeoxycholic acid and chenodeoxycholic acid in human prostate cancer cells [J]. Cancer Lett, 2003; 199: 157 167. [8] Zhou CS, Yin ZY, Zhao WX, et al. Study of bear bile on immunologic feature of hepatic stellate cells in vivo [J]. China J Tradit Chin Med Pharm ( ), 2011, 26: 2251 2254. [9] Luo YQ, Wu MC, Chen H, et al. Gene expression of HGF and its receptor in experimental hepatomas [J]. Natl Med J China ( ), 1996, 76: 822 825. [10] Yang M, Chen Q. Expression and significances of resistance protein P-gp and Topo- in B cell non-hodgkin lymphoma [J]. China Pharm ( ), 2012, 23: 1684 1687. [11] Zhang ZM, Wang G, Chen C, et al. Pathologic and morphologic study on modified DEN-induced hepatocarcinoma model in

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