Brief Reports Open Access
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Aug 1, 2004; 10(15): 2295-2298
Published online Aug 1, 2004. doi: 10.3748/wjg.v10.i15.2295
Inhibitory effect of Huangqi Zhechong decoction on liver fibrosis in rat
Shuang-Suo Dang, Xiao-Li Jia, Yan-An Cheng, Yun-Ru Chen, Department of Infectious Diseases, Second Hospital of Xi’an Jiaotong University, Xi’an 710004, Shaanxi Province, China
En-Qi Liu, Center of Experimental Animal, Xi’an Jiaotong University, Xi’an 710004, Shaanxi Province, China
Zong-Fang Li, Department of Surgery, Second Hospital of Xi’an Jiaotong University, Xi’an 710004, Shaanxi Province, China
Author contributions: All authors contributed equally to the work.
Supported by the Science and Technology Foundation of Shaanxi Province, No. 2002k11-G7
Correspondence to: Shuang-Suo Dang, Department of Infectious Disease, Second Hospital of Xi’an Jiaotong University, Xi’an 710004, Shaanxi Province, China. shuangsuo640212@sohu.com
Telephone: +86-29-83036998
Received: December 19, 2003
Revised: December 23, 2003
Accepted: January 15, 2004
Published online: August 1, 2004

Abstract

AIM: To assess the inhibitory effect of Huangqi Zhechong decoction on hepatic fibrosis in rats induced by CCl4 plus alcohol and high fat low protein diet.

METHODS: Male SD rats were randomly divided into hepatic fibrosis model group, control group and 3 treatment groups consisting of 12 rats in each group. Except for the normal control group, all the rats were subcutaneously injected with CCl4 at a dosage of 3 mL/kg. In 3 treated groups, either high-dose group (9 mL/kg), or medium-dose group (6 mL/kg), or low-dose group (3 mL/kg) was daily gavaged with Huangqi Zhechong decoction, and saline vehicle was given to model and normal control rats. Enzyme-linked immunosorbent assay (ELISA) and biochemical examinations were used to determine the changes of alanine aminotransferase (ALT), aspartate aminotransferase (AST), hyaluronic acid (HA), laminin (LN), type-III-procollagen-N- peptide (PIIIP), and type IV collagen content in serum, and hydroxyproline (Hyp) content in liver after sacrificing the rats. Pathologic changes, particularly fibrosis were examined by hematoxylin and eosin (HE) and Van Gieson staining.

RESULTS: Compared with the model control group, serum ALT, AST, HA, LN, PIIIP and type IV collagen levels dropped markedly in Huangqi Zhechong decoction groups, especially in the medium-dose Huangqi Zhechong decoction group (1 954 ± 576 U/L vs 759 ± 380 U/L, 2 735 ± 786 U/L vs 1 259 ± 829 U/L, 42.74 ± 7.04 ng/mL vs 20.68 ± 5.85 ng/mL, 31.62 ± 5.84 ng/mL vs 14.87 ± 1.45 ng/mL, 3.26 ± 0.69 ng/mL vs 1.47 ± 0.46 ng/mL, 77.68 ± 20.23 ng/mL vs 25.64 ± 4.68 ng/mL, respectively) (P < 0.05). The Hyp content in liver tissue was also markedly decreased (26.47 ± 11.24 mg/mgprot vs 9.89 ± 3.74 mg/mgprot) (P < 0.01). Moreover, the stage of the rat liver fibrosis in Huangqi Zhechong decoction groups was lower than that in model group, and more dramatic drop was observed in medium-dose Huangqi Zhechong decoction group (P < 0.01).

CONCLUSION: Huangqi Zhechong decoction can inhibit hepatic fibrosis resulted from chronic liver injure, retard the development of cirrhosis, and notably ameliorate the liver function. It may be a safe and effective therapeutic drug for patients with fibrosis.




INTRODUCTION

Liver fibrosis is common in most chronic liver diseases regardless of the etiology[1-8]. Although new therapeutic approaches have recently been proposed, there is no established therapy for liver fibrosis[9]. Huangqi Zhechong decoction is a traditional Chinese medicine. The aim of the present study was to investigate the protective effects of Huangqi Zhechong decoction on liver fibrosis in rats of CCl4-induced cirrhosis.

MATERIALS AND METHODS
Reagents

CCl4 (Xi’an Chemical Factory) was diluted into 400 g/L in olive oil (Xi’an Chemical Factory). Huangqi Zhechong decoction was self-made by the Pharmaceutical Department of the Second Hospital, Xi’an Jiaotong University. The kit for Hyp was bought from Nianjing Jiancheng Biological Institute. Kits for HA, LN, PIIIP and type IV collagen were bought from Senxiong Company, Shanghai.

Animals

Sixty adult male SD rats weighing 150-200 g were provided by the Laboratory Animal Center of the College of Medicine, Xi’an Jiaotong University. The rats were randomly divided into 5 groups of 12 each: control group; model group; and 3 treatment groups. Except for the control rats, all rats were subcutaneously injected with 400 g/L CCl4 (CCl4:Olive oil 2: 3), 3 mL/kg·b.w., at every 3 d for 6 wk, and fed with high fat low protein diet (75% pure maize plus 20% lard and 0.5% cholesterol) and 300 mL/L alcohol as drinks. In the 3 treatment groups, Huangqi Zhechong decoction was administered daily via gastric tube to high-dose, medium-dose and low -dose groups at a dosage of 9 mL/kg, 6 mL/kg and 3 mL/kg for 6 wk, respectively. After 6 wk, except the dead, all the rats were anesthetized with 200 g/L urethane (5 mL/kg, abdominal injection). Blood was taken from abdominal aorta, centrifuged at 4 °C, and plasma were kept at -20 °C for assays.

Pathological observations

Hepatic tissues were fixed in 40 g/L solutions of formaldehyde in 0.1% mol/L phosphate-buffered saline (pH 7.4), and embedded in paraffin. Five-micrometer thick section slides were prepared. All the sections stained with HE and standard van Gieson staining (VG) were coded and scored by blind reading. Van Gieson’s method was used to detect collagen fibers[10]. Liver condition was classified according to the standard formulated by China Medical Association in 1995[11], and fibrosis was graded from 0 to 4 (0: no fibrosis; 1: portal area fibrosis; 2: fibrotic septa between portal tracts; 3: fibrosis septa and structure disturbance of hepatic lobule; and 4: cirrhosis).

Statistical analysis

Results were expressed as mean ± SD. Quantitative data were analyzed by using ANOVA in statistical software SPSS 11.0. A value of P < 0.05 was considered statistically significant. Ridit test was used for statistical analysis of the qualitative data.

RESULTS
Hyp content in liver tissues

Liver Hyp level was significantly lower in rats treated with CCl4 and Huangqi Zhechong decoction compared to the rats treated with CCl4 alone (P < 0.01). And the liver Hyp level of rat in 3 Huangqi Zhechong decoction treatment groups has no significant difference from control group (Table 1).

Table 1 Level of serum ALT, AST and liver Hyp.
GroupnALT (U/L)AST (U/L)Liver Hyp (μg/mgprot)
Control1286.0 ± 17.7329 ± 4010.02 ± 1.05
Model111 954 ± 576d2735 ± 786d26.47 ± 11.24d
High-dose group9989 ± 576ad1 584 ± 988c15.01 ± 7.59b
Medium-dose group10759 ± 380bc1259 ± 829a9.89 ± 3.74b
Low-dose group101 003 ± 530ad1 650 ± 928c10.06 ± 2.58b
Plasma levels of ALT and AST

Plasma levels of ALT and AST in model group were higher than those in the controls (P < 0.01), while the Huangqi Zhechong decoction treatment groups showed significant lower ALT and AST levels than the model group. Furthermore, among the 3 treatment groups the medium-dose group showed the best effect and the levels of ALT and AST in serum showed no difference compared with the normal group (Table 1).

HA, LN, PIIIP and type IV collagen levels in serum

Serum levels of HA, LN, PIIIP and type IV collagen in model group, compared with the controls, were all markedly increased (P < 0.01). And compared with the model group, the serum levels of HA, LN, PIIIP and type IVcollagen were significant decreased in the 3 treatment groups (P < 0.01) (Table 2).

Table 2 Serum levels of HA, LN, PIIIP and type IV collagen.
GroupnPIIIP (ng/mL)Type IV collagen (ng/mL)LN (ng/mL)HA (ng/mL)
Control120.34 ± 0.6718.47 ± 3.4310.07 ± 1.7417.96 ± 5.86
Model113.26 ± 0.69d77.68 ± 20.23d31.62 ± 5.84d42.74 ± 7.04d
High-dose group92.01 ± 0.40bd39.14 ± 4.97 bd16.32 ± 2.73bd21.71 ± 5.69b
Medium-dose group101.47 ± 0.46bd25.64 ± 4.68b14.87 ± 1.45 bd20.68 ± 5.85b
Low-dose group101.84 ± 0.27bd29.09 ± 2.78b17.02 ± 2.74 bd24.18 ± 7.89b
Pathological assay

At the end of the study, the liver of control rats had no appreciable alterations (Figure 1A). In the model group, the margin of liver was uneven; more fibrous tissues formed and extended into the hepatic lobules to separate them incompletely; a large amount of inflammatory cells infiltrated in the intralobular and the interlobular regions; the liver structure was disordered with some displacement of central veins, and there were more necrotic and degenerated liver cells compared with the control (Figure 1B). While in the 3 treatment groups, especially in the medium-dose group, the pathological changes of liver was rather milder, showing less fibrous tissue proliferation and inflammatory cell infiltration in the interlobular space; the hepatic cell cords arranged radially with less displacement of central veins and less degenerated or necrosis hepatic cells,without any pseudolobule observed (Figure 1C). Compared with the model group, the liver condition of the rats was significantly improved in Huangqi Zhechong decoction groups (Table 3).

Figure 1
Figure 1 Liver tissue under light microscope. A: Normal liver tissue in control group (HE staining, original magnification: × 400); B: Liver fibrosis tissue in model group, more fibrous tissue was formed in liver. A large amount of inflammatory cells soaked into the intralobular and the interlobular (van Gieson staining, original magnification: × 200); C: Liver fibrosis tissue in Huangqi Zhechong decoction group. The pathological change of liver was rather lighter compared with the model (van Gieson staining, original magnification: × 200).
Table 3 Pathological observation of liver condition.
GroupnLiver condition
U
0IIIIIIIV
Model1100038
High-dose group9023312.98a
Medium-dose group10044204.01b
Low-dose group10024313.75b
DISCUSSION

The incidence rate of chronic hepatopathy in China is high, which afflicts the patients by progressively developing irreversible cirrhosis[12,13]. Hepatic fibrosis is the intermediate and crucial stage of this process, characterized by reversibility. If treated properly in this stage, cirrhosis could be successfully prevented[14]. But it remains a problem to prevent cirrhosis or to control its progression in patients with a chronic liver disease[15]. Great efforts have been made to find safe and effective drugs. Recent clinical and experimental observations have demonstrated that Chinese medicines might be of some preventive and therapeutic values against fibrosis[16-18].

Of Huangqi Zhechong decoction, the Chinese traditional medicine, the Astragalus has the effects of activating blood circulation to relieve stasis, strengthening “spleen”, supplementing and smoothening “qi” to eliminate fullness, reinforcement body’s immunological function. It also could preserve the integrity of hepatocytes, eliminate toxic free radicals, inhibit lipid peroxidation of cytomembrane, relieve necrosis of hepatocytes, and obviously antifibrosis[19-23]. Thoroughfare is mainly used to activate blood circulation, remove stasis, and dredge the liver[24].

Huangqi Zhechong decoction has been used in clinic for many years to prevent liver fibrosis and shown good effect. However, its effect and the associated mechanisms need further experimental evidence. CCl4 is a super-hepatotoxin, with which the CCl3 free radical is produced during metabolic processes and acts on liver cells to covalently conjugate with the membranous unsaturated lipid to cause lipid peroxidation and necrosis of hepatocytes[25-27]. For this reason, CCl4 was used to induce liver fibrosis.

We started to treat the rats with Huangqi Zhechong decoction at the same time of subcutaneous injection with CCl4. After 6 wk, the histological features showed that there were no appreciable alterations in control group. But pathological evaluation showed that the rats in model group almost had integrity fibrosis septum, and pseudolobular could be seen in nearly every section. While the rats received Huangqi Zhechong decoction had less fibrosis, the reticular fibrosis in the interlobular septum was limited remarkably, and no pseudolobular could be seen. In addition, Huangqi Zhechong decoction, especially the medium-dose administration could decrease the scores of hepatic fibrosis grading.

ALT and AST are indexes to describe liver functions. Most part of ALT is presented in the cytoplasm of liver cell, discharged in blood when degeneration, hyper permeability and necrosis of liver cells occur. So the increase of ALT level in serum reflects the degree of liver cell injury. Our study showed that the Huangqi Zhechong decoction could decrease serum levels of ALT and AST in rats with hepatic injury caused by CCl4. It indicates that Huangqi Zhechong decoction may work through protecting the liver cells.

HA, LN, PIIIP and type IV collagen are good serum markers of hepatic fibrosis. In this study, the serum contents of these 4 markers in the model group were much higher than those of the controls (P < 0.01). And the Huangqi Zhechong decoction groups had significantly low HA, LN, PIIIP and type IV collagen levels in serum than those in the controls, which indicated that Huangqi Zhechong decoction could successfully prevent hepatic fibrosis.

Hyp content in liver is another important index to react the hepatic fibrosis. In fibrotic liver, collagen fibers increase, which induced the rise of Hyp content in liver[28]. So Hyp level could provide the information about the degree and variant process of cirrhosis. In this study, we observed that the liver Hyp level in the model group was much higher than that of the controls and Huangqi Zhechong decoction groups.

In summary, Huangqi Zhechong decoction may play a role in antifibrotic therapy. It can protect the liver cells and inhibit the deposition of collagen fibers in liver. It may provide a safe and effective strategy for inhibition of cirrhosis in clinic use.

Footnotes

Edited by Kumar M and Chen WW Proofread by Xu FM

References
1.  Ma X, Qiu DK, Peng YS. Immunohistochemical study of hepatic oval cells in human chronic viral hepatitis. World J Gastroenterol. 2001;7:238-242.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Reshetnyak VI, Sharafanova TI, Ilchenko LU, Golovanova EV, Poroshenko GG. Peripheral blood lymphocytes DNA in patients with chronic liver diseases. World J Gastroenterol. 2001;7:235-237.  [PubMed]  [DOI]  [Cited in This Article: ]
3.  McCaughan GW, Gorrell MD, Bishop GA, Abbott CA, Shackel NA, McGuinness PH, Levy MT, Sharland AF, Bowen DG, Yu D. Molecular pathogenesis of liver disease: an approach to hepatic inflammation, cirrhosis and liver transplant tolerance. Immunol Rev. 2000;174:172-191.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 61]  [Cited by in F6Publishing: 67]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
4.  Okazaki I, Watanabe T, Hozawa S, Arai M, Maruyama K. Molecular mechanism of the reversibility of hepatic fibrosis: with special reference to the role of matrix metalloproteinases. J Gastroenterol Hepatol. 2000;15 Suppl:D26-D32.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 57]  [Cited by in F6Publishing: 64]  [Article Influence: 2.7]  [Reference Citation Analysis (0)]
5.  Jung SA, Chung YH, Park NH, Lee SS, Kim JA, Yang SH, Song IH, Lee YS, Suh DJ, Moon IH. Experimental model of hepatic fibrosis following repeated periportal necrosis induced by allylalcohol. Scand J Gastroenterol. 2000;35:969-975.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 17]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
6.  Plummer JL, Ossowicz CJ, Whibley C, Ilsley AH, Hall PD. Influence of intestinal flora on the development of fibrosis and cirrhosis in a rat model. J Gastroenterol Hepatol. 2000;15:1307-1311.  [PubMed]  [DOI]  [Cited in This Article: ]
7.  Croquet V, Moal F, Veal N, Wang J, Oberti F, Roux J, Vuillemin E, Gallois Y, Douay O, Chappard D. Hemodynamic and antifibrotic effects of losartan in rats with liver fibrosis and/or portal hypertension. J Hepatol. 2002;37:773-780.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 86]  [Cited by in F6Publishing: 84]  [Article Influence: 3.8]  [Reference Citation Analysis (0)]
8.  Marcellin P, Asselah T, Boyer N. Fibrosis and disease progression in hepatitis C. Hepatology. 2002;36:S47-S56.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 40]  [Cited by in F6Publishing: 97]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
9.  Friedman SL. Molecular regulation of hepatic fibrosis, an integrated cellular response to tissue injury. J Biol Chem. 2000;275:2247-2250.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1567]  [Cited by in F6Publishing: 1567]  [Article Influence: 65.3]  [Reference Citation Analysis (0)]
10.  Zhu H, Zeng L, Zhu D, Yuan Y. The role of TGF-beta 1 in mice hepatic fibrosis by Schistosomiasis Japonica. J Tongji Med Univ. 2000;20:320-321, 329.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 8]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
11.  China Medical Association infectious branch. The standard of grading and staging of viral hepatitis. Zhonghua Chuanranbing Zazhi. 1995;13:241-247.  [PubMed]  [DOI]  [Cited in This Article: ]
12.  Lamireau T, Desmoulière A, Bioulac-Sage P, Rosenbaum J. [Mechanisms of hepatic fibrogenesis]. Arch Pediatr. 2002;9:392-405.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 18]  [Cited by in F6Publishing: 25]  [Article Influence: 1.1]  [Reference Citation Analysis (0)]
13.  Brenner DA, Waterboer T, Choi SK, Lindquist JN, Stefanovic B, Burchardt E, Yamauchi M, Gillan A, Rippe RA. New aspects of hepatic fibrosis. J Hepatol. 2000;32:32-38.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 138]  [Cited by in F6Publishing: 148]  [Article Influence: 6.2]  [Reference Citation Analysis (0)]
14.  Riley TR, Bhatti AM. Preventive strategies in chronic liver disease: part II. Cirrhosis. Am Fam Physician. 2001;64:1735-1740.  [PubMed]  [DOI]  [Cited in This Article: ]
15.  Murphy F, Arthur M, Iredale J. Developing strategies for liver fibrosis treatment. Expert Opin Investig Drugs. 2002;11:1575-1585.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 17]  [Cited by in F6Publishing: 20]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
16.  Liu C, Jiang CM, Liu CH, Liu P, Hu YY. Effect of Fuzhenghuayu decoction on vascular endothelial growth factor secretion in hepatic stellate cells. Hepatobiliary Pancreat Dis Int. 2002;1:207-210.  [PubMed]  [DOI]  [Cited in This Article: ]
17.  Liu P, Liu CH, Wang HN, Hu YY, Liu C. Effect of salvianolic acid B on collagen production and mitogen-activated protein kinase activity in rat hepatic stellate cells. Acta Pharmacol Sin. 2002;23:733-738.  [PubMed]  [DOI]  [Cited in This Article: ]
18.  Kusunose M, Qiu B, Cui T, Hamada A, Yoshioka S, Ono M, Miyamura M, Kyotani S, Nishioka Y. Effect of Sho-saiko-to extract on hepatic inflammation and fibrosis in dimethylnitrosamine induced liver injury rats. Biol Pharm Bull. 2002;25:1417-1421.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 43]  [Cited by in F6Publishing: 47]  [Article Influence: 2.1]  [Reference Citation Analysis (0)]
19.  Wang RT, Shan BE, Li QX. [Extracorporeal experimental study on immuno-modulatory activity of Astragalus memhranaceus extract]. Zhongguo Zhongxiyi Jiehe Zazhi. 2002;22:453-456.  [PubMed]  [DOI]  [Cited in This Article: ]
20.  Chu DT, Lin JR, Wong W. [The in vitro potentiation of LAK cell cytotoxicity in cancer and aids patients induced by F3--a fractionated extract of Astragalus membranaceus]. Zhonghua Zhongliu Zazhi. 1994;16:167-171.  [PubMed]  [DOI]  [Cited in This Article: ]
21.  Zhang YD, Shen JP, Zhu SH, Huang DK, Ding Y, Zhang XL. [Effects of astragalus (ASI, SK) on experimental liver injury]. Yaoxue Xuebao. 1992;27:401-406.  [PubMed]  [DOI]  [Cited in This Article: ]
22.  Tan YW, Yin YM, Yu XJ. [Influence of Salvia miltiorrhizae and Astragalus membranaceus on hemodynamics and liver fibrosis indexes in liver cirrhotic patients with portal hypertension]. Zhongguo Zhongxiyi Jiehe Zazhi. 2001;21:351-353.  [PubMed]  [DOI]  [Cited in This Article: ]
23.  Fu QL. [Experimental study on yiqi-huoxue therapy of liver fibrosis]. Zhongguo Zhongxiyi Jiehe Zazhi. 1992;12:228-229, 198.  [PubMed]  [DOI]  [Cited in This Article: ]
24.  Chen H, Weng L. [Comparison on efficacy in treating liver fibrosis of chronic hepatitis B between Astragalus Polygonum anti-fibrosis decoction and jinshuibao capsule]. Zhongguo Zhongxiyi Jiehe Zazhi. 2000;20:255-257.  [PubMed]  [DOI]  [Cited in This Article: ]
25.  Kanta J, Dooley S, Delvoux B, Breuer S, D'Amico T, Gressner AM. Tropoelastin expression is up-regulated during activation of hepatic stellate cells and in the livers of CCl(4)-cirrhotic rats. Liver. 2002;22:220-227.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 16]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
26.  Yan JC, Ma Y, Chen WB, Xu CJ. Dynamic observation on vascu-lar diseases of liver tissues of rats induced by CCl4. Shijie Huaren Xiaohua Zazhi. 2000;8:42-45.  [PubMed]  [DOI]  [Cited in This Article: ]
27.  Yan JC, Chen WB, Ma Y, Xu CJ. Immunohistochemical study on hepatic vascular forming factors in liver fibrosis induced by CCl4 in rats. Shijie Huaren Xiaohua Zazhi. 2000;8:1238-1241.  [PubMed]  [DOI]  [Cited in This Article: ]
28.  García L, Hernández I, Sandoval A, Salazar A, Garcia J, Vera J, Grijalva G, Muriel P, Margolin S, Armendariz-Borunda J. Pirfenidone effectively reverses experimental liver fibrosis. J Hepatol. 2002;37:797-805.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 116]  [Cited by in F6Publishing: 121]  [Article Influence: 5.5]  [Reference Citation Analysis (0)]