Medicinal Herbs for HCV (oxymatrin)

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NATAP - www.natap.orgMedicinal Herbs for HCV (oxymatrin), Part I of IIThis report contains several recent publications of a clinical studies in patients infected with hepatitis B and/or C and using for treatment a Chinese herb called oxymatrin in the Dec 2004 issue of World Journal of Gastroenterology. Following this full report is a journal article of a systematic review of randomized trials on medicinal herbs published in the American Journal of Gastroenterology in March 2003 prior to the recent Dec article on oxymatrine. [Preliminary study on therapeutic effect of oxymatrine in treating patients with chronic hepatitis C][Article in Chinese]Li J, Li C, Zeng M.Renji Hospital of Shanghai, Second Medical University, Shanghai 200001.OBJECTIVE: To evaluate the efficacy of oxymatrine in treating chronic hepatitis C and its mechanism. METHODS: Forty-three patient were divided randomly into the treated group (20 cases) and the control group (23 cases). The treated group was given oxymatrine 600 mg per day intramuscularly, and the control group was given the general liver protective agents such as vitamins. The therapeutic course of both groups was 3 months. RESULTS: HCVRNA of 8 in 17 cases (47.1%) of the treated group converted to negative, while in 18 cases of the control group, the negative conversion only took place in 1 patient (5.6%), the negative conversion rate was significantly higher in the treated group than that in the control group (P < 0.05). The normalization rates of serum alanine transaminase (ALT) of the treated group after 1 month and 2 months treatment was higher than that of the control group, but after 3 months treatment, the normalization rates of the two groups were not different significantly. Plasma level of soluble interleukin-2 receptor and serum level of collagen type IV in the treated group were lowered significantly after treatment, but in the control group, there were no significant change, the difference between the two groups was significant (P < 0.01, P < 0.05). CONCLUSION: Oxymatrine is effective in inhibiting proliferation of HCV, antagonisting liver fibrosis and regulating immune reaction of the host, so it could be a safe, effective drug in treating chronic hepatitis C.[Oxymatrine in the treatment of chronic hepatitis B for one year: a multicenter random double-blind placebo-controlled trial.][Article in Chinese]Lu LG, Zeng MD, Mao YM, Wan MB, Li CZ, Chen CW, Fu QC, Wang JY, She WM.Shanghai Institute of Digestive Diseases, Renji Hospital, Shanghai Second Medical University, Shanghai 200001 China.OBJECTIVE: To evaluate the efficacy and safety of oxymatrine in the treatment of chronic hepatitis B. METHODS: A multicenter randomized double-blind placebo-controlled trial was conducted. A total of 144 patients with chronic hepatitis B entered the study for 52 weeks; of them 72 received oxymatrine, and 72 received a placebo. Before and after the treatment, clinical symptoms, liver function, serum hepatitis B virus markers, and adverse drug reactions were observed. RESULTS: In 144 patients, 14 were dropped and excluded due to inconsistencies in the included standard. Therefore, the efficacy and safety of 130 patients were analyzed. After being treated for 52 weeks, 70.77% of the patients in the study group had a normal ALT level, and in 43.08% and 33.33% their HBV DNA and HBeAg became negative. In the placebo group, 39.68% had normal ALT level, and 12.31% and 3.33% had their HBV DNA and HBeAg become negative. The rates of complete response and partial response in the oxymatrine group were 23.08% and 58.46%, and in the placebo group they were 3.08% and 44.62%. They were significantly higher in the oxymatrine group than in the placebo group. In the oxymatrine treated patients, 12 weeks after its withdrawal, 60.00% had a normal ALT level, 41.54% and 23.33% had both HBV DNA and HBeAg negative. In the placebo group, 31.75% had a normal ALT level, 3.08% and 1.67% had both HBV DNA and HBeAg negative. The rates of complete response and partial response in the oxymatrine group were 21.54% and 47.69%, and in the placebo group they were 0 and 41.54%. They were significantly higher in the study group than in the placebo group. The adverse reaction rates of oxymatrine in the study and the placebo group were 7.69% and 6.15%, respectively, but there was no statistical significant difference between them. CONCLUSION: Oxymatrine is an effective and safe agent for the treatment of chronic hepatitis B.Oxymatrine therapy for chronic hepatitis B: a randomized double-blind and placebo-controlled multi-center trial.World J Gastroenterol. 2003 Nov;9(11):2480-3.Lu LG, Zeng MD, Mao YM, Li JQ, Wan MB, Li CZ, Chen CW, Fu QC, Wang JY, She WM, Cai X, Ye J, Zhou XQ, Wang H, Wu SM, Tang MF, Zhu JS, Chen WX, Zhang HQsease, Renji Hospital, Shanghai Second Medical University, Shanghai 200001, China. AIM: To evaluate the efficacy and safety of capsule oxymatrine in the treatment of chronic hepatitis B. METHODS: A randomised double-blind and placebo-controlled multicenter trial was conducted. Injection of oxymatrine was used as positive-control drug. A total of 216 patients with chronic hepatitis B entered the study for 24 weeks, of them 108 received capsule oxymatrine, 36 received injection of oxymatrine, and 72 received placebo. After and before the treatment, clinical symptoms, liver function, serum hepatitis B virus markers, and adverse drug reaction were observed. RESULTS: Among the 216 patients, six were dropped off, and 11 inconsistent with the standard were excluded. Therefore, the efficacy and safety of oxymatrine in patients were analysed. In the capsule treated patients, 76.47% became normal in ALT level, 38.61% and 31.91% became negative both in HBV DNA and in HBeAg. In the injection treated patients, 83.33% became normal in ALT level, 43.33% and 39.29% became negative both in HBV DNA and in HBeAg. In the placebo treated patients, 40.00% became normal in ALT level, 7.46% and 6.45% became negative both in HBV DNA and in HBeAg. The rates of complete response and partial response were 24.51% and 57.84% in the capsule treated patients, and 33.33% and 50.00% in the injection treated patients, and 2.99% and 41.79% in the placebo treated patients, respectively. There was no significance between the two groups of patients, but both were significantly higher than the placebo. The adverse drug reaction rates of the capsule, injection and placebo were 7.77%, 6.67% and 8.82%, respectively. There was no statistically significant difference among them. CONCLUSION: Oxymatrine is an effective and safe agent for the treatment of chronic hepatitis B.Capsule oxymatrine in treatment of hepatic fibrosis due to chronic viral hepatitis: A randomized, double blind, placebo-controlled, multicenter clinical studyWorld J Gastroenterol 2004 November 15;10(22):3269-3273Yi-Min Mao (Shanghai Institute of Digestive Disease, Renji Hospital, Shanghai Second Medical University, Shanghai 200001, China), Min-De Zeng, Lun-Gen Lu, Mo-Bin Wan, Cheng-Zhong Li, Cheng-Wei Chen, Qing-Chuen Fu, Ji-Yao Wang, Wei-Min She, Xiong Cai, Jun Ye, Xia-Qiu Zhou, Hui Wang, Shan-Ming Wu, Mei-Fang Tang, Jin-Shui Zhu, Wei-Xiong Chen, Hui-Quan ZhangAbstractAIM: To evaluate the efficacy and safety of oxymatrine capsule in treatment of hepatic fibrosis in patients with chronic viral hepatitis.METHODS: It was a randomized, double blind, placebo-controlled, multicenter clinical study. One hundred and forty-four patients were divided into oxymatrine capsule group(group A) and placebo group (group .The course was 52 wk. Patients were visited once every 12 wk and the last visit was at 12 wk after cessation of the treatment. All patients had liver biopsy before treatment. part of them had a second biopsy at the end of therapy. Clinical symptoms, liver function test, serum markers of hepatic fibrosis were tested. Ultrasound evaluation was performed before, during and at the end of therapy.RESULTS: One hundred and forty-four patients enrolled in the study. Of them 132 patients completed the study according to the protocol,49 patients had liver biopsy twice (25 patients in group A and 24 in group . At the end of therapy, significant improvements in hepatic fibrosis and inflammatory activity based on Semi-quantitative scoring system (SSS) were achieved in group A. The total effective rate of the treatment was 48.00%, much higher than that of 4.17% in group B (P<0.05). Significant improvement in serum markers of hepatic fibrosis such as hyaluronic acid (HA) and type III procollagenic peptide (P III P) in group A was seen (P<0.05). The total effective rate of serum markers at the end of therapy in group A was 68.19%, much higher than that of 34.85% in group B (P<0.05). The total effective rate of noninvasive markers at the end of therapy in group A was 66.67%, much higher than that of 30.30% in group B (P<0.05). The rate of adverse events was similar in two groups.CONCLUSION: Oxymatrine capsule is effective and safe in treatment of hepatic fibrosis due to chronic viral hepatitis.INTRODUCTIONHepatic fibrosis is a kind of compensating and healing response in the liver to liver injury induced by a variety of causes and also a common pathological process of many chronic liver diseases characterized by hyperplasia and deposition of fibro-connective tissues. It is essential to block the genesis and progress of hepatic fibrosis[1-5,30,31]. Oxymatrine is a kind of alkaloid extracted from a Chinese herb Sophora alopecuraides L. which has been proved to have antihepatic fibrosis effect[6,7,18-20]. In this paper, we reported the clinical study data of oxymatrine capsule in treatment of hepatic fibrosis in patients with chronic viral hepatitis.MATERIALS AND METHODSResarch designThis study was a clinical trial characterized by multicentre, randomization, double blinding, and placebo-control. Enrolled patients were randomly assigned into oxymatrine capsule group(group A) or vacant placebo control group (group , with 72 cases in each group and a treatment course of 52 wk. This study was conformed to the Good Clinical Practice (GCP) of China. The research protocol was discussed and approved by the Ethic Committee of National Clinical Research Base of Drugs in the Institute of Digestive Disease of Renji Hospital. Informed consent was obtained from each patient.Selection of subjectsEnrolled criteria were age: 18-65 years regardless of sex; positive serum markers of hepatitis B virus (HBV) and hepatitis C virus(HCV) for at least 6 mo before enrollment; abnormal serum value of alanine transaminase (ALT) twice or more within 6 mo before enrollment; liver biopsy examination during 1 mo before enrollment indicating the stage of hepatic fibrosis from 1 to 4 according to National Criteria of Grading and Staging for chronic viral hepatitis amended in 1995 and the scores of stage equal or more than 1 assessed by the semi-quantitative scoring system(SSS) of hepatic fibrosis; total serum bilirubin level less than or equal to 85.5 mmol/L; no history of administrating following drugs: antiviral drugs, immunoregulating drugs and other antifibrotic agents; promising not to receive other systemic antiviral agents, cytotoxic agents, immunoregulators, drugs capable of reducing serum enzyme activity and bilirubin level, and Chinese traditional medicines, etc. Following situations should be excluded: patients with positive laboratory test of HIV; uncompensable liver diseases; suggestive of autoimmune diseases with antinuclear antibody (ANA) titer greater than a 1:160 dilution; bone marrow inhibition; abnormality of serum creatinine with a value 1.5 times greater than normal; concurrence of other associated diseases which might affect the present treatment such as unstable diabetes, renal insufficiency, unstable angina pectoris, alcoholic liver disease, epilepsy, obvious manifestations of neurosis, drug abuser, psychosis, pancreatitis, disability of absorption and malignant disease, and so on; Having taken other drugs in clinical trial within 30 d before the first medication; hypersensitive to oxymatrine capsule; pregnancy and during breast-feeding period; female conceptive patients not adopting any contraceptives.Treatment procedures and drugsAfter completion of selection and assessment, qualified subjects were allocated into group A or B randomly. The patients in group A took 300 mg oxymatrine capsules orally 3 times a day, and 2 tablets of complex vitamins B and C at the same time for 52 wk. The patients in group B took 3 tablets of vacant capsules instead of oxymatrine capsules and complex vitamins B and C at the same frequency as described above for 52 wk. All patients received follow-up once every 12 wk during treatment and were followed up at out-patient department 12 wk after treatment. Oxymatrine capsule, vacant placebo capsule, complex vitamins B and C tablets were manufactured and provided by Ningxia Pharmaceutic Institute and Shanghai Green Valley Ecological Engineering Co.LTD.Observation of indexes and assessmentClinical manifestations Clinical symptoms and signs were divided into grades from 0 to 3 according to the symptomatic grading criteria , evaluated at each follow-up visit, and examined 24 and 52 wk after treatment and 12 wk after drug withdrawal.Analysis of blood and urine routines and related liver function indexes These indexes were evaluated at each follow-up visit and examined 52 wk after treatment and 12 wk after drug withdrawal.Analysis of serum markers of hepatic fibrosis Tests of serum hyaluronic acid (HA), laminin (LN), type III procollagenic peptide (p III p), type IV collagen-7S (IV-7S) were fulfilled by Military Clinical Immunologic Research Centre of Changzheng Hospital, Second Military Medical University. The above markers were evaluated before treatment, 24 and 52 wk after treatment,12 wk after drug withdrawal respectively, and examined 24 and 52 wk after treatment,12 wk after drug withdrawal, respectively.Imaging examination (type B ultrasound) The detection included 5 indexes: maximal oblique radius of right liver lobe, main trunk diameter of portal vein and its blood flow parameters per minute; width of spleen at the hilus and the diameter of spleenic vein. Ultrasound examination was performed on fixed machines and by fixed operators and the data were recorded and input in computers which were read by experts. All the indexes were evaluated before treatment and 52 wk after therapy, examined 52 wk after drug withdrawal.Histopathological detection Histopathological specimens were independently observed and assessed based on National Criteria of Grading and Staging for chronic viral hepatitis amended in 1995 and SSS by 3 pathologists from Department of Pathology, Medical College, Fudan University. The observed results were checked by another 3 pathologists who did not anticipate in the study by Kappa test. The reciprocal consistence among the above pathologists was satisfactory. The observed results in all patients were evaluated before therapy and part of them were evaluated 52 wk after therapy. All data were examined 52 wk after therapy. During treatment and after therapy was terminated, the following events were recorded: combined medication, adverse reactions and the compliance of patients.Assessment of therapeutic effectsIndexes of histopathology The curative effect was evaluated based on SSS. Distinctly effective: the scores of hepatic fibrosis based on SSS from liver biopsy decreased at least 6 scores compared with that before treatment. Effective: the above scores decreased at least 2 scores. Ineffective: the effect did not meet the effective criteria.Assessment of indexes of noninvasive tests These indexes were evaluated comprehensively in terms of clinical manifestations, serum liver fibrotic markers and ultrasound detection data. Distinctly effective: any two values among serum liver fibrotic indexes decreased by at least 80% compared with that before treatment, at least the main trunk diameter of portal vein and splenic width returned to normal after treatment, clinical symptoms and signs disappeared or their total scores decreased by at least 75% compared with that before treatment. Effective: any two values among serum liver fibrotic indexes decreased by at least 40% compared with that before treatment, the main trunk diameter of portal vein and splenic width reduced after treatment, clinical symptoms and signs disappeared basically or their total scores decreased by at least 25% compared with that before treatment. Ineffective: the effect did not meet the effective criteria.Assessment of safetyAny abnormal clinical manifestations and laboratory tests occurred during treatment were recorded and divided into 4 grades according to the criteria published by WHO and the Ministry of Public Health of China in 1994.Statistical analysisStatistical analyses were performed by professor Su BH and He QB from Department of Statistics, Shanghai Second Medical University, and SAS 6.12 software kit was used.RESULTSSelected patientsA total of 144 patients satisfied the selection criteria. Of them,12 cases withdrew or were excluded during treatment, 132 cases fulfilled the treatment course according to the required protocol(66 cases in group A and 66 cases in group . Before treatment, the following general data between two groups were similar (P>0.05, respectively): sex, age, drinking history, duration of hepatitis, duration of abnormality of liver function and a more than 2-fold normal elevation of serum ALT, etc. Each qualified patient received liver biopsy before treatment. A total of 49 cases had a second liver biopsy (25 cases in group A and 24 cases in group .Analysis of observed indexesClinical symptoms and signs Clinical manifestations in group A were obviously improved 52 wk after therapy (P<0.05), except for epistaxis (P = 1.0000). Heptomegaly was also improved significantly after therapy (P = 0.0313), symptoms of gum bleeding and epistaxis were not improved obviously in group B (P>0.05). Signs of hepatomegaly, splenomegaly and liver palm were significantly improved in group B (P<0.05), improvement of anorexia in group A was greater than that in group B (P = 0.0263).Liver function Indexes of liver function in group A were significantly improved 52 wk after treatment (P<0.05) except for serum gamma glutamino transpeptidase (GGT) and TB (P>0.05). In group B, indexes such as serum ALT, AST, TB and alkaline phosphatase (ALP) had no obvious difference before and after therapy (P>0.05). Compared with group B, the improvement of ALT and AST in group A was much greater (P = 0.0007 and 0.0025). Fifty-two wk after therapy, the normalization rate of ALT in group A was 70.77%, much higher than 39.68% in group B (P = 0.0003). In groups A and B, 14 out of 46 cases (30.43%) and 12 out of 25 cases (48.00%) had their serum ALT levels returned to normal 52 wk after treatment ,and their serum ALT levels became abnormal again after drug withdrawal.Liver histologic examination Evaluation of hepatic fibrosis based on SSS: In group A, the scores of hepatic fibrosis after therapy were 4.72±5.63, much smaller than 6.76±6.67 before therapy (P = 0.0001), while the scores in group B after therapy increased significantly (P = 0.0009). There was an obvious difference between two groups (P = 0) (Table 1). Evaluation of histolgic inflammatory activity based on SSS: In group A, the scores of histologic activity decreased from 46.08±3.84 before treatment to 4.00±2.97 after therapy (P = 0.0002), while the scores in group B after therapy did not decrease obviously (P = 0.2344). There was an obvious difference between two groups (P = 0008) (Table 2).Evaluation of serum markers of hepatic fibrosis In group A, serum levels of HA, LN, p III p and IV-7S decreased significantly 24 and 52 wk after treatment (P<0.05). In group B, serum levels of LN, p III p and IV-7S also decreased obviously after treatment(P<0.05). However, degrees of improvement in HA and p III p between two groups were distinctly different (P<0.05). In group A, except for LN (P = 0.1493), the other 3 liver fibrotic markers increased significantly 12 wk after drug withdrawal compared with that 52 wk after treatment (P<0.05). In group B, except for HA (P = 0.4212), the other markers also increased obviously 12 wk after drug withdrawal compared with that 52 wk after treatment(P<0.05). The increase of HA in group A was more than that in group B (P = 0.0002) and the increase of IV-7S in group B was more than that in group A (P = 0.0048).Imaging examination After treatment, the average values of main trunk diameters of portal vein and splenic width in group A obviously decreased (P<0.05). However, in group B, the above two parameters and the parameters of blood flow volume per minute of portal vein and diameters of splenic vein all increased significantly compared with those before therapy (P<0.05). The changes in main trunk diameters of portal vein and splenic width between two groups were statistically significant (P<0.05).Analysis of therapeutic effectAssessment of histopathology based on SSS After treatment, the rates of distinct effectiveness and effectiveness in group A were both 24.00%, and the total effective rate was 48.00%. In group B, none achieved distinct effectiveness and the effective rate was only 4.17%; Comparison of the rates of distinct effectiveness and effectiveness between two groups had a significant difference (P = 0.004) (Table 3).Assessment of serum markers of hepatic fibrosis The total effective rate of group A 24 and 52 wk after therapy was 57.43% and 68.19%, more than 24.24% and 34.85% of group B (P = 0.0002 and 0.0004, respectively). Twelve weeks after treatment, the total effective rate of group A was 50.00%, more than 15.16% of group B (P =0.00).Assessment of noninvasive indexes of hepatic fibrosis After treatment, the rates of distinct effectiveness and effectiveness in group A were respectively 3.03% and 63.64%, and the total effective rate was 66.67%. In group B, the rates of distinct effectiveness and effectiveness were respectively 0% and 30.30%, and the total effective rate was 30.30%. The comparison of the above statistics between two groups had a significant difference (P = 0.0001) (Table 4).Adverse effectsIn group A, there were 5 patients who suffered from adverse drug reactions and the incidence was 6.94%. The adverse drug reactions mainly included nausea, rash, chest discomfort, fever, epigastric comfort, diarrhea and poor taste, and most of them were mild or moderate. None of the patients withdrew because of adverse drug reactions. In group B, adverse effects occurred in 7 patients and the incidence was 9.72%. The manifestations were similar to those in group A and 1 patient withdrew because of weakness, anorexia, epigastric discomfort after taking drugs.DISCUSSIONHepatic fibrosis, a precuror of cirrhosis, is a consequence of sever liver damage that occurred in many patients with chronic liver disease, and involves the abnormal accumulation of extracellular matrix[3,4,11,12]. Liver fibrosis represents a major worldwide healthcare burden. Current therapy is limited to removing the causal agent. This approach has been successful in some diseases, particularly in haemochromatosis and chronic viral hepatitis[9,10,17,28]. However, for many patients treatment was not possible, while other patients presenting to medical attention were at an advanced stage of fibrosis[8,9]. There is therefore a great need for novel therapies for liver fibrosis. Tremendous insights into the understanding of hepatic fibrosis have taken place over the past ten years. Foremost among these is the recognition that hepatic stellate cells (formerly known as lipocytes, Ito cells, or fat-storing cells) play a central role based on their ability to undergo activation following liver injury of any cause[11,15,16,29]. Hepatic stellate cells have been recognised to be responsible for most of the excess extracellular matrix observed in chronic liver fibrosis. The detailed understanding of hepatic stellate cell biology has allowed the rational design of novel antifibrotic therapies[29]. Effective therapy for hepatic fibrogenesis would probably also be multifactorial, based on the basic mechanisms underlying the fibrogenic process[13,14,21-23].At present, it is considered that treatment of hepatic fibrosis and antihepatic fibrosis are two different concepts and antifibrotic drugs should act on various parts of the genesis and development of hepatic fibrosis. Firstly, as for etiological treatment, oxymatrine could effectively treat chronic viral hepatitis and promote the serum markers of hepatitis B virus (HBV) and hepatitis C virus(HCV) in chronic hepatitis B and C to convert to negative and reduce serum level of ALT[6,7]. Secondly, oxymatrine could inhibit the proliferation of hepatic stellate cells (HSC) at the concentrations of 0.5-16 mg/mL in vitro. In addition, oxygen stress and lipid peroxidation are important mechanisms responsible for hepatic injury and hepatic stellate cell activation. Therefore, inhibition of lipid peroxidation is an essential strategy of antihepatic fibrosis[12-16]. By establishing D-galactosamine-induced rat liver fibrosis model, we observed the effect of oxymatrine on serum and tissue biochemical indexes, content of liver hydroxyline, expression of TGFb1 mRNA and changes of tissue pathology, the results showed oxymatrine had prophylactic and therapeutic effects on D-galactosamine induced rat liver fibrosis. This was partly by protecting hepatocytes and suppressing fibrosis accumulation through anti-lipoperoxidation[10]. In present study, We found that the scores of hepatic fibrosis after therapy in group A were 4.72±5.63, much smaller than 6.76±6.67 before therapy, and the scores in group B after therapy increased significantly. There was an obvious difference between two groups. 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