Effect of anluohuaxian tablet combined with γ-IFN on schistosomal liver fibrosis

Jiaquan Huang , Haiyan Huang , Yuntao Jiao , Guo Ai , Tiejun Huang , Lan Li , Haijing Yu , Ke Ma , Fei Xiao

Current Medical Science ›› 2009, Vol. 29 ›› Issue (1) : 53 -58.

PDF
Current Medical Science ›› 2009, Vol. 29 ›› Issue (1) : 53 -58. DOI: 10.1007/s11596-009-0111-7
Article

Effect of anluohuaxian tablet combined with γ-IFN on schistosomal liver fibrosis

Author information +
History +
PDF

Abstract

The therapeutic effects of anluohuaxian tablet combined with γ-IFN on schistosomal liver fibrosis and its mechanism were studied in a murine model and clinical cases of schistosomal liver fibrosis. Fifty Kunming mice were randomly divided into 5 groups: normal control group, infection control group, anluohuaxian tablet-treated group, γ-IFN-treated group and combined treatment (anluohuaian tablet+γ-IFN) group. Pathologic changes in liver, including hepatic pigmentation and the size of schistosomal egg granuloma, were observed by HE staining after treatment for 8 weeks. The expression of the type I and collagen III, and TIMP-1 was detected by immunohistochemistry. TGF-β1 mRNA expression was examined by real-time fluorescent quantitative PCR. Sixty patients with schistosomal liver fibrosis were divided into treatment group and control group. The patients in treatment group were treated with anluohuaxian tablet in combination with γ-IFN for 6 months. Before and after treatment, the changes of symptoms and signs, liver function, serum liver fibrosis indexes and imaging indexes were observed. The results showed that as compared with infection control group, all forms of treatments relieved the hepatic pathological injury with apparently diminished size of schistosomal egg nodules and decreased percentage of pigmentation (P<0.05). Furthermore, the expression of collagen I and III, TIMP-1, and TGF-β1 mRNA in combined treatment group was significantly decreased as compared with anluohuaxian tablet-treated and γ-IFN-treated groups (P<0.05). In the clinical observation, the serum liver fibrosis indexes, the portal vein width as well as the spleen thickness was significantly reduced in treatment group as compared with control group (P<0.05). It was concluded that the combined use of anluohuaxian tablet with γ-IFN in schistosomal liver fibrosis could protect liver function, alleviate liver fibrosis, and could be used as a choice in treating patients with schiatosomal liver fibrosis.

Keywords

Schistosomiasis japonica / liver fibrosis / anluohuaxian tablet / γ-interferon / hepatic pigmentation / TIMP-1 / TGF-β1 mRNA

Cite this article

Download citation ▾
Jiaquan Huang, Haiyan Huang, Yuntao Jiao, Guo Ai, Tiejun Huang, Lan Li, Haijing Yu, Ke Ma, Fei Xiao. Effect of anluohuaxian tablet combined with γ-IFN on schistosomal liver fibrosis. Current Medical Science, 2009, 29(1): 53-58 DOI:10.1007/s11596-009-0111-7

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

WengH.L., CaiW.M., WangB.E., et al. . Clinical study of anti-hepatic fibrosis effect of γ-IFN in patients with chronic hepatitis B. Chin Med J (Chinese), 2003, 83(11): 943-947

[2]

ChengG.Z., MaoD.W., LiG.X., et al. . Effects of Anluohuaxian capsule on hepatic fibrosis indexes in patients with chronic hepatitis. Chin J Integ Tradit Western Med Dig (Chinese), 2005, 13(2): 1099

[3]

National Standard GB15977-1995 (China). Diagnostic criteria and principles of management of schistosomiasis[S]

[4]

Hepatic fibrosis Group under Chinese Liver Disease Association.. Common understanding of diagnosis and effect of hepatic fibrosis. Chin J Hepatol (Chinese), 2002, 10(5): 327-328

[5]

WuW.L., CaiW.M., ChenM.G., et al. . Blueprint for the diagnosis and assessment of therapeutic efficacy in liver fibrosis due to schistosomiasis. Chin J Schistosomiasis Control (Chinese), 2004, 16(3): 229-230

[6]

FriedmanS.L.. Liver fibrosis—from bench to bedside. J Hepatol, 2003, 38(Suppl1): 38

[7]

WuW.L., ZhouX.Z., HuangY.Y., et al. . Long-term efficacy of pyquiton on Schistosomiasis japonica. Chin J Infect Dis (Chinese), 2004, 22(4): 238-241

[8]

BatallerR., BrennerD.A.. Liver fibrosis. J Clin Invest, 2005, 1(2): 209-218

[9]

ShekF.W., BenyonR.C.. How can transforming growth factor beta be targeted usefully to combat liver fibrosis?. J Eur J Gastro Enterol Hepato, 2004, 16(2): 123-126

[10]

HerbsT.H., WegeT., MilaniS., et al. . Tissue inhibitor of metalloproteinase-1 and -2 RNA expression in rat and human liver fibrosis. Am J Pathol, 1997, 150: 1647-1659

[11]

MurphyF.R., IssaR., ZhouX., et al. . Inhibition of apoptosis of activated hepatic stellate cells by tissue inhibitor of metalloproteinase-1 is mediated via effects on matrix metalloproteinase inhibition: implications for reversibility of liver fibrosis. J Biol Chem, 2002, 277: 11 069-11 076

[12]

ChenX.B., WuG.L., SunX., et al. . Modern Parasitology (Chinese), 2002, Beijing, People’s Military Medical Press: 638

[13]

MaH., ZhuY.K., MaX.M., et al. . Effects of γ-interferon on gene expression of collagen I, III and tissue inhibito of metalloproteinase 1 in dimethylnitrosamine-induced liver fibrosis in rats. Chin Hepatol, 2005, 10: 92-94

[14]

TaoJ., CaiW.M., ZhangB.B., et al. . Pigment deposit in liver of BALB/c mice infected by Schistosoma japonicum and its relation to the effect of praziquantel treatment. Chin J Parasitol Parasitic Dis (Chinese), 2006, 24(1): 79-80

[15]

HurstM.H., WillinghamA.L.3rd, LindbergR.. Tissue responses in experimental schistosomiasis japonica in the pig: a histopathologic study of different stages of single low- or high-dose infections. Am J Trop Med Hyg, 2000, 62(1): 45-50

AI Summary AI Mindmap
PDF

80

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/