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Article: Effect of WeiJia on carbon tetrachloride induced chronic liver injury
Title | Effect of WeiJia on carbon tetrachloride induced chronic liver injury |
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Authors | |
Keywords | Carbon tetrachloride Liver fibrosis WeiJia |
Issue Date | 2006 |
Publisher | Baishideng Publishing Group. The Journal's web site is located at http://www.wjgnet.com/1007-9327/index.htm |
Citation | World Journal Of Gastroenterology, 2006, v. 12 n. 12, p. 1912-1917 How to Cite? |
Abstract | Aim: To study the effect of WeiJia on chronic liver injury using carbon tetrachloride (CCl 4) induced liver injury animal model. Methods: Wista r rats weighing 180-220g were randomly divided into three groups: normal control group (Group A), CCl 4 induced liver injury control group (Group B) and CCl 4 induction with WeiJia treatment group (Group C). Each group consisted of 14 rats. Liver damage and fibrosis was induced by subcutaneous injection with 40% CCl 4 in olive oil at 3 mL/kg body weight twice a week for eight weeks for Groups B and C rats whereas olive oil was used for Group A rats. Starting from the third week, Group C rats also received daily intraperitoneal injection of WeiJia at a dose of 1.25 μg/kg body weight. Animals were sacrificed at the fifth week (4 male, 3 female), and eighth week (4 male, 3 female) respectively. Degree of fibrosis were measured and serological markers for liver fibrosis and function including hyaluronic acid (HA), type IV collagen (CIV), γ-glutamyl transferase (γ-GT), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were determined. Alpha smooth muscle actin (α-SMA) and proliferating cell nuclear antigen (PCNA) immunohistochemistry were also performed. Results: CCl 4 induction led to the damage of liver and development of fibrosis in Group B and Group C rats when compared to Group A rats. The treatment of WeiJia in Group C rats could reduce the fibrosis condition significantly compared to Group B rats. The effect could be observed after three weeks of treatment and was more obvious after eight weeks of treatment. Serum HA, CIV, ALT, AST and γ-GT levels after eight weeks of treatment for Group C rats were 58±22 μg/L (P<0.01), 57±21 μg/L (P<0.01), 47±10 U/L (P<0.01), 139±13 U/L (P<0.05) and 52±21 U/L (P> 0.05) respectively, similar to normal control group (Group A), but significantly different from CCl 4 induced liver injury control group (Group B). An increase in PCNA and decrease in α-SMA expression level was also observed. Conclusion: WeiJia could improve liver function and reduce liver fibrosis which might be through the inhibition of stellate cell activity. © 2006 The WJG Press. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/69299 |
ISSN | 2023 Impact Factor: 4.3 2023 SCImago Journal Rankings: 1.063 |
PubMed Central ID | |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Cheung, PY | en_HK |
dc.contributor.author | Zhang, Q | en_HK |
dc.contributor.author | Zhang, YO | en_HK |
dc.contributor.author | Bai, GR | en_HK |
dc.contributor.author | Lin, MCM | en_HK |
dc.contributor.author | Chan, B | en_HK |
dc.contributor.author | Fong, CC | en_HK |
dc.contributor.author | Shi, L | en_HK |
dc.contributor.author | Shi, YF | en_HK |
dc.contributor.author | Chun, J | en_HK |
dc.contributor.author | Kung, HF | en_HK |
dc.contributor.author | Yang, MS | en_HK |
dc.date.accessioned | 2010-09-06T06:12:23Z | - |
dc.date.available | 2010-09-06T06:12:23Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | World Journal Of Gastroenterology, 2006, v. 12 n. 12, p. 1912-1917 | en_HK |
dc.identifier.issn | 1007-9327 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/69299 | - |
dc.description.abstract | Aim: To study the effect of WeiJia on chronic liver injury using carbon tetrachloride (CCl 4) induced liver injury animal model. Methods: Wista r rats weighing 180-220g were randomly divided into three groups: normal control group (Group A), CCl 4 induced liver injury control group (Group B) and CCl 4 induction with WeiJia treatment group (Group C). Each group consisted of 14 rats. Liver damage and fibrosis was induced by subcutaneous injection with 40% CCl 4 in olive oil at 3 mL/kg body weight twice a week for eight weeks for Groups B and C rats whereas olive oil was used for Group A rats. Starting from the third week, Group C rats also received daily intraperitoneal injection of WeiJia at a dose of 1.25 μg/kg body weight. Animals were sacrificed at the fifth week (4 male, 3 female), and eighth week (4 male, 3 female) respectively. Degree of fibrosis were measured and serological markers for liver fibrosis and function including hyaluronic acid (HA), type IV collagen (CIV), γ-glutamyl transferase (γ-GT), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were determined. Alpha smooth muscle actin (α-SMA) and proliferating cell nuclear antigen (PCNA) immunohistochemistry were also performed. Results: CCl 4 induction led to the damage of liver and development of fibrosis in Group B and Group C rats when compared to Group A rats. The treatment of WeiJia in Group C rats could reduce the fibrosis condition significantly compared to Group B rats. The effect could be observed after three weeks of treatment and was more obvious after eight weeks of treatment. Serum HA, CIV, ALT, AST and γ-GT levels after eight weeks of treatment for Group C rats were 58±22 μg/L (P<0.01), 57±21 μg/L (P<0.01), 47±10 U/L (P<0.01), 139±13 U/L (P<0.05) and 52±21 U/L (P> 0.05) respectively, similar to normal control group (Group A), but significantly different from CCl 4 induced liver injury control group (Group B). An increase in PCNA and decrease in α-SMA expression level was also observed. Conclusion: WeiJia could improve liver function and reduce liver fibrosis which might be through the inhibition of stellate cell activity. © 2006 The WJG Press. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Baishideng Publishing Group. The Journal's web site is located at http://www.wjgnet.com/1007-9327/index.htm | en_HK |
dc.relation.ispartof | World Journal of Gastroenterology | en_HK |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Carbon tetrachloride | en_HK |
dc.subject | Liver fibrosis | en_HK |
dc.subject | WeiJia | en_HK |
dc.title | Effect of WeiJia on carbon tetrachloride induced chronic liver injury | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1007-9327&volume=12&issue=12&spage=1912&epage=1917&date=2006&atitle=Effect+of+WeiJia+on+carbon+tetrachloride+induced+chronic+liver+injury | en_HK |
dc.identifier.email | Lin, MCM:mcllin@hkucc.hku.hk | en_HK |
dc.identifier.authority | Lin, MCM=rp00746 | en_HK |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.3748/wjg.v12.i12.1912 | - |
dc.identifier.pmid | 16609998 | - |
dc.identifier.pmcid | PMC4087517 | - |
dc.identifier.scopus | eid_2-s2.0-33645963113 | en_HK |
dc.identifier.hkuros | 115278 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33645963113&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 12 | en_HK |
dc.identifier.issue | 12 | en_HK |
dc.identifier.spage | 1912 | en_HK |
dc.identifier.epage | 1917 | en_HK |
dc.identifier.isi | WOS:000239996000012 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Cheung, PY=7202595426 | en_HK |
dc.identifier.scopusauthorid | Zhang, Q=35515964300 | en_HK |
dc.identifier.scopusauthorid | Zhang, YO=16176894000 | en_HK |
dc.identifier.scopusauthorid | Bai, GR=7103085757 | en_HK |
dc.identifier.scopusauthorid | Lin, MCM=7404816359 | en_HK |
dc.identifier.scopusauthorid | Chan, B=13005652300 | en_HK |
dc.identifier.scopusauthorid | Fong, CC=11739503800 | en_HK |
dc.identifier.scopusauthorid | Shi, L=55254757000 | en_HK |
dc.identifier.scopusauthorid | Shi, YF=7404963405 | en_HK |
dc.identifier.scopusauthorid | Chun, J=13005621200 | en_HK |
dc.identifier.scopusauthorid | Kung, HF=7402514190 | en_HK |
dc.identifier.scopusauthorid | Yang, MS=35204210300 | en_HK |
dc.identifier.issnl | 1007-9327 | - |