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Conference Paper: Comparison on the therapeutic action of coptis and bear bile on experimental liver fibrosis
Title | Comparison on the therapeutic action of coptis and bear bile on experimental liver fibrosis |
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Authors | |
Issue Date | 2013 |
Publisher | OMICS Group Conferences. The Conference abstract's web site is located at http://omicsgroup.com/conferences/bioequivalence-bioavailability-2013/posters.php |
Citation | The 4th World Congress on Bioavailability and Bioequivalence: Pharmaceutical R&D Summit, Beijing, China, 20-22 May 2013 How to Cite? |
Abstract | Bear bile is a Chinese Medicine that was used to treat liver diseases for thousands of years. However, the use of
bear bile in Chinese Medicine clinical practice has received a lot of challenges since bears are currently
endangered. It is a ethical problem that obtaining bile juice from the animals. Coptis is a Chinese Medicine that
has been used to treat heat-related diseases in clinical practice and our clinical observation has found that Coptis is
effective in curing liver diseases. The aim of study is to investigate if the therapeutic effect of Coptis is
comparable with bear bile on the experimental hepatic fibrosis models. CCl4-, bile duct ligation- (BDL-) and
alcohol-induced liver fibrosis models were used in this study and the therapeutic effects of Coptis and bear bile
were evaluated. The chemical composition of Coptis and bear bile was analyzed by high performance liquid
chromatography (HPLC). It was observed that the major active components of Coptis was berberine and
berberine-like alkaloids and the major compounds in bear bile was Tauroursodeoxycholic acid (TUDCA).
Significant induction on the Hyp content, the biomarker of liver fibrosis in tissue, was observed (p < 0.05). Drug
intervention could reduce the Hyp content in modeled rats (p < 0.05). The effect of Coptis is comparable with Bear
bile (p > 0.05). However, it was observed that BB (TUDCA) might exhibit better effect in inhibiting Hyp content
than Coptis did in hepatic fibrosis though no statistical significance could be found (p > 0.05). Both Coptis and
Bear bile exhibited potent therapeutic effect regarding the combined scores based on the examination of
hepatocyte death, inflammatory cell infiltration and fibrosis It was observed that both Coptis and Bear bile could
completely combat the liver fibrosis induced by alcohol, while Bear bile exhibited better effect on chemical toxin
CCl4-induced hepatic damage and fibrosis and Coptis showed potent action on BDL-induced fibrosis. In
conclusion, the anti-fibrotic action of Coptis was comparable to bear bile on the all three experimental animal
models. Coptis had the potential to replace bear bile for the treatment of liver diseases. |
Description | Poster Presentations |
Persistent Identifier | http://hdl.handle.net/10722/185193 |
DC Field | Value | Language |
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dc.contributor.author | Wang, N | en_US |
dc.contributor.author | Feng, Y | en_US |
dc.date.accessioned | 2013-07-15T10:40:18Z | - |
dc.date.available | 2013-07-15T10:40:18Z | - |
dc.date.issued | 2013 | en_US |
dc.identifier.citation | The 4th World Congress on Bioavailability and Bioequivalence: Pharmaceutical R&D Summit, Beijing, China, 20-22 May 2013 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/185193 | - |
dc.description | Poster Presentations | - |
dc.description.abstract | Bear bile is a Chinese Medicine that was used to treat liver diseases for thousands of years. However, the use of bear bile in Chinese Medicine clinical practice has received a lot of challenges since bears are currently endangered. It is a ethical problem that obtaining bile juice from the animals. Coptis is a Chinese Medicine that has been used to treat heat-related diseases in clinical practice and our clinical observation has found that Coptis is effective in curing liver diseases. The aim of study is to investigate if the therapeutic effect of Coptis is comparable with bear bile on the experimental hepatic fibrosis models. CCl4-, bile duct ligation- (BDL-) and alcohol-induced liver fibrosis models were used in this study and the therapeutic effects of Coptis and bear bile were evaluated. The chemical composition of Coptis and bear bile was analyzed by high performance liquid chromatography (HPLC). It was observed that the major active components of Coptis was berberine and berberine-like alkaloids and the major compounds in bear bile was Tauroursodeoxycholic acid (TUDCA). Significant induction on the Hyp content, the biomarker of liver fibrosis in tissue, was observed (p < 0.05). Drug intervention could reduce the Hyp content in modeled rats (p < 0.05). The effect of Coptis is comparable with Bear bile (p > 0.05). However, it was observed that BB (TUDCA) might exhibit better effect in inhibiting Hyp content than Coptis did in hepatic fibrosis though no statistical significance could be found (p > 0.05). Both Coptis and Bear bile exhibited potent therapeutic effect regarding the combined scores based on the examination of hepatocyte death, inflammatory cell infiltration and fibrosis It was observed that both Coptis and Bear bile could completely combat the liver fibrosis induced by alcohol, while Bear bile exhibited better effect on chemical toxin CCl4-induced hepatic damage and fibrosis and Coptis showed potent action on BDL-induced fibrosis. In conclusion, the anti-fibrotic action of Coptis was comparable to bear bile on the all three experimental animal models. Coptis had the potential to replace bear bile for the treatment of liver diseases. | - |
dc.language | eng | en_US |
dc.publisher | OMICS Group Conferences. The Conference abstract's web site is located at http://omicsgroup.com/conferences/bioequivalence-bioavailability-2013/posters.php | - |
dc.relation.ispartof | World Congress on Bioavailability and Bioequivalence: Pharmaceutical R&D Summit | en_US |
dc.title | Comparison on the therapeutic action of coptis and bear bile on experimental liver fibrosis | en_US |
dc.type | Conference_Paper | en_US |
dc.identifier.email | Wang, N: ckwang@hku.hk | en_US |
dc.identifier.email | Feng, Y: yfeng@hku.hk | en_US |
dc.identifier.authority | Feng, Y=rp00466 | en_US |
dc.identifier.hkuros | 215002 | en_US |
dc.identifier.hkuros | 217212 | - |
dc.publisher.place | United States | - |