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- Publisher Website: 10.1016/j.jep.2011.09.032
- Scopus: eid_2-s2.0-82455210880
- PMID: 21963555
- WOS: WOS:000298897800006
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Article: Hepatoprotective effect and its possible mechanism of Coptidis rhizoma aqueous extract on carbon tetrachloride-induced chronic liver hepatotoxicity in rats
Title | Hepatoprotective effect and its possible mechanism of Coptidis rhizoma aqueous extract on carbon tetrachloride-induced chronic liver hepatotoxicity in rats |
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Authors | |
Keywords | Anti-oxidant agent Chronic liver damage Coptidis rhizoma Erk1/2 inhibition Hepatoprotective effect |
Issue Date | 2011 |
Publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/jethpharm |
Citation | Journal of Ethnopharmacology, 2011, v. 138 n. 3, p. 683-690 How to Cite? |
Abstract | Ethnopharmacological relevance: Coptidis rhizoma is traditionally used for heat-clearing and toxic-scavenging and it belongs to liver meridian in Chinese medicine practice. Clinically, Coptidis rhizoma can be used for hepatic and biliary disorders, yet details in the therapies of liver diseases and underlying mechanism(s) remain unclear. Our previous study demonstrated that Coptidis rhizoma aqueous extract (CRAE) against CCl 4-induced acute liver damage was related to antioxidant property. In the present study, the protection of CRAE on chronic liver damage induced by carbon tetrachloride (CCl 4) in rats and its related mechanism were explored. Materials and methods: The CCl 4-induced chronic liver damage model was established, and CRAE's protective effect was examined. Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activity, serum and liver superoxide dismutase (SOD) activity were then measured. The histological changes were observed under microscopy and then computed in numerical score. The normal or damaged cells were isolated and related signaling pathway was evaluated. Result: Serum AST and ALT activities were significantly decreased in rats treated with different doses of CRAE, indicating its protective effect against CCl 4-induced chronic liver damage. Observation on serum SOD activity revealed that CRAE might act as an anti-oxidant agent against CCl 4-induced chronic oxide stress. Histological study supported these observations. Erk1/2 inhibition may take part into CRAE's effect on preventing hepatocyte from apoptosis when exposed to oxidative stress. Conclusion: CRAE showed protective effect against CCl 4-induced chronic liver damage in rats and its potential as an agent in the treatment of chronic liver diseases by protecting hepatocyte from injury. © 2011 Elsevier Ireland Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/166186 |
ISSN | 2023 Impact Factor: 4.8 2023 SCImago Journal Rankings: 0.936 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Feng, Y | en_HK |
dc.contributor.author | Wang, N | en_HK |
dc.contributor.author | Ye, X | en_HK |
dc.contributor.author | Li, H | en_HK |
dc.contributor.author | Feng, YG | en_HK |
dc.contributor.author | Cheung, F | en_HK |
dc.contributor.author | Nagamatsu, T | en_HK |
dc.date.accessioned | 2012-09-20T08:30:00Z | - |
dc.date.available | 2012-09-20T08:30:00Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Journal of Ethnopharmacology, 2011, v. 138 n. 3, p. 683-690 | en_US |
dc.identifier.issn | 0378-8741 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/166186 | - |
dc.description.abstract | Ethnopharmacological relevance: Coptidis rhizoma is traditionally used for heat-clearing and toxic-scavenging and it belongs to liver meridian in Chinese medicine practice. Clinically, Coptidis rhizoma can be used for hepatic and biliary disorders, yet details in the therapies of liver diseases and underlying mechanism(s) remain unclear. Our previous study demonstrated that Coptidis rhizoma aqueous extract (CRAE) against CCl 4-induced acute liver damage was related to antioxidant property. In the present study, the protection of CRAE on chronic liver damage induced by carbon tetrachloride (CCl 4) in rats and its related mechanism were explored. Materials and methods: The CCl 4-induced chronic liver damage model was established, and CRAE's protective effect was examined. Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activity, serum and liver superoxide dismutase (SOD) activity were then measured. The histological changes were observed under microscopy and then computed in numerical score. The normal or damaged cells were isolated and related signaling pathway was evaluated. Result: Serum AST and ALT activities were significantly decreased in rats treated with different doses of CRAE, indicating its protective effect against CCl 4-induced chronic liver damage. Observation on serum SOD activity revealed that CRAE might act as an anti-oxidant agent against CCl 4-induced chronic oxide stress. Histological study supported these observations. Erk1/2 inhibition may take part into CRAE's effect on preventing hepatocyte from apoptosis when exposed to oxidative stress. Conclusion: CRAE showed protective effect against CCl 4-induced chronic liver damage in rats and its potential as an agent in the treatment of chronic liver diseases by protecting hepatocyte from injury. © 2011 Elsevier Ireland Ltd. All rights reserved. | en_HK |
dc.language | eng | en_US |
dc.publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/jethpharm | en_HK |
dc.relation.ispartof | Journal of Ethnopharmacology | en_HK |
dc.subject | Anti-oxidant agent | - |
dc.subject | Chronic liver damage | - |
dc.subject | Coptidis rhizoma | - |
dc.subject | Erk1/2 inhibition | - |
dc.subject | Hepatoprotective effect | - |
dc.subject.mesh | Rats, Sprague-Dawley | en_HK |
dc.subject.mesh | Rats | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | MAP Kinase Signaling System - drug effects | en_HK |
dc.subject.mesh | Hepatocytes - drug effects - metabolism | en_HK |
dc.subject.mesh | Drugs, Chinese Herbal - analysis - therapeutic use | en_HK |
dc.subject.mesh | Drug-Induced Liver Injury - blood - drug therapy - pathology | en_HK |
dc.subject.mesh | DNA Fragmentation - drug effects | en_HK |
dc.subject.mesh | Caspase 3 - metabolism | en_HK |
dc.subject.mesh | Carbon Tetrachloride | en_HK |
dc.subject.mesh | Aspartate Aminotransferases - blood | en_HK |
dc.subject.mesh | Apoptosis - drug effects | en_HK |
dc.subject.mesh | Animals | en_HK |
dc.subject.mesh | Alanine Transaminase - blood | en_HK |
dc.title | Hepatoprotective effect and its possible mechanism of Coptidis rhizoma aqueous extract on carbon tetrachloride-induced chronic liver hepatotoxicity in rats | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0378-8741&volume=138&issue=3&spage=683&epage=690&date=2011&atitle=Hepatoprotective+effect+and+its+possible+mechanism+of+Coptidis+rhizoma+aqueous+extract+on+carbon+tetrachloride-induced+chronic+liver+hepatotoxicity+in+rats | en_US |
dc.identifier.email | Feng, Y: yfeng@hku.hk | en_HK |
dc.identifier.email | Wang, N: ckwang@hku.hk | - |
dc.identifier.email | Ye, X: xiujuany@hku.hk | - |
dc.identifier.email | Cheung, F: h0180012@HKUSUC.hku.hk | - |
dc.identifier.email | Nagamatsu, T: nagamats@ccmfs.meijo-u.ac.jp | - |
dc.identifier.authority | Feng, Y=rp00466 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.jep.2011.09.032 | en_HK |
dc.identifier.pmid | 21963555 | - |
dc.identifier.scopus | eid_2-s2.0-82455210880 | en_HK |
dc.identifier.hkuros | 208639 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-82455210880&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 138 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 683 | en_HK |
dc.identifier.epage | 690 | en_HK |
dc.identifier.eissn | 1872-7573 | - |
dc.identifier.isi | WOS:000298897800006 | - |
dc.publisher.place | Ireland | en_HK |
dc.identifier.scopusauthorid | Nagamatsu, T=7006510058 | en_HK |
dc.identifier.scopusauthorid | Cheung, F=54796436400 | en_HK |
dc.identifier.scopusauthorid | Feng, Y=36983738700 | en_HK |
dc.identifier.scopusauthorid | Li, H=54796615400 | en_HK |
dc.identifier.scopusauthorid | Ye, X=35277763000 | en_HK |
dc.identifier.scopusauthorid | Wang, N=35072317700 | en_HK |
dc.identifier.scopusauthorid | Feng, Y=24467969600 | en_HK |
dc.identifier.citeulike | 9824250 | - |
dc.identifier.issnl | 0378-8741 | - |