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San Huang Shel Shin Tang beta-cyclodextrin complex augmented the hepatoprotective effects against carbon tetrachloride-induced acute hepatotoxicity in rats

BACKGROUND: San Huang Shel Shin Tang (SHSST) is a traditional herbal decoction used as a hepato-protective agent and is composed of Rheum officinale Baill, Scutellaria baicalnsis Geprgi and Coptis chinensis Franch (2:1:1 w/w). Beta-cyclodextrin (β-CD) modification may potentially increase the solubi...

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Autores principales: Yeh, Yu-Lan, Ting, Wei-Jen, Kuo, Wei-Wen, Hsu, Hsi-Hsien, Lin, Yueh-Min, Shen, Chia-Yao, Chang, Chung-Ho, Padma, Viswanadha Vijaya, Tsai, Yuhsin, Huang, Chih-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884430/
https://www.ncbi.nlm.nih.gov/pubmed/27234802
http://dx.doi.org/10.1186/s12906-016-1127-8
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author Yeh, Yu-Lan
Ting, Wei-Jen
Kuo, Wei-Wen
Hsu, Hsi-Hsien
Lin, Yueh-Min
Shen, Chia-Yao
Chang, Chung-Ho
Padma, Viswanadha Vijaya
Tsai, Yuhsin
Huang, Chih-Yang
author_facet Yeh, Yu-Lan
Ting, Wei-Jen
Kuo, Wei-Wen
Hsu, Hsi-Hsien
Lin, Yueh-Min
Shen, Chia-Yao
Chang, Chung-Ho
Padma, Viswanadha Vijaya
Tsai, Yuhsin
Huang, Chih-Yang
author_sort Yeh, Yu-Lan
collection PubMed
description BACKGROUND: San Huang Shel Shin Tang (SHSST) is a traditional herbal decoction used as a hepato-protective agent and is composed of Rheum officinale Baill, Scutellaria baicalnsis Geprgi and Coptis chinensis Franch (2:1:1 w/w). Beta-cyclodextrin (β-CD) modification may potentially increase the solubility and spectral properties of SHSST. METHODS: In this research, the hepato-protective effects of unmodified SHSST, β-CD modified SHSST complex (SHSSTc) and silymarin were evaluated in carbon tetrachloride (CCl(4)) induced acute hepatotoxicity in rats. RESULTS: SHHSTc (40 mg/kg/day) and silymarin (100 mg/kg/day) both decreased the CCl(4)-induced cirrhosis pathway-related transforming growth factor beta (TGF-β) and apoptosis pathway-related caspase-8 protein expressions, but SHSST (40 mg/kg/day) did not reduce TGF-β and caspase-8 significantly . Moreover, SHHSTc (40 mg/kg/day) enhanced the activation of insulin-like growth factor 1 receptor (IGF1R) mediated survival pathway than the silymarin (100 mg/kg/day) to protect the liver from damage induced by CCl(4). CONCLUSIONS: β-CD modification promotes hepato-protective effects of SHSST and reduces the required-dosage of the SHSST.
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spelling pubmed-48844302016-05-29 San Huang Shel Shin Tang beta-cyclodextrin complex augmented the hepatoprotective effects against carbon tetrachloride-induced acute hepatotoxicity in rats Yeh, Yu-Lan Ting, Wei-Jen Kuo, Wei-Wen Hsu, Hsi-Hsien Lin, Yueh-Min Shen, Chia-Yao Chang, Chung-Ho Padma, Viswanadha Vijaya Tsai, Yuhsin Huang, Chih-Yang BMC Complement Altern Med Research Article BACKGROUND: San Huang Shel Shin Tang (SHSST) is a traditional herbal decoction used as a hepato-protective agent and is composed of Rheum officinale Baill, Scutellaria baicalnsis Geprgi and Coptis chinensis Franch (2:1:1 w/w). Beta-cyclodextrin (β-CD) modification may potentially increase the solubility and spectral properties of SHSST. METHODS: In this research, the hepato-protective effects of unmodified SHSST, β-CD modified SHSST complex (SHSSTc) and silymarin were evaluated in carbon tetrachloride (CCl(4)) induced acute hepatotoxicity in rats. RESULTS: SHHSTc (40 mg/kg/day) and silymarin (100 mg/kg/day) both decreased the CCl(4)-induced cirrhosis pathway-related transforming growth factor beta (TGF-β) and apoptosis pathway-related caspase-8 protein expressions, but SHSST (40 mg/kg/day) did not reduce TGF-β and caspase-8 significantly . Moreover, SHHSTc (40 mg/kg/day) enhanced the activation of insulin-like growth factor 1 receptor (IGF1R) mediated survival pathway than the silymarin (100 mg/kg/day) to protect the liver from damage induced by CCl(4). CONCLUSIONS: β-CD modification promotes hepato-protective effects of SHSST and reduces the required-dosage of the SHSST. BioMed Central 2016-05-27 /pmc/articles/PMC4884430/ /pubmed/27234802 http://dx.doi.org/10.1186/s12906-016-1127-8 Text en © Yeh et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yeh, Yu-Lan
Ting, Wei-Jen
Kuo, Wei-Wen
Hsu, Hsi-Hsien
Lin, Yueh-Min
Shen, Chia-Yao
Chang, Chung-Ho
Padma, Viswanadha Vijaya
Tsai, Yuhsin
Huang, Chih-Yang
San Huang Shel Shin Tang beta-cyclodextrin complex augmented the hepatoprotective effects against carbon tetrachloride-induced acute hepatotoxicity in rats
title San Huang Shel Shin Tang beta-cyclodextrin complex augmented the hepatoprotective effects against carbon tetrachloride-induced acute hepatotoxicity in rats
title_full San Huang Shel Shin Tang beta-cyclodextrin complex augmented the hepatoprotective effects against carbon tetrachloride-induced acute hepatotoxicity in rats
title_fullStr San Huang Shel Shin Tang beta-cyclodextrin complex augmented the hepatoprotective effects against carbon tetrachloride-induced acute hepatotoxicity in rats
title_full_unstemmed San Huang Shel Shin Tang beta-cyclodextrin complex augmented the hepatoprotective effects against carbon tetrachloride-induced acute hepatotoxicity in rats
title_short San Huang Shel Shin Tang beta-cyclodextrin complex augmented the hepatoprotective effects against carbon tetrachloride-induced acute hepatotoxicity in rats
title_sort san huang shel shin tang beta-cyclodextrin complex augmented the hepatoprotective effects against carbon tetrachloride-induced acute hepatotoxicity in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884430/
https://www.ncbi.nlm.nih.gov/pubmed/27234802
http://dx.doi.org/10.1186/s12906-016-1127-8
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