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Protective effects of Huangqin Decoction against ulcerative colitis and associated cancer in mice

Individuals with ulcerative colitis (UC) are at a high risk for developing colorectal cancer (CRC). Huangqin Decoction (HQD), a traditional Chinese medicinal formula chronicled in the Shang Han Lun, is commonly used to treat gastrointestinal symptoms. However, experimental evidence for supporting th...

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Autores principales: Chen, Gang, Yang, Yang, Hu, Chunping, Cheng, Xiaolan, Xu, Yuehua, Cai, Xueting, Wang, Min, Yang, Chung S., Cao, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308679/
https://www.ncbi.nlm.nih.gov/pubmed/27557503
http://dx.doi.org/10.18632/oncotarget.11426
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author Chen, Gang
Yang, Yang
Hu, Chunping
Cheng, Xiaolan
Xu, Yuehua
Cai, Xueting
Wang, Min
Yang, Chung S.
Cao, Peng
author_facet Chen, Gang
Yang, Yang
Hu, Chunping
Cheng, Xiaolan
Xu, Yuehua
Cai, Xueting
Wang, Min
Yang, Chung S.
Cao, Peng
author_sort Chen, Gang
collection PubMed
description Individuals with ulcerative colitis (UC) are at a high risk for developing colorectal cancer (CRC). Huangqin Decoction (HQD), a traditional Chinese medicinal formula chronicled in the Shang Han Lun, is commonly used to treat gastrointestinal symptoms. However, experimental evidence for supporting the clinical practice is lacking. This study used modern biomedical approaches to investigate the protective/preventive effects of HQD in dextran sulfate sodium (DSS)-induced acute/chronic UC and azoxymethane (AOM)/DSS-induced CRC in mice. HQDs were prepared in 4 different ways: HQD-1 and HQD-2 were prepared in boiling water, whereas HQD-3 and HQD-4 were prepared in heated ethanol (70%). For HQD-1 and HQD-3, the 4 constituent herbs were processed together, whereas for HQD-2 and HQD4, these herbs were processed individually and then combined. The mice were administered 9.1 g/kg HQD via oral gavage daily. HQD-1 significantly inhibited DSS-induced acute UC, whereas HQD-3 and HQD-4 exhibited mild ameliorative effects; but HQD-2 had no protective effect and resulted in a higher mortality rate. This higher mortality rate may be due to the greater abundance of baicalein and wogonin in HQD-2 than HQD-1. Furthermore, HQD-1 protected against DSS-induced chronic UC and significantly inhibited AOM/DSS-induced CRC in mice. HQD-1 also inhibited the production of inflammatory cytokines and increased antioxidant capacity both in chronic DSS and AOM/DSS treated mice. Overall, HQD-1 inhibits the development of acute/chronic colitis and prevents colitis-associated CRC, possibly by inhibiting inflammation and preventing oxidative stress induced cellular damage.
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spelling pubmed-53086792017-03-09 Protective effects of Huangqin Decoction against ulcerative colitis and associated cancer in mice Chen, Gang Yang, Yang Hu, Chunping Cheng, Xiaolan Xu, Yuehua Cai, Xueting Wang, Min Yang, Chung S. Cao, Peng Oncotarget Research Paper Individuals with ulcerative colitis (UC) are at a high risk for developing colorectal cancer (CRC). Huangqin Decoction (HQD), a traditional Chinese medicinal formula chronicled in the Shang Han Lun, is commonly used to treat gastrointestinal symptoms. However, experimental evidence for supporting the clinical practice is lacking. This study used modern biomedical approaches to investigate the protective/preventive effects of HQD in dextran sulfate sodium (DSS)-induced acute/chronic UC and azoxymethane (AOM)/DSS-induced CRC in mice. HQDs were prepared in 4 different ways: HQD-1 and HQD-2 were prepared in boiling water, whereas HQD-3 and HQD-4 were prepared in heated ethanol (70%). For HQD-1 and HQD-3, the 4 constituent herbs were processed together, whereas for HQD-2 and HQD4, these herbs were processed individually and then combined. The mice were administered 9.1 g/kg HQD via oral gavage daily. HQD-1 significantly inhibited DSS-induced acute UC, whereas HQD-3 and HQD-4 exhibited mild ameliorative effects; but HQD-2 had no protective effect and resulted in a higher mortality rate. This higher mortality rate may be due to the greater abundance of baicalein and wogonin in HQD-2 than HQD-1. Furthermore, HQD-1 protected against DSS-induced chronic UC and significantly inhibited AOM/DSS-induced CRC in mice. HQD-1 also inhibited the production of inflammatory cytokines and increased antioxidant capacity both in chronic DSS and AOM/DSS treated mice. Overall, HQD-1 inhibits the development of acute/chronic colitis and prevents colitis-associated CRC, possibly by inhibiting inflammation and preventing oxidative stress induced cellular damage. Impact Journals LLC 2016-08-19 /pmc/articles/PMC5308679/ /pubmed/27557503 http://dx.doi.org/10.18632/oncotarget.11426 Text en Copyright: © 2016 Chen et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Chen, Gang
Yang, Yang
Hu, Chunping
Cheng, Xiaolan
Xu, Yuehua
Cai, Xueting
Wang, Min
Yang, Chung S.
Cao, Peng
Protective effects of Huangqin Decoction against ulcerative colitis and associated cancer in mice
title Protective effects of Huangqin Decoction against ulcerative colitis and associated cancer in mice
title_full Protective effects of Huangqin Decoction against ulcerative colitis and associated cancer in mice
title_fullStr Protective effects of Huangqin Decoction against ulcerative colitis and associated cancer in mice
title_full_unstemmed Protective effects of Huangqin Decoction against ulcerative colitis and associated cancer in mice
title_short Protective effects of Huangqin Decoction against ulcerative colitis and associated cancer in mice
title_sort protective effects of huangqin decoction against ulcerative colitis and associated cancer in mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308679/
https://www.ncbi.nlm.nih.gov/pubmed/27557503
http://dx.doi.org/10.18632/oncotarget.11426
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