Cargando…

Protective Effect of Daikenchuto on Dextran Sulfate Sodium-Induced Colitis in Mice

Aim. To investigate the effect of daikenchuto (TJ-100; DKT) for ulcerative colitis (UC) model mouse and assess its anti-inflammatory mechanisms. Methods. We evaluated the effects of DKT on dextran sulfate sodium- (DSS-) induced experimental colitis. First, we assessed the short-term effects of DKT u...

Descripción completa

Detalles Bibliográficos
Autores principales: Matsunaga, Takaharu, Hashimoto, Shinichi, Yamamoto, Naoki, Kawasato, Ryo, Shirasawa, Tomohiro, Goto, Atsushi, Fujisawa, Koichi, Takami, Taro, Okamoto, Takeshi, Nishikawa, Jun, Sakaida, Isao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292124/
https://www.ncbi.nlm.nih.gov/pubmed/28210268
http://dx.doi.org/10.1155/2017/1298263
_version_ 1782504877523468288
author Matsunaga, Takaharu
Hashimoto, Shinichi
Yamamoto, Naoki
Kawasato, Ryo
Shirasawa, Tomohiro
Goto, Atsushi
Fujisawa, Koichi
Takami, Taro
Okamoto, Takeshi
Nishikawa, Jun
Sakaida, Isao
author_facet Matsunaga, Takaharu
Hashimoto, Shinichi
Yamamoto, Naoki
Kawasato, Ryo
Shirasawa, Tomohiro
Goto, Atsushi
Fujisawa, Koichi
Takami, Taro
Okamoto, Takeshi
Nishikawa, Jun
Sakaida, Isao
author_sort Matsunaga, Takaharu
collection PubMed
description Aim. To investigate the effect of daikenchuto (TJ-100; DKT) for ulcerative colitis (UC) model mouse and assess its anti-inflammatory mechanisms. Methods. We evaluated the effects of DKT on dextran sulfate sodium- (DSS-) induced experimental colitis. First, we assessed the short-term effects of DKT using two groups: 5% DSS group and 5% DSS with DKT group. Colon length; histological scores; and interleukin- (IL-) 10, IL-1β, and tumor necrosis factor-α mRNA expression profiles were analyzed using real-time PCR. Second, we assessed the long-term effects of DKT, by comparing survival time between 2% DSS and 2% DSS with DKT groups. Results. After 7 days, the colon lengths of DSS + DKT group were longer than those of the DSS group (mean values: 6.11 versus 5.69 cm, p < 0.05). Furthermore, compared to DSS group, the DSS + DKT group maintained significantly higher levels of serum hemoglobin (13.1 versus 10.7 g/dL, p < 0.05) and exhibited significantly higher expression levels of IL-10 (p < 0.05). The 2% DSS + DKT group exhibited significantly longer survival time than the 2% DSS group (70 versus 44 days, p < 0.01). Conclusion. Our results indicate that DKT prevented inflammation in the colon, indicating its potential as a new therapeutic agent for UC.
format Online
Article
Text
id pubmed-5292124
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-52921242017-02-16 Protective Effect of Daikenchuto on Dextran Sulfate Sodium-Induced Colitis in Mice Matsunaga, Takaharu Hashimoto, Shinichi Yamamoto, Naoki Kawasato, Ryo Shirasawa, Tomohiro Goto, Atsushi Fujisawa, Koichi Takami, Taro Okamoto, Takeshi Nishikawa, Jun Sakaida, Isao Gastroenterol Res Pract Research Article Aim. To investigate the effect of daikenchuto (TJ-100; DKT) for ulcerative colitis (UC) model mouse and assess its anti-inflammatory mechanisms. Methods. We evaluated the effects of DKT on dextran sulfate sodium- (DSS-) induced experimental colitis. First, we assessed the short-term effects of DKT using two groups: 5% DSS group and 5% DSS with DKT group. Colon length; histological scores; and interleukin- (IL-) 10, IL-1β, and tumor necrosis factor-α mRNA expression profiles were analyzed using real-time PCR. Second, we assessed the long-term effects of DKT, by comparing survival time between 2% DSS and 2% DSS with DKT groups. Results. After 7 days, the colon lengths of DSS + DKT group were longer than those of the DSS group (mean values: 6.11 versus 5.69 cm, p < 0.05). Furthermore, compared to DSS group, the DSS + DKT group maintained significantly higher levels of serum hemoglobin (13.1 versus 10.7 g/dL, p < 0.05) and exhibited significantly higher expression levels of IL-10 (p < 0.05). The 2% DSS + DKT group exhibited significantly longer survival time than the 2% DSS group (70 versus 44 days, p < 0.01). Conclusion. Our results indicate that DKT prevented inflammation in the colon, indicating its potential as a new therapeutic agent for UC. Hindawi Publishing Corporation 2017 2017-01-22 /pmc/articles/PMC5292124/ /pubmed/28210268 http://dx.doi.org/10.1155/2017/1298263 Text en Copyright © 2017 Takaharu Matsunaga et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Matsunaga, Takaharu
Hashimoto, Shinichi
Yamamoto, Naoki
Kawasato, Ryo
Shirasawa, Tomohiro
Goto, Atsushi
Fujisawa, Koichi
Takami, Taro
Okamoto, Takeshi
Nishikawa, Jun
Sakaida, Isao
Protective Effect of Daikenchuto on Dextran Sulfate Sodium-Induced Colitis in Mice
title Protective Effect of Daikenchuto on Dextran Sulfate Sodium-Induced Colitis in Mice
title_full Protective Effect of Daikenchuto on Dextran Sulfate Sodium-Induced Colitis in Mice
title_fullStr Protective Effect of Daikenchuto on Dextran Sulfate Sodium-Induced Colitis in Mice
title_full_unstemmed Protective Effect of Daikenchuto on Dextran Sulfate Sodium-Induced Colitis in Mice
title_short Protective Effect of Daikenchuto on Dextran Sulfate Sodium-Induced Colitis in Mice
title_sort protective effect of daikenchuto on dextran sulfate sodium-induced colitis in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292124/
https://www.ncbi.nlm.nih.gov/pubmed/28210268
http://dx.doi.org/10.1155/2017/1298263
work_keys_str_mv AT matsunagatakaharu protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice
AT hashimotoshinichi protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice
AT yamamotonaoki protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice
AT kawasatoryo protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice
AT shirasawatomohiro protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice
AT gotoatsushi protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice
AT fujisawakoichi protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice
AT takamitaro protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice
AT okamototakeshi protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice
AT nishikawajun protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice
AT sakaidaisao protectiveeffectofdaikenchutoondextransulfatesodiuminducedcolitisinmice