Preventive Effect of TU-100 on a Type-2 Model of Colitis in Mice: Possible Involvement of Enhancing Adrenomedullin in Intestinal Epithelial Cells
Purpose. Crohn's disease (CD) and ulcerative colitis (UC), the two major forms of inflammatory bowel disease (IBD), have histopathologically and immunologically different characteristics. We previously reported that a traditional Japanese medicine, daikenchuto (TU-100), ameliorated a trinitrobe...
Saved in:
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2013-01-01
|
Series: | Gastroenterology Research and Practice |
Online Access: | http://dx.doi.org/10.1155/2013/384057 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832560433092886528 |
---|---|
author | Atsushi Kaneko Toru Kono Naoko Miura Naoko Tsuchiya Masahiro Yamamoto |
author_facet | Atsushi Kaneko Toru Kono Naoko Miura Naoko Tsuchiya Masahiro Yamamoto |
author_sort | Atsushi Kaneko |
collection | DOAJ |
description | Purpose. Crohn's disease (CD) and ulcerative colitis (UC), the two major forms of inflammatory bowel disease (IBD), have histopathologically and immunologically different characteristics. We previously reported that a traditional Japanese medicine, daikenchuto (TU-100), ameliorated a trinitrobenzenesulfonic acid- (TNBS-) induced type-1 model colitis exhibiting histopathological features of CD through adrenomedullin (ADM) enhancement. Our current aims were to examine whether TU-100 ameliorates a type-2 model colitis that histologically resembles UC and identify the active ingredients. Methods. TU-100 was administered orally to mice with oxazolone- (OXN-) induced type-2 model colitis. The morbidity was evaluated by body weight loss and the macroscopic score of colonic lesions. ADM was quantified using an EIA kit. Results. TU-100 prevented weight loss and colon ulceration. ADM production by intestinal epithelial cells was increased by TU-100 addition. Screening to identify active ingredients showed that [6]-shogaol and hydroxy α-sanshool enhanced ADM production. Conclusions. TU-100 exerted a protective effect in OXN-induced type-2 model colitis, indicating that TU-100 may be a beneficial agent for treatment of UC. |
format | Article |
id | doaj-art-1b423dfae26343428e84f68c2b4f5664 |
institution | Kabale University |
issn | 1687-6121 1687-630X |
language | English |
publishDate | 2013-01-01 |
publisher | Wiley |
record_format | Article |
series | Gastroenterology Research and Practice |
spelling | doaj-art-1b423dfae26343428e84f68c2b4f56642025-02-03T01:27:35ZengWileyGastroenterology Research and Practice1687-61211687-630X2013-01-01201310.1155/2013/384057384057Preventive Effect of TU-100 on a Type-2 Model of Colitis in Mice: Possible Involvement of Enhancing Adrenomedullin in Intestinal Epithelial CellsAtsushi Kaneko0Toru Kono1Naoko Miura2Naoko Tsuchiya3Masahiro Yamamoto4Tsumura Research Laboratories, Tsumura & Co., 3586 Yoshiwara, Ami-machi, Inashiki-gun, Ibaraki 300-1192, JapanFaculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, JapanTsumura Research Laboratories, Tsumura & Co., 3586 Yoshiwara, Ami-machi, Inashiki-gun, Ibaraki 300-1192, JapanTsumura Research Laboratories, Tsumura & Co., 3586 Yoshiwara, Ami-machi, Inashiki-gun, Ibaraki 300-1192, JapanTsumura Research Laboratories, Tsumura & Co., 3586 Yoshiwara, Ami-machi, Inashiki-gun, Ibaraki 300-1192, JapanPurpose. Crohn's disease (CD) and ulcerative colitis (UC), the two major forms of inflammatory bowel disease (IBD), have histopathologically and immunologically different characteristics. We previously reported that a traditional Japanese medicine, daikenchuto (TU-100), ameliorated a trinitrobenzenesulfonic acid- (TNBS-) induced type-1 model colitis exhibiting histopathological features of CD through adrenomedullin (ADM) enhancement. Our current aims were to examine whether TU-100 ameliorates a type-2 model colitis that histologically resembles UC and identify the active ingredients. Methods. TU-100 was administered orally to mice with oxazolone- (OXN-) induced type-2 model colitis. The morbidity was evaluated by body weight loss and the macroscopic score of colonic lesions. ADM was quantified using an EIA kit. Results. TU-100 prevented weight loss and colon ulceration. ADM production by intestinal epithelial cells was increased by TU-100 addition. Screening to identify active ingredients showed that [6]-shogaol and hydroxy α-sanshool enhanced ADM production. Conclusions. TU-100 exerted a protective effect in OXN-induced type-2 model colitis, indicating that TU-100 may be a beneficial agent for treatment of UC.http://dx.doi.org/10.1155/2013/384057 |
spellingShingle | Atsushi Kaneko Toru Kono Naoko Miura Naoko Tsuchiya Masahiro Yamamoto Preventive Effect of TU-100 on a Type-2 Model of Colitis in Mice: Possible Involvement of Enhancing Adrenomedullin in Intestinal Epithelial Cells Gastroenterology Research and Practice |
title | Preventive Effect of TU-100 on a Type-2 Model of Colitis in Mice: Possible Involvement of Enhancing Adrenomedullin in Intestinal Epithelial Cells |
title_full | Preventive Effect of TU-100 on a Type-2 Model of Colitis in Mice: Possible Involvement of Enhancing Adrenomedullin in Intestinal Epithelial Cells |
title_fullStr | Preventive Effect of TU-100 on a Type-2 Model of Colitis in Mice: Possible Involvement of Enhancing Adrenomedullin in Intestinal Epithelial Cells |
title_full_unstemmed | Preventive Effect of TU-100 on a Type-2 Model of Colitis in Mice: Possible Involvement of Enhancing Adrenomedullin in Intestinal Epithelial Cells |
title_short | Preventive Effect of TU-100 on a Type-2 Model of Colitis in Mice: Possible Involvement of Enhancing Adrenomedullin in Intestinal Epithelial Cells |
title_sort | preventive effect of tu 100 on a type 2 model of colitis in mice possible involvement of enhancing adrenomedullin in intestinal epithelial cells |
url | http://dx.doi.org/10.1155/2013/384057 |
work_keys_str_mv | AT atsushikaneko preventiveeffectoftu100onatype2modelofcolitisinmicepossibleinvolvementofenhancingadrenomedullininintestinalepithelialcells AT torukono preventiveeffectoftu100onatype2modelofcolitisinmicepossibleinvolvementofenhancingadrenomedullininintestinalepithelialcells AT naokomiura preventiveeffectoftu100onatype2modelofcolitisinmicepossibleinvolvementofenhancingadrenomedullininintestinalepithelialcells AT naokotsuchiya preventiveeffectoftu100onatype2modelofcolitisinmicepossibleinvolvementofenhancingadrenomedullininintestinalepithelialcells AT masahiroyamamoto preventiveeffectoftu100onatype2modelofcolitisinmicepossibleinvolvementofenhancingadrenomedullininintestinalepithelialcells |