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©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 7, 2016; 22(5): 1826-1833
Published online Feb 7, 2016. doi: 10.3748/wjg.v22.i5.1826
Published online Feb 7, 2016. doi: 10.3748/wjg.v22.i5.1826
Chymase inhibitor TY-51469 in therapy of inflammatory bowel disease
Wei-Xin Liu, Ying Wang, Shen Zhang, Ting Wang, Feng Zhou, Department of Gastroenterology, First Affiliated Hospital, China Medical University, Shenyang 110001, Liaoning Province, China
Li-Xuan Sang, Department of Cadre Ward II, First Affiliated Hospital of China Medical University, Shenyang 110001, Liaoning Province, China
Shou-Zhi Gu, Department of Anatomy, Seirei Christopher College, Hamamatsu 4338558, Japan
Author contributions: Liu WX and Gu SZ designed the research; Sang LX, Zhang S, Wang Y and Zhou F performed the research; Liu WX and Wang T analyzed the data; Liu WX and Wang Y wrote the paper.
Supported by Science and Technology Project of Liaoning Province, No. 2013225303; and Science and Technology Project of Shenyang City, No. F13-316-1-40.
Institutional review board statement: This study was approved by the Institute Research Medical Ethics Committee of the First Affiliated Hospital of China Medical University.
Institutional animal care and use committee statement: All procedures involving animals were reviewed and approved by the Institutional Animal Care and Use Committee of China Medical University.
Conflict-of-interest statement: All of the authors declare that there is no conflict of interest.
Data sharing statement: No additional data are available.
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Wei-Xin Liu, Professor, Department of Gastroenterology, First Affiliated Hospital, China Medical University, No. 155 North Nanjing Street, Heping District, Shenyang 110001, Liaoning Province, China. weixinliu@yahoo.com
Telephone: +86-24-83282863 Fax: +86-24-83282863
Received: March 15, 2015
Peer-review started: March 15, 2015
First decision: April 13, 2015
Revised: June 10, 2015
Accepted: August 25, 2015
Article in press: August 25, 2015
Published online: February 7, 2016
Processing time: 312 Days and 4.8 Hours
Peer-review started: March 15, 2015
First decision: April 13, 2015
Revised: June 10, 2015
Accepted: August 25, 2015
Article in press: August 25, 2015
Published online: February 7, 2016
Processing time: 312 Days and 4.8 Hours
Core Tip
Core tip: Until now, little is known of the role of chymase inhibitor in the immune system and no investigation has been performed in inflammatory bowel disease (IBD). In the present study, we built a Sprague-Dawley rat model of colitis induced with dextran sulfate sodium (DSS) and treated the model rats with chymase inhibitor TY-51469. The changes of Tregs were further detected to investigate the effect of chymase inhibitor TY-51469 on IBD and to explore the underlying mechanism. The results indicated that chymase inhibitor TY-51469 might ameliorate the progression of DSS-induced colitis possibly by increasing the expression of Tregs and cytokines.