Literature DB >> 19905913

Effects of tranilast and pentoxifylline in a mouse model of chronic asthma using house dust mite antigen.

Seung Joon Kim1, Jin Woo Kim, Yong Hyun Kim, Sang Haak Lee, Hyoung Kyu Yoon, Chi Hong Kim, Joong Hyun Ahn, Jung Mi Lee, Jin Sook Kim, Seok Chan Kim, Sook Young Lee, Soon Seog Kwon, Young Kyoon Kim.   

Abstract

Tranilast has been used in allergic diseases because of its inhibitory effect on mast cells; it also has an anti-fibrotic effect in several diseases. Pentoxifylline (PTX), a methylxanthine derivative, is a potent anti-inflammatory drug that is known to manifest its effect through the inhibition of Th1 cytokine, but with an uncertain effect on Th2 cytokine. Seven-week-old female BALB/c mice were studied as a chronic asthma model. The mice were challenged with house dust mite (HDM) antigen for 7 weeks. Each group of mice was given an intraperitoneal injection of tranilast, PTX, or tranilast plus PTX before antigen administration. In this mouse model of chronic asthma, tranilast, and PTX each had an inhibitory effect on airway remodeling as well as on airway hyperresponsiveness (AHR) and airway inflammation. The improved events of these drugs were related with the inhibition of the Th2 cytokine IL-13 and TGF-beta 1. Immunohistochemical analysis showed that decreases in the peribronchial trichrome stained area in each treatment group were associated with improvements in the peribronchial smooth muscle hyperplasia, collagen type I, and collagen type III deposition. These drugs could have potential beneficial effects on chronic asthma, especially with respect to airway remodeling.

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Year:  2009        PMID: 19905913     DOI: 10.3109/02770900903089998

Source DB:  PubMed          Journal:  J Asthma        ISSN: 0277-0903            Impact factor:   2.515


  7 in total

1.  Ex vivo host and parasite response to antileishmanial drugs and immunomodulators.

Authors:  Laura Gonzalez-Fajardo; Olga Lucía Fernández; Diane McMahon-Pratt; Nancy Gore Saravia
Journal:  PLoS Negl Trop Dis       Date:  2015-05-29

2.  Low-molecular-weight heparin and unfractionated heparin decrease Th-1, 2, and 17 expressions.

Authors:  Jing-Ning Huang; Ming-Chin Tsai; Shun-Lung Fang; Margaret Dah-Tsyr Chang; Yu-Rou Wu; Jaw-Ji Tsai; Lin-Shien Fu; Heng-Kuei Lin; Yi-Jun Chen; Tsai-Wei Li
Journal:  PLoS One       Date:  2014-11-03       Impact factor: 3.240

3.  Cytochrome P450s in human immune cells regulate IL-22 and c-Kit via an AHR feedback loop.

Authors:  Renate Effner; Julia Hiller; Stefanie Eyerich; Claudia Traidl-Hoffmann; Knut Brockow; Massimo Triggiani; Heidrun Behrendt; Carsten B Schmidt-Weber; Jeroen T M Buters
Journal:  Sci Rep       Date:  2017-03-09       Impact factor: 4.379

4.  Tranilast Treatment Attenuates Cerebral Ischemia-Reperfusion Injury in Rats Through the Inhibition of Inflammatory Responses Mediated by NF-κB and PPARs.

Authors:  Yue Zhuo; Jun Zhuo
Journal:  Clin Transl Sci       Date:  2018-12-31       Impact factor: 4.689

5.  The NF-κB Transcription Factor c-Rel Modulates Group 2 Innate Lymphoid Cell Effector Functions and Drives Allergic Airway Inflammation.

Authors:  Barbara C Mindt; Sai Sakktee Krisna; Claudia U Duerr; Mathieu Mancini; Lara Richer; Silvia M Vidal; Steven Gerondakis; David Langlais; Jörg H Fritz
Journal:  Front Immunol       Date:  2021-11-16       Impact factor: 7.561

6.  The role of IgE-receptors in IgE-dependent airway smooth muscle cell remodelling.

Authors:  Michael Roth; Jun Zhong; Celine Zumkeller; Chong Teck S'ng; Stephanie Goulet; Michael Tamm
Journal:  PLoS One       Date:  2013-02-14       Impact factor: 3.240

7.  Tranilast administration reduces fibrosis and improves fatigue resistance in muscles of mdx dystrophic mice.

Authors:  Kristy Swiderski; Michelle Todorov; Stefan M Gehrig; Timur Naim; Annabel Chee; David I Stapleton; René Koopman; Gordon S Lynch
Journal:  Fibrogenesis Tissue Repair       Date:  2014-01-30
  7 in total

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