Literature DB >> 19959748

3-(2,4-dichlorophenyl)-4-(1-methyl-1H-indol-3-yl)-1H-pyrrole-2,5-dione (SB216763), a glycogen synthase kinase-3 inhibitor, displays therapeutic properties in a mouse model of pulmonary inflammation and fibrosis.

Carmela Gurrieri1, Francesco Piazza, Marianna Gnoato, Barbara Montini, Lucia Biasutto, Cristina Gattazzo, Enrico Brunetta, Anna Cabrelle, Francesco Cinetto, Raffaele Niero, Monica Facco, Spiridione Garbisa, Fiorella Calabrese, Gianpietro Semenzato, Carlo Agostini.   

Abstract

Glycogen synthase kinase (GSK)-3 modulates the production of inflammatory cytokines. Because bleomycin (BLM) causes lung injury, which is characterized by an inflammatory response followed by a fibrotic degeneration, we postulated that blocking GSK-3 activity with a specific inhibitor could affect the inflammatory and profibrotic cytokine network generated in the BLM-induced process of pulmonary inflammation and fibrosis. Thus, here we investigated the effects of the GSK-3 inhibitor 3-(2,4-dichlorophenyl)-4-(1-methyl-1H-indol-3-yl)-1H-pyrrole-2,5-dione (SB216763) on a BLM-induced lung fibrosis model in mice. SB216763 prevented lung inflammation and the subsequent fibrosis when coadministered with BLM. Bronchoalveolar lavage fluid analysis of mice treated with BLM plus SB216763 revealed a significant reduction in BLM-induced alveolitis. Furthermore, SB216763 treatment was associated with a significantly lower production of inflammatory cytokines by macrophages. BLM-treated mice that received SB216763 developed alveolar epithelial cell damage and pulmonary fibrosis to a significantly lower extent compared with BLM-treated controls. These findings suggest that GSK-3 inhibition has a protective effect on lung fibrosis induced by BLM and candidate GSK-3 as a potential therapeutic target for preventing pulmonary fibrosis.

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Year:  2009        PMID: 19959748     DOI: 10.1124/jpet.109.153049

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  20 in total

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2.  Glycogen synthase kinase 3 (GSK3)-inhibitor SB216763 promotes the conversion of human umbilical cord mesenchymal stem cells into neural precursors in adherent culture.

Authors:  Liyang Gao; Mingyan Zhao; Peng Li; Junchao Kong; Zhijun Liu; Yonghua Chen; Rui Huang; Jiaqi Chu; Juanhua Quan; Rong Zeng
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4.  Glycogen synthase kinase-3 (GSK-3) regulates TGF-β₁-induced differentiation of pulmonary fibroblasts.

Authors:  Hoeke A Baarsma; Lilian H J M Engelbertink; Lonneke J van Hees; Mark H Menzen; Herman Meurs; Wim Timens; Dirkje S Postma; Huib A M Kerstjens; Reinoud Gosens
Journal:  Br J Pharmacol       Date:  2013-06       Impact factor: 8.739

5.  GSK3β-dependent inhibition of AMPK potentiates activation of neutrophils and macrophages and enhances severity of acute lung injury.

Authors:  Dae Won Park; Shaoning Jiang; Yanping Liu; Gene P Siegal; Ken Inoki; Edward Abraham; Jaroslaw W Zmijewski
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2014-09-19       Impact factor: 5.464

Review 6.  Perspectives on Wnt Signal Pathway in the Pathogenesis and Therapeutics of Chronic Obstructive Pulmonary Disease.

Authors:  Jiao Qu; Li Yue; Jian Gao; Hongwei Yao
Journal:  J Pharmacol Exp Ther       Date:  2019-04-05       Impact factor: 4.030

7.  Inhibition of GSK3α/β promotes increased pulmonary endothelial permeability to albumin by reactive oxygen/nitrogen species.

Authors:  Paul Neumann; Hiba Alsaffar; Nancy Gertzberg; Arnold Johnson
Journal:  Pulm Pharmacol Ther       Date:  2013-06-11       Impact factor: 3.410

8.  Regulation by glycogen synthase kinase-3 of inflammation and T cells in CNS diseases.

Authors:  Eléonore Beurel
Journal:  Front Mol Neurosci       Date:  2011-08-31       Impact factor: 5.639

9.  Pharmacological inhibition of GSK-3 in a guinea pig model of LPS-induced pulmonary inflammation: I. Effects on lung remodeling and pathology.

Authors:  Hoeke A Baarsma; Sophie Bos; Herman Meurs; Kim H Visser; Marieke Smit; Annemie M W J Schols; Ramon C Langen; Huib A M Kerstjens; Reinoud Gosens
Journal:  Respir Res       Date:  2013-10-23

10.  Genome-wide RNAi screen reveals a new role of a WNT/CTNNB1 signaling pathway as negative regulator of virus-induced innate immune responses.

Authors:  Martin Baril; Salwa Es-Saad; Laurent Chatel-Chaix; Karin Fink; Tram Pham; Valérie-Ann Raymond; Karine Audette; Anne-Sophie Guenier; Jean Duchaine; Marc Servant; Marc Bilodeau; Eric Cohen; Nathalie Grandvaux; Daniel Lamarre
Journal:  PLoS Pathog       Date:  2013-06-13       Impact factor: 6.823

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