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Evaluation of the Anti-Inflammatory Effect of Chalcone and Chalcone Analogues in a Zebrafish Model

The aim of this study was to investigate novel chalcones with potent anti-inflammatory activities in vivo. Chalcone and two chalcone analogues (compound 5 and 9) were evaluated using a caudal fin-wounded transgenic zebrafish line “Tg(mpx:gfp)” to visualize the effect of neutrophil recruitment dynami...

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Autores principales: Chen, Yau-Hung, Wang, Wei-Hua, Wang, Yun-Hsin, Lin, Zi-Yu, Wen, Chi-Chung, Chern, Ching-Yuh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270403/
https://www.ncbi.nlm.nih.gov/pubmed/23385341
http://dx.doi.org/10.3390/molecules18022052
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author Chen, Yau-Hung
Wang, Wei-Hua
Wang, Yun-Hsin
Lin, Zi-Yu
Wen, Chi-Chung
Chern, Ching-Yuh
author_facet Chen, Yau-Hung
Wang, Wei-Hua
Wang, Yun-Hsin
Lin, Zi-Yu
Wen, Chi-Chung
Chern, Ching-Yuh
author_sort Chen, Yau-Hung
collection PubMed
description The aim of this study was to investigate novel chalcones with potent anti-inflammatory activities in vivo. Chalcone and two chalcone analogues (compound 5 and 9) were evaluated using a caudal fin-wounded transgenic zebrafish line “Tg(mpx:gfp)” to visualize the effect of neutrophil recruitment dynamically. Results showed that treatment with compound 9 not only affected wound-induced neutrophil recruitment, but also affected Mpx enzymatic activity. Moreover, protein expression levels of pro-inflammatory factors (Mpx, NFκB, and TNFα) were also regulated by compound 9. Taken together, our results provide in vivo evidence of the anti-inflammatory effects of synthesized chalcone analogues on wound-induced inflammation.
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spelling pubmed-62704032018-12-14 Evaluation of the Anti-Inflammatory Effect of Chalcone and Chalcone Analogues in a Zebrafish Model Chen, Yau-Hung Wang, Wei-Hua Wang, Yun-Hsin Lin, Zi-Yu Wen, Chi-Chung Chern, Ching-Yuh Molecules Article The aim of this study was to investigate novel chalcones with potent anti-inflammatory activities in vivo. Chalcone and two chalcone analogues (compound 5 and 9) were evaluated using a caudal fin-wounded transgenic zebrafish line “Tg(mpx:gfp)” to visualize the effect of neutrophil recruitment dynamically. Results showed that treatment with compound 9 not only affected wound-induced neutrophil recruitment, but also affected Mpx enzymatic activity. Moreover, protein expression levels of pro-inflammatory factors (Mpx, NFκB, and TNFα) were also regulated by compound 9. Taken together, our results provide in vivo evidence of the anti-inflammatory effects of synthesized chalcone analogues on wound-induced inflammation. MDPI 2013-02-05 /pmc/articles/PMC6270403/ /pubmed/23385341 http://dx.doi.org/10.3390/molecules18022052 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Chen, Yau-Hung
Wang, Wei-Hua
Wang, Yun-Hsin
Lin, Zi-Yu
Wen, Chi-Chung
Chern, Ching-Yuh
Evaluation of the Anti-Inflammatory Effect of Chalcone and Chalcone Analogues in a Zebrafish Model
title Evaluation of the Anti-Inflammatory Effect of Chalcone and Chalcone Analogues in a Zebrafish Model
title_full Evaluation of the Anti-Inflammatory Effect of Chalcone and Chalcone Analogues in a Zebrafish Model
title_fullStr Evaluation of the Anti-Inflammatory Effect of Chalcone and Chalcone Analogues in a Zebrafish Model
title_full_unstemmed Evaluation of the Anti-Inflammatory Effect of Chalcone and Chalcone Analogues in a Zebrafish Model
title_short Evaluation of the Anti-Inflammatory Effect of Chalcone and Chalcone Analogues in a Zebrafish Model
title_sort evaluation of the anti-inflammatory effect of chalcone and chalcone analogues in a zebrafish model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270403/
https://www.ncbi.nlm.nih.gov/pubmed/23385341
http://dx.doi.org/10.3390/molecules18022052
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