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Polyphenol derivatives – potential regulators of neutrophil activity

The study provides new information on the effect of natural polyphenols (derivatives of stilbene – resveratrol, pterostilbene, pinosylvin and piceatannol and derivatives of ferulic acid – curcumin, N-feruloylserotonin) on the activity of human neutrophils in influencing oxidative burst. All the poly...

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Autores principales: Drábiková, Katarína, Perečko, Tomáš, Nosáľ, Radomír, Harmatha, Juraj, Šmidrkal, Jan, Jančinová, Viera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Slovak Toxicology Society SETOX 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485655/
https://www.ncbi.nlm.nih.gov/pubmed/23118589
http://dx.doi.org/10.2478/v10102-012-0011-8
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author Drábiková, Katarína
Perečko, Tomáš
Nosáľ, Radomír
Harmatha, Juraj
Šmidrkal, Jan
Jančinová, Viera
author_facet Drábiková, Katarína
Perečko, Tomáš
Nosáľ, Radomír
Harmatha, Juraj
Šmidrkal, Jan
Jančinová, Viera
author_sort Drábiková, Katarína
collection PubMed
description The study provides new information on the effect of natural polyphenols (derivatives of stilbene – resveratrol, pterostilbene, pinosylvin and piceatannol and derivatives of ferulic acid – curcumin, N-feruloylserotonin) on the activity of human neutrophils in influencing oxidative burst. All the polyphenols tested were found to reduce markedly the production of reactive oxygen species released by human neutrophils on extra-and intracellular levels as well as in cell free system. Moreover, pinosylvin, curcumin, N-feruloylserotonin and resveratrol decreased protein kinase C activity involved in neutrophil signalling and reactive oxygen species production. Our results suggest that due to their anti-neutrophil activity, the polyphenols tested might be attractive candidates in therapeutic development.
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spelling pubmed-34856552012-11-01 Polyphenol derivatives – potential regulators of neutrophil activity Drábiková, Katarína Perečko, Tomáš Nosáľ, Radomír Harmatha, Juraj Šmidrkal, Jan Jančinová, Viera Interdiscip Toxicol Review Article The study provides new information on the effect of natural polyphenols (derivatives of stilbene – resveratrol, pterostilbene, pinosylvin and piceatannol and derivatives of ferulic acid – curcumin, N-feruloylserotonin) on the activity of human neutrophils in influencing oxidative burst. All the polyphenols tested were found to reduce markedly the production of reactive oxygen species released by human neutrophils on extra-and intracellular levels as well as in cell free system. Moreover, pinosylvin, curcumin, N-feruloylserotonin and resveratrol decreased protein kinase C activity involved in neutrophil signalling and reactive oxygen species production. Our results suggest that due to their anti-neutrophil activity, the polyphenols tested might be attractive candidates in therapeutic development. Slovak Toxicology Society SETOX 2012-06 2012-06 /pmc/articles/PMC3485655/ /pubmed/23118589 http://dx.doi.org/10.2478/v10102-012-0011-8 Text en Copyright © 2012 Slovak Toxicology Society SETOX http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Drábiková, Katarína
Perečko, Tomáš
Nosáľ, Radomír
Harmatha, Juraj
Šmidrkal, Jan
Jančinová, Viera
Polyphenol derivatives – potential regulators of neutrophil activity
title Polyphenol derivatives – potential regulators of neutrophil activity
title_full Polyphenol derivatives – potential regulators of neutrophil activity
title_fullStr Polyphenol derivatives – potential regulators of neutrophil activity
title_full_unstemmed Polyphenol derivatives – potential regulators of neutrophil activity
title_short Polyphenol derivatives – potential regulators of neutrophil activity
title_sort polyphenol derivatives – potential regulators of neutrophil activity
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485655/
https://www.ncbi.nlm.nih.gov/pubmed/23118589
http://dx.doi.org/10.2478/v10102-012-0011-8
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