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Comparative Immunomodulatory Activity of Nigella sativa L. Preparations on Proinflammatory Mediators: A Focus on Asthma

Introduction: A range of traditional and commercial preparations of NS is frequently used in the treatment of several inflammatory diseases. Often, these preparations have poor preclinical characterization that may lead to variable pharmacological effects. Objective: To assess the in vitro effects o...

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Autores principales: Koshak, Abdulrahman E., Yousif, Nizar M., Fiebich, Bernd L., Koshak, Emad A., Heinrich, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176110/
https://www.ncbi.nlm.nih.gov/pubmed/30333747
http://dx.doi.org/10.3389/fphar.2018.01075
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author Koshak, Abdulrahman E.
Yousif, Nizar M.
Fiebich, Bernd L.
Koshak, Emad A.
Heinrich, Michael
author_facet Koshak, Abdulrahman E.
Yousif, Nizar M.
Fiebich, Bernd L.
Koshak, Emad A.
Heinrich, Michael
author_sort Koshak, Abdulrahman E.
collection PubMed
description Introduction: A range of traditional and commercial preparations of NS is frequently used in the treatment of several inflammatory diseases. Often, these preparations have poor preclinical characterization that may lead to variable pharmacological effects. Objective: To assess the in vitro effects of different chemically defined preparations of NS on some asthma-related mediators of inflammation. Methods: Different NS preparations were obtained by either seed extraction with a spectrum of solvents ranging from lipophilic to hydrophilic, or commercial products were collected. The TQ concentration of NS was analyzed by HPLC. Immunomodulatory activity was assessed by the release of mediators (IL-2, IL-6, PGE(2)) in primary human T-lymphocytes, monocytes, and A549 human lung epithelial cells. Results: Ten distinct NS preparations showed variability in TQ concentration, being highest in the oily preparations extract-7 (2.4% w/w), followed by extract-10 (0.7%w/w). Similarly, the release of mediators was varied, being greatest in extract-7 and 10 via significantly (<0.05) suppressing IL-2, IL-6, and PGE(2) in T-lymphocytes as well as IL-6 and PGE(2) in monocytes. Also, PGE(2) release in A549 cells was significantly enhanced by both extracts. Conclusion: The TQ concentration and in vitro activity were variable among the different NS preparations. TQ-rich oily NS preparations produced potent favorable immunomodulation in asthma inflammation and can be used in future studies.
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spelling pubmed-61761102018-10-17 Comparative Immunomodulatory Activity of Nigella sativa L. Preparations on Proinflammatory Mediators: A Focus on Asthma Koshak, Abdulrahman E. Yousif, Nizar M. Fiebich, Bernd L. Koshak, Emad A. Heinrich, Michael Front Pharmacol Pharmacology Introduction: A range of traditional and commercial preparations of NS is frequently used in the treatment of several inflammatory diseases. Often, these preparations have poor preclinical characterization that may lead to variable pharmacological effects. Objective: To assess the in vitro effects of different chemically defined preparations of NS on some asthma-related mediators of inflammation. Methods: Different NS preparations were obtained by either seed extraction with a spectrum of solvents ranging from lipophilic to hydrophilic, or commercial products were collected. The TQ concentration of NS was analyzed by HPLC. Immunomodulatory activity was assessed by the release of mediators (IL-2, IL-6, PGE(2)) in primary human T-lymphocytes, monocytes, and A549 human lung epithelial cells. Results: Ten distinct NS preparations showed variability in TQ concentration, being highest in the oily preparations extract-7 (2.4% w/w), followed by extract-10 (0.7%w/w). Similarly, the release of mediators was varied, being greatest in extract-7 and 10 via significantly (<0.05) suppressing IL-2, IL-6, and PGE(2) in T-lymphocytes as well as IL-6 and PGE(2) in monocytes. Also, PGE(2) release in A549 cells was significantly enhanced by both extracts. Conclusion: The TQ concentration and in vitro activity were variable among the different NS preparations. TQ-rich oily NS preparations produced potent favorable immunomodulation in asthma inflammation and can be used in future studies. Frontiers Media S.A. 2018-10-02 /pmc/articles/PMC6176110/ /pubmed/30333747 http://dx.doi.org/10.3389/fphar.2018.01075 Text en Copyright © 2018 Koshak, Yousif, Fiebich, Koshak and Heinrich. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Koshak, Abdulrahman E.
Yousif, Nizar M.
Fiebich, Bernd L.
Koshak, Emad A.
Heinrich, Michael
Comparative Immunomodulatory Activity of Nigella sativa L. Preparations on Proinflammatory Mediators: A Focus on Asthma
title Comparative Immunomodulatory Activity of Nigella sativa L. Preparations on Proinflammatory Mediators: A Focus on Asthma
title_full Comparative Immunomodulatory Activity of Nigella sativa L. Preparations on Proinflammatory Mediators: A Focus on Asthma
title_fullStr Comparative Immunomodulatory Activity of Nigella sativa L. Preparations on Proinflammatory Mediators: A Focus on Asthma
title_full_unstemmed Comparative Immunomodulatory Activity of Nigella sativa L. Preparations on Proinflammatory Mediators: A Focus on Asthma
title_short Comparative Immunomodulatory Activity of Nigella sativa L. Preparations on Proinflammatory Mediators: A Focus on Asthma
title_sort comparative immunomodulatory activity of nigella sativa l. preparations on proinflammatory mediators: a focus on asthma
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176110/
https://www.ncbi.nlm.nih.gov/pubmed/30333747
http://dx.doi.org/10.3389/fphar.2018.01075
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