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Anti-inflammatory activities of Coleus forsteri (formerly Plectranthus forsteri) extracts on human macrophages and chemical characterization

Introduction: Formerly named Plectranthus forsteri, Coleus forsteri (Benth.) A.J.Paton, 2019 is a Lamiaceae traditionally used to treat flu-like symptoms and shock-related ecchymosis, especially in the Pacific region. Few studies investigated chemical composition and anti-inflammatory potential of t...

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Autores principales: Nicolas, Mael, Lasalo, Malia, Chow, Sharron, Antheaume, Cyril, Huet, Karl, Hnawia, Edouard, Guillemin, Gilles J., Nour, Mohammed, Matsui, Mariko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868419/
https://www.ncbi.nlm.nih.gov/pubmed/36699063
http://dx.doi.org/10.3389/fphar.2022.1081310
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author Nicolas, Mael
Lasalo, Malia
Chow, Sharron
Antheaume, Cyril
Huet, Karl
Hnawia, Edouard
Guillemin, Gilles J.
Nour, Mohammed
Matsui, Mariko
author_facet Nicolas, Mael
Lasalo, Malia
Chow, Sharron
Antheaume, Cyril
Huet, Karl
Hnawia, Edouard
Guillemin, Gilles J.
Nour, Mohammed
Matsui, Mariko
author_sort Nicolas, Mael
collection PubMed
description Introduction: Formerly named Plectranthus forsteri, Coleus forsteri (Benth.) A.J.Paton, 2019 is a Lamiaceae traditionally used to treat flu-like symptoms and shock-related ecchymosis, especially in the Pacific region. Few studies investigated chemical composition and anti-inflammatory potential of this plant. Method: Herein, we investigated anti-inflammatory potential of C. forsteri ethanolic (ePE) and cyclohexane (cPE) plant extract on LPS-induced human macrophages models and quantified cytokines and quinolinic acid (QUIN) as inflammatory markers. Results: Our results show that extract of ePE and cPE significantly inhibit inflammatory cytokine IL-6 and TNF-α induced by LPS on PMA-derived THP-1 macrophages. QUIN production is also diminished under ePE and cPE treatment in activated human monocyte-derived macrophages (MDMs). Seven abietane diterpenes were characterized from C. forsteri cPE including coleon U (1), coleon U-quinone (2), 8α,9α-epoxycoleon U-quinone (3), horminone or 7α-hydroxyroyleanone (4), 6β,7α-dihydroxyroyleanone (5), 7α-acetoxy-6β-hydroxyroyleanone (6) and 7α-formyloxy-6β-hydroxyroyleanone (7). Discussion: We discussed potential contributions of these molecules from C. forsteri extracts for their anti-inflammatory activities.
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spelling pubmed-98684192023-01-24 Anti-inflammatory activities of Coleus forsteri (formerly Plectranthus forsteri) extracts on human macrophages and chemical characterization Nicolas, Mael Lasalo, Malia Chow, Sharron Antheaume, Cyril Huet, Karl Hnawia, Edouard Guillemin, Gilles J. Nour, Mohammed Matsui, Mariko Front Pharmacol Pharmacology Introduction: Formerly named Plectranthus forsteri, Coleus forsteri (Benth.) A.J.Paton, 2019 is a Lamiaceae traditionally used to treat flu-like symptoms and shock-related ecchymosis, especially in the Pacific region. Few studies investigated chemical composition and anti-inflammatory potential of this plant. Method: Herein, we investigated anti-inflammatory potential of C. forsteri ethanolic (ePE) and cyclohexane (cPE) plant extract on LPS-induced human macrophages models and quantified cytokines and quinolinic acid (QUIN) as inflammatory markers. Results: Our results show that extract of ePE and cPE significantly inhibit inflammatory cytokine IL-6 and TNF-α induced by LPS on PMA-derived THP-1 macrophages. QUIN production is also diminished under ePE and cPE treatment in activated human monocyte-derived macrophages (MDMs). Seven abietane diterpenes were characterized from C. forsteri cPE including coleon U (1), coleon U-quinone (2), 8α,9α-epoxycoleon U-quinone (3), horminone or 7α-hydroxyroyleanone (4), 6β,7α-dihydroxyroyleanone (5), 7α-acetoxy-6β-hydroxyroyleanone (6) and 7α-formyloxy-6β-hydroxyroyleanone (7). Discussion: We discussed potential contributions of these molecules from C. forsteri extracts for their anti-inflammatory activities. Frontiers Media S.A. 2023-01-09 /pmc/articles/PMC9868419/ /pubmed/36699063 http://dx.doi.org/10.3389/fphar.2022.1081310 Text en Copyright © 2023 Nicolas, Lasalo, Chow, Antheaume, Huet, Hnawia, Guillemin, Nour and Matsui. https://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
Nicolas, Mael
Lasalo, Malia
Chow, Sharron
Antheaume, Cyril
Huet, Karl
Hnawia, Edouard
Guillemin, Gilles J.
Nour, Mohammed
Matsui, Mariko
Anti-inflammatory activities of Coleus forsteri (formerly Plectranthus forsteri) extracts on human macrophages and chemical characterization
title Anti-inflammatory activities of Coleus forsteri (formerly Plectranthus forsteri) extracts on human macrophages and chemical characterization
title_full Anti-inflammatory activities of Coleus forsteri (formerly Plectranthus forsteri) extracts on human macrophages and chemical characterization
title_fullStr Anti-inflammatory activities of Coleus forsteri (formerly Plectranthus forsteri) extracts on human macrophages and chemical characterization
title_full_unstemmed Anti-inflammatory activities of Coleus forsteri (formerly Plectranthus forsteri) extracts on human macrophages and chemical characterization
title_short Anti-inflammatory activities of Coleus forsteri (formerly Plectranthus forsteri) extracts on human macrophages and chemical characterization
title_sort anti-inflammatory activities of coleus forsteri (formerly plectranthus forsteri) extracts on human macrophages and chemical characterization
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868419/
https://www.ncbi.nlm.nih.gov/pubmed/36699063
http://dx.doi.org/10.3389/fphar.2022.1081310
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