Anti-Inflammatory Activity of Bryophytes Extracts in LPS-Stimulated RAW264.7 Murine Macrophages

Bryophytes produce rare and bioactive compounds with a broad range of therapeutic potential, and many species are reported in ethnomedicinal uses. However, only a few studies have investigated their potential as natural anti-inflammatory drug candidate compounds. The present study investigates the a...

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Main Authors: Raíssa Volpatto Marques, Stefania Enza Sestito, Frédéric Bourgaud, Sissi Miguel, Frédéric Cailotto, Pascal Reboul, Jean-Yves Jouzeau, Sophie Rahuel-Clermont, Sandrine Boschi-Muller, Henrik Toft Simonsen, David Moulin
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Molecules
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Online Access:https://www.mdpi.com/1420-3049/27/6/1940
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author Raíssa Volpatto Marques
Stefania Enza Sestito
Frédéric Bourgaud
Sissi Miguel
Frédéric Cailotto
Pascal Reboul
Jean-Yves Jouzeau
Sophie Rahuel-Clermont
Sandrine Boschi-Muller
Henrik Toft Simonsen
David Moulin
author_facet Raíssa Volpatto Marques
Stefania Enza Sestito
Frédéric Bourgaud
Sissi Miguel
Frédéric Cailotto
Pascal Reboul
Jean-Yves Jouzeau
Sophie Rahuel-Clermont
Sandrine Boschi-Muller
Henrik Toft Simonsen
David Moulin
author_sort Raíssa Volpatto Marques
collection DOAJ
description Bryophytes produce rare and bioactive compounds with a broad range of therapeutic potential, and many species are reported in ethnomedicinal uses. However, only a few studies have investigated their potential as natural anti-inflammatory drug candidate compounds. The present study investigates the anti-inflammatory effects of thirty-two species of bryophytes, including mosses and liverworts, on Raw 264.7 murine macrophages stimulated with lipopolysaccharide (LPS) or recombinant human peroxiredoxin (hPrx1). The 70% ethanol extracts of bryophytes were screened for their potential to reduce the production of nitric oxide (NO), an important pro-inflammatory mediator. Among the analyzed extracts, two moss species significantly inhibited LPS-induced NO production without cytotoxic effects. The bioactive extracts of <i>Dicranum majus</i> and <i>Thuidium delicatulum</i> inhibited NO production in a concentration-dependent manner with IC<sub>50</sub> values of 1.04 and 1.54 µg/mL, respectively. The crude 70% ethanol and ethyl acetate extracts were then partitioned with different solvents in increasing order of polarity (n-hexane, diethyl ether, chloroform, ethyl acetate, and n-butanol). The fractions were screened for their inhibitory effects on NO production stimulated with LPS at 1 ng/mL or 10 ng/mL. The NO production levels were significantly affected by the fractions of decreasing polarity such as n-hexane and diethyl ether ones. Therefore, the potential of these extracts to inhibit the LPS-induced NO pathway suggests their effective properties in attenuating inflammation and could represent a perspective for the development of innovative therapeutic agents.
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spelling doaj.art-d94e0c4bbfff4d85904afe3381ad78cc2023-11-30T21:43:34ZengMDPI AGMolecules1420-30492022-03-01276194010.3390/molecules27061940Anti-Inflammatory Activity of Bryophytes Extracts in LPS-Stimulated RAW264.7 Murine MacrophagesRaíssa Volpatto Marques0Stefania Enza Sestito1Frédéric Bourgaud2Sissi Miguel3Frédéric Cailotto4Pascal Reboul5Jean-Yves Jouzeau6Sophie Rahuel-Clermont7Sandrine Boschi-Muller8Henrik Toft Simonsen9David Moulin10Department of Biotechnology and Biomedicine, Technical University of Denmark, Søltoft Plads 223, 2800 Kongens Lyngby, DenmarkUMR 7365 CNRS, Ingénierie Moléculaire et Physiopathologie Articulaire IMoPA, Université de Lorraine, 54500 Vandœuvre-lès-Nancy, FrancePlant Advanced Technologies, 19 Avenue de la Forêt de Haye, 54500 Vandœuvre-lès-Nancy, FranceCellengo, 19 Avenue de la Forêt de Haye, 54500 Vandœuvre-lès-Nancy, FranceUMR 7365 CNRS, Ingénierie Moléculaire et Physiopathologie Articulaire IMoPA, Université de Lorraine, 54500 Vandœuvre-lès-Nancy, FranceUMR 7365 CNRS, Ingénierie Moléculaire et Physiopathologie Articulaire IMoPA, Université de Lorraine, 54500 Vandœuvre-lès-Nancy, FranceUMR 7365 CNRS, Ingénierie Moléculaire et Physiopathologie Articulaire IMoPA, Université de Lorraine, 54500 Vandœuvre-lès-Nancy, FranceUMR 7365 CNRS, Ingénierie Moléculaire et Physiopathologie Articulaire IMoPA, Université de Lorraine, 54500 Vandœuvre-lès-Nancy, FranceUMR 7365 CNRS, Ingénierie Moléculaire et Physiopathologie Articulaire IMoPA, Université de Lorraine, 54500 Vandœuvre-lès-Nancy, FranceDepartment of Biotechnology and Biomedicine, Technical University of Denmark, Søltoft Plads 223, 2800 Kongens Lyngby, DenmarkUMR 7365 CNRS, Ingénierie Moléculaire et Physiopathologie Articulaire IMoPA, Université de Lorraine, 54500 Vandœuvre-lès-Nancy, FranceBryophytes produce rare and bioactive compounds with a broad range of therapeutic potential, and many species are reported in ethnomedicinal uses. However, only a few studies have investigated their potential as natural anti-inflammatory drug candidate compounds. The present study investigates the anti-inflammatory effects of thirty-two species of bryophytes, including mosses and liverworts, on Raw 264.7 murine macrophages stimulated with lipopolysaccharide (LPS) or recombinant human peroxiredoxin (hPrx1). The 70% ethanol extracts of bryophytes were screened for their potential to reduce the production of nitric oxide (NO), an important pro-inflammatory mediator. Among the analyzed extracts, two moss species significantly inhibited LPS-induced NO production without cytotoxic effects. The bioactive extracts of <i>Dicranum majus</i> and <i>Thuidium delicatulum</i> inhibited NO production in a concentration-dependent manner with IC<sub>50</sub> values of 1.04 and 1.54 µg/mL, respectively. The crude 70% ethanol and ethyl acetate extracts were then partitioned with different solvents in increasing order of polarity (n-hexane, diethyl ether, chloroform, ethyl acetate, and n-butanol). The fractions were screened for their inhibitory effects on NO production stimulated with LPS at 1 ng/mL or 10 ng/mL. The NO production levels were significantly affected by the fractions of decreasing polarity such as n-hexane and diethyl ether ones. Therefore, the potential of these extracts to inhibit the LPS-induced NO pathway suggests their effective properties in attenuating inflammation and could represent a perspective for the development of innovative therapeutic agents.https://www.mdpi.com/1420-3049/27/6/1940bryophytesmosses<i>Dicranum majus</i><i>Thuidium delicatulum</i>anti-inflammatory activitynitric oxide
spellingShingle Raíssa Volpatto Marques
Stefania Enza Sestito
Frédéric Bourgaud
Sissi Miguel
Frédéric Cailotto
Pascal Reboul
Jean-Yves Jouzeau
Sophie Rahuel-Clermont
Sandrine Boschi-Muller
Henrik Toft Simonsen
David Moulin
Anti-Inflammatory Activity of Bryophytes Extracts in LPS-Stimulated RAW264.7 Murine Macrophages
Molecules
bryophytes
mosses
<i>Dicranum majus</i>
<i>Thuidium delicatulum</i>
anti-inflammatory activity
nitric oxide
title Anti-Inflammatory Activity of Bryophytes Extracts in LPS-Stimulated RAW264.7 Murine Macrophages
title_full Anti-Inflammatory Activity of Bryophytes Extracts in LPS-Stimulated RAW264.7 Murine Macrophages
title_fullStr Anti-Inflammatory Activity of Bryophytes Extracts in LPS-Stimulated RAW264.7 Murine Macrophages
title_full_unstemmed Anti-Inflammatory Activity of Bryophytes Extracts in LPS-Stimulated RAW264.7 Murine Macrophages
title_short Anti-Inflammatory Activity of Bryophytes Extracts in LPS-Stimulated RAW264.7 Murine Macrophages
title_sort anti inflammatory activity of bryophytes extracts in lps stimulated raw264 7 murine macrophages
topic bryophytes
mosses
<i>Dicranum majus</i>
<i>Thuidium delicatulum</i>
anti-inflammatory activity
nitric oxide
url https://www.mdpi.com/1420-3049/27/6/1940
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