Cargando…

An extract of the medicinal plant Artemisia annua modulates production of inflammatory markers in activated neutrophils

PURPOSE: To investigate the ability of a commercial extract from the medicinal plant Artemisia annua to modulate production of the cytokine, tumor necrosis factor-alpha (TNF-α), and the cyclooxygenase (COX) inflammatory marker, prostaglandin E(2) (PGE(2)) in activated neutrophils. METHODS: Neutrophi...

Descripción completa

Detalles Bibliográficos
Autores principales: Hunt, Sheena, Yoshida, Mayumi, Davis, Catherine EJ, Greenhill, Nicholas S, Davis, Paul F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298291/
https://www.ncbi.nlm.nih.gov/pubmed/25609991
http://dx.doi.org/10.2147/JIR.S75484
_version_ 1782353246921162752
author Hunt, Sheena
Yoshida, Mayumi
Davis, Catherine EJ
Greenhill, Nicholas S
Davis, Paul F
author_facet Hunt, Sheena
Yoshida, Mayumi
Davis, Catherine EJ
Greenhill, Nicholas S
Davis, Paul F
author_sort Hunt, Sheena
collection PubMed
description PURPOSE: To investigate the ability of a commercial extract from the medicinal plant Artemisia annua to modulate production of the cytokine, tumor necrosis factor-alpha (TNF-α), and the cyclooxygenase (COX) inflammatory marker, prostaglandin E(2) (PGE(2)) in activated neutrophils. METHODS: Neutrophils were harvested from rat whole blood and cultured in the presence of plant extract or control samples. Neutrophils, except unactivated control cells, were activated with 10 μg/mL lipopolysaccharide (LPS). The cells were cultured with a range of different concentrations of the A. annua extracts (400–1 μg/mL) and artemisinin (200 and 100 μg/mL) and the supernatants were then tested by enzyme-linked immunosorbent assay (ELISA) for the concentrations of TNF-α and PGE(2). Each sample was assayed in triplicate. Positive controls with an inhibitor were assayed in triplicate: chloroquine 2.58 and 5.16 μg/mL for TNF-α, and ibuprofen 400 μg/mL for PGE(2). An unsupplemented group was also assessed in triplicate as a baseline control. RESULTS: Neutrophils were stimulated to an inflammatory state by the addition of LPS. A. annua extract significantly inhibited TNF-α production by activated neutrophils in a dose-dependent manner. There was complete inhibition by the A. annua extract at 200, 100, and 50 μg/mL (all P≤0.0003). At A. annua extract concentrations of 25, 10, and 5 μg/mL, TNF-α production was inhibited by 89% (P<0.0001), 54% (P=0.0002), and 38% (P=0.0014), respectively. A. annua 1 μg/mL did not significantly inhibit TNF-α production (8.8%; P>0.05). Concentrations of 400, 200, and 100 μg/mL A. annua extract significantly inhibited PGE(2) production by 87% (P=0.0128), 91% (P=0.0017), and 93% (P=0.0114), respectively. CONCLUSION: An extract of A. annua was shown to be a potent inhibitor of TNF-α and a strong inhibitor of PGE(2) production in activated neutrophils at the concentrations tested. Further studies are warranted with this promising plant extract.
format Online
Article
Text
id pubmed-4298291
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-42982912015-01-21 An extract of the medicinal plant Artemisia annua modulates production of inflammatory markers in activated neutrophils Hunt, Sheena Yoshida, Mayumi Davis, Catherine EJ Greenhill, Nicholas S Davis, Paul F J Inflamm Res Original Research PURPOSE: To investigate the ability of a commercial extract from the medicinal plant Artemisia annua to modulate production of the cytokine, tumor necrosis factor-alpha (TNF-α), and the cyclooxygenase (COX) inflammatory marker, prostaglandin E(2) (PGE(2)) in activated neutrophils. METHODS: Neutrophils were harvested from rat whole blood and cultured in the presence of plant extract or control samples. Neutrophils, except unactivated control cells, were activated with 10 μg/mL lipopolysaccharide (LPS). The cells were cultured with a range of different concentrations of the A. annua extracts (400–1 μg/mL) and artemisinin (200 and 100 μg/mL) and the supernatants were then tested by enzyme-linked immunosorbent assay (ELISA) for the concentrations of TNF-α and PGE(2). Each sample was assayed in triplicate. Positive controls with an inhibitor were assayed in triplicate: chloroquine 2.58 and 5.16 μg/mL for TNF-α, and ibuprofen 400 μg/mL for PGE(2). An unsupplemented group was also assessed in triplicate as a baseline control. RESULTS: Neutrophils were stimulated to an inflammatory state by the addition of LPS. A. annua extract significantly inhibited TNF-α production by activated neutrophils in a dose-dependent manner. There was complete inhibition by the A. annua extract at 200, 100, and 50 μg/mL (all P≤0.0003). At A. annua extract concentrations of 25, 10, and 5 μg/mL, TNF-α production was inhibited by 89% (P<0.0001), 54% (P=0.0002), and 38% (P=0.0014), respectively. A. annua 1 μg/mL did not significantly inhibit TNF-α production (8.8%; P>0.05). Concentrations of 400, 200, and 100 μg/mL A. annua extract significantly inhibited PGE(2) production by 87% (P=0.0128), 91% (P=0.0017), and 93% (P=0.0114), respectively. CONCLUSION: An extract of A. annua was shown to be a potent inhibitor of TNF-α and a strong inhibitor of PGE(2) production in activated neutrophils at the concentrations tested. Further studies are warranted with this promising plant extract. Dove Medical Press 2015-01-14 /pmc/articles/PMC4298291/ /pubmed/25609991 http://dx.doi.org/10.2147/JIR.S75484 Text en © 2015 Hunt et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Hunt, Sheena
Yoshida, Mayumi
Davis, Catherine EJ
Greenhill, Nicholas S
Davis, Paul F
An extract of the medicinal plant Artemisia annua modulates production of inflammatory markers in activated neutrophils
title An extract of the medicinal plant Artemisia annua modulates production of inflammatory markers in activated neutrophils
title_full An extract of the medicinal plant Artemisia annua modulates production of inflammatory markers in activated neutrophils
title_fullStr An extract of the medicinal plant Artemisia annua modulates production of inflammatory markers in activated neutrophils
title_full_unstemmed An extract of the medicinal plant Artemisia annua modulates production of inflammatory markers in activated neutrophils
title_short An extract of the medicinal plant Artemisia annua modulates production of inflammatory markers in activated neutrophils
title_sort extract of the medicinal plant artemisia annua modulates production of inflammatory markers in activated neutrophils
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298291/
https://www.ncbi.nlm.nih.gov/pubmed/25609991
http://dx.doi.org/10.2147/JIR.S75484
work_keys_str_mv AT huntsheena anextractofthemedicinalplantartemisiaannuamodulatesproductionofinflammatorymarkersinactivatedneutrophils
AT yoshidamayumi anextractofthemedicinalplantartemisiaannuamodulatesproductionofinflammatorymarkersinactivatedneutrophils
AT daviscatherineej anextractofthemedicinalplantartemisiaannuamodulatesproductionofinflammatorymarkersinactivatedneutrophils
AT greenhillnicholass anextractofthemedicinalplantartemisiaannuamodulatesproductionofinflammatorymarkersinactivatedneutrophils
AT davispaulf anextractofthemedicinalplantartemisiaannuamodulatesproductionofinflammatorymarkersinactivatedneutrophils
AT huntsheena extractofthemedicinalplantartemisiaannuamodulatesproductionofinflammatorymarkersinactivatedneutrophils
AT yoshidamayumi extractofthemedicinalplantartemisiaannuamodulatesproductionofinflammatorymarkersinactivatedneutrophils
AT daviscatherineej extractofthemedicinalplantartemisiaannuamodulatesproductionofinflammatorymarkersinactivatedneutrophils
AT greenhillnicholass extractofthemedicinalplantartemisiaannuamodulatesproductionofinflammatorymarkersinactivatedneutrophils
AT davispaulf extractofthemedicinalplantartemisiaannuamodulatesproductionofinflammatorymarkersinactivatedneutrophils