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Anti-inflammatory effect of Prunus yedoensis through inhibition of nuclear factor-κB in macrophages
BACKGROUND: Prunus yedoensis (PY) is a traditional anti-allergy and anti-inflammatory herb medicine used in South Korea. However, until date, little is known regarding its mechanism of action. METHODS: In order to elucidate the mechanism of anti-inflammatory effect of PY, the constituents of PY were...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659032/ https://www.ncbi.nlm.nih.gov/pubmed/23631356 http://dx.doi.org/10.1186/1472-6882-13-92 |
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author | Lee, Juyeong Yang, Gabsik Lee, Kyungjin Lee, Mi-Hwa Eom, Ji-Whan Ham, Inhye Choi, Ho-Young |
author_facet | Lee, Juyeong Yang, Gabsik Lee, Kyungjin Lee, Mi-Hwa Eom, Ji-Whan Ham, Inhye Choi, Ho-Young |
author_sort | Lee, Juyeong |
collection | PubMed |
description | BACKGROUND: Prunus yedoensis (PY) is a traditional anti-allergy and anti-inflammatory herb medicine used in South Korea. However, until date, little is known regarding its mechanism of action. METHODS: In order to elucidate the mechanism of anti-inflammatory effect of PY, the constituents of PY were analysed by high performance liquid chromatography (HPLC), and nitric oxide (NO) and prostaglandin E(2) (PGE(2)) production were measured enzyme-linked immuno sorbent assay (ELISA). The expression levels of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and nuclear factor-κB (NF-κB) were also measured by western blotting in lipopolysaccharide (LPS)-induced RAW 264.7 macrophage cells treated with PY. RESULTS: The results indicate that (50, 100 μg/mL) methanol and ethyl acetate fractionation extracts of PY not only inhibited LPS-mediated NO production and iNOS expression, but also decreased LPS-induced PGE(2) production and COX-2 expression. The anti-inflammatory effects of PY were also due to the attenuation of nuclear translocation of NF-κB, as evaluated by the use of anti-p50 on nuclear fractions. LPS-induced nuclear translocation of NF-κB decreased significantly by the methanol extract and ethyl acetate fraction of PY. High performance liquid chromatography (HPLC) analyses revealed that methanol extract and ethyl acetate fraction have similar patterns of retention time and peaks. CONCLUSION: Our results demonstrate that methanol extracts and the ethyl acetate fraction of PY have anti-inflammatory properties, thus emphasizing the potential of PY as a natural health product. |
format | Online Article Text |
id | pubmed-3659032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36590322013-05-21 Anti-inflammatory effect of Prunus yedoensis through inhibition of nuclear factor-κB in macrophages Lee, Juyeong Yang, Gabsik Lee, Kyungjin Lee, Mi-Hwa Eom, Ji-Whan Ham, Inhye Choi, Ho-Young BMC Complement Altern Med Research Article BACKGROUND: Prunus yedoensis (PY) is a traditional anti-allergy and anti-inflammatory herb medicine used in South Korea. However, until date, little is known regarding its mechanism of action. METHODS: In order to elucidate the mechanism of anti-inflammatory effect of PY, the constituents of PY were analysed by high performance liquid chromatography (HPLC), and nitric oxide (NO) and prostaglandin E(2) (PGE(2)) production were measured enzyme-linked immuno sorbent assay (ELISA). The expression levels of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and nuclear factor-κB (NF-κB) were also measured by western blotting in lipopolysaccharide (LPS)-induced RAW 264.7 macrophage cells treated with PY. RESULTS: The results indicate that (50, 100 μg/mL) methanol and ethyl acetate fractionation extracts of PY not only inhibited LPS-mediated NO production and iNOS expression, but also decreased LPS-induced PGE(2) production and COX-2 expression. The anti-inflammatory effects of PY were also due to the attenuation of nuclear translocation of NF-κB, as evaluated by the use of anti-p50 on nuclear fractions. LPS-induced nuclear translocation of NF-κB decreased significantly by the methanol extract and ethyl acetate fraction of PY. High performance liquid chromatography (HPLC) analyses revealed that methanol extract and ethyl acetate fraction have similar patterns of retention time and peaks. CONCLUSION: Our results demonstrate that methanol extracts and the ethyl acetate fraction of PY have anti-inflammatory properties, thus emphasizing the potential of PY as a natural health product. BioMed Central 2013-04-30 /pmc/articles/PMC3659032/ /pubmed/23631356 http://dx.doi.org/10.1186/1472-6882-13-92 Text en Copyright © 2013 Lee et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lee, Juyeong Yang, Gabsik Lee, Kyungjin Lee, Mi-Hwa Eom, Ji-Whan Ham, Inhye Choi, Ho-Young Anti-inflammatory effect of Prunus yedoensis through inhibition of nuclear factor-κB in macrophages |
title | Anti-inflammatory effect of Prunus yedoensis through inhibition of nuclear factor-κB in macrophages |
title_full | Anti-inflammatory effect of Prunus yedoensis through inhibition of nuclear factor-κB in macrophages |
title_fullStr | Anti-inflammatory effect of Prunus yedoensis through inhibition of nuclear factor-κB in macrophages |
title_full_unstemmed | Anti-inflammatory effect of Prunus yedoensis through inhibition of nuclear factor-κB in macrophages |
title_short | Anti-inflammatory effect of Prunus yedoensis through inhibition of nuclear factor-κB in macrophages |
title_sort | anti-inflammatory effect of prunus yedoensis through inhibition of nuclear factor-κb in macrophages |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659032/ https://www.ncbi.nlm.nih.gov/pubmed/23631356 http://dx.doi.org/10.1186/1472-6882-13-92 |
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