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Silibinin inhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast cells

BACKGROUND: Silibinin is the major active molecule of silymarin, the mixture of flavonolignans extracted from Cirsium japonicum. It has been used for the treatment of hepatitis and inflammation-related diseases. In the present study, the effects of silibinin on allergic inflammation and its signalin...

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Autores principales: Kim, Beom-Rak, Seo, Hye-Sook, Ku, Jin-Mo, Kim, Gyung-Jun, Jeon, Chan Yong, Park, Jong Hyeong, Jang, Bo-Hyoung, Park, Sun-Ju, Shin, Yong-Cheol, Ko, Seong-Gyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Basel 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825293/
https://www.ncbi.nlm.nih.gov/pubmed/24045679
http://dx.doi.org/10.1007/s00011-013-0640-1
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author Kim, Beom-Rak
Seo, Hye-Sook
Ku, Jin-Mo
Kim, Gyung-Jun
Jeon, Chan Yong
Park, Jong Hyeong
Jang, Bo-Hyoung
Park, Sun-Ju
Shin, Yong-Cheol
Ko, Seong-Gyu
author_facet Kim, Beom-Rak
Seo, Hye-Sook
Ku, Jin-Mo
Kim, Gyung-Jun
Jeon, Chan Yong
Park, Jong Hyeong
Jang, Bo-Hyoung
Park, Sun-Ju
Shin, Yong-Cheol
Ko, Seong-Gyu
author_sort Kim, Beom-Rak
collection PubMed
description BACKGROUND: Silibinin is the major active molecule of silymarin, the mixture of flavonolignans extracted from Cirsium japonicum. It has been used for the treatment of hepatitis and inflammation-related diseases. In the present study, the effects of silibinin on allergic inflammation and its signaling were investigated in the induced human mast cells. METHODS: Cell growth inhibition induced by silibinin was measured by MTS assay. Histamine release was measured by enzyme immunoassay. The tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-8 (IL-8) secreted protein levels and mRNA levels were measured by the ELISA assay and RT-PCR, respectively. The NF-κB promoter activity was examined by a luciferase assay. RESULTS: Silibinin suppressed the growth of HMC-1 cells and also reduced the production and mRNA expression of pro-inflammatory cytokines such as TNF-α, IL-6, and IL-8. Moreover, silibinin inhibited the nuclear translocation of nuclear factor (NF)-κB through inhibition of the phosphorylation of IκBα and suppressed NF-κB transcriptional activity in stimulated HMC-1 cells. CONCLUSIONS: Taken together, these results indicate that silibinin inhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast cells, suggesting that silibinin could be used for the treatment of mast cell-derived allergic inflammatory diseases.
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spelling pubmed-38252932013-11-21 Silibinin inhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast cells Kim, Beom-Rak Seo, Hye-Sook Ku, Jin-Mo Kim, Gyung-Jun Jeon, Chan Yong Park, Jong Hyeong Jang, Bo-Hyoung Park, Sun-Ju Shin, Yong-Cheol Ko, Seong-Gyu Inflamm Res Original Research Paper BACKGROUND: Silibinin is the major active molecule of silymarin, the mixture of flavonolignans extracted from Cirsium japonicum. It has been used for the treatment of hepatitis and inflammation-related diseases. In the present study, the effects of silibinin on allergic inflammation and its signaling were investigated in the induced human mast cells. METHODS: Cell growth inhibition induced by silibinin was measured by MTS assay. Histamine release was measured by enzyme immunoassay. The tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-8 (IL-8) secreted protein levels and mRNA levels were measured by the ELISA assay and RT-PCR, respectively. The NF-κB promoter activity was examined by a luciferase assay. RESULTS: Silibinin suppressed the growth of HMC-1 cells and also reduced the production and mRNA expression of pro-inflammatory cytokines such as TNF-α, IL-6, and IL-8. Moreover, silibinin inhibited the nuclear translocation of nuclear factor (NF)-κB through inhibition of the phosphorylation of IκBα and suppressed NF-κB transcriptional activity in stimulated HMC-1 cells. CONCLUSIONS: Taken together, these results indicate that silibinin inhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast cells, suggesting that silibinin could be used for the treatment of mast cell-derived allergic inflammatory diseases. Springer Basel 2013-09-18 2013 /pmc/articles/PMC3825293/ /pubmed/24045679 http://dx.doi.org/10.1007/s00011-013-0640-1 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Research Paper
Kim, Beom-Rak
Seo, Hye-Sook
Ku, Jin-Mo
Kim, Gyung-Jun
Jeon, Chan Yong
Park, Jong Hyeong
Jang, Bo-Hyoung
Park, Sun-Ju
Shin, Yong-Cheol
Ko, Seong-Gyu
Silibinin inhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast cells
title Silibinin inhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast cells
title_full Silibinin inhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast cells
title_fullStr Silibinin inhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast cells
title_full_unstemmed Silibinin inhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast cells
title_short Silibinin inhibits the production of pro-inflammatory cytokines through inhibition of NF-κB signaling pathway in HMC-1 human mast cells
title_sort silibinin inhibits the production of pro-inflammatory cytokines through inhibition of nf-κb signaling pathway in hmc-1 human mast cells
topic Original Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825293/
https://www.ncbi.nlm.nih.gov/pubmed/24045679
http://dx.doi.org/10.1007/s00011-013-0640-1
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