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21-O-Angeloyltheasapogenol E3, a Novel Triterpenoid Saponin from the Seeds of Tea Plants, Inhibits Macrophage-Mediated Inflammatory Responses in a NF-κB-Dependent Manner

21-O-Angeloyltheasapogenol E3 (ATS-E3) is a triterpenoid saponin recently isolated from the seeds of the tea tree Camellia sinensis (L.) O. Kuntze. ATS-E3 has several beneficial properties including anti-inflammatory, antidiabetic, antiatherosclerotic, and anticancer effects. Unlike other phenolic c...

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Autores principales: Yang, Woo Seok, Ko, Jaeyoung, Kim, Eunji, Kim, Ji Hye, Park, Jae Gwang, Sung, Nak Yoon, Kim, Han Gyung, Yang, Sungjae, Rho, Ho Sik, Hong, Yong Deog, Shin, Song Seok, Cho, Jae Youl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245502/
https://www.ncbi.nlm.nih.gov/pubmed/25477714
http://dx.doi.org/10.1155/2014/658351
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author Yang, Woo Seok
Ko, Jaeyoung
Kim, Eunji
Kim, Ji Hye
Park, Jae Gwang
Sung, Nak Yoon
Kim, Han Gyung
Yang, Sungjae
Rho, Ho Sik
Hong, Yong Deog
Shin, Song Seok
Cho, Jae Youl
author_facet Yang, Woo Seok
Ko, Jaeyoung
Kim, Eunji
Kim, Ji Hye
Park, Jae Gwang
Sung, Nak Yoon
Kim, Han Gyung
Yang, Sungjae
Rho, Ho Sik
Hong, Yong Deog
Shin, Song Seok
Cho, Jae Youl
author_sort Yang, Woo Seok
collection PubMed
description 21-O-Angeloyltheasapogenol E3 (ATS-E3) is a triterpenoid saponin recently isolated from the seeds of the tea tree Camellia sinensis (L.) O. Kuntze. ATS-E3 has several beneficial properties including anti-inflammatory, antidiabetic, antiatherosclerotic, and anticancer effects. Unlike other phenolic compounds isolated from tea plants, there are no studies reporting the pharmacological action of ATS-E3. In this study, we therefore aimed to explore the cellular and molecular inhibitory activities of ATS-E3 in macrophage-mediated inflammatory responses. ATS-E3 remarkably diminished cellular responses of macrophages such as FITC-dextran-induced phagocytic uptake, sodium nitroprusside- (SNP-) induced radical generation, and LPS-induced nitric oxide (NO) production. Analysis of its molecular activity showed that this compound significantly suppressed the expression of inducible NO synthase (iNOS), nuclear translocation of nuclear factor- (NF-) κB subunits (p50 and p65), phosphorylation of inhibitor of κB kinase (IKK), and the enzyme activity of AKT1. Taken together, the novel triterpenoid saponin compound ATS-E3 contributes to the beneficial effects of tea plants by exerting anti-inflammatory and antioxidative activities in an AKT/IKK/NF-κB-dependent manner.
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spelling pubmed-42455022014-12-04 21-O-Angeloyltheasapogenol E3, a Novel Triterpenoid Saponin from the Seeds of Tea Plants, Inhibits Macrophage-Mediated Inflammatory Responses in a NF-κB-Dependent Manner Yang, Woo Seok Ko, Jaeyoung Kim, Eunji Kim, Ji Hye Park, Jae Gwang Sung, Nak Yoon Kim, Han Gyung Yang, Sungjae Rho, Ho Sik Hong, Yong Deog Shin, Song Seok Cho, Jae Youl Mediators Inflamm Research Article 21-O-Angeloyltheasapogenol E3 (ATS-E3) is a triterpenoid saponin recently isolated from the seeds of the tea tree Camellia sinensis (L.) O. Kuntze. ATS-E3 has several beneficial properties including anti-inflammatory, antidiabetic, antiatherosclerotic, and anticancer effects. Unlike other phenolic compounds isolated from tea plants, there are no studies reporting the pharmacological action of ATS-E3. In this study, we therefore aimed to explore the cellular and molecular inhibitory activities of ATS-E3 in macrophage-mediated inflammatory responses. ATS-E3 remarkably diminished cellular responses of macrophages such as FITC-dextran-induced phagocytic uptake, sodium nitroprusside- (SNP-) induced radical generation, and LPS-induced nitric oxide (NO) production. Analysis of its molecular activity showed that this compound significantly suppressed the expression of inducible NO synthase (iNOS), nuclear translocation of nuclear factor- (NF-) κB subunits (p50 and p65), phosphorylation of inhibitor of κB kinase (IKK), and the enzyme activity of AKT1. Taken together, the novel triterpenoid saponin compound ATS-E3 contributes to the beneficial effects of tea plants by exerting anti-inflammatory and antioxidative activities in an AKT/IKK/NF-κB-dependent manner. Hindawi Publishing Corporation 2014 2014-11-10 /pmc/articles/PMC4245502/ /pubmed/25477714 http://dx.doi.org/10.1155/2014/658351 Text en Copyright © 2014 Woo Seok Yang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yang, Woo Seok
Ko, Jaeyoung
Kim, Eunji
Kim, Ji Hye
Park, Jae Gwang
Sung, Nak Yoon
Kim, Han Gyung
Yang, Sungjae
Rho, Ho Sik
Hong, Yong Deog
Shin, Song Seok
Cho, Jae Youl
21-O-Angeloyltheasapogenol E3, a Novel Triterpenoid Saponin from the Seeds of Tea Plants, Inhibits Macrophage-Mediated Inflammatory Responses in a NF-κB-Dependent Manner
title 21-O-Angeloyltheasapogenol E3, a Novel Triterpenoid Saponin from the Seeds of Tea Plants, Inhibits Macrophage-Mediated Inflammatory Responses in a NF-κB-Dependent Manner
title_full 21-O-Angeloyltheasapogenol E3, a Novel Triterpenoid Saponin from the Seeds of Tea Plants, Inhibits Macrophage-Mediated Inflammatory Responses in a NF-κB-Dependent Manner
title_fullStr 21-O-Angeloyltheasapogenol E3, a Novel Triterpenoid Saponin from the Seeds of Tea Plants, Inhibits Macrophage-Mediated Inflammatory Responses in a NF-κB-Dependent Manner
title_full_unstemmed 21-O-Angeloyltheasapogenol E3, a Novel Triterpenoid Saponin from the Seeds of Tea Plants, Inhibits Macrophage-Mediated Inflammatory Responses in a NF-κB-Dependent Manner
title_short 21-O-Angeloyltheasapogenol E3, a Novel Triterpenoid Saponin from the Seeds of Tea Plants, Inhibits Macrophage-Mediated Inflammatory Responses in a NF-κB-Dependent Manner
title_sort 21-o-angeloyltheasapogenol e3, a novel triterpenoid saponin from the seeds of tea plants, inhibits macrophage-mediated inflammatory responses in a nf-κb-dependent manner
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245502/
https://www.ncbi.nlm.nih.gov/pubmed/25477714
http://dx.doi.org/10.1155/2014/658351
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