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Anti-inflammatory activity of cinnamon water extract in vivo and in vitro LPS-induced models

BACKGROUND: Cinnamon bark is one of the most popular herbal ingredients in traditional oriental medicine and possesses diverse pharmacological activities including anti-bacterial, anti-viral, and anti-cancer properties. The goal of this study is to investigate the in vivo and in vitro inhibitory eff...

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Autores principales: Hong, Joung-Woo, Yang, Ga-Eun, Kim, Yoon Bum, Eom, Seok Hyun, Lew, Jae-Hwan, Kang, Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533872/
https://www.ncbi.nlm.nih.gov/pubmed/23190501
http://dx.doi.org/10.1186/1472-6882-12-237
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author Hong, Joung-Woo
Yang, Ga-Eun
Kim, Yoon Bum
Eom, Seok Hyun
Lew, Jae-Hwan
Kang, Hee
author_facet Hong, Joung-Woo
Yang, Ga-Eun
Kim, Yoon Bum
Eom, Seok Hyun
Lew, Jae-Hwan
Kang, Hee
author_sort Hong, Joung-Woo
collection PubMed
description BACKGROUND: Cinnamon bark is one of the most popular herbal ingredients in traditional oriental medicine and possesses diverse pharmacological activities including anti-bacterial, anti-viral, and anti-cancer properties. The goal of this study is to investigate the in vivo and in vitro inhibitory effect of cinnamon water extract (CWE) on lipopolysaccharide (LPS)-induced tumor necrosis factor (TNF)-α and its underlying intracellular mechanisms. METHODS: CWE was orally administrated to mice for 6 days prior to intraperitoneal injection of LPS. Serum levels of TNF-α and interleukin (IL)-6 were determined 1 hour after LPS stimulation. Peritoneal macrophages from thioglycollate-injected mice were isolated and assayed for viability, cytokine expression and signaling molecules upon LPS stimulation. CWE was further fractioned according to molecular size, and the levels of total polyphenols and biological activities of each fraction were measured. RESULTS: The oral administration of CWE to mice significantly decreased the serum levels of TNF-α and IL-6. CWE treatment in vitro decreased the mRNA expression of TNF-α. CWE blocked the LPS-induced degradation of IκBα as well as the activation of JNK, p38 and ERK1/2. Furthermore, size-based fractionation of CWE showed that the observed inhibitory effect of CWE in vitro occurred in the fraction containing the highest level of total polyphenols. CONCLUSIONS: Treatment with CWE decreased LPS-induced TNF-α in serum. In vitro inhibition of TNF-α gene by CWE may occur via the modulation of IκBα degradation and JNK, p38, and ERK1/2 activation. Our results also indicate that the observed anti-inflammatory action of CWE may originate from the presence of polyphenols.
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spelling pubmed-35338722013-01-07 Anti-inflammatory activity of cinnamon water extract in vivo and in vitro LPS-induced models Hong, Joung-Woo Yang, Ga-Eun Kim, Yoon Bum Eom, Seok Hyun Lew, Jae-Hwan Kang, Hee BMC Complement Altern Med Research Article BACKGROUND: Cinnamon bark is one of the most popular herbal ingredients in traditional oriental medicine and possesses diverse pharmacological activities including anti-bacterial, anti-viral, and anti-cancer properties. The goal of this study is to investigate the in vivo and in vitro inhibitory effect of cinnamon water extract (CWE) on lipopolysaccharide (LPS)-induced tumor necrosis factor (TNF)-α and its underlying intracellular mechanisms. METHODS: CWE was orally administrated to mice for 6 days prior to intraperitoneal injection of LPS. Serum levels of TNF-α and interleukin (IL)-6 were determined 1 hour after LPS stimulation. Peritoneal macrophages from thioglycollate-injected mice were isolated and assayed for viability, cytokine expression and signaling molecules upon LPS stimulation. CWE was further fractioned according to molecular size, and the levels of total polyphenols and biological activities of each fraction were measured. RESULTS: The oral administration of CWE to mice significantly decreased the serum levels of TNF-α and IL-6. CWE treatment in vitro decreased the mRNA expression of TNF-α. CWE blocked the LPS-induced degradation of IκBα as well as the activation of JNK, p38 and ERK1/2. Furthermore, size-based fractionation of CWE showed that the observed inhibitory effect of CWE in vitro occurred in the fraction containing the highest level of total polyphenols. CONCLUSIONS: Treatment with CWE decreased LPS-induced TNF-α in serum. In vitro inhibition of TNF-α gene by CWE may occur via the modulation of IκBα degradation and JNK, p38, and ERK1/2 activation. Our results also indicate that the observed anti-inflammatory action of CWE may originate from the presence of polyphenols. BioMed Central 2012-11-28 /pmc/articles/PMC3533872/ /pubmed/23190501 http://dx.doi.org/10.1186/1472-6882-12-237 Text en Copyright ©2012 Hong 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
Hong, Joung-Woo
Yang, Ga-Eun
Kim, Yoon Bum
Eom, Seok Hyun
Lew, Jae-Hwan
Kang, Hee
Anti-inflammatory activity of cinnamon water extract in vivo and in vitro LPS-induced models
title Anti-inflammatory activity of cinnamon water extract in vivo and in vitro LPS-induced models
title_full Anti-inflammatory activity of cinnamon water extract in vivo and in vitro LPS-induced models
title_fullStr Anti-inflammatory activity of cinnamon water extract in vivo and in vitro LPS-induced models
title_full_unstemmed Anti-inflammatory activity of cinnamon water extract in vivo and in vitro LPS-induced models
title_short Anti-inflammatory activity of cinnamon water extract in vivo and in vitro LPS-induced models
title_sort anti-inflammatory activity of cinnamon water extract in vivo and in vitro lps-induced models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533872/
https://www.ncbi.nlm.nih.gov/pubmed/23190501
http://dx.doi.org/10.1186/1472-6882-12-237
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