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Protective effect of Rhei Rhizoma on reflux esophagitis in rats via Nrf2-mediated inhibition of NF-κB signaling pathway

BACKGROUND: Rhei Rhizoma has been widely used as a traditional herbal medicine to treat various inflammatory diseases. The present study was conducted to evaluate its anti-inflammatory activity against experimental reflux-induced esophagitis (RE) in SD rats. METHODS: Rhei Rhizoma was administered at...

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Autores principales: Kwon, O Jun, Choo, Byung Kil, Lee, Joo Young, Kim, Min Yeong, Shin, Sung Ho, Seo, Bu-Il, Seo, Young-Bae, Rhee, Man Hee, Shin, Mi-Rae, Kim, Gyo-Nam, Park, Chan Hum, Roh, Seong-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707002/
https://www.ncbi.nlm.nih.gov/pubmed/26748627
http://dx.doi.org/10.1186/s12906-015-0974-z
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author Kwon, O Jun
Choo, Byung Kil
Lee, Joo Young
Kim, Min Yeong
Shin, Sung Ho
Seo, Bu-Il
Seo, Young-Bae
Rhee, Man Hee
Shin, Mi-Rae
Kim, Gyo-Nam
Park, Chan Hum
Roh, Seong-Soo
author_facet Kwon, O Jun
Choo, Byung Kil
Lee, Joo Young
Kim, Min Yeong
Shin, Sung Ho
Seo, Bu-Il
Seo, Young-Bae
Rhee, Man Hee
Shin, Mi-Rae
Kim, Gyo-Nam
Park, Chan Hum
Roh, Seong-Soo
author_sort Kwon, O Jun
collection PubMed
description BACKGROUND: Rhei Rhizoma has been widely used as a traditional herbal medicine to treat various inflammatory diseases. The present study was conducted to evaluate its anti-inflammatory activity against experimental reflux-induced esophagitis (RE) in SD rats. METHODS: Rhei Rhizoma was administered at 125 or 250 mg/kg body weight per day for 7 days prior to the induction of reflux esophagitis, and its effect was compared with RE control and normal rats. RESULTS: Rhei Rhizoma administration markedly ameliorated mucosal damage on histological evaluation. The elevated reactive oxygen species in the esophageal tissue of RE control rats decreased with the administration of Rhei Rhizoma. RE control rats exhibited the down-regulation of antioxidant-related proteins, such as nuclear factor-erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1) expression levels, in the presence of esophagitis; however, the levels with Rhei Rhizoma treatment were significantly higher than those in RE control rats. Moreover, RE control rats exhibited the up-regulation of protein expressions related to oxidative stress in the presence of esophagitis, but Rhei Rhizoma administration significantly reduced the expression of inflammatory proteins through mitogen-activated protein kinase (MAPK)-related signaling pathways. The protein expressions of inflammatory mediators and cytokines by nuclear factor-kappa B (NF-κB) activation were modulated through blocking the phosphorylation of inhibitor of nuclear factor kappa B (IκB)α. CONCLUSION: Our findings support the therapeutic evidence for Rhei Rhizoma ameliorating the development of esophagitis via regulating inflammation through the activation of the antioxidant pathway. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-015-0974-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-47070022016-01-11 Protective effect of Rhei Rhizoma on reflux esophagitis in rats via Nrf2-mediated inhibition of NF-κB signaling pathway Kwon, O Jun Choo, Byung Kil Lee, Joo Young Kim, Min Yeong Shin, Sung Ho Seo, Bu-Il Seo, Young-Bae Rhee, Man Hee Shin, Mi-Rae Kim, Gyo-Nam Park, Chan Hum Roh, Seong-Soo BMC Complement Altern Med Research Article BACKGROUND: Rhei Rhizoma has been widely used as a traditional herbal medicine to treat various inflammatory diseases. The present study was conducted to evaluate its anti-inflammatory activity against experimental reflux-induced esophagitis (RE) in SD rats. METHODS: Rhei Rhizoma was administered at 125 or 250 mg/kg body weight per day for 7 days prior to the induction of reflux esophagitis, and its effect was compared with RE control and normal rats. RESULTS: Rhei Rhizoma administration markedly ameliorated mucosal damage on histological evaluation. The elevated reactive oxygen species in the esophageal tissue of RE control rats decreased with the administration of Rhei Rhizoma. RE control rats exhibited the down-regulation of antioxidant-related proteins, such as nuclear factor-erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1) expression levels, in the presence of esophagitis; however, the levels with Rhei Rhizoma treatment were significantly higher than those in RE control rats. Moreover, RE control rats exhibited the up-regulation of protein expressions related to oxidative stress in the presence of esophagitis, but Rhei Rhizoma administration significantly reduced the expression of inflammatory proteins through mitogen-activated protein kinase (MAPK)-related signaling pathways. The protein expressions of inflammatory mediators and cytokines by nuclear factor-kappa B (NF-κB) activation were modulated through blocking the phosphorylation of inhibitor of nuclear factor kappa B (IκB)α. CONCLUSION: Our findings support the therapeutic evidence for Rhei Rhizoma ameliorating the development of esophagitis via regulating inflammation through the activation of the antioxidant pathway. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-015-0974-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-09 /pmc/articles/PMC4707002/ /pubmed/26748627 http://dx.doi.org/10.1186/s12906-015-0974-z Text en © Kwon et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kwon, O Jun
Choo, Byung Kil
Lee, Joo Young
Kim, Min Yeong
Shin, Sung Ho
Seo, Bu-Il
Seo, Young-Bae
Rhee, Man Hee
Shin, Mi-Rae
Kim, Gyo-Nam
Park, Chan Hum
Roh, Seong-Soo
Protective effect of Rhei Rhizoma on reflux esophagitis in rats via Nrf2-mediated inhibition of NF-κB signaling pathway
title Protective effect of Rhei Rhizoma on reflux esophagitis in rats via Nrf2-mediated inhibition of NF-κB signaling pathway
title_full Protective effect of Rhei Rhizoma on reflux esophagitis in rats via Nrf2-mediated inhibition of NF-κB signaling pathway
title_fullStr Protective effect of Rhei Rhizoma on reflux esophagitis in rats via Nrf2-mediated inhibition of NF-κB signaling pathway
title_full_unstemmed Protective effect of Rhei Rhizoma on reflux esophagitis in rats via Nrf2-mediated inhibition of NF-κB signaling pathway
title_short Protective effect of Rhei Rhizoma on reflux esophagitis in rats via Nrf2-mediated inhibition of NF-κB signaling pathway
title_sort protective effect of rhei rhizoma on reflux esophagitis in rats via nrf2-mediated inhibition of nf-κb signaling pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707002/
https://www.ncbi.nlm.nih.gov/pubmed/26748627
http://dx.doi.org/10.1186/s12906-015-0974-z
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