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Inhibitory effects of Camellia japonica on cell inflammation and acute rat reflux esophagitis
BACKGROUND: Excessive and continuous inflammation may be the main cause of various immune system diseases. Reflux esophagitis (RE) is a common gastroesophageal reflux disease (GERD). Camellia japonica has high medicinal value and has long been used as a traditional herbal hemostatic medicine in Chin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791640/ https://www.ncbi.nlm.nih.gov/pubmed/33413538 http://dx.doi.org/10.1186/s13020-020-00411-0 |
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author | Nam, Hyeon Hwa Nan, Li Choo, Byung Kil |
author_facet | Nam, Hyeon Hwa Nan, Li Choo, Byung Kil |
author_sort | Nam, Hyeon Hwa |
collection | PubMed |
description | BACKGROUND: Excessive and continuous inflammation may be the main cause of various immune system diseases. Reflux esophagitis (RE) is a common gastroesophageal reflux disease (GERD). Camellia japonica has high medicinal value and has long been used as a traditional herbal hemostatic medicine in China and Korea. The purpose of this study is to explore the antioxidant and anti-inflammatory activities of CJE and its protective effect on RE. MATERIALS AND METHODS: Buds from C. japonica plants were collected in the mountain area of Jeju, South Korea. Dried C. japonica buds were extracted with 75% ethanol. DPPH and ABTS radical scavenging assay were evaluated according to previous method. The ROS production and anti-inflammatory effects of C. japonica buds ethanol extract (CJE) were evaluated on LPS-induced RAW 264.7 cell inflammation. The protective effects of CJE on RE were conducted in a RE rat model. RESULTS: CJE eliminated over 50% of DPPH and ABTS radical at concentration of 100 and 200 µg/mL, respectively. CJE alleviated changes in cell morphology, reduced production of ROS, NO and IL-1β. Also, down-regulated expression levels of iNOS, TNF-α, phosphorylated NF-κB, IκBα, and JNK/p38/MAPK. CJE reduced esophageal tissue damage ratio (40.3%) and attenuation of histological changes. In addition, CJE down-regulated the expression levels of TNF-α, IL-1β, COX-2 and phosphorylation levels of NF-κB and IκBα in esophageal tissue. CONCLUSIONS: CJE possesses good anti-oxidation and anti-inflammatory activity, and can improve RE in rats caused by gastric acid reflux. Therefore, CJE is a natural material with good anti-oxidant and anti-inflammatory activity and has the possibility of being a candidate phytomedicine source for the treatment of RE. |
format | Online Article Text |
id | pubmed-7791640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77916402021-01-11 Inhibitory effects of Camellia japonica on cell inflammation and acute rat reflux esophagitis Nam, Hyeon Hwa Nan, Li Choo, Byung Kil Chin Med Research BACKGROUND: Excessive and continuous inflammation may be the main cause of various immune system diseases. Reflux esophagitis (RE) is a common gastroesophageal reflux disease (GERD). Camellia japonica has high medicinal value and has long been used as a traditional herbal hemostatic medicine in China and Korea. The purpose of this study is to explore the antioxidant and anti-inflammatory activities of CJE and its protective effect on RE. MATERIALS AND METHODS: Buds from C. japonica plants were collected in the mountain area of Jeju, South Korea. Dried C. japonica buds were extracted with 75% ethanol. DPPH and ABTS radical scavenging assay were evaluated according to previous method. The ROS production and anti-inflammatory effects of C. japonica buds ethanol extract (CJE) were evaluated on LPS-induced RAW 264.7 cell inflammation. The protective effects of CJE on RE were conducted in a RE rat model. RESULTS: CJE eliminated over 50% of DPPH and ABTS radical at concentration of 100 and 200 µg/mL, respectively. CJE alleviated changes in cell morphology, reduced production of ROS, NO and IL-1β. Also, down-regulated expression levels of iNOS, TNF-α, phosphorylated NF-κB, IκBα, and JNK/p38/MAPK. CJE reduced esophageal tissue damage ratio (40.3%) and attenuation of histological changes. In addition, CJE down-regulated the expression levels of TNF-α, IL-1β, COX-2 and phosphorylation levels of NF-κB and IκBα in esophageal tissue. CONCLUSIONS: CJE possesses good anti-oxidation and anti-inflammatory activity, and can improve RE in rats caused by gastric acid reflux. Therefore, CJE is a natural material with good anti-oxidant and anti-inflammatory activity and has the possibility of being a candidate phytomedicine source for the treatment of RE. BioMed Central 2021-01-07 /pmc/articles/PMC7791640/ /pubmed/33413538 http://dx.doi.org/10.1186/s13020-020-00411-0 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Nam, Hyeon Hwa Nan, Li Choo, Byung Kil Inhibitory effects of Camellia japonica on cell inflammation and acute rat reflux esophagitis |
title | Inhibitory effects of Camellia japonica on cell inflammation and acute rat reflux esophagitis |
title_full | Inhibitory effects of Camellia japonica on cell inflammation and acute rat reflux esophagitis |
title_fullStr | Inhibitory effects of Camellia japonica on cell inflammation and acute rat reflux esophagitis |
title_full_unstemmed | Inhibitory effects of Camellia japonica on cell inflammation and acute rat reflux esophagitis |
title_short | Inhibitory effects of Camellia japonica on cell inflammation and acute rat reflux esophagitis |
title_sort | inhibitory effects of camellia japonica on cell inflammation and acute rat reflux esophagitis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791640/ https://www.ncbi.nlm.nih.gov/pubmed/33413538 http://dx.doi.org/10.1186/s13020-020-00411-0 |
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