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Anti-inflammatory effects of a traditional Korean medicine: Ojayeonjonghwan
Objective: To study the anti-inflammatory properties of OJ. Context: Ojayeonjonghwan (OJ) is a traditional Korean prescription, which has been widely used for the treatment of prostatitis. However, no scientific study has been performed of the anti-inflammatory effects of OJ. Materials and methods:...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130514/ https://www.ncbi.nlm.nih.gov/pubmed/28614972 http://dx.doi.org/10.1080/13880209.2017.1339282 |
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author | Nam, Sun-Young Kim, Kyu-Yeob Kim, Mi Hye Jang, Jae-Bum Rah, So-Young Lee, Jin-Man Kim, Hyung-Min Jeong, Hyun-Ja |
author_facet | Nam, Sun-Young Kim, Kyu-Yeob Kim, Mi Hye Jang, Jae-Bum Rah, So-Young Lee, Jin-Man Kim, Hyung-Min Jeong, Hyun-Ja |
author_sort | Nam, Sun-Young |
collection | PubMed |
description | Objective: To study the anti-inflammatory properties of OJ. Context: Ojayeonjonghwan (OJ) is a traditional Korean prescription, which has been widely used for the treatment of prostatitis. However, no scientific study has been performed of the anti-inflammatory effects of OJ. Materials and methods: Peritoneal macrophages were isolated 3–4 days after injecting a C57BL/6J mouse with thioglycollate. They were then treated with OJ water extract (0.01, 0.1, and 1 mg/mL) for 1 h and stimulated with lipopolysaccharide (LPS) for different times. Nitric oxide (NO), inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX)-2, and proinflammatory cytokine levels were determined by NO assay, Western blotting, RT-PCR and ELISA. Results: NO generation and iNOS induction were increased in the LPS-activated mouse peritoneal macrophages. However, NO generation and iNOS induction by LPS were suppressed by treatment with OJ for the first time. The IC(50) value of OJ with respect to NO production was 0.09 mg/mL. OJ did not influence LPS-stimulated COX-2 induction, but did significantly decrease LPS-stimulated secretions and mRNA expressions of tumour necrosis factor (TNF)-α, interleukin (IL)-6, and IL-1β. Inhibition rates of TNF-α, IL-6, and IL-1β at an OJ concentration of 1 mg/mL were 77%, 88%, and 50%, respectively. OJ also suppressed the LPS-induced nuclear translocation of NF-κB. High-performance liquid chromatography showed schizandrin and gomisin A are major components of OJ. Conclusions: OJ reduces inflammatory response, and this probably explains its positive impact on the prostatitis associated inflammation. |
format | Online Article Text |
id | pubmed-6130514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-61305142018-09-27 Anti-inflammatory effects of a traditional Korean medicine: Ojayeonjonghwan Nam, Sun-Young Kim, Kyu-Yeob Kim, Mi Hye Jang, Jae-Bum Rah, So-Young Lee, Jin-Man Kim, Hyung-Min Jeong, Hyun-Ja Pharm Biol Research Article Objective: To study the anti-inflammatory properties of OJ. Context: Ojayeonjonghwan (OJ) is a traditional Korean prescription, which has been widely used for the treatment of prostatitis. However, no scientific study has been performed of the anti-inflammatory effects of OJ. Materials and methods: Peritoneal macrophages were isolated 3–4 days after injecting a C57BL/6J mouse with thioglycollate. They were then treated with OJ water extract (0.01, 0.1, and 1 mg/mL) for 1 h and stimulated with lipopolysaccharide (LPS) for different times. Nitric oxide (NO), inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX)-2, and proinflammatory cytokine levels were determined by NO assay, Western blotting, RT-PCR and ELISA. Results: NO generation and iNOS induction were increased in the LPS-activated mouse peritoneal macrophages. However, NO generation and iNOS induction by LPS were suppressed by treatment with OJ for the first time. The IC(50) value of OJ with respect to NO production was 0.09 mg/mL. OJ did not influence LPS-stimulated COX-2 induction, but did significantly decrease LPS-stimulated secretions and mRNA expressions of tumour necrosis factor (TNF)-α, interleukin (IL)-6, and IL-1β. Inhibition rates of TNF-α, IL-6, and IL-1β at an OJ concentration of 1 mg/mL were 77%, 88%, and 50%, respectively. OJ also suppressed the LPS-induced nuclear translocation of NF-κB. High-performance liquid chromatography showed schizandrin and gomisin A are major components of OJ. Conclusions: OJ reduces inflammatory response, and this probably explains its positive impact on the prostatitis associated inflammation. Taylor & Francis 2017-06-14 /pmc/articles/PMC6130514/ /pubmed/28614972 http://dx.doi.org/10.1080/13880209.2017.1339282 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Nam, Sun-Young Kim, Kyu-Yeob Kim, Mi Hye Jang, Jae-Bum Rah, So-Young Lee, Jin-Man Kim, Hyung-Min Jeong, Hyun-Ja Anti-inflammatory effects of a traditional Korean medicine: Ojayeonjonghwan |
title | Anti-inflammatory effects of a traditional Korean medicine: Ojayeonjonghwan |
title_full | Anti-inflammatory effects of a traditional Korean medicine: Ojayeonjonghwan |
title_fullStr | Anti-inflammatory effects of a traditional Korean medicine: Ojayeonjonghwan |
title_full_unstemmed | Anti-inflammatory effects of a traditional Korean medicine: Ojayeonjonghwan |
title_short | Anti-inflammatory effects of a traditional Korean medicine: Ojayeonjonghwan |
title_sort | anti-inflammatory effects of a traditional korean medicine: ojayeonjonghwan |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130514/ https://www.ncbi.nlm.nih.gov/pubmed/28614972 http://dx.doi.org/10.1080/13880209.2017.1339282 |
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