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Oryeongsan (Goreisan) Ameliorates Experimental Autoimmune Encephalomyelitis
OBJECTIVE: Oryeongsan (Goreisan), a formula composed of five herbal medicines, has long been used to treat impairments of the regulation of body fluid homeostasis. Goreisan has been revealed to have anti-inflammatory actions and inhibit a water channel, the aquaporin (AQP). We herein report the ther...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Internal Medicine
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995709/ https://www.ncbi.nlm.nih.gov/pubmed/31484905 http://dx.doi.org/10.2169/internalmedicine.3030-19 |
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author | Inada, Rino Miyamoto, Katsuichi Tanaka, Noriko Moriguchi, Kota Kusunoki, Susumu |
author_facet | Inada, Rino Miyamoto, Katsuichi Tanaka, Noriko Moriguchi, Kota Kusunoki, Susumu |
author_sort | Inada, Rino |
collection | PubMed |
description | OBJECTIVE: Oryeongsan (Goreisan), a formula composed of five herbal medicines, has long been used to treat impairments of the regulation of body fluid homeostasis. Goreisan has been revealed to have anti-inflammatory actions and inhibit a water channel, the aquaporin (AQP). We herein report the therapeutic effect of Goreisan on experimental autoimmune encephalomyelitis (EAE in, an animal model of inflammatory demyelinating diseases. MATERIALS AND METHODS: EAE mice immunized with MOG(35-55) peptide were divided into Goreisan- and sham-treated groups. The clinical EAE score and histopathological finding of the central nervous system (CNS) were analyzed. For the proliferation assay, prepared spleen cells from immunized mice were cultured and analyzed for the [(3)H]-thymidine uptake and cytokine concentrations of the culture supernatant. The relative quantification of AQP4 mRNA in the CNS of EAE mice was analyzed quantitatively. RESULTS: The EAE score of the Goreisan-treated mice was significantly lower than that of the sham-treated mice. The CD4-positive cell number in the CNS of Goreisan-treated mice was lower than that of sham-treated mice. In the recall response to MOG(35-55) peptide, the cell proliferation did not differ markedly between the spleen cells from Goreisan- and sham-treated mice. Furthermore, Goreisan decreased the mRNA level of AQP4 in the spinal cord during EAE. CONCLUSION: Goreisan prevented the disease activity of EAE by inhibiting the migration of pathogenic cells into the CNS by suppressing the AQP4 expression in the CNS. Goreisan may have a therapeutic effect on inflammatory demyelinating diseases. |
format | Online Article Text |
id | pubmed-6995709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Japanese Society of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-69957092020-02-03 Oryeongsan (Goreisan) Ameliorates Experimental Autoimmune Encephalomyelitis Inada, Rino Miyamoto, Katsuichi Tanaka, Noriko Moriguchi, Kota Kusunoki, Susumu Intern Med Original Article OBJECTIVE: Oryeongsan (Goreisan), a formula composed of five herbal medicines, has long been used to treat impairments of the regulation of body fluid homeostasis. Goreisan has been revealed to have anti-inflammatory actions and inhibit a water channel, the aquaporin (AQP). We herein report the therapeutic effect of Goreisan on experimental autoimmune encephalomyelitis (EAE in, an animal model of inflammatory demyelinating diseases. MATERIALS AND METHODS: EAE mice immunized with MOG(35-55) peptide were divided into Goreisan- and sham-treated groups. The clinical EAE score and histopathological finding of the central nervous system (CNS) were analyzed. For the proliferation assay, prepared spleen cells from immunized mice were cultured and analyzed for the [(3)H]-thymidine uptake and cytokine concentrations of the culture supernatant. The relative quantification of AQP4 mRNA in the CNS of EAE mice was analyzed quantitatively. RESULTS: The EAE score of the Goreisan-treated mice was significantly lower than that of the sham-treated mice. The CD4-positive cell number in the CNS of Goreisan-treated mice was lower than that of sham-treated mice. In the recall response to MOG(35-55) peptide, the cell proliferation did not differ markedly between the spleen cells from Goreisan- and sham-treated mice. Furthermore, Goreisan decreased the mRNA level of AQP4 in the spinal cord during EAE. CONCLUSION: Goreisan prevented the disease activity of EAE by inhibiting the migration of pathogenic cells into the CNS by suppressing the AQP4 expression in the CNS. Goreisan may have a therapeutic effect on inflammatory demyelinating diseases. The Japanese Society of Internal Medicine 2019-09-03 2020-01-01 /pmc/articles/PMC6995709/ /pubmed/31484905 http://dx.doi.org/10.2169/internalmedicine.3030-19 Text en Copyright © 2020 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Inada, Rino Miyamoto, Katsuichi Tanaka, Noriko Moriguchi, Kota Kusunoki, Susumu Oryeongsan (Goreisan) Ameliorates Experimental Autoimmune Encephalomyelitis |
title | Oryeongsan (Goreisan) Ameliorates Experimental Autoimmune Encephalomyelitis |
title_full | Oryeongsan (Goreisan) Ameliorates Experimental Autoimmune Encephalomyelitis |
title_fullStr | Oryeongsan (Goreisan) Ameliorates Experimental Autoimmune Encephalomyelitis |
title_full_unstemmed | Oryeongsan (Goreisan) Ameliorates Experimental Autoimmune Encephalomyelitis |
title_short | Oryeongsan (Goreisan) Ameliorates Experimental Autoimmune Encephalomyelitis |
title_sort | oryeongsan (goreisan) ameliorates experimental autoimmune encephalomyelitis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995709/ https://www.ncbi.nlm.nih.gov/pubmed/31484905 http://dx.doi.org/10.2169/internalmedicine.3030-19 |
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