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Adenosine A2A Receptors Mediate Anti-Inflammatory Effects of Electroacupuncture on Synovitis in Mice with Collagen-Induced Arthritis
To study the role of adenosine A2A receptor (A(2A)R) in mediating the anti-inflammatory effect of electroacupuncture (EA) on synovitis in collagen-induced arthritis (CIA), C57BL/6 mice were divided into five treatment groups: Sham-control, CIA-control, CIA-EA, CIA-SCH58261 (A(2A)R antagonist), and C...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345253/ https://www.ncbi.nlm.nih.gov/pubmed/25784951 http://dx.doi.org/10.1155/2015/809560 |
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author | Li, Qi-hui Xie, Wen-xia Li, Xiao-pei Huang, Ka-te Du, Zhong-heng Cong, Wen-jie Zhou, Long-hua Ye, Tian-shen Chen, Jiang-Fan |
author_facet | Li, Qi-hui Xie, Wen-xia Li, Xiao-pei Huang, Ka-te Du, Zhong-heng Cong, Wen-jie Zhou, Long-hua Ye, Tian-shen Chen, Jiang-Fan |
author_sort | Li, Qi-hui |
collection | PubMed |
description | To study the role of adenosine A2A receptor (A(2A)R) in mediating the anti-inflammatory effect of electroacupuncture (EA) on synovitis in collagen-induced arthritis (CIA), C57BL/6 mice were divided into five treatment groups: Sham-control, CIA-control, CIA-EA, CIA-SCH58261 (A(2A)R antagonist), and CIA-EA-SCH58261. All mice except those in the Sham-control group were immunized with collagen II for arthritis induction. EA treatment was administered using the stomach 36 and spleen 6 points, and stimulated with a continuous rectangular wave for 30 min daily. EA treatment and SCH58261 were administered daily from days 35 to 49 (n = 10). After treatment, X-ray radiography of joint bone morphology was established at day 60 and mouse blood was collected for ELISA determination of tumor necrosis factor alpha (TNF-α) levels. Mice were sacrificed and processed for histological examination of pathological changes of joint tissue, including hematoxylin-eosin staining and immunohistochemistry of A(2A)R expression. EA treatment resulted in significantly reduced pathological scores, TNF-α concentrations, and bone damage X-ray scores. Importantly, the anti-inflammatory and tissue-protective effect of EA treatment was reversed by coadministration of SCH58261. Thus, EA treatment exerts an anti-inflammatory effect resulting in significant protection of cartilage by activation of A(2A)R in the synovial tissue of CIA. |
format | Online Article Text |
id | pubmed-4345253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-43452532015-03-17 Adenosine A2A Receptors Mediate Anti-Inflammatory Effects of Electroacupuncture on Synovitis in Mice with Collagen-Induced Arthritis Li, Qi-hui Xie, Wen-xia Li, Xiao-pei Huang, Ka-te Du, Zhong-heng Cong, Wen-jie Zhou, Long-hua Ye, Tian-shen Chen, Jiang-Fan Evid Based Complement Alternat Med Research Article To study the role of adenosine A2A receptor (A(2A)R) in mediating the anti-inflammatory effect of electroacupuncture (EA) on synovitis in collagen-induced arthritis (CIA), C57BL/6 mice were divided into five treatment groups: Sham-control, CIA-control, CIA-EA, CIA-SCH58261 (A(2A)R antagonist), and CIA-EA-SCH58261. All mice except those in the Sham-control group were immunized with collagen II for arthritis induction. EA treatment was administered using the stomach 36 and spleen 6 points, and stimulated with a continuous rectangular wave for 30 min daily. EA treatment and SCH58261 were administered daily from days 35 to 49 (n = 10). After treatment, X-ray radiography of joint bone morphology was established at day 60 and mouse blood was collected for ELISA determination of tumor necrosis factor alpha (TNF-α) levels. Mice were sacrificed and processed for histological examination of pathological changes of joint tissue, including hematoxylin-eosin staining and immunohistochemistry of A(2A)R expression. EA treatment resulted in significantly reduced pathological scores, TNF-α concentrations, and bone damage X-ray scores. Importantly, the anti-inflammatory and tissue-protective effect of EA treatment was reversed by coadministration of SCH58261. Thus, EA treatment exerts an anti-inflammatory effect resulting in significant protection of cartilage by activation of A(2A)R in the synovial tissue of CIA. Hindawi Publishing Corporation 2015 2015-02-16 /pmc/articles/PMC4345253/ /pubmed/25784951 http://dx.doi.org/10.1155/2015/809560 Text en Copyright © 2015 Qi-hui Li et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Qi-hui Xie, Wen-xia Li, Xiao-pei Huang, Ka-te Du, Zhong-heng Cong, Wen-jie Zhou, Long-hua Ye, Tian-shen Chen, Jiang-Fan Adenosine A2A Receptors Mediate Anti-Inflammatory Effects of Electroacupuncture on Synovitis in Mice with Collagen-Induced Arthritis |
title | Adenosine A2A Receptors Mediate Anti-Inflammatory Effects of Electroacupuncture on Synovitis in Mice with Collagen-Induced Arthritis |
title_full | Adenosine A2A Receptors Mediate Anti-Inflammatory Effects of Electroacupuncture on Synovitis in Mice with Collagen-Induced Arthritis |
title_fullStr | Adenosine A2A Receptors Mediate Anti-Inflammatory Effects of Electroacupuncture on Synovitis in Mice with Collagen-Induced Arthritis |
title_full_unstemmed | Adenosine A2A Receptors Mediate Anti-Inflammatory Effects of Electroacupuncture on Synovitis in Mice with Collagen-Induced Arthritis |
title_short | Adenosine A2A Receptors Mediate Anti-Inflammatory Effects of Electroacupuncture on Synovitis in Mice with Collagen-Induced Arthritis |
title_sort | adenosine a2a receptors mediate anti-inflammatory effects of electroacupuncture on synovitis in mice with collagen-induced arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345253/ https://www.ncbi.nlm.nih.gov/pubmed/25784951 http://dx.doi.org/10.1155/2015/809560 |
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