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Wu-Tou Decoction Inhibits Chronic Inflammatory Pain in Mice: Participation of TRPV1 and TRPA1 Ion Channels

Wu-tou decoction (WTD) is a classic traditional Chinese medicine formula and has been used effectively to treat joint diseases clinically. Previous reports indicated that WTD possesses anti-inflammatory activity; however, its actions on pain have not been clarified. Here, we investigated the antinoc...

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Autores principales: Wang, Chao, Liu, Chunfang, Wan, Hongye, Wang, Danhua, Sun, Danni, Xu, Tengfei, Yang, Yue, Qu, Yakun, Xu, Ying, Jing, Xianghong, Liu, Junling, Chen, Shuping, Liu, Zhiqiang, Lin, Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369886/
https://www.ncbi.nlm.nih.gov/pubmed/25839032
http://dx.doi.org/10.1155/2015/328707
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author Wang, Chao
Liu, Chunfang
Wan, Hongye
Wang, Danhua
Sun, Danni
Xu, Tengfei
Yang, Yue
Qu, Yakun
Xu, Ying
Jing, Xianghong
Liu, Junling
Chen, Shuping
Liu, Zhiqiang
Lin, Na
author_facet Wang, Chao
Liu, Chunfang
Wan, Hongye
Wang, Danhua
Sun, Danni
Xu, Tengfei
Yang, Yue
Qu, Yakun
Xu, Ying
Jing, Xianghong
Liu, Junling
Chen, Shuping
Liu, Zhiqiang
Lin, Na
author_sort Wang, Chao
collection PubMed
description Wu-tou decoction (WTD) is a classic traditional Chinese medicine formula and has been used effectively to treat joint diseases clinically. Previous reports indicated that WTD possesses anti-inflammatory activity; however, its actions on pain have not been clarified. Here, we investigated the antinociceptive activity of WTD in CFA-induced mice, and its possible mechanism of the action associated with transient receptor potential (TRP) ion channels was also explored. Our results showed that 1.58, 3.15, and 6.30 g/kg WTD significantly attenuated mechanical, cold, and heat hypersensitivities. Moreover, WTD effectively inhibited spontaneous nociceptive responses to intraplantar injections of capsaicin and cinnamaldehyde, respectively. WTD also effectively suppressed jumping and wet-dog-shake behaviors to intraperitoneal injection of icilin. Additionally, WTD significantly reduced protein expression of TRPV1 and TRPA1 in dorsal root ganglia and skins of injured paw. Collectively, our data demonstrate firstly that WTD exerts antinociceptive activity in inflammatory conditions by attenuating mechanical, cold, and heat hypersensitivities. This antinociceptive effect may result in part from inhibiting the activities of TRPV1, TRPA1, and TRPM8, and the suppression of TRPV1 and TRPA1 protein by WTD was also highly effective. These findings suggest that WTD might be an attractive and suitable therapeutic agent for the management of chronic inflammatory pain.
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spelling pubmed-43698862015-04-02 Wu-Tou Decoction Inhibits Chronic Inflammatory Pain in Mice: Participation of TRPV1 and TRPA1 Ion Channels Wang, Chao Liu, Chunfang Wan, Hongye Wang, Danhua Sun, Danni Xu, Tengfei Yang, Yue Qu, Yakun Xu, Ying Jing, Xianghong Liu, Junling Chen, Shuping Liu, Zhiqiang Lin, Na Biomed Res Int Research Article Wu-tou decoction (WTD) is a classic traditional Chinese medicine formula and has been used effectively to treat joint diseases clinically. Previous reports indicated that WTD possesses anti-inflammatory activity; however, its actions on pain have not been clarified. Here, we investigated the antinociceptive activity of WTD in CFA-induced mice, and its possible mechanism of the action associated with transient receptor potential (TRP) ion channels was also explored. Our results showed that 1.58, 3.15, and 6.30 g/kg WTD significantly attenuated mechanical, cold, and heat hypersensitivities. Moreover, WTD effectively inhibited spontaneous nociceptive responses to intraplantar injections of capsaicin and cinnamaldehyde, respectively. WTD also effectively suppressed jumping and wet-dog-shake behaviors to intraperitoneal injection of icilin. Additionally, WTD significantly reduced protein expression of TRPV1 and TRPA1 in dorsal root ganglia and skins of injured paw. Collectively, our data demonstrate firstly that WTD exerts antinociceptive activity in inflammatory conditions by attenuating mechanical, cold, and heat hypersensitivities. This antinociceptive effect may result in part from inhibiting the activities of TRPV1, TRPA1, and TRPM8, and the suppression of TRPV1 and TRPA1 protein by WTD was also highly effective. These findings suggest that WTD might be an attractive and suitable therapeutic agent for the management of chronic inflammatory pain. Hindawi Publishing Corporation 2015 2015-03-09 /pmc/articles/PMC4369886/ /pubmed/25839032 http://dx.doi.org/10.1155/2015/328707 Text en Copyright © 2015 Chao Wang 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
Wang, Chao
Liu, Chunfang
Wan, Hongye
Wang, Danhua
Sun, Danni
Xu, Tengfei
Yang, Yue
Qu, Yakun
Xu, Ying
Jing, Xianghong
Liu, Junling
Chen, Shuping
Liu, Zhiqiang
Lin, Na
Wu-Tou Decoction Inhibits Chronic Inflammatory Pain in Mice: Participation of TRPV1 and TRPA1 Ion Channels
title Wu-Tou Decoction Inhibits Chronic Inflammatory Pain in Mice: Participation of TRPV1 and TRPA1 Ion Channels
title_full Wu-Tou Decoction Inhibits Chronic Inflammatory Pain in Mice: Participation of TRPV1 and TRPA1 Ion Channels
title_fullStr Wu-Tou Decoction Inhibits Chronic Inflammatory Pain in Mice: Participation of TRPV1 and TRPA1 Ion Channels
title_full_unstemmed Wu-Tou Decoction Inhibits Chronic Inflammatory Pain in Mice: Participation of TRPV1 and TRPA1 Ion Channels
title_short Wu-Tou Decoction Inhibits Chronic Inflammatory Pain in Mice: Participation of TRPV1 and TRPA1 Ion Channels
title_sort wu-tou decoction inhibits chronic inflammatory pain in mice: participation of trpv1 and trpa1 ion channels
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369886/
https://www.ncbi.nlm.nih.gov/pubmed/25839032
http://dx.doi.org/10.1155/2015/328707
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