Cargando…

Resveratrol mediates mechanical allodynia through modulating inflammatory response via the TREM2-autophagy axis in SNI rat model

BACKGROUND: Neuropathic pain (NeuP) is a chronic and challenging clinical problem, with little effective treatment. Resveratrol has shown neuroprotection by inhibiting inflammatory response in NeuP. Recently, the triggering receptor expressed on myeloid cells 2 (TREM2) expressed by microglia was ide...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Yaping, Shi, Yu, Huang, Yongquan, Liu, Wei, Cai, Guiyuan, Huang, Shimin, Zeng, Yanyan, Ren, Siqiang, Zhan, Hongrui, Wu, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576710/
https://www.ncbi.nlm.nih.gov/pubmed/33081801
http://dx.doi.org/10.1186/s12974-020-01991-2
_version_ 1783598067603210240
author Wang, Yaping
Shi, Yu
Huang, Yongquan
Liu, Wei
Cai, Guiyuan
Huang, Shimin
Zeng, Yanyan
Ren, Siqiang
Zhan, Hongrui
Wu, Wen
author_facet Wang, Yaping
Shi, Yu
Huang, Yongquan
Liu, Wei
Cai, Guiyuan
Huang, Shimin
Zeng, Yanyan
Ren, Siqiang
Zhan, Hongrui
Wu, Wen
author_sort Wang, Yaping
collection PubMed
description BACKGROUND: Neuropathic pain (NeuP) is a chronic and challenging clinical problem, with little effective treatment. Resveratrol has shown neuroprotection by inhibiting inflammatory response in NeuP. Recently, the triggering receptor expressed on myeloid cells 2 (TREM2) expressed by microglia was identified as a critical factor of inflammation in nervous system diseases. In this study, we explored whether resveratrol could ameliorate neuroinflammation and produce anti-mechanical allodynia effects via regulating TREM2 in spared nerve injury rats, as well as investigated the underlying mechanisms. METHODS: A spared nerve injury (SNI) rat model was performed to investigate whether resveratrol could exert anti-mechanical allodynia effects via inhibiting neuroinflammation. To evaluate the role of TREM2 in anti-neuroinflammatory function of resveratrol, lentivirus coding TREM2 was intrathecally injected into SNI rats to activate TREM2, and the pain behavior was detected by the von Frey test. Furthermore, 3-methyladenine (3-MA, an autophagy inhibitor) was applied to study the molecular mechanisms of resveratrol-mediated anti-neuroinflammation using Western blot, qPCR, and immunofluorescence. RESULTS: The TREM2 expression and number of the microglial cells were significantly increased in the ipsilateral spinal dorsal horn after SNI. We found that intrathecal administration of resveratrol (300ug/day) alleviated mechanical allodynia; obviously enhanced autophagy; and markedly reduced the levels of interleukin-1β, interleukin-6, and tumor necrosis factor-α in the ipsilateral spinal dorsal horn after SNI. Moreover, the number of Iba-1(+) microglial cells and TREM2 expression were downregulated after resveratrol treatment. Intrathecal administration of lentivirus coding TREM2 and/or 3-MA in those rats induced deficiencies in resveratrol-mediated anti-inflammation, leading to mechanical allodynia that could be rescued via administration of Res. Furthermore, 3-MA treatment contributed to TREM2-mediated mechanical allodynia. CONCLUSIONS: Taken together, these data reveal that resveratrol relieves neuropathic pain through suppressing microglia-mediated neuroinflammation via regulating the TREM2-autophagy axis in SNI rats.
format Online
Article
Text
id pubmed-7576710
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-75767102020-10-21 Resveratrol mediates mechanical allodynia through modulating inflammatory response via the TREM2-autophagy axis in SNI rat model Wang, Yaping Shi, Yu Huang, Yongquan Liu, Wei Cai, Guiyuan Huang, Shimin Zeng, Yanyan Ren, Siqiang Zhan, Hongrui Wu, Wen J Neuroinflammation Research BACKGROUND: Neuropathic pain (NeuP) is a chronic and challenging clinical problem, with little effective treatment. Resveratrol has shown neuroprotection by inhibiting inflammatory response in NeuP. Recently, the triggering receptor expressed on myeloid cells 2 (TREM2) expressed by microglia was identified as a critical factor of inflammation in nervous system diseases. In this study, we explored whether resveratrol could ameliorate neuroinflammation and produce anti-mechanical allodynia effects via regulating TREM2 in spared nerve injury rats, as well as investigated the underlying mechanisms. METHODS: A spared nerve injury (SNI) rat model was performed to investigate whether resveratrol could exert anti-mechanical allodynia effects via inhibiting neuroinflammation. To evaluate the role of TREM2 in anti-neuroinflammatory function of resveratrol, lentivirus coding TREM2 was intrathecally injected into SNI rats to activate TREM2, and the pain behavior was detected by the von Frey test. Furthermore, 3-methyladenine (3-MA, an autophagy inhibitor) was applied to study the molecular mechanisms of resveratrol-mediated anti-neuroinflammation using Western blot, qPCR, and immunofluorescence. RESULTS: The TREM2 expression and number of the microglial cells were significantly increased in the ipsilateral spinal dorsal horn after SNI. We found that intrathecal administration of resveratrol (300ug/day) alleviated mechanical allodynia; obviously enhanced autophagy; and markedly reduced the levels of interleukin-1β, interleukin-6, and tumor necrosis factor-α in the ipsilateral spinal dorsal horn after SNI. Moreover, the number of Iba-1(+) microglial cells and TREM2 expression were downregulated after resveratrol treatment. Intrathecal administration of lentivirus coding TREM2 and/or 3-MA in those rats induced deficiencies in resveratrol-mediated anti-inflammation, leading to mechanical allodynia that could be rescued via administration of Res. Furthermore, 3-MA treatment contributed to TREM2-mediated mechanical allodynia. CONCLUSIONS: Taken together, these data reveal that resveratrol relieves neuropathic pain through suppressing microglia-mediated neuroinflammation via regulating the TREM2-autophagy axis in SNI rats. BioMed Central 2020-10-21 /pmc/articles/PMC7576710/ /pubmed/33081801 http://dx.doi.org/10.1186/s12974-020-01991-2 Text en © The Author(s) 2020 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
Wang, Yaping
Shi, Yu
Huang, Yongquan
Liu, Wei
Cai, Guiyuan
Huang, Shimin
Zeng, Yanyan
Ren, Siqiang
Zhan, Hongrui
Wu, Wen
Resveratrol mediates mechanical allodynia through modulating inflammatory response via the TREM2-autophagy axis in SNI rat model
title Resveratrol mediates mechanical allodynia through modulating inflammatory response via the TREM2-autophagy axis in SNI rat model
title_full Resveratrol mediates mechanical allodynia through modulating inflammatory response via the TREM2-autophagy axis in SNI rat model
title_fullStr Resveratrol mediates mechanical allodynia through modulating inflammatory response via the TREM2-autophagy axis in SNI rat model
title_full_unstemmed Resveratrol mediates mechanical allodynia through modulating inflammatory response via the TREM2-autophagy axis in SNI rat model
title_short Resveratrol mediates mechanical allodynia through modulating inflammatory response via the TREM2-autophagy axis in SNI rat model
title_sort resveratrol mediates mechanical allodynia through modulating inflammatory response via the trem2-autophagy axis in sni rat model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576710/
https://www.ncbi.nlm.nih.gov/pubmed/33081801
http://dx.doi.org/10.1186/s12974-020-01991-2
work_keys_str_mv AT wangyaping resveratrolmediatesmechanicalallodyniathroughmodulatinginflammatoryresponseviathetrem2autophagyaxisinsniratmodel
AT shiyu resveratrolmediatesmechanicalallodyniathroughmodulatinginflammatoryresponseviathetrem2autophagyaxisinsniratmodel
AT huangyongquan resveratrolmediatesmechanicalallodyniathroughmodulatinginflammatoryresponseviathetrem2autophagyaxisinsniratmodel
AT liuwei resveratrolmediatesmechanicalallodyniathroughmodulatinginflammatoryresponseviathetrem2autophagyaxisinsniratmodel
AT caiguiyuan resveratrolmediatesmechanicalallodyniathroughmodulatinginflammatoryresponseviathetrem2autophagyaxisinsniratmodel
AT huangshimin resveratrolmediatesmechanicalallodyniathroughmodulatinginflammatoryresponseviathetrem2autophagyaxisinsniratmodel
AT zengyanyan resveratrolmediatesmechanicalallodyniathroughmodulatinginflammatoryresponseviathetrem2autophagyaxisinsniratmodel
AT rensiqiang resveratrolmediatesmechanicalallodyniathroughmodulatinginflammatoryresponseviathetrem2autophagyaxisinsniratmodel
AT zhanhongrui resveratrolmediatesmechanicalallodyniathroughmodulatinginflammatoryresponseviathetrem2autophagyaxisinsniratmodel
AT wuwen resveratrolmediatesmechanicalallodyniathroughmodulatinginflammatoryresponseviathetrem2autophagyaxisinsniratmodel