Microglia P2X4R-BDNF signalling contributes to central sensitization in a recurrent nitroglycerin-induced chronic migraine model

Abstract Background According to our previous study, microglia P2X4 receptors (P2X4Rs) play a pivotal role in the central sensitization of chronic migraine (CM). However, the molecular mechanism that underlies the crosstalk between microglia P2X4Rs and neurons of the trigeminal nucleus caudalis (TNC...

Full description

Bibliographic Details
Main Authors: Ting Long, Wei He, Qi Pan, Shanshan Zhang, Dunke Zhang, Guangcheng Qin, Lixue Chen, Jiying Zhou
Format: Article
Language:English
Published: BMC 2020-01-01
Series:The Journal of Headache and Pain
Subjects:
Online Access:https://doi.org/10.1186/s10194-019-1070-4
_version_ 1811270813890904064
author Ting Long
Wei He
Qi Pan
Shanshan Zhang
Dunke Zhang
Guangcheng Qin
Lixue Chen
Jiying Zhou
author_facet Ting Long
Wei He
Qi Pan
Shanshan Zhang
Dunke Zhang
Guangcheng Qin
Lixue Chen
Jiying Zhou
author_sort Ting Long
collection DOAJ
description Abstract Background According to our previous study, microglia P2X4 receptors (P2X4Rs) play a pivotal role in the central sensitization of chronic migraine (CM). However, the molecular mechanism that underlies the crosstalk between microglia P2X4Rs and neurons of the trigeminal nucleus caudalis (TNC) is not fully understood. Therefore, the aim of this study is to examine the exact P2X4Rs signalling pathway in the development of central sensitization in a CM animal model. Methods We used an animal model with recurrent intermittent administration of nitroglycerin (NTG), which closely mimics CM. NTG-induced basal mechanical and thermal hypersensitivity were evaluated using a von Frey filament test and an increasing-temperature hot plate apparatus (IITC). We detected P2X4Rs, brain-derived neurotrophic factor (BDNF) and phosphorylated p38 mitogen-activated protein kinase (p-p38-MAPK) expression profiles in the TNC. We investigated the effects of a P2X4R inhibitor (5-BDBD) and an agonist (IVM) on NTG-induced hyperalgesia and neurochemical changes as well as on the expression of p-p38-MAPK and BDNF. We also detected the effects of a tropomyosin-related kinase B (TrkB) inhibitor (ANA-12) on the CM animal model in vivo. Then, we evaluated the effect of 5-BDBD and SB203580 (a p38-MAPK inhibitors) on the release and synthesis of BDNF in BV2 microglia cells treated with 50 μM adenosine triphosphate (ATP). Results Chronic intermittent administration of NTG resulted in chronic mechanical and thermal hyperalgesia, accompanied by the upregulation of P2X4Rs and BDNF expression. 5-BDBD or ANA-12 prevented hyperalgesia induced by NTG, which was associated with a significant inhibition of the NTG-induced increase in phosphorylated extracellular regulated protein kinases (p-ERK) and calcitonin gene related peptide (CGRP) release in the TNC. Repeated administration of IVM produced sustained hyperalgesia and significantly increased the levels of p-ERK and CGRP release in the TNC. Activating P2X4Rs with ATP triggered BDNF release and increased BDNF synthesis in BV2 microglia, and these results were then reduced by 5-BDBD or SB203580. Conclusions Our results indicated that the P2X4R contributes to the central sensitization of CM by releasing BDNF and promoting TNC neuronal hyper-excitability. Blocking microglia P2X4R-BDNF signalling may have an effect on the prevention of migraine chronification.
first_indexed 2024-04-12T22:08:52Z
format Article
id doaj.art-a694e47d024842aea9e952b7711a09c1
institution Directory Open Access Journal
issn 1129-2369
1129-2377
language English
last_indexed 2024-04-12T22:08:52Z
publishDate 2020-01-01
publisher BMC
record_format Article
series The Journal of Headache and Pain
spelling doaj.art-a694e47d024842aea9e952b7711a09c12022-12-22T03:14:50ZengBMCThe Journal of Headache and Pain1129-23691129-23772020-01-0121111710.1186/s10194-019-1070-4Microglia P2X4R-BDNF signalling contributes to central sensitization in a recurrent nitroglycerin-induced chronic migraine modelTing Long0Wei He1Qi Pan2Shanshan Zhang3Dunke Zhang4Guangcheng Qin5Lixue Chen6Jiying Zhou7Department of Neurology, The Affiliated Hospital of Southwest Medical UniversityDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical UniversityDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical UniversityDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical UniversityLaboratory Research Center, The First Affiliated Hospital of Chongqing Medical UniversityLaboratory Research Center, The First Affiliated Hospital of Chongqing Medical UniversityLaboratory Research Center, The First Affiliated Hospital of Chongqing Medical UniversityDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical UniversityAbstract Background According to our previous study, microglia P2X4 receptors (P2X4Rs) play a pivotal role in the central sensitization of chronic migraine (CM). However, the molecular mechanism that underlies the crosstalk between microglia P2X4Rs and neurons of the trigeminal nucleus caudalis (TNC) is not fully understood. Therefore, the aim of this study is to examine the exact P2X4Rs signalling pathway in the development of central sensitization in a CM animal model. Methods We used an animal model with recurrent intermittent administration of nitroglycerin (NTG), which closely mimics CM. NTG-induced basal mechanical and thermal hypersensitivity were evaluated using a von Frey filament test and an increasing-temperature hot plate apparatus (IITC). We detected P2X4Rs, brain-derived neurotrophic factor (BDNF) and phosphorylated p38 mitogen-activated protein kinase (p-p38-MAPK) expression profiles in the TNC. We investigated the effects of a P2X4R inhibitor (5-BDBD) and an agonist (IVM) on NTG-induced hyperalgesia and neurochemical changes as well as on the expression of p-p38-MAPK and BDNF. We also detected the effects of a tropomyosin-related kinase B (TrkB) inhibitor (ANA-12) on the CM animal model in vivo. Then, we evaluated the effect of 5-BDBD and SB203580 (a p38-MAPK inhibitors) on the release and synthesis of BDNF in BV2 microglia cells treated with 50 μM adenosine triphosphate (ATP). Results Chronic intermittent administration of NTG resulted in chronic mechanical and thermal hyperalgesia, accompanied by the upregulation of P2X4Rs and BDNF expression. 5-BDBD or ANA-12 prevented hyperalgesia induced by NTG, which was associated with a significant inhibition of the NTG-induced increase in phosphorylated extracellular regulated protein kinases (p-ERK) and calcitonin gene related peptide (CGRP) release in the TNC. Repeated administration of IVM produced sustained hyperalgesia and significantly increased the levels of p-ERK and CGRP release in the TNC. Activating P2X4Rs with ATP triggered BDNF release and increased BDNF synthesis in BV2 microglia, and these results were then reduced by 5-BDBD or SB203580. Conclusions Our results indicated that the P2X4R contributes to the central sensitization of CM by releasing BDNF and promoting TNC neuronal hyper-excitability. Blocking microglia P2X4R-BDNF signalling may have an effect on the prevention of migraine chronification.https://doi.org/10.1186/s10194-019-1070-4Chronic migraineCentral sensitizationMicrogliaP2X4RBDNF
spellingShingle Ting Long
Wei He
Qi Pan
Shanshan Zhang
Dunke Zhang
Guangcheng Qin
Lixue Chen
Jiying Zhou
Microglia P2X4R-BDNF signalling contributes to central sensitization in a recurrent nitroglycerin-induced chronic migraine model
The Journal of Headache and Pain
Chronic migraine
Central sensitization
Microglia
P2X4R
BDNF
title Microglia P2X4R-BDNF signalling contributes to central sensitization in a recurrent nitroglycerin-induced chronic migraine model
title_full Microglia P2X4R-BDNF signalling contributes to central sensitization in a recurrent nitroglycerin-induced chronic migraine model
title_fullStr Microglia P2X4R-BDNF signalling contributes to central sensitization in a recurrent nitroglycerin-induced chronic migraine model
title_full_unstemmed Microglia P2X4R-BDNF signalling contributes to central sensitization in a recurrent nitroglycerin-induced chronic migraine model
title_short Microglia P2X4R-BDNF signalling contributes to central sensitization in a recurrent nitroglycerin-induced chronic migraine model
title_sort microglia p2x4r bdnf signalling contributes to central sensitization in a recurrent nitroglycerin induced chronic migraine model
topic Chronic migraine
Central sensitization
Microglia
P2X4R
BDNF
url https://doi.org/10.1186/s10194-019-1070-4
work_keys_str_mv AT tinglong microgliap2x4rbdnfsignallingcontributestocentralsensitizationinarecurrentnitroglycerininducedchronicmigrainemodel
AT weihe microgliap2x4rbdnfsignallingcontributestocentralsensitizationinarecurrentnitroglycerininducedchronicmigrainemodel
AT qipan microgliap2x4rbdnfsignallingcontributestocentralsensitizationinarecurrentnitroglycerininducedchronicmigrainemodel
AT shanshanzhang microgliap2x4rbdnfsignallingcontributestocentralsensitizationinarecurrentnitroglycerininducedchronicmigrainemodel
AT dunkezhang microgliap2x4rbdnfsignallingcontributestocentralsensitizationinarecurrentnitroglycerininducedchronicmigrainemodel
AT guangchengqin microgliap2x4rbdnfsignallingcontributestocentralsensitizationinarecurrentnitroglycerininducedchronicmigrainemodel
AT lixuechen microgliap2x4rbdnfsignallingcontributestocentralsensitizationinarecurrentnitroglycerininducedchronicmigrainemodel
AT jiyingzhou microgliap2x4rbdnfsignallingcontributestocentralsensitizationinarecurrentnitroglycerininducedchronicmigrainemodel