The Localization Research of Brain Plasticity Changes after Brachial Plexus Pain: Sensory Regions or Cognitive Regions?

Objective. Neuropathic pain after brachial plexus injury remains an increasingly prevalent and intractable disease due to inadequacy of satisfactory treatment strategies. A detailed mapping of cortical regions concerning the brain plasticity was the first step of therapeutic intervention. However, t...

Full description

Saved in:
Bibliographic Details
Main Authors: Shuai Wang, Zhen-zhen Ma, Ye-chen Lu, Jia-jia Wu, Xu-yun Hua, Mou-xiong Zheng, Jian-guang Xu
Format: Article
Language:English
Published: Wiley 2019-01-01
Series:Neural Plasticity
Online Access:http://dx.doi.org/10.1155/2019/7381609
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832549667545546752
author Shuai Wang
Zhen-zhen Ma
Ye-chen Lu
Jia-jia Wu
Xu-yun Hua
Mou-xiong Zheng
Jian-guang Xu
author_facet Shuai Wang
Zhen-zhen Ma
Ye-chen Lu
Jia-jia Wu
Xu-yun Hua
Mou-xiong Zheng
Jian-guang Xu
author_sort Shuai Wang
collection DOAJ
description Objective. Neuropathic pain after brachial plexus injury remains an increasingly prevalent and intractable disease due to inadequacy of satisfactory treatment strategies. A detailed mapping of cortical regions concerning the brain plasticity was the first step of therapeutic intervention. However, the specific mapping research of brachial plexus pain was limited. We aimed to provide some localization information about the brain plasticity changes after brachial plexus pain in this preliminary study. Methods. 24 Sprague-Dawley rats received complete brachial plexus avulsion with neuropathic pain on the right forelimb successfully. Through functional imaging of both resting-state and block-design studies, we compared the amplitude of low-frequency fluctuations (ALFF) of premodeling and postmodeling groups and the changes of brain activation when applying sensory stimulation. Results. The postmodeling group showed significant decreases on the mechanical withdrawal threshold (MWT) in the bilateral hindpaws and thermal withdrawal latency (TWL) in the left hindpaw than the premodeling group (P<0.05). The amplitude of low-frequency fluctuations (ALFF) of the postmodeling group manifested increases in regions of the left anterodorsal hippocampus, left mesencephalic region, left dorsal midline thalamus, and so on. Decreased ALFF was observed in the bilateral entorhinal cortex compared to that of the premodeling group. The results of block-design scan showed significant differences in regions including the limbic/paralimbic system and somatosensory cortex. Conclusion. We concluded that the entorhinal-hippocampus pathway, which was part of the Papez circuit, was involved in the functional integrated areas of brachial plexus pain processing. The regions in the “pain matrix” showed expected activation when applying instant nociceptive stimulus but remained silent in the resting status. This research confirmed the involvement of cognitive function, which brought novel information to the potential new therapy for brachial plexus pain.
format Article
id doaj-art-906343c802c44f9db51db24d5145feab
institution Kabale University
issn 2090-5904
1687-5443
language English
publishDate 2019-01-01
publisher Wiley
record_format Article
series Neural Plasticity
spelling doaj-art-906343c802c44f9db51db24d5145feab2025-02-03T06:10:48ZengWileyNeural Plasticity2090-59041687-54432019-01-01201910.1155/2019/73816097381609The Localization Research of Brain Plasticity Changes after Brachial Plexus Pain: Sensory Regions or Cognitive Regions?Shuai Wang0Zhen-zhen Ma1Ye-chen Lu2Jia-jia Wu3Xu-yun Hua4Mou-xiong Zheng5Jian-guang Xu6School of Rehabilitation Science, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaSchool of Rehabilitation Science, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaSchool of Rehabilitation Science, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaSchool of Rehabilitation Science, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaSchool of Rehabilitation Science, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaSchool of Rehabilitation Science, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaSchool of Rehabilitation Science, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaObjective. Neuropathic pain after brachial plexus injury remains an increasingly prevalent and intractable disease due to inadequacy of satisfactory treatment strategies. A detailed mapping of cortical regions concerning the brain plasticity was the first step of therapeutic intervention. However, the specific mapping research of brachial plexus pain was limited. We aimed to provide some localization information about the brain plasticity changes after brachial plexus pain in this preliminary study. Methods. 24 Sprague-Dawley rats received complete brachial plexus avulsion with neuropathic pain on the right forelimb successfully. Through functional imaging of both resting-state and block-design studies, we compared the amplitude of low-frequency fluctuations (ALFF) of premodeling and postmodeling groups and the changes of brain activation when applying sensory stimulation. Results. The postmodeling group showed significant decreases on the mechanical withdrawal threshold (MWT) in the bilateral hindpaws and thermal withdrawal latency (TWL) in the left hindpaw than the premodeling group (P<0.05). The amplitude of low-frequency fluctuations (ALFF) of the postmodeling group manifested increases in regions of the left anterodorsal hippocampus, left mesencephalic region, left dorsal midline thalamus, and so on. Decreased ALFF was observed in the bilateral entorhinal cortex compared to that of the premodeling group. The results of block-design scan showed significant differences in regions including the limbic/paralimbic system and somatosensory cortex. Conclusion. We concluded that the entorhinal-hippocampus pathway, which was part of the Papez circuit, was involved in the functional integrated areas of brachial plexus pain processing. The regions in the “pain matrix” showed expected activation when applying instant nociceptive stimulus but remained silent in the resting status. This research confirmed the involvement of cognitive function, which brought novel information to the potential new therapy for brachial plexus pain.http://dx.doi.org/10.1155/2019/7381609
spellingShingle Shuai Wang
Zhen-zhen Ma
Ye-chen Lu
Jia-jia Wu
Xu-yun Hua
Mou-xiong Zheng
Jian-guang Xu
The Localization Research of Brain Plasticity Changes after Brachial Plexus Pain: Sensory Regions or Cognitive Regions?
Neural Plasticity
title The Localization Research of Brain Plasticity Changes after Brachial Plexus Pain: Sensory Regions or Cognitive Regions?
title_full The Localization Research of Brain Plasticity Changes after Brachial Plexus Pain: Sensory Regions or Cognitive Regions?
title_fullStr The Localization Research of Brain Plasticity Changes after Brachial Plexus Pain: Sensory Regions or Cognitive Regions?
title_full_unstemmed The Localization Research of Brain Plasticity Changes after Brachial Plexus Pain: Sensory Regions or Cognitive Regions?
title_short The Localization Research of Brain Plasticity Changes after Brachial Plexus Pain: Sensory Regions or Cognitive Regions?
title_sort localization research of brain plasticity changes after brachial plexus pain sensory regions or cognitive regions
url http://dx.doi.org/10.1155/2019/7381609
work_keys_str_mv AT shuaiwang thelocalizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT zhenzhenma thelocalizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT yechenlu thelocalizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT jiajiawu thelocalizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT xuyunhua thelocalizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT mouxiongzheng thelocalizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT jianguangxu thelocalizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT shuaiwang localizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT zhenzhenma localizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT yechenlu localizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT jiajiawu localizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT xuyunhua localizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT mouxiongzheng localizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions
AT jianguangxu localizationresearchofbrainplasticitychangesafterbrachialplexuspainsensoryregionsorcognitiveregions