Central sensitization-related changes of effective and functional connectivity in the rat inflammatory trigeminal pain model.

Central sensitization is a key mechanism in the pathology of several neuropathic pain disorders. We aimed to investigate the underlying brain connectivity changes in a rat model of chronic pain. Non-noxious whisker stimulation was used to evoke blood-oxygen-level-dependent (BOLD) responses in a bloc...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Spisák Tamás
Pozsgay Zsófia
Aranyi Sándor Csaba
David Szabolcs
Kocsis Pál
Nyitrai Gabriella
Gajári Dávid
Emri Miklós
Czurkó András
Kincses Zsigmond Tamás
Dokumentumtípus: Cikk
Megjelent: 2017
Sorozat:NEUROSCIENCE 344
doi:10.1016/j.neuroscience.2016.12.018

mtmt:3182042
Online Access:http://publicatio.bibl.u-szeged.hu/19017
Leíró adatok
Tartalmi kivonat:Central sensitization is a key mechanism in the pathology of several neuropathic pain disorders. We aimed to investigate the underlying brain connectivity changes in a rat model of chronic pain. Non-noxious whisker stimulation was used to evoke blood-oxygen-level-dependent (BOLD) responses in a block-design functional Magnetic Resonance Imaging (fMRI) experiment on 9.4T. Measurements were repeated two days and one week after injecting complete Freund's adjuvant into the rats' whisker pad. We found that acute pain reduced activation in the barrel cortex, most probably due to a plateau effect. After one week, increased activation of the anterior cingulate cortex was found. Analyses of effective connectivity driven by stimulus-related activation revealed that chronic pain-related central sensitization manifested as a widespread alteration in the activity of the somatosensory network. Changes were mainly mediated by the anterior cingulate cortex and the striatum and affected the somatosensory and motor cortices and the superior colliculus. Functional connectivity analysis of nested BOLD oscillations justified that the anterior cingular-somatosensory interplay is a key element of network changes. Additionally, a decreased cingulo-motor functional connectivity implies that alterations also involve the output tract of the network. Our results extend the knowledge about the role of the cingulate cortex in the chronification of pain and indicate that integration of multiple connectivity analysis could be fruitful in studying the central sensitization in the pain matrix.
Terjedelem/Fizikai jellemzők:133-147
ISSN:0306-4522