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    Brainstem pain-control circuitry connectivity in chronic neuropathic pain

    79644.pdf (1.434Mb)
    Access Status
    Open access
    Authors
    Mills, E.P.
    Di Pietro, Flavia
    Alshelh, Z.
    Peck, C.C.
    Murray, G.M.
    Vickers, E.R.
    Henderson, L.A.
    Date
    2018
    Type
    Journal Article
    
    Metadata
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    Citation
    Mills, E.P. and Di Pietro, F. and Alshelh, Z. and Peck, C.C. and Murray, G.M. and Vickers, E.R. and Henderson, L.A. 2018. Brainstem pain-control circuitry connectivity in chronic neuropathic pain. Journal of Neuroscience. 38 (2): pp. 465-473.
    Source Title
    Journal of Neuroscience
    DOI
    10.1523/JNEUROSCI.1647-17.2017
    ISSN
    0270-6474
    Faculty
    Faculty of Health Sciences
    School
    School of Pharmacy and Biomedical Sciences
    Funding and Sponsorship
    http://purl.org/au-research/grants/nhmrc/1032072
    http://purl.org/au-research/grants/nhmrc/1059182
    URI
    http://hdl.handle.net/20.500.11937/79562
    Collection
    • Curtin Research Publications
    Abstract

    © 2018 the authors.

    Preclinical investigations have suggested that altered functioning of brainstem pain-modulation circuits may be crucial for the maintenance of some chronic pain conditions. While some human psychophysical studies show that patients with chronic pain display altered pain-modulation efficacy, it remains unknown whether brainstem pain-modulation circuits are altered in individuals with chronic pain. The aim of the present investigation was to determine whether, in humans, chronic pain following nerve injury is associated with altered ongoing functioning of the brainstem descending modulation systems. Using resting-state functional magnetic resonance imaging, we found that male and female patients with chronic neuropathic orofacial pain show increased functional connectivity between the rostral ventromedial medulla (RVM) and other brainstem pain-modulatory regions, including the ventrolateral periaqueductal gray (vlPAG) and locus ceruleus (LC). We also identified an increase in RVM functional connectivity with the region that receives orofacial nociceptor afferents, the spinal trigeminal nucleus. In addition, the vlPAG and LC displayed increased functional connectivity strengths with higher brain regions, including the hippocampus, nucleus accumbens, and anterior cingulate cortex, in individuals with chronic pain. These data reveal that chronic pain is associated with altered ongoing functioning within the endogenous pain-modulation network. These changes may underlie enhanced descending facilitation of processing at the primary synapse, resulting in increased nociceptive transmission to higher brain centers. Further, our findings show that higher brain regions interact with the brainstem modulation system differently in chronic pain, possibly reflecting top–down engagement of the circuitry alongside altered reward processing in pain conditions.

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