Tonic pain alters functional connectivity of the descending pain modulatory network involving amygdala, periaqueductal gray, parabrachial nucleus and anterior cingulate cortex

Introduction: Resting state functional connectivity (FC) is widely used to assess functional brain alterations in patients with chronic pain. However, reports of FC accompanying tonic pain in pain-free persons are rare. A network we term the Descending Pain Modulatory Network (DPMN) is implicated in...

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Main Authors: Dorsey, S.G (Author), Greenspan, J.D (Author), Gullapalli, R.P (Author), Keaser, M.L (Author), Khan, S.A (Author), Meeker, T.J (Author), Schmid, A.-C (Author), Seminowicz, D.A (Author)
Format: Article
Language:English
Published: Academic Press Inc. 2022
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Online Access:View Fulltext in Publisher
LEADER 03613nam a2200289Ia 4500
001 10.1016-j.neuroimage.2022.119278
008 220517s2022 CNT 000 0 und d
020 |a 10538119 (ISSN) 
245 1 0 |a Tonic pain alters functional connectivity of the descending pain modulatory network involving amygdala, periaqueductal gray, parabrachial nucleus and anterior cingulate cortex 
260 0 |b Academic Press Inc.  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1016/j.neuroimage.2022.119278 
520 3 |a Introduction: Resting state functional connectivity (FC) is widely used to assess functional brain alterations in patients with chronic pain. However, reports of FC accompanying tonic pain in pain-free persons are rare. A network we term the Descending Pain Modulatory Network (DPMN) is implicated in healthy and pathologic pain modulation. Here, we evaluate the effect of tonic pain on FC of specific nodes of this network: anterior cingulate cortex (ACC), amygdala (AMYG), periaqueductal gray (PAG), and parabrachial nuclei (PBN). Methods: In 50 pain-free participants (30F), we induced tonic pain using a capsaicin-heat pain model. functional MRI measured resting BOLD signal during pain-free rest with a 32 °C thermode and then tonic pain where participants experienced a previously warm temperature combined with capsaicin. We evaluated FC from ACC, AMYG, PAG, and PBN with correlation of self-report pain intensity during both states. We hypothesized tonic pain would diminish FC dyads within the DPMN. Results: Of all hypothesized FC dyads, only PAG and subgenual ACC was weakly altered during pain (F = 3.34; p = 0.074; pain-free>pain d = 0.25). After pain induction sACC-PAG FC became positively correlated with pain intensity (R = 0.38; t = 2.81; p = 0.007). Right PBN-PAG FC during pain-free rest positively correlated with subsequently experienced pain (R = 0.44; t = 3.43; p = 0.001). During pain, this connection's FC was diminished (paired t=-3.17; p = 0.0026). In whole-brain analyses, during pain-free rest, FC between left AMYG and right superior parietal lobule and caudate nucleus were positively correlated with subsequent pain. During pain, FC between left AMYG and right inferior temporal gyrus negatively correlated with pain. Subsequent pain positively correlated with right AMYG FC with right claustrum; right primary visual cortex and right temporo-occipitoparietal junction Conclusion: We demonstrate sACC-PAG tonic pain FC positively correlates with experienced pain and resting right PBN-PAG FC correlates with subsequent pain and is diminished during tonic pain. Finally, we reveal PAG- and right AMYG-anchored networks which correlate with subsequently experienced pain intensity. Our findings suggest specific connectivity patterns within the DPMN at rest are associated with subsequently experienced pain and modulated by tonic pain. These nodes and their functional modulation may reveal new therapeutic targets for neuromodulation or biomarkers to guide interventions. © 2022 The Authors 
650 0 4 |a Capsaicin-heat pain model 
650 0 4 |a Central sensitization 
650 0 4 |a Descending pain modulatory network 
650 0 4 |a Parabrachial nuclei 
650 0 4 |a Periaqueductal gray 
650 0 4 |a Seed-driven functional connectivity 
700 1 |a Dorsey, S.G.  |e author 
700 1 |a Greenspan, J.D.  |e author 
700 1 |a Gullapalli, R.P.  |e author 
700 1 |a Keaser, M.L.  |e author 
700 1 |a Khan, S.A.  |e author 
700 1 |a Meeker, T.J.  |e author 
700 1 |a Schmid, A.-C.  |e author 
700 1 |a Seminowicz, D.A.  |e author 
773 |t NeuroImage