Simultaneous brain, brainstem, and spinal cord pharmacological-fMRI reveals involvement of an endogenous opioid network in attentional analgesia
Adult
Male
Hot Temperature
Adolescent
QH301-705.5
brain
Science
610
Pain
/dk/atira/pure/core/keywords/anaesthesia_pain_and_critical_care; name=Anaesthesia Pain and Critical Care
/dk/atira/pure/core/keywords/anaesthesia_pain_and_critical_care
Reboxetine
Young Adult
03 medical and health sciences
0302 clinical medicine
617
Humans
pain
human
name=Anaesthesia Pain and Critical Care
Biology (General)
Pain Measurement
fMRI
Q
R
spinal cord
Brain
Pain Perception
Middle Aged
Magnetic Resonance Imaging
Naltrexone
Analgesics, Opioid
Spinal Cord
opioid
Medicine
Female
Neuroscience
Brain Stem
DOI:
10.7554/elife.71877
Publication Date:
2022-01-26T12:15:17Z
AUTHORS (5)
ABSTRACT
Pain perception is decreased by shifting attentional focus away from a threatening event. This attentional analgesia engages parallel descending control pathways from anterior cingulate (ACC) to locus coeruleus, and ACC to periaqueductal grey (PAG) – rostral ventromedial medulla (RVM), indicating possible roles for noradrenergic or opioidergic neuromodulators. To determine which pathway modulates nociceptive activity in humans, we used simultaneous whole brain-spinal cord pharmacological-fMRI (N = 39) across three sessions. Noxious thermal forearm stimulation generated somatotopic-activation of dorsal horn (DH) whose activity correlated with pain report and mirrored attentional pain modulation. Activity in an adjacent cluster reported the interaction between task and noxious stimulus. Effective connectivity analysis revealed that ACC interacts with PAG and RVM to modulate spinal cord activity. Blocking endogenous opioids with Naltrexone impairs attentional analgesia and disrupts RVM-spinal and ACC-PAG connectivity. Noradrenergic augmentation with Reboxetine did not alter attentional analgesia. Cognitive pain modulation involves opioidergic ACC-PAG-RVM descending control which suppresses spinal nociceptive activity.
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