Evidence for a spinal involvement in temporal pain contrast enhancement

Standard

Evidence for a spinal involvement in temporal pain contrast enhancement. / Sprenger, Christian; Stenmans, Philip; Tinnermann, Alexandra; Büchel, Christian.

in: NEUROIMAGE, Jahrgang 183, 12.2018, S. 788-799.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

APA

Vancouver

Bibtex

@article{cf508c0e4bca4b57848304038c94ffc8,
title = "Evidence for a spinal involvement in temporal pain contrast enhancement",
abstract = "Spatiotemporal filtering and amplification of sensory information at multiple levels during the generation of perceptual representations is a fundamental processing principle of the nervous system. While for the visual and auditory system temporal filtering of sensory signals has been noticed for a long time, respective contrast mechanisms within the nociceptive system became only recently subject of investigations, mainly in the context of offset analgesia (OA) subsequent to noxious stimulus decreases. In the present study we corroborate in a first experiment the assumption that offset analgesia involves a central component by showing that an OA-like effect accounting for 74% of a corresponding OA reference can be evoked by decomposing the stimulus offset into two separate box-car stimuli applied within the same dermatome but to separate populations of primary afferent neurons. In order to draw conclusions about the levels of the CNS at which temporal filtering of nociceptive information takes place during OA we investigate in a second experiment neuronal activity in the spinal cord during a painful thermal stimulus offset employing high-resolution fMRI in healthy volunteers. Pain-related BOLD responses in the spinal cord were significantly reduced during OA and their time course followed widely behavioral hypoalgesia, but not the thermal stimulation profile. In summary, the results suggest that temporal pain contrast enhancement during OA comprises a central mechanism and this mechanism becomes already effective at the level of the spinal cord.",
keywords = "Adult, Female, Hot Temperature, Humans, Image Processing, Computer-Assisted/methods, Magnetic Resonance Imaging/methods, Male, Pain, Pain Threshold/physiology, Spinal Cord/physiology, Young Adult",
author = "Christian Sprenger and Philip Stenmans and Alexandra Tinnermann and Christian B{\"u}chel",
note = "Copyright {\textcopyright} 2018 Elsevier Inc. All rights reserved.",
year = "2018",
month = dec,
doi = "10.1016/j.neuroimage.2018.09.003",
language = "English",
volume = "183",
pages = "788--799",
journal = "NEUROIMAGE",
issn = "1053-8119",
publisher = "Academic Press",

}

RIS

TY - JOUR

T1 - Evidence for a spinal involvement in temporal pain contrast enhancement

AU - Sprenger, Christian

AU - Stenmans, Philip

AU - Tinnermann, Alexandra

AU - Büchel, Christian

N1 - Copyright © 2018 Elsevier Inc. All rights reserved.

PY - 2018/12

Y1 - 2018/12

N2 - Spatiotemporal filtering and amplification of sensory information at multiple levels during the generation of perceptual representations is a fundamental processing principle of the nervous system. While for the visual and auditory system temporal filtering of sensory signals has been noticed for a long time, respective contrast mechanisms within the nociceptive system became only recently subject of investigations, mainly in the context of offset analgesia (OA) subsequent to noxious stimulus decreases. In the present study we corroborate in a first experiment the assumption that offset analgesia involves a central component by showing that an OA-like effect accounting for 74% of a corresponding OA reference can be evoked by decomposing the stimulus offset into two separate box-car stimuli applied within the same dermatome but to separate populations of primary afferent neurons. In order to draw conclusions about the levels of the CNS at which temporal filtering of nociceptive information takes place during OA we investigate in a second experiment neuronal activity in the spinal cord during a painful thermal stimulus offset employing high-resolution fMRI in healthy volunteers. Pain-related BOLD responses in the spinal cord were significantly reduced during OA and their time course followed widely behavioral hypoalgesia, but not the thermal stimulation profile. In summary, the results suggest that temporal pain contrast enhancement during OA comprises a central mechanism and this mechanism becomes already effective at the level of the spinal cord.

AB - Spatiotemporal filtering and amplification of sensory information at multiple levels during the generation of perceptual representations is a fundamental processing principle of the nervous system. While for the visual and auditory system temporal filtering of sensory signals has been noticed for a long time, respective contrast mechanisms within the nociceptive system became only recently subject of investigations, mainly in the context of offset analgesia (OA) subsequent to noxious stimulus decreases. In the present study we corroborate in a first experiment the assumption that offset analgesia involves a central component by showing that an OA-like effect accounting for 74% of a corresponding OA reference can be evoked by decomposing the stimulus offset into two separate box-car stimuli applied within the same dermatome but to separate populations of primary afferent neurons. In order to draw conclusions about the levels of the CNS at which temporal filtering of nociceptive information takes place during OA we investigate in a second experiment neuronal activity in the spinal cord during a painful thermal stimulus offset employing high-resolution fMRI in healthy volunteers. Pain-related BOLD responses in the spinal cord were significantly reduced during OA and their time course followed widely behavioral hypoalgesia, but not the thermal stimulation profile. In summary, the results suggest that temporal pain contrast enhancement during OA comprises a central mechanism and this mechanism becomes already effective at the level of the spinal cord.

KW - Adult

KW - Female

KW - Hot Temperature

KW - Humans

KW - Image Processing, Computer-Assisted/methods

KW - Magnetic Resonance Imaging/methods

KW - Male

KW - Pain

KW - Pain Threshold/physiology

KW - Spinal Cord/physiology

KW - Young Adult

U2 - 10.1016/j.neuroimage.2018.09.003

DO - 10.1016/j.neuroimage.2018.09.003

M3 - SCORING: Journal article

C2 - 30189340

VL - 183

SP - 788

EP - 799

JO - NEUROIMAGE

JF - NEUROIMAGE

SN - 1053-8119

ER -