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A nociresponsive specific area of human somatosensory cortex within BA3a: BA3c?

It is well recognized that in primates, including humans, noxious body stimulation evokes a neural response in the posterior bank of the central sulcus, in Brodmann cytoarchitectonic subdivisions 3b and 1 of the primary somatosensory cortex. This response is associated with the 1st/sharp pain and co...

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Autores principales: Panchuelo, Rosa M. Sanchez, Eldeghaidy, Sally, Marshall, Andrew, McGlone, Francis, Francis, Susan T., Favorov, Oleg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762820/
https://www.ncbi.nlm.nih.gov/pubmed/32711068
http://dx.doi.org/10.1016/j.neuroimage.2020.117187
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author Panchuelo, Rosa M. Sanchez
Eldeghaidy, Sally
Marshall, Andrew
McGlone, Francis
Francis, Susan T.
Favorov, Oleg
author_facet Panchuelo, Rosa M. Sanchez
Eldeghaidy, Sally
Marshall, Andrew
McGlone, Francis
Francis, Susan T.
Favorov, Oleg
author_sort Panchuelo, Rosa M. Sanchez
collection PubMed
description It is well recognized that in primates, including humans, noxious body stimulation evokes a neural response in the posterior bank of the central sulcus, in Brodmann cytoarchitectonic subdivisions 3b and 1 of the primary somatosensory cortex. This response is associated with the 1st/sharp pain and contributes to sensory discriminative aspects of pain perception and spatial localization of the noxious stimulus. However, neurophysiological studies in New World monkeys predict that in humans noxious stimulation also evokes a separate neural response—mediated by C-afferent drive and associated with the 2nd/burning pain—in the depth of the central sulcus in Brodmann area 3a (BA3a) at the transition between the somatosensory and motor cortices. To evoke such a response, it is necessary to use multi-second duration noxious stimulation, rather than brief laser pulses. Given the limited human pain-imaging literature on cortical responses induced by C-nociceptive input specifically within BA3a, here we used high spatial resolution 7T fMRI to study the response to thermonoxious skin stimulation. We observed the predicted response of BA3a in the depth of the central sulcus in five human volunteers. Review of the available evidence suggests that the nociresponsive region in the depth of the central sulcus is a structurally and functionally distinct cortical area that should not be confused with proprioceptive BA3a. It is most likely engaged in interoception and control of the autonomic nervous system, and contributes to the sympathetic response to noxious stimulation, arguably the most intolerable aspect of pain experience. Ablation of this region has been shown to reduce pain sensibility and might offer an effective means of ameliorating some pathological pain conditions.
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spelling pubmed-77628202020-12-28 A nociresponsive specific area of human somatosensory cortex within BA3a: BA3c? Panchuelo, Rosa M. Sanchez Eldeghaidy, Sally Marshall, Andrew McGlone, Francis Francis, Susan T. Favorov, Oleg Neuroimage Full Length Article It is well recognized that in primates, including humans, noxious body stimulation evokes a neural response in the posterior bank of the central sulcus, in Brodmann cytoarchitectonic subdivisions 3b and 1 of the primary somatosensory cortex. This response is associated with the 1st/sharp pain and contributes to sensory discriminative aspects of pain perception and spatial localization of the noxious stimulus. However, neurophysiological studies in New World monkeys predict that in humans noxious stimulation also evokes a separate neural response—mediated by C-afferent drive and associated with the 2nd/burning pain—in the depth of the central sulcus in Brodmann area 3a (BA3a) at the transition between the somatosensory and motor cortices. To evoke such a response, it is necessary to use multi-second duration noxious stimulation, rather than brief laser pulses. Given the limited human pain-imaging literature on cortical responses induced by C-nociceptive input specifically within BA3a, here we used high spatial resolution 7T fMRI to study the response to thermonoxious skin stimulation. We observed the predicted response of BA3a in the depth of the central sulcus in five human volunteers. Review of the available evidence suggests that the nociresponsive region in the depth of the central sulcus is a structurally and functionally distinct cortical area that should not be confused with proprioceptive BA3a. It is most likely engaged in interoception and control of the autonomic nervous system, and contributes to the sympathetic response to noxious stimulation, arguably the most intolerable aspect of pain experience. Ablation of this region has been shown to reduce pain sensibility and might offer an effective means of ameliorating some pathological pain conditions. Academic Press 2020-11-01 /pmc/articles/PMC7762820/ /pubmed/32711068 http://dx.doi.org/10.1016/j.neuroimage.2020.117187 Text en © 2020 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Full Length Article
Panchuelo, Rosa M. Sanchez
Eldeghaidy, Sally
Marshall, Andrew
McGlone, Francis
Francis, Susan T.
Favorov, Oleg
A nociresponsive specific area of human somatosensory cortex within BA3a: BA3c?
title A nociresponsive specific area of human somatosensory cortex within BA3a: BA3c?
title_full A nociresponsive specific area of human somatosensory cortex within BA3a: BA3c?
title_fullStr A nociresponsive specific area of human somatosensory cortex within BA3a: BA3c?
title_full_unstemmed A nociresponsive specific area of human somatosensory cortex within BA3a: BA3c?
title_short A nociresponsive specific area of human somatosensory cortex within BA3a: BA3c?
title_sort nociresponsive specific area of human somatosensory cortex within ba3a: ba3c?
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762820/
https://www.ncbi.nlm.nih.gov/pubmed/32711068
http://dx.doi.org/10.1016/j.neuroimage.2020.117187
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