Literature DB >> 21906686

The primary somatosensory cortex largely contributes to the early part of the cortical response elicited by nociceptive stimuli.

E Valentini1, L Hu, B Chakrabarti, Y Hu, S M Aglioti, G D Iannetti.   

Abstract

Research on the cortical sources of nociceptive laser-evoked brain potentials (LEPs) began almost two decades ago (Tarkka and Treede, 1993). Whereas there is a large consensus on the sources of the late part of the LEP waveform (N2 and P2 waves), the relative contribution of the primary somatosensory cortex (S1) to the early part of the LEP waveform (N1 wave) is still debated. To address this issue we recorded LEPs elicited by the stimulation of four limbs in a large population (n=35). Early LEP generators were estimated both at single-subject and group level, using three different approaches: distributed source analysis, dipolar source modeling, and probabilistic independent component analysis (ICA). We show that the scalp distribution of the earliest LEP response to hand stimulation was maximal over the central-parietal electrodes contralateral to the stimulated side, while that of the earliest LEP response to foot stimulation was maximal over the central-parietal midline electrodes. Crucially, all three approaches indicated hand and foot S1 areas as generators of the earliest LEP response. Altogether, these findings indicate that the earliest part of the scalp response elicited by a selective nociceptive stimulus is largely explained by activity in the contralateral S1, with negligible contribution from the secondary somatosensory cortex (S2).
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21906686     DOI: 10.1016/j.neuroimage.2011.08.069

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


  48 in total

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Authors:  Diana M E Torta
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2.  Human primary somatosensory cortex is differentially involved in vibrotaction and nociception.

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3.  Novelty is not enough: laser-evoked potentials are determined by stimulus saliency, not absolute novelty.

Authors:  I Ronga; E Valentini; A Mouraux; G D Iannetti
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4.  Evidence-based source modeling of nociceptive cortical responses: A direct comparison of scalp and intracranial activity in humans.

Authors:  Claire Bradley; Hélène Bastuji; Luis Garcia-Larrea
Journal:  Hum Brain Mapp       Date:  2017-09-18       Impact factor: 5.038

5.  Event-related brain potentials elicited by high-speed cooling of the skin: A robust and non-painful method to assess the spinothalamic system in humans.

Authors:  Roxane De Keyser; Emanuel N van den Broeke; Arthur Courtin; André Dufour; André Mouraux
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Authors:  Elisa Raffaella Ferrè; Patrick Haggard; Gabriella Bottini; Gian Domenico Iannetti
Journal:  Exp Brain Res       Date:  2015-08-18       Impact factor: 1.972

7.  TrpM8-mediated somatosensation in mouse neocortex.

Authors:  Patrick Beukema; Katherine L Cecil; Elena Peterson; Victor R Mann; Megumi Matsushita; Yoshio Takashima; Saket Navlakha; Alison L Barth
Journal:  J Comp Neurol       Date:  2018-03-25       Impact factor: 3.215

8.  Fine-grained nociceptive maps in primary somatosensory cortex.

Authors:  Flavia Mancini; Patrick Haggard; Gian Domenico Iannetti; Matthew R Longo; Martin I Sereno
Journal:  J Neurosci       Date:  2012-11-28       Impact factor: 6.167

9.  Dishabituation of laser-evoked EEG responses: dissecting the effect of certain and uncertain changes in stimulus spatial location.

Authors:  D M Torta; M Liang; E Valentini; A Mouraux; G D Iannetti
Journal:  Exp Brain Res       Date:  2012-02-17       Impact factor: 1.972

10.  Anodal Transcutaneous Spinal Direct Current Stimulation (tsDCS) Selectively Inhibits the Synaptic Efficacy of Nociceptive Transmission at Spinal Cord Level.

Authors:  Cédric Lenoir; Aleksandar Jankovski; André Mouraux
Journal:  Neuroscience       Date:  2018-10-12       Impact factor: 3.590

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