<HashMap><database>biostudies-literature</database><scores/><additional><submitter>De Martino E</submitter><funding>Danmarks Grundforskningsfond</funding><funding>European Research Council</funding><funding>Novo Nordisk Fonden</funding><pagination>e26679</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11034005</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>45(6)</volume><pubmed_abstract>Temporal dynamics of local cortical rhythms during acute pain remain largely unknown. The current study used a novel approach based on transcranial magnetic stimulation combined with electroencephalogram (TMS-EEG) to investigate evoked-oscillatory cortical activity during acute pain. Motor (M1) and dorsolateral prefrontal cortex (DLPFC) were probed by TMS, respectively, to record oscillatory power (event-related spectral perturbation and relative spectral power) and phase synchronization (inter-trial coherence) by 63 EEG channels during experimentally induced acute heat pain in 24 healthy participants. TMS-EEG was recorded before, during, and after noxious heat (acute pain condition) and non-noxious warm (Control condition), delivered in a randomized sequence. The main frequency bands (α, β1, and β2) of TMS-evoked potentials after M1 and DLPFC stimulation were recorded close to the TMS coil and remotely. Cold and heat pain thresholds were measured before TMS-EEG. Over M1, acute pain decreased α-band oscillatory power locally and α-band phase synchronization remotely in parietal-occipital clusters compared with non-noxious warm (all p &lt; .05). The remote (parietal-occipital) decrease in α-band phase synchronization during acute pain correlated with the cold (p = .001) and heat pain thresholds (p = .023) and to local (M1) α-band oscillatory power decrease (p = .024). Over DLPFC, acute pain only decreased β1-band power locally compared with non-noxious warm (p = .015). Thus, evoked-oscillatory cortical activity to M1 stimulation is reduced by acute pain in central and parietal-occipital regions and correlated with pain sensitivity, in contrast to DLPFC, which had only local effects. This finding expands the significance of α and β band oscillations and may have relevance for pain therapies.</pubmed_abstract><journal>Human brain mapping</journal><pubmed_title>Evoked oscillatory cortical activity during acute pain: Probing brain in pain by transcranial magnetic stimulation combined with electroencephalogram.</pubmed_title><pmcid>PMC11034005</pmcid><funding_grant_id>NNF21OC0072828</funding_grant_id><funding_grant_id>101087925</funding_grant_id><funding_grant_id>DNRF121</funding_grant_id><pubmed_authors>Couto BA</pubmed_authors><pubmed_authors>Casali A</pubmed_authors><pubmed_authors>De Martino E</pubmed_authors><pubmed_authors>Rosanova M</pubmed_authors><pubmed_authors>Graven-Nielsen T</pubmed_authors><pubmed_authors>Hassan G</pubmed_authors><pubmed_authors>de Andrade DC</pubmed_authors><pubmed_authors>Casarotto S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evoked oscillatory cortical activity during acute pain: Probing brain in pain by transcranial magnetic stimulation combined with electroencephalogram.</name><description>Temporal dynamics of local cortical rhythms during acute pain remain largely unknown. The current study used a novel approach based on transcranial magnetic stimulation combined with electroencephalogram (TMS-EEG) to investigate evoked-oscillatory cortical activity during acute pain. Motor (M1) and dorsolateral prefrontal cortex (DLPFC) were probed by TMS, respectively, to record oscillatory power (event-related spectral perturbation and relative spectral power) and phase synchronization (inter-trial coherence) by 63 EEG channels during experimentally induced acute heat pain in 24 healthy participants. TMS-EEG was recorded before, during, and after noxious heat (acute pain condition) and non-noxious warm (Control condition), delivered in a randomized sequence. The main frequency bands (α, β1, and β2) of TMS-evoked potentials after M1 and DLPFC stimulation were recorded close to the TMS coil and remotely. Cold and heat pain thresholds were measured before TMS-EEG. Over M1, acute pain decreased α-band oscillatory power locally and α-band phase synchronization remotely in parietal-occipital clusters compared with non-noxious warm (all p &lt; .05). The remote (parietal-occipital) decrease in α-band phase synchronization during acute pain correlated with the cold (p = .001) and heat pain thresholds (p = .023) and to local (M1) α-band oscillatory power decrease (p = .024). Over DLPFC, acute pain only decreased β1-band power locally compared with non-noxious warm (p = .015). Thus, evoked-oscillatory cortical activity to M1 stimulation is reduced by acute pain in central and parietal-occipital regions and correlated with pain sensitivity, in contrast to DLPFC, which had only local effects. This finding expands the significance of α and β band oscillations and may have relevance for pain therapies.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-07-01T03:21:49.341Z</modification><creation>2026-07-01T03:12:29.559Z</creation></dates><accession>S-EPMC11034005</accession><cross_references><pubmed>38647038</pubmed><doi>10.1002/hbm.26679</doi></cross_references></HashMap>