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Alterations in cortical excitability during pain: A combined TMS-EEG Study.
Chowdhury, Nahian S; Chiang, Alan Ki; Millard, Samantha K; Skippen, Patrick; Chang, Wei-Ju; Seminowicz, David A; Schabrun, Siobhan M.
Afiliação
  • Chowdhury NS; Center for Pain IMPACT, Neuroscience Research Australia, Sydney, New South Wales, Australia.
  • Chiang AK; University of New South Wales, Sydney, New South Wales, Australia.
  • Millard SK; Center for Pain IMPACT, Neuroscience Research Australia, Sydney, New South Wales, Australia.
  • Skippen P; University of New South Wales, Sydney, New South Wales, Australia.
  • Chang WJ; Center for Pain IMPACT, Neuroscience Research Australia, Sydney, New South Wales, Australia.
  • Seminowicz DA; University of New South Wales, Sydney, New South Wales, Australia.
  • Schabrun SM; Center for Pain IMPACT, Neuroscience Research Australia, Sydney, New South Wales, Australia.
bioRxiv ; 2023 Aug 07.
Article em En | MEDLINE | ID: mdl-37131586
Transcranial magnetic stimulation (TMS) has been used to examine inhibitory and facilitatory circuits during experimental pain and in chronic pain populations. However, current applications of TMS to pain have been restricted to measurements of motor evoked potentials (MEPs) from peripheral muscles. Here, TMS was combined with electroencephalography (EEG) to determine whether experimental pain could induce alterations in cortical inhibitory/facilitatory activity observed in TMS-evoked potentials (TEPs). In Experiment 1 (n = 29), multiple sustained thermal stimuli were administered to the forearm, with the first, second and third block of thermal stimuli consisting of warm but non-painful (pre-pain block), painful (pain block) and warm but non-painful (post-pain block) temperatures respectively. During each stimulus, TMS pulses were delivered while EEG (64 channels) was simultaneously recorded. Verbal pain ratings were collected between TMS pulses. Relative to pre-pain warm stimuli, painful stimuli led to an increase in the amplitude of the frontocentral negative peak ~45ms post-TMS (N45), with a larger increase associated with higher pain ratings. Experiments 2 and 3 (n = 10 in each) showed that the increase in the N45 in response to pain was not due to changes in sensory potentials associated with TMS, or a result of stronger reafferent muscle feedback during pain. This is the first study to use combined TMS-EEG to examine alterations in cortical excitability in response to pain. These results suggest that the N45 TEP peak, which indexes GABAergic neurotransmission, is implicated in pain perception and is a potential marker of individual differences in pain sensitivity.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália