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Cortical inhibition of distinct mechanisms in the dorsolateral prefrontal cortex is related to working memory performance

dc.contributor.authorRogasch, Nigel C.en
dc.contributor.authorDaskalakis, Zafiris J.en
dc.contributor.authorFitzgerald, Paul B.en
dc.date.accessioned2025-03-16T20:27:02Z
dc.date.available2025-03-16T20:27:02Z
dc.date.issued2015-03-01en
dc.description.abstractPaired-pulse transcranial magnetic stimulation combined with electroencephalography (TMS-EEG) is a method for studying cortical inhibition from the dorsolateral prefrontal cortex (DLPFC). However, little is known about the mechanisms underlying TMS-evoked cortical potentials (TEPs) from this region, letalone inhibition of these components. The aim of this study was to assess cortical inhibition of distinct TEPs and oscillations in the DLPFC using TMS-EEG and to investigate the relationship of these mechanisms to working memory. 30 healthy volunteers received single and paired (interstimulus interval=100msec) TMS to the left DLPFC. Variations in long-interval cortical inhibition (LICI) of different TEP peaks (N40, P60, N100) and different TMS-evoked oscillations (alpha, lower beta, upper beta, gamma) were compared between individuals. Variation in N100 slope following single pulse TMS, another putative marker of inhibition, was also compared with LICI of each measure. Finally, these measures were correlated with performance of a working memory task. LICI resulted in significant suppression of all TEP peaks and TMS-evoked oscillations (all p< 05). There were no significant correlations between LICI of different TEP peaks or TMS-evoked oscillations with the exception of P60 and N100. Variation in N100 slope correlated with LICI of N40 and beta oscillations. In addition, LICI of P60 and N100 were differentially correlated with working memory performance. The results suggest that both the LICI paradigm and N100 following single pulse TMS reflect complementary methods for assessing GABAB-mediated cortical inhibition in the DLPFC. Furthermore, these measures demonstrate the importance of prefrontal GABAB-mediated inhibitory control for working memory performance.en
dc.description.sponsorshipThe authors wish to thank all volunteers for their participation. The following work contributed to the doctoral thesis of NCR. NCR was supported by a postgraduate biomedical research scholarship ( 607223 ) and currently holds a research fellowship ( 1072057 ) from the National Health and Medical Research Council (NHMRC) of Australia. PBF is supported by an NHMRC Practitioner Fellowship.en
dc.description.statustrueen
dc.format.extent10en
dc.identifier.otherresearchoutputwizard:a383154xPUB33364en
dc.identifier.otherScopus:84909606120en
dc.identifier.urihttps://dspace-test.anu.edu.au/handle/1885/733719036
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=84909606120&partnerID=8YFLogxKen
dc.language.isoEnglishen
dc.rightsPublisher Copyright: © 2014 Elsevier Ltd.en
dc.sourceCortexen
dc.subjectAPBen
dc.subjectCortical inhibitionen
dc.subjectDLPFCen
dc.subjectDorsolateral prefrontal cortexen
dc.subjectEEGen
dc.subjectElectroencephalographyen
dc.subjectGABAen
dc.subjectLICIen
dc.subjectMEPen
dc.subjectRMTen
dc.subjectTEPen
dc.subjectTMSen
dc.subjectTranscranial magnetic stimulationen
dc.subjectWorking memoryen
dc.titleCortical inhibition of distinct mechanisms in the dorsolateral prefrontal cortex is related to working memory performanceen
dc.typeArticleen
local.bibliographicCitation.lastpage77en
local.bibliographicCitation.startpage68en
local.contributor.affiliationRogasch, Nigel C.; Monash Universityen
local.contributor.affiliationDaskalakis, Zafiris J.; University of Torontoen
local.contributor.affiliationFitzgerald, Paul B.; Monash Universityen
local.identifier.citationvolume64en
local.identifier.doi10.1016/j.cortex.2014.10.003en
local.identifier.purec23c9847-4f05-4069-ac6f-ccd44677e5e6en
local.type.statusPublisheden

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