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dc.contributor.authorYaakub, SN
dc.contributor.authorWhite, TA
dc.contributor.authorRoberts, J
dc.contributor.authorMartin, E
dc.contributor.authorVerhagen, L
dc.contributor.authorStagg, CJ
dc.contributor.authorHall, S
dc.contributor.authorFouragnan, EF
dc.date.accessioned2023-11-07T13:54:52Z
dc.date.available2023-11-07T13:54:52Z
dc.date.issued2023-09-01
dc.identifier.issn2041-1723
dc.identifier.issn2041-1723
dc.identifier.other5318
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/21610
dc.description.abstract

Low-intensity transcranial ultrasound stimulation (TUS) is an emerging non-invasive technique for focally modulating human brain function. The mechanisms and neurochemical substrates underlying TUS neuromodulation in humans and how these relate to excitation and inhibition are still poorly understood. In 24 healthy controls, we separately stimulated two deep cortical regions and investigated the effects of theta-burst TUS, a protocol shown to increase corticospinal excitability, on the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) and functional connectivity. We show that theta-burst TUS in humans selectively reduces GABA levels in the posterior cingulate, but not the dorsal anterior cingulate cortex. Functional connectivity increased following TUS in both regions. Our findings suggest that TUS changes overall excitability by reducing GABAergic inhibition and that changes in TUS-mediated neuroplasticity last at least 50 mins after stimulation. The difference in TUS effects on the posterior and anterior cingulate could suggest state- or location-dependency of the TUS effect—both mechanisms increasingly recognized to influence the brain’s response to neuromodulation.

dc.format.extent5318-
dc.format.mediumElectronic
dc.languageen
dc.publisherSpringer Science and Business Media LLC
dc.subjectHumans
dc.subjectAnimals
dc.subjectGastropoda
dc.subjectGyrus Cinguli
dc.subjectInhibition, Psychological
dc.subjectLight
dc.subjectgamma-Aminobutyric Acid
dc.titleTranscranial focused ultrasound-mediated neurochemical and functional connectivity changes in deep cortical regions in humans
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37658076
plymouth.issue1
plymouth.volume14
plymouth.publisher-urlhttp://dx.doi.org/10.1038/s41467-023-40998-0
plymouth.publication-statusPublished online
plymouth.journalNature Communications
dc.identifier.doi10.1038/s41467-023-40998-0
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Research Groups
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|Faculty of Health|School of Psychology
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA04 Psychology, Psychiatry and Neuroscience
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA04 Psychology, Psychiatry and Neuroscience|UoA04 REF peer reviewers
plymouth.organisational-group|Plymouth|Research Groups|FoH - Applied Parkinson's Research
plymouth.organisational-group|Plymouth|Users by role|Researchers in ResearchFish submission
dc.publisher.placeEngland
dcterms.dateAccepted2023-08-17
dc.date.updated2023-11-07T13:54:30Z
dc.rights.embargodate2023-11-9
dc.identifier.eissn2041-1723
dc.rights.embargoperiod
rioxxterms.versionofrecord10.1038/s41467-023-40998-0


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