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Article: Asymmetric Left–right Hippocampal Glutamatergic Modulation Of Cognitive Control In Apoe‐isoform Subjects Is Unrelated To Neuroinflammation

TitleAsymmetric Left–right Hippocampal Glutamatergic Modulation Of Cognitive Control In Apoe‐isoform Subjects Is Unrelated To Neuroinflammation
Authors
KeywordsApoE4
functional magnetic resonance imaging
glutamatergic system
magnetic resonance spectroscopy
Issue Date2021
PublisherWiley-Blackwell Publishing Ltd. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1460-9568
Citation
European Journal of Neuroscience, 2021, v. 54 n. 4, p. 5310-5326 How to Cite?
AbstractThe glutamatergic cycle is essential in modulating memory processing by the hippocampal circuitry. Our combined proton magnetic resonance spectroscopy (1H-MRS) and task-based functional magnetic resonance imaging (fMRI) study (using face-name paired-associates encoding and retrieval task) of a cognitively normal cohort of 67 healthy adults (18 ApoE4 carriers and 49 non-ApoE4 carriers) found altered patterns of relationships between glutamatergic-modulated synaptic signalling and neuronal activity or functional hyperaemia in the ApoE4 isoforms. Our study highlighted the asymmetric left–right hippocampal glutamatergic system in modulating neuronal activities in ApoE4 carriers versus non-carriers. Such brain differentiation might be developmental cognitive advantages or compensatory due to impaired synaptic integrity and plasticity in ApoE4 carriers. As there was no difference in myoinositol levels measured by MRS between the ApoE4 and non-ApoE4 subgroups, the mechanism is unlikely to be a response to neuroinflammation.
DescriptionHybrid open access
Persistent Identifierhttp://hdl.handle.net/10722/304191
ISSN
2023 Impact Factor: 2.7
2023 SCImago Journal Rankings: 1.129
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhang, H-
dc.contributor.authorChiu, PW-
dc.contributor.authorIp, I-
dc.contributor.authorLiu, T-
dc.contributor.authorWong, GHY-
dc.contributor.authorSong, YQ-
dc.contributor.authorWong, SWH-
dc.contributor.authorHerrup, K-
dc.contributor.authorMak, HKF-
dc.date.accessioned2021-09-23T08:56:30Z-
dc.date.available2021-09-23T08:56:30Z-
dc.date.issued2021-
dc.identifier.citationEuropean Journal of Neuroscience, 2021, v. 54 n. 4, p. 5310-5326-
dc.identifier.issn0953-816X-
dc.identifier.urihttp://hdl.handle.net/10722/304191-
dc.descriptionHybrid open access-
dc.description.abstractThe glutamatergic cycle is essential in modulating memory processing by the hippocampal circuitry. Our combined proton magnetic resonance spectroscopy (1H-MRS) and task-based functional magnetic resonance imaging (fMRI) study (using face-name paired-associates encoding and retrieval task) of a cognitively normal cohort of 67 healthy adults (18 ApoE4 carriers and 49 non-ApoE4 carriers) found altered patterns of relationships between glutamatergic-modulated synaptic signalling and neuronal activity or functional hyperaemia in the ApoE4 isoforms. Our study highlighted the asymmetric left–right hippocampal glutamatergic system in modulating neuronal activities in ApoE4 carriers versus non-carriers. Such brain differentiation might be developmental cognitive advantages or compensatory due to impaired synaptic integrity and plasticity in ApoE4 carriers. As there was no difference in myoinositol levels measured by MRS between the ApoE4 and non-ApoE4 subgroups, the mechanism is unlikely to be a response to neuroinflammation.-
dc.languageeng-
dc.publisherWiley-Blackwell Publishing Ltd. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1460-9568-
dc.relation.ispartofEuropean Journal of Neuroscience-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectApoE4-
dc.subjectfunctional magnetic resonance imaging-
dc.subjectglutamatergic system-
dc.subjectmagnetic resonance spectroscopy-
dc.titleAsymmetric Left–right Hippocampal Glutamatergic Modulation Of Cognitive Control In Apoe‐isoform Subjects Is Unrelated To Neuroinflammation-
dc.typeArticle-
dc.identifier.emailZhang, H: shirlzh7@hku.hk-
dc.identifier.emailLiu, T: tianyin@hku.hk-
dc.identifier.emailWong, GHY: ghywong@hku.hk-
dc.identifier.emailSong, YQ: songy@hku.hk-
dc.identifier.emailMak, HKF: makkf@hku.hk-
dc.identifier.authorityLiu, T=rp02466-
dc.identifier.authorityWong, GHY=rp01850-
dc.identifier.authoritySong, YQ=rp00488-
dc.identifier.authorityMak, HKF=rp00533-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1111/ejn.15399-
dc.identifier.pmid34309092-
dc.identifier.scopuseid_2-s2.0-85111620862-
dc.identifier.hkuros325379-
dc.identifier.volume54-
dc.identifier.issue4-
dc.identifier.spage5310-
dc.identifier.epage5326-
dc.identifier.isiWOS:000680045300001-
dc.publisher.placeUnited Kingdom-

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