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題名 Vascular-metabolic and GABAergic Inhibitory Correlates of Neural Variability Modulation. A Combined fMRI and PET Study
作者 Qin, Pengmin;Duncan, Niall W.;Chen, David Yen-Ting;Chen, Chi-Jen;Huang, Li-Kai;Huang, Zirui;Lin, Chien-Yuan E.;Wiebking, Christine;Yang, Che-Ming;Northoff, Georg;Lane, Timothy J.
Northoff, Georg
藍亭
Lane, Timothy J.
貢獻者 心腦中心
關鍵詞 temporal variability ; brain state ; cerebral blood flow ; visual cortex ; GABAA receptor ; flumazenil
日期 2018-05
上傳時間 13-Sep-2018 17:43:12 (UTC+8)
摘要 Neural activity varies continually from moment to moment. Such temporal variability (TV) has been highlighted as a functionally specific brain property playing a fundamental role in cognition. We sought to investigate the mechanisms involved in TV changes between two basic behavioral states, namely having the eyes open (EO) or eyes closed (EC) in vivo in humans. To these ends we acquired BOLD fMRI, ASL, and [18F]-fluoro-deoxyglucose PET in a group of healthy participants (n = 15), along with BOLD fMRI and [18F]-flumazenil PET in a separate group (n = 19). Focusing on an EO- vs EC-sensitive region in the occipital cortex (identified in an independent sample), we show that TV is constrained in the EO condition compared to EC. This reduction is correlated with an increase in energy consumption and with regional GABAA receptor density. This suggests that the modulation of TV by behavioral state involves an increase in overall neural activity that is related to an increased effect from GABAergic inhibition in addition to any excitatory changes. These findings contribute to our understanding of the mechanisms underlying activity variability in the human brain and its control.
關聯 Neuroscience, Volume 379, 21 May 2018, Pages 142-151
資料類型 article
DOI https://doi.org/10.1016/j.neuroscience.2018.02.041
dc.contributor 心腦中心
dc.creator (作者) Qin, Pengmin;Duncan, Niall W.;Chen, David Yen-Ting;Chen, Chi-Jen;Huang, Li-Kai;Huang, Zirui;Lin, Chien-Yuan E.;Wiebking, Christine;Yang, Che-Ming;Northoff, Georg;Lane, Timothy J.en_US
dc.creator (作者) Northoff, Georgen_US
dc.creator (作者) 藍亭zh_TW
dc.creator (作者) Lane, Timothy J.en_US
dc.date (日期) 2018-05
dc.date.accessioned 13-Sep-2018 17:43:12 (UTC+8)-
dc.date.available 13-Sep-2018 17:43:12 (UTC+8)-
dc.date.issued (上傳時間) 13-Sep-2018 17:43:12 (UTC+8)-
dc.identifier.uri (URI) http://nccur.lib.nccu.edu.tw/handle/140.119/120082-
dc.description.abstract (摘要) Neural activity varies continually from moment to moment. Such temporal variability (TV) has been highlighted as a functionally specific brain property playing a fundamental role in cognition. We sought to investigate the mechanisms involved in TV changes between two basic behavioral states, namely having the eyes open (EO) or eyes closed (EC) in vivo in humans. To these ends we acquired BOLD fMRI, ASL, and [18F]-fluoro-deoxyglucose PET in a group of healthy participants (n = 15), along with BOLD fMRI and [18F]-flumazenil PET in a separate group (n = 19). Focusing on an EO- vs EC-sensitive region in the occipital cortex (identified in an independent sample), we show that TV is constrained in the EO condition compared to EC. This reduction is correlated with an increase in energy consumption and with regional GABAA receptor density. This suggests that the modulation of TV by behavioral state involves an increase in overall neural activity that is related to an increased effect from GABAergic inhibition in addition to any excitatory changes. These findings contribute to our understanding of the mechanisms underlying activity variability in the human brain and its control.en_US
dc.format.extent 817623 bytes-
dc.format.mimetype application/pdf-
dc.relation (關聯) Neuroscience, Volume 379, 21 May 2018, Pages 142-151
dc.subject (關鍵詞) temporal variability ; brain state ; cerebral blood flow ; visual cortex ; GABAA receptor ; flumazenilen_US
dc.title (題名) Vascular-metabolic and GABAergic Inhibitory Correlates of Neural Variability Modulation. A Combined fMRI and PET Studyen_US
dc.type (資料類型) article
dc.identifier.doi (DOI) 10.1016/j.neuroscience.2018.02.041
dc.doi.uri (DOI) https://doi.org/10.1016/j.neuroscience.2018.02.041