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題名 Resting GABA concentration predicts inhibitory control during an auditory Go-Nogo task
作者 蔡尚岳
Cheng, Chia-Hsiung
Niddam, David M.
Hsu, Shih-Chieh
Liu, Chia-Yih
Tsai, Shang-Yueh
貢獻者 應物所
關鍵詞 Response inhibition ; M100 ; Sensory gating ; Magnetic resonance spectroscopy (MRS) ; Magnetoencephalography (MEG)
日期 2017-12
上傳時間 18-Apr-2018 14:33:01 (UTC+8)
摘要 Inhibitory control plays an important role in goal-directed behavior. Although substantial inter-individual variability exists in the behavioral performance of response inhibition, the corresponding modulating neurochemical and neurophysiological mechanisms remain unclear. Thus, the present study aimed to explore the relationship between behavioral response inhibition, GABA+ concentrations and automatic sensory gating (SG) in the auditory cortices. We recruited 19 healthy adults to undergo magnetoencephalography, magnetic resonance spectroscopy (MRS), and behavioral experiments. A paired-stimulus paradigm was used to study SG of the auditory cortices, and an auditory-driven Go-Nogo task was used to evaluate the behavioral response inhibition. Resting GABA+ concentrations were measured in the bilateral superior temporal gyri by means of MRS. Neither GABA+ concentrations nor auditory SG showed significant hemispheric asymmetry. However, an enhanced SG (lower ratio) was found to correlate with improved behavioral inhibition. Moreover, a higher GABA+ concentration was strongly related to improved inhibitory control. These findings highlight the important role of automatic neurophysiological processes and inhibitory neurotransmitters in the prediction of the behavioral performance of inhibitory control.
關聯 Experimental Brain Research, Volume 235, Issue 12, pp. 3833-3841
資料類型 article
DOI https://doi.org/10.1007/s00221-017-5101-6
dc.contributor 應物所zh_Tw
dc.creator (作者) 蔡尚岳zh_TW
dc.creator (作者) Cheng, Chia-Hsiungen_US
dc.creator (作者) Niddam, David M.en_US
dc.creator (作者) Hsu, Shih-Chiehen_US
dc.creator (作者) Liu, Chia-Yihen_US
dc.creator (作者) Tsai, Shang-Yuehen_US
dc.date (日期) 2017-12-
dc.date.accessioned 18-Apr-2018 14:33:01 (UTC+8)-
dc.date.available 18-Apr-2018 14:33:01 (UTC+8)-
dc.date.issued (上傳時間) 18-Apr-2018 14:33:01 (UTC+8)-
dc.identifier.uri (URI) http://nccur.lib.nccu.edu.tw/handle/140.119/116893-
dc.description.abstract (摘要) Inhibitory control plays an important role in goal-directed behavior. Although substantial inter-individual variability exists in the behavioral performance of response inhibition, the corresponding modulating neurochemical and neurophysiological mechanisms remain unclear. Thus, the present study aimed to explore the relationship between behavioral response inhibition, GABA+ concentrations and automatic sensory gating (SG) in the auditory cortices. We recruited 19 healthy adults to undergo magnetoencephalography, magnetic resonance spectroscopy (MRS), and behavioral experiments. A paired-stimulus paradigm was used to study SG of the auditory cortices, and an auditory-driven Go-Nogo task was used to evaluate the behavioral response inhibition. Resting GABA+ concentrations were measured in the bilateral superior temporal gyri by means of MRS. Neither GABA+ concentrations nor auditory SG showed significant hemispheric asymmetry. However, an enhanced SG (lower ratio) was found to correlate with improved behavioral inhibition. Moreover, a higher GABA+ concentration was strongly related to improved inhibitory control. These findings highlight the important role of automatic neurophysiological processes and inhibitory neurotransmitters in the prediction of the behavioral performance of inhibitory control.en_US
dc.format.extent 1547505 bytes-
dc.format.mimetype application/pdf-
dc.relation (關聯) Experimental Brain Research, Volume 235, Issue 12, pp. 3833-3841-
dc.subject (關鍵詞) Response inhibition ; M100 ; Sensory gating ; Magnetic resonance spectroscopy (MRS) ; Magnetoencephalography (MEG)en_US
dc.title (題名) Resting GABA concentration predicts inhibitory control during an auditory Go-Nogo tasken_US
dc.type (資料類型) article-
dc.identifier.doi (DOI) 10.1007/s00221-017-5101-6-
dc.doi.uri (DOI) https://doi.org/10.1007/s00221-017-5101-6-