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运动皮层 GABA 能抑制解释高危赌徒和非赌徒控制反应能力的差异。

Variations in response control within at-risk gamblers and non-gambling controls explained by GABAergic inhibition in the motor cortex.

机构信息

The University of Sydney, Australia.

The University of Sydney, Australia.

出版信息

Cortex. 2018 Jun;103:153-163. doi: 10.1016/j.cortex.2018.03.004. Epub 2018 Mar 17.

Abstract

Paired-pulse Transcranial Magnetic Stimulation (TMS) is used to study inhibitory and excitatory mechanisms in the motor cortex through the measurement of short-interval intracortical inhibition (SICI), indicative of GABAergic activity, and intracortical facilitation (ICF), indicative of glutamatergic activity. In the present study, TMS was delivered to the left motor cortex of 40 participants while we measured SICI and ICF at rest. We were interested in whether variation between individuals in these modulatory mechanisms is related to inhibitory control over responding measured as stop signal reaction time (SSRT). Within the same group of participants, we investigated whether SICI, ICF, SSRT, and self-reported impulsivity, are impaired in participants identified as At-Risk gamblers (n = 20) compared to non-gambling controls (n = 20). We found a significant negative correlation between SICI strength and SSRT, but no correlation between ICF strength and SSRT after controlling for the correlation between SICI and SSRT. Thus, poor inhibitory control of responding was associated with weak GABAergic activity. When taking into account the effects of substance/alcohol use and attention-deficit hyperactivity disorder (ADHD) symptom severity, At-Risk gamblers showed elevated self-reported impulsivity, but did not differ from controls on SSRT or SICI/ICF. Our study is the first to show that individual differences in motor cortex inhibition can predict stopping performance, and the first to investigate paired-pulse TMS parameters (together with other impulse control measures) in a gambling population.

摘要

成对脉冲经颅磁刺激(TMS)用于通过测量短程抑制(SICI)和皮质内易化(ICF)来研究运动皮质中的抑制和兴奋机制,SICI 指示 GABA 能活动,而 ICF 指示谷氨酸能活动。在本研究中,我们在测量静息时的 SICI 和 ICF 的同时,向 40 名参与者的左运动皮质施加 TMS。我们感兴趣的是,这些调节机制个体之间的差异是否与抑制控制反应有关,该抑制控制反应通过停止信号反应时间(SSRT)来衡量。在同一组参与者中,我们研究了 SICI、ICF、SSRT 和自我报告的冲动性,在被确定为高危赌博者(n=20)与非赌博对照组(n=20)的参与者中是否受损。我们发现 SICI 强度与 SSRT 之间存在显著负相关,但在控制 SICI 和 SSRT 之间的相关性后,ICF 强度与 SSRT 之间没有相关性。因此,反应抑制不良与 GABA 能活动减弱有关。当考虑物质/酒精使用和注意缺陷多动障碍(ADHD)症状严重程度的影响时,高危赌博者表现出更高的自我报告冲动性,但在 SSRT 或 SICI/ICF 上与对照组没有差异。我们的研究首次表明,运动皮质抑制的个体差异可以预测停止表现,并且首次在赌博人群中调查了成对脉冲 TMS 参数(与其他冲动控制措施一起)。

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