刺激间期和试验间期对体感门控的影响

Aoi Mase, Manabu Shibasaki, Hiroki Nakata
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摘要

研究目的感觉门控是人类的一种高级认知功能,其作用是抑制过多的感觉信息,防止大脑过度活跃。为了阐明这一功能,研究人员在记录脑电图(EEG)时使用了成对脉冲刺激范式,并以对第二个刺激(S2)的反应与对第一个刺激(S1)的反应的振幅比来进行评估。本研究利用体感诱发电位(SEPs)研究了刺激间歇(ISI)和试验间歇(ITI)对体感门控的影响:在实验 1 中,ISI 设置为五种条件:方法:在实验 1 中,ISI 设置为五种条件:200、400、600、800 和 1000 毫秒。实验 2 中,ITI 设置为四种情况:结果:ISI影响了S2/S1:ISI影响了C3'处P22和N27以及Fz处N30的S2/S1振幅比,这些S2/S1振幅比在200和400毫秒条件下下降最大。ITI 影响了 C3'处 P22、N27 和 N60 的 S2/S1 振幅比,尤其是在 1 秒条件下,体感门控不起作用。这些结果表明,随着 ISI 和 ITI 的变化,并非所有 SEP 成分都以相同的方式受到调节。ISI和ITI对体感门控的影响是独立的:根据我们的研究结果,在评估 SEP 中躯体感觉门控的功能机制时,ISI 的参数最好为 200-400 毫秒,ITI 的参数最好为 4 秒或更长。
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Effects of inter-stimulus and inter-trial intervals on somatosensory gating.

Aim of the study: Sensory gating is a human higher cognitive function that serves to suppress excessive sensory information and prevent brain overactivity. To elucidate this function, a paired-pulse stimulation paradigm has been used while recording electroencephalography (EEG), and evaluated as an amplitude ratio of responses to a second stimulus (S2) over responses to the first stimulus (S1). The present study investigated the effects of the inter-stimulus interval (ISI) and inter-trial interval (ITI) on somatosensory gating using somatosensory-evoked potentials (SEPs).

Methods: In Experiment 1, ISI was set at five conditions: 200, 400, 600, 800, and 1000 ms. In Experiment 2, ITI was set at four conditions: 1, 2, 4, and 8 s.

Results: ISI affected the S2/S1 amplitude ratios of P22 and N27 at C3' and N30 at Fz, and these S2/S1 amplitude ratios decreased the most under the 200 and 400-ms conditions. ITI affected the S2/S1 amplitude ratios of P22, N27, and N60 at C3', and especially, the somatosensory gating did not work under the 1-s condition. These results suggest that not all SEP components are modulated in the same manner with changing ISI and ITI. The effects of ISI and ITI independently affected the somatosensory gating.

Conclusions: Based on our findings, preferable parameters are 200-400 ms for ISI and 4 s or longer for ITI to evaluate the functional mechanisms on somatosensory gating in SEPs.

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