The effects of alterations in conditioning stimulus intensity on short interval intracortical inhibition

Short interval intracortical inhibition [SICI] is mediated by cortical inhibitory interneurons, with two physiologically distinct phases at interstimulus interval [ISI] < 1 ms and 2.5–3 ms. The second phase of SICI is mediated by synaptic mechanisms, while the first phase has been attributed to a...

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Bibliographic Details
Published inBrain research Vol. 1273; pp. 39 - 47
Main Authors Vucic, Steve, Cheah, Benjamin C., Krishnan, Arun V., Burke, David, Kiernan, Matthew C.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.06.2009
Elsevier
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Summary:Short interval intracortical inhibition [SICI] is mediated by cortical inhibitory interneurons, with two physiologically distinct phases at interstimulus interval [ISI] < 1 ms and 2.5–3 ms. The second phase of SICI is mediated by synaptic mechanisms, while the first phase has been attributed to axonal refractoriness, synaptic mechanisms or both. In the present study, threshold-tracking transcranial magnetic stimulation was used to explore mechanisms underlying SICI. SICI was studied in 10 normal subjects at three different conditioning stimulus [CS] intensities [40%, 70% and 90% of resting motor threshold, RMT, defined as the threshold for a MEP of ∼ 0.2 mV]. Motor responses were recorded from abductor pollicis brevis. Maximal SICI developed with CS set to 70% RMT [SICI 70%], with two phases evident, at ISI 1 ms [12.7 ± 3.4%] and ISI 2.5 ms [19.3 ± 2.9%]. With CS set to 40% RMT, SICI occurred between 1 ms and 5 ms, peaking at 2.5 ms and was reduced [1.9 ± 1.4%, P < 0.0001] compared to peak SICI 70%. The small SICI peak at 1 ms was absent. With CS at 90% RMT, SICI developed between 2 and 5 ms, peaking at 4 ms [11.2 ± 7.8%]. Facilitation was evident at 1 ms. The findings from the present study suggest that inhibitory circuits with different thresholds underlie the phases of SICI, with synaptic mechanisms also critical to the development of SICI at 1 ms.
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ISSN:0006-8993
1872-6240
1872-6240
DOI:10.1016/j.brainres.2009.03.043