NeuroImage · 2019
Normative event-related potentials from sensory and cognitive tasks reveal occipital and frontal activities prior and following visual events.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Di Russo F, M Berchicci, V Bianco, Rl Perri, S Pitzalis, F Quinzi, D Spinelli
Аннотация
In the present study, we report the results from a large sample of participants (N = 136), selected based on their EEG quality, to obtain event-related potential (ERP) normative data. All participants were tested in Simple Response Task (SRT) and Discriminative Response Task (DRT). A subset of 36 participants was tested also in Passive Vision task. Both pre- and post-stimulus ERPs were analyzed and compared among different tasks. Spatiotemporal patterns of all the observed components were analyzed using source analysis. Beside the well-known ERP components, we also described recently identified prefrontal components: the pre-stimulus prefrontal negativity (pN) associated to proactive cognitive (mainly inhibitory) control within the inferior frontal gyrus (iFg); the post-stimulus prefrontal N1, P1 and P2 (pN1, pP1 and pP2) involved in perceptual and visual-motor awareness (pN1 and pP1), and in stimulus-response mapping and decision-making (pP2) localized within the insular cortex. The large sample of high-quality EEG datasets allowed to identify four additional components: the pre-stimulus visual negativity (vN) originating in extrastriate visual areas and interpreted as a visual readiness activity; the post-stimulus prefrontal N2 and N3 (pN2 and pN3) components interpreted as feedback reactivation of the anterior insular cortex; and the post-stimulus prefrontal P3 (pP3), interpreted as persisting inhibitory activity of the iFg for inhibited trials.