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DOI 10.1016/j.clinph.2004.02.013

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2004

Magnetoencephalographic study of occipitotemporal activity elicited by viewing mouth movements.

Miki Kensaku, Watanabe Shoko, Kakigi Ryusuke, Puce Aina

Клиническое исследованиеСтатьяПеревод пока не подготовлен

Аннотация

OBJECTIVE

We studied the temporal and spatial characteristics of neural responses elicited by viewing mouth movements using magnetoencephalography.

METHODS

We focused on differences in responses to mouth opening and closing movements by apparent motion, using an averting eyes condition as a control.

RESULTS

A large clear MEG component, 1 M (mean peak latency of approximately 160 ms), was elicited by both mouth movements. We modeled the neural sources using a brain electric source analysis (BESA) method and placed the sources around: (1) the occipitotemporal border at human MT/V5, (2) the primary visual cortex (V1), and (3) fusiform gyrus. The calculated activity of Source (1) was large whereas the activity of the others was small or negligible. Source (1), as calculated separately for mouth closing and opening movements and eye movement, showed no significant different amplitude and locations. We did not find any activity in the superior temporal sulcus (STS).

CONCLUSIONS

Our results indicate that human MT/V5 is active in the perception of both mouth and eye motions. Viewing mouth and eye movements elicits no significant differences in MT/V5 activity, indicating that the perception of movement of facial parts is probably processed in the same manner.

SIGNIFICANCE: Characteristic activities in the human MT/V5 elicited by viewing mouth movement were clarified by MEG.

Для цитирования: Miki Kensaku, Watanabe Shoko, Kakigi Ryusuke, Puce Aina. Magnetoencephalographic study of occipitotemporal activity elicited by viewing mouth movements.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2004. DOI: 10.1016/j.clinph.2004.02.013.

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