Kensaku Miki

Gaze direction affects face perception in humans

We recorded event-related potentials (ERP) in response to images of faces with a straight gaze (straight eyes) and eyes averted (averted eyes). Peak latencies of ERP components showed no significant change between straight eyes and averted eyes, but amplitude for averted eyes, particularly when averted to the right, was significantly larger than that for straight eyes at the lateral temporal electrode of the right hemisphere. Single-unit recordings in monkeys and neuroimaging studies in humans have revealed activity in the lateral temporal region, mainly the superior temporal sulcus, and a clinical study demonstrated the importance of the right hemisphere when viewing gaze direction. This is the first systematic neurophysiological report to confirm these findings using ERP.

Sensory perception during sleep in humans: a magnetoencephalograhic study

We reported the changes of brain responses during sleep following auditory, visual, somatosensory and painful somatosensory stimulation by using magnetoencephalography (MEG). Surprisingly, very large changes were found under all conditions, although the changes in each were not the same. However, there are some common findings. Short-latency components, reflecting the primary cortical activities generated in the primary sensory cortex for each stimulus kind, show no significant change, or are slightly prolonged in latency and decreased in amplitude. These findings indicate that the neuronal activities in the primary sensory cortex are not affected or are only slightly inhibited during sleep. By contrast, middle- and long-latency components, probably reflecting secondary activities, are much affected during sleep. Since the dipole location is changed (auditory stimulation), unchanged (somatosensory stimulation) or vague (visual stimulation) between the state of being awake and asleep, different regions responsible for such changes of activity may be one explanation, although the activated regions are very close to each other. The enhancement of activities probably indicates two possibilities, an increase in the activity of excitatory systems during sleep, or a decrease in the activity of some inhibitory systems, which are active in the awake state. We have no evidence to support either, but we prefer the latter, since it is difficult to consider why neuronal activities would be increased during sleep.

Human MT/V5 activity on viewing eye gaze changes in others : A magnetoencephalographic study

The present study used magnetoencephalography (MEG) to investigate human MT/V5 activity when observing changes in eye gaze. Subjects viewed a face in which the eyes changed to look either directly at (BACK) or away from (AWAY) the subject in a series of apparent motion conditions. BACK involved 2 directions, from left to center (LC) and from right to center (RC). Likewise, AWAY involved 2 directions, from center to left (CL) and from center to right (CR). A clear MEG component, 1M, was elicited with all eye gaze changes. Mean peak latency was 157 ms and was unaffected by stimulus condition. The equivalent current dipole (ECD) was localized to human MT/V5. Two main effects were noted: (1) ECD moment was significantly larger for BACK than for AWAY; and (2) 1M ECD locations were more posterior for AWAY than for BACK. Gaze direction, with LEFT involving CL and RC and RIGHT involving CR and LC, showed no significant effects. These data indicate that MT/V5 responds to gaze direction rather than eye position, and that eye movements directed at the viewer elicit the strongest effects. Processing of gaze change is NOT sensitive to eye direction per se but rather is modulated by eye gaze relative to the viewer.

Mechanisms of face perception in humans : A magneto- and electro-encephalographic study

We have been studying the underlying mechanisms of face perception in humans using magneto‐ (MEG) and electro‐encephalography (EEG) including (1) perception by viewing the static face, (2) differences in perception by viewing the eyes and whole face, (3) the face inversion effect, (4) the effect of gaze direction, (5) perception of eye motion, (6) perception of mouth motion, and (7) the interaction between auditory and visual stimuli related to the vowel sounds. In this review article, we mainly summarize our results obtained on 3, 5, and 6 above.

Magnetoencephalographic study of occipitotemporal activity elicited by viewing mouth movements

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.

Timing of early activity in the visual cortex as revealed by simultaneous MEG and ERG recordings.

To clarify the latency of the earliest cortical activity in visual processing, electroretinograms (ERGs) and visual evoked magnetic fields (VEFs) following flash stimulation were recorded simultaneously in six human subjects. Flash stimuli were applied to the right eye and ERGs were recorded from a skin electrode placed on the lower lid. ERGs showed two major deflections in all subjects: an eyelid-negativity around 20 ms and a positivity around 60 ms corresponding to an a- and b-waves, respectively. The mean onset and peak latency of the earliest component of VEFs (37 M) was 30.2 and 36.9 ms, respectively. There was a linear correlation between the peak latency of the a-wave and the onset latency of the 37 M (r=0.90, P=0.011). When a single equivalent current dipole analysis was applied to the 37 M, four out of six subjects showed highly reliable results. The generator of the 37 M was estimated to be located in the striate cortex in all four subjects. Since post-receptoral activities in the retina are expected to start around the peak of the a-wave (20 ms), the early cortical activity, which appears 10 ms later than the a-wave peak, is considered to be the earliest cortical activity following flash stimulation.

Brain responses for the subconscious recognition of faces.

We investigated the event-related responses following subthreshold and suprathreshold stimulation with facial and non-facial figures using magnetoencephalography (MEG) and EEG recordings to clarify the physiological nature of subconscious perception. Event-related magnetic fields and potentials were recorded from the right hemisphere in eight healthy subjects. Three types of stimulus, i.e., facial image (Face), letters of the alphabet (Letters) and random patterns of dots (Dots), with different presentation periods, subthreshold (16 ms), intermediate (32 ms) and suprathreshold (48 ms) were visually presented in a random order. A psychological discrimination task using the same stimuli was also employed. Clear MEG and EEG responses were recorded for all the stimuli, but the amplitude of the responses was largest for Face and smallest for Dots even in the subthreshold stimulation. The equivalent current dipoles (ECDs) for Face were located around the fusiform gyrus, although the correlation coefficients for ECDs were low under subthreshold and intermediate conditions. The ECDs for Letters and Dots were not estimated with reliable correlation coefficients. The results from the psychological task correlated with the dominancy of face recognition. Face perception was processed differently in the subthreshold condition as well as suprathreshold condition. The subconscious recognition of face might be processed around the fusiform gyrus.

Effects of inverting contour and features on processing for static and dynamic face perception: An MEG study

We investigated the effects of inverting facial contour (hair and chin) and features (eyes, nose and mouth) on processing for static and dynamic face perception using magnetoencephalography (MEG). We used apparent motion, in which the first stimulus (S1) was replaced by a second stimulus (S2) with no interstimulus interval and subjects perceived visual motion, and presented three conditions as follows: (1) U&U: Upright contour and Upright features, (2) U&I: Upright contour and Inverted features, and (3) I&I: Inverted contour and Inverted features. In static face perception (S1 onset), the peak latency of the fusiform areas activity, which was related to static face perception, was significantly longer for U&I and I&I than for U&U in the right hemisphere and for U&I than for U&U and I&I in the left. In dynamic face perception (S2 onset), the strength (moment) of the occipitotemporal areas activity, which was related to dynamic face perception, was significantly larger for I&I than for U&U and U&I in the right hemisphere, but not the left. These results can be summarized as follows: (1) in static face perception, the activity of the right fusiform area was more affected by the inversion of features while that of the left fusiform area was more affected by the disruption of the spatial relation between the contour and features, and (2) in dynamic face perception, the activity of the right occipitotemporal area was affected by the inversion of the facial contour.

The development of the perception of facial emotional change examined using ERPs

OBJECTIVE The development of the perception of changes in facial emotion was investigated using event-related potentials (ERPs) in children and adults. METHODS Four different conditions were presented: (1) N-H: a neutral face that suddenly changed to a happy face. (2) H-N: reverse of N-H. (3) N-A: a neutral face that suddenly changed to an angry face. (4) A-N: reverse of N-A. RESULTS In the bilateral posterior temporal areas, a negative component was evoked by all conditions in younger children (7-10 years old), older children (11-14 years old), and adults (23-33 years old) within 150-300 ms. Peak latency was significantly shorter and amplitude was significantly smaller in adults than younger and older children. Moreover, maximum amplitude was significantly larger for N-H and N-A than H-N and A-N in younger children and for N-H than the other three conditions in adults. CONCLUSION The areas of the brain involved in perceiving changes in facial emotion have not matured by 14 years of age. SIGNIFICANCE Our study is the first to clarify a difference between children and adults in the perception of facial emotional change.

Differential priming effects of color-opponent subliminal stimulation on visual magnetic responses.

We investigated the effects of subliminal stimulation on visible stimulation to demonstrate the priority of facial discrimination processing, using a unique, indiscernible, color‐opponent subliminal (COS) stimulation. We recorded event‐related magnetic cortical fields (ERF) by magnetoencephalography (MEG) after the presentation of a face or flower stimulus with COS conditioning using a face, flower, random pattern, and blank. The COS stimulation enhanced the response to visible stimulation when the figure in the COS stimulation was identical to the target visible stimulus, but more so for the face than for the flower stimulus. The ERF component modulated by the COS stimulation was estimated to be located in the ventral temporal cortex. We speculated that the enhancement was caused by an interaction of the responses after subthreshold stimulation by the COS stimulation and the suprathreshold stimulation after target stimulation, such as in the processing for categorization or discrimination. We also speculated that the face was processed with priority at the level of the ventral temporal cortex during visual processing outside of consciousness. Hum Brain Mapp, 2006.