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PubMed1999

Affective attitudes to face images associated with intracerebral EEG source location before face viewing.

We investigated whether different, personality-related affective attitudes are associated with different brain electric field (EEG) sources before any emotional challenge (stimulus exposure). A 27-channel EEG was recorded in 15 subjects during eyes-closed resting. After recording, subjects rated 32 images of human faces for affective appeal. The subjects in the first (i.e., most negative) and fourth (i.e., most positive) quartile of general affective attitude were further analyzed. The EEG data (mean=25+/-4. 8 s/subject) were subjected to frequency-domain model dipole source analysis (FFT-Dipole-Approximation), resulting in 3-dimensional intracerebral source locations and strengths for the delta-theta, alpha, and beta EEG frequency band, and for the full range (1.5-30 Hz) band. Subjects with negative attitude (compared to those with positive attitude) showed the following source locations: more inferior for all frequency bands, more anterior for the delta-theta band, more posterior and more right for the alpha, beta and 1.5-30 Hz bands. One year later, the subjects were asked to rate the face images again. The rating scores for the same face images were highly correlated for all subjects, and original and retest affective mean attitude was highly correlated across subjects. The present results show that subjects with different affective attitudes to face images had different active, cerebral, neural populations in a task-free condition prior to viewing the images. We conclude that the brain functional state which implements affective attitude towards face images as a personality feature exists without elicitors, as a continuously present, dynamic feature of brain functioning.

Adult↗
PubMed2000

Spatiotemporal source analysis of vocalization-associated magnetic fields.

The vocalization-related cortical fields (VRCF) following vowel vocalization were studied by magnetoencephalography (MEG) in eight normal subjects. A multiple-source model, BESA (Brain Electric Source Analysis), was applied to elucidate the generating mechanism of VRCF in the period from 150 ms before to 150 ms after the onset of vocalization. Six sources provided satisfactory solutions for VRCF activities during that period. Sources 1 and 2, which were activated from approximately 150 ms before the vocalization onset, were located in laryngeal motor areas of the left and right hemispheres, respectively. Sources 5 and 6 were located in the truncal motor area in each hemisphere, and they were very similar to sources 1 and 2 in terms of temporal change of activities. Sources 3 and 4 were located in the auditory cortices of the left and right hemispheres, respectively, and they appeared to be activated just after the vocalization onset. However, all six sources were temporally overlapped in the period approximately 0-100 ms after the vocalization onset. The present results suggested that the bilateral motor cortices, probably laryngeal and truncal areas, were activated just before the vocalization. We considered that the activities of the bilateral auditory areas after the vocalization were the response of the subject's central auditory system to his/her own voice. The motor and auditory activities were temporally overlapped, and BESA was very useful to separate the activities of each source.

Adult↗
PubMed2002

Novel schemes for hearing and orientation in insects.

Severe size constraints are imposed on the hearing organs of insects, yet they perform sophisticated tasks of auditory processing. Recent research has shown how flies acoustically locate targets in space, how mosquitoes afford highly sensitive ears, and how crickets avoid deafening themselves with their songs. These findings unveil the exquisite analytical capabilities of highly specialized microscale auditory systems.

Animals↗
PubMed2002

A common cortical substrate activated by horizontal and vertical sound movement in the human brain.

Perception of movement in acoustic space depends on comparison of the sound waveforms reaching the two ears (binaural cues) as well as spectrotemporal analysis of the waveform at each ear (monaural cues). The relative importance of these two cues is different for perception of vertical or horizontal motion, with spectrotemporal analysis likely to be more important for perceiving vertical shifts. In humans, functional imaging studies have shown that sound movement in the horizontal plane activates brain areas distinct from the primary auditory cortex, in parietal and frontal lobes and in the planum temporale. However, no previous work has examined activations for vertical sound movement. It is therefore difficult to generalize previous imaging studies, based on horizontal movement only, to multidimensional auditory space perception. Using externalized virtual-space sounds in a functional magnetic resonance imaging (fMRI) paradigm to investigate this, we compared vertical and horizontal shifts in sound location. A common bilateral network of brain areas was activated in response to both horizontal and vertical sound movement. This included the planum temporale, superior parietal cortex, and premotor cortex. Sounds perceived laterally in virtual space were associated with contralateral activation of the auditory cortex. These results demonstrate that sound movement in vertical and horizontal dimensions engages a common processing network in the human cerebral cortex and show that multidimensional spatial properties of sounds are processed at this level.

Acoustic Stimulation↗
PubMed2003

Auditory neuroscience: the salience of looming sounds.

Sounds that move towards us have a greater biological salience than those that move away. Recent studies in human and non-human primates have demonstrated a perceptual and behavioural priority for such looming sounds that is also reflected in an asymmetric pattern of cortical activation.

Animals↗
PubMed2003

Eye position affects activity in primary auditory cortex of primates.

BACKGROUND: Neurons in primary auditory cortex are known to be sensitive to the locations of sounds in space, but the reference frame for this spatial sensitivity has not been investigated. Conventional wisdom holds that the auditory and visual pathways employ different reference frames, with the auditory pathway using a head-centered reference frame and the visual pathway using an eye-centered reference frame. Reconciling these discrepant reference frames is therefore a critical component of multisensory integration. RESULTS: We tested the reference frame of neurons in the auditory cortex of primates trained to fixate visual stimuli at different orbital positions. We found that eye position altered the activity of about one third of the neurons in this region (35 of 113, or 31%). Eye position affected not only the responses to sounds (26 of 113, or 23%), but also the spontaneous activity (14 of 113, or 12%). Such effects were also evident when monkeys moved their eyes freely in the dark. Eye position and sound location interacted to produce a representation for auditory space that was neither head- nor eye-centered in reference frame. CONCLUSIONS: Taken together with emerging results in both visual and other auditory areas, these findings suggest that neurons whose responses reflect complex interactions between stimulus position and eye position set the stage for the eventual convergence of auditory and visual information.

Acoustic Stimulation↗
PubMed2003

Asymmetry in the human primary somatosensory cortex and handedness.

Brain asymmetry is a phenomenon well known for handedness and language specialization and has also been studied in motor cortex. Less is known about hemispheric asymmetries in the somatosensory cortex. In the present study, we systematically investigated the representation of somatosensory function analyzing early subcortical and cortical somatosensory-evoked potentials (SEP) after electrical stimulation of the right and left median nerve. In 16 subjects, we compared thresholds, the peripheral neurogram at Erb point, and, using MRI-based EEG source analysis, the P14 brainstem component as well as N20 and P22, the earliest cortical responses from the primary sensorimotor cortex. Handedness was documented using the Edinburgh Inventory and a dichotic listening test was performed as a measure for language dominance. Whereas thresholds, Erb potential, and P14 were symmetrical, amplitudes of the cortical N20 showed significant hemispheric asymmetry. In the left hemisphere, the N20 amplitude was higher, its generator was located further medial, and it had a stronger dipole moment. There was no difference in dipole orientation. As a possible morphological correlate, the size of the left postcentral gyrus exceeded that of the right. The cortical P22 component showed a lower amplitude and a trend toward weaker dipole strength in the left hemisphere. Across subjects, there were no significant correlations between laterality indices of N20, the size of the postcentral gyrus, handedness, or ear advantage. These data show that asymmetry of median nerve SEP occurs at the cortical level, only. However, both functional and morphological cortical asymmetry of somatosensory representation appears to vary independently of motor and language functions.

Adult↗
PubMed2003

Magnetoencephalographic evidence of the interhemispheric asymmetry in echoic memory lifetime and its dependence on handedness and gender.

The echoic memory trace (EMT) refers to neuronal activity associated with the short-term retention of stimulus-related information, especially within the primary and association auditory cortex. Using magnetoencephalography it is possible to determine quantitatively the lifetime of the EMT. Previous studies assumed that each new stimulus drives the EMT to its full strength, which then passively decays. In this study we show the limitations of this assumption using trains of auditory stimuli designed specifically for computing the EMT lifetime and its contextual sensitivity. We estimated a time-dependent EMT using a data-driven approach, which allows contributions from a relatively wide area around the auditory cortex in our quantitative measures. We identified: (1) internally generated cortical activations during the silent period between stimuli well separated in time from each other, which had influence on the morphology of the neuromagnetic response to the next external stimulus; and (2) EMTs with different lifetimes that modulate the amplitude of the evoked responses at different latencies, suggesting the existence of multiple neural delay lines. Long EMT lifetimes were observed on the descending part of the M100 complex, which showed handedness and gender-dependent interhemispheric asymmetry. Specifically, all subjects showed longer EMT lifetimes on the left hemisphere, except left-handed males. Distributed source analysis of the data for one left- and one right-handed male subject identified a secondary generator in the right-handed subject, which was located posterior to the early primary generator and dominated the auditory response at late latencies, where EMT lifetime asymmetry was high. The identified multiple neural delay lines and their laterality may provide a link between macroneuronal activity and left hemisphere specialization for processing linguistic material.

Acoustic Stimulation↗
PubMed2003

Auditory what, where, and when: a sensory somatotopy in lateral premotor cortex.

Recent findings have demonstrated that attention to visual events engages the lateral premotor cortex even in the absence of motor planning. Here, we used functional magnetic resonance imaging to explore acoustically triggered activations within the lateral premotor cortex. Temporal (when), object-related (what), and spatial (where) auditory patterns were to be monitored for violations in a serial prediction task. As a result, we found a modality-dependent modulation for auditory events within the inferior ventrolateral premotor cortex, an area engaged in vocal plans. In addition, however, auditory activations were distributed within the entire premotor cortex depending on which stimulus property was attended to. Attention to where patterns was found to engage fields for gaze and reaching (dorsolateral premotor cortex), what patterns to engage fields for hand movements (superior ventrolateral premotor cortex), and when patterns to engage fields for vocal plans. Together, the findings confirm the idea of a sensory somatotopy in lateral premotor cortex, according to which a perceptual pattern triggers representations within that motor effector which would be most appropriate to generate it as an action effect.

Acoustic Stimulation↗
PubMed2003

Differences between auditory evoked responses recorded during spatial and nonspatial working memory tasks.

Results from several recent studies suggest that neuronal processing of sound content and its spatial location may be dissociated. The use of modern neuroimaging techniques has allowed for the determination that different brain structures may be specifically activated during working memory processing of pitch and location of sound. The time course of these task-related differences, however, remains uncertain. In the present study, we performed simultaneous whole-head electroencephalogram and magnetoencephalogram recordings, using a new behavioral paradigm, to investigate the dynamics of differences between "what" and "where" evoked responses in the auditory system as a function of memory load. In the location task the latency of the N1m was shorter and its generator was situated more inferiorly than in the pitch task. Working memory processing of the tonal frequency enhanced the amplitude of the N2 component, as well as the negative-going deflection at a latency around 400 ms. A memory-load-dependent task-related difference was found in the positive slow wave which was higher during the location than pitch task at the low load. Late slow waves were affected by memory load but not type of task. These results suggest that separate neuronal networks are involved in the attribute-specific analysis of auditory stimuli and their encoding into working memory, whereas the maintenance of auditory information is accomplished by a common, nonspecific neuronal network.

Acoustic Stimulation↗
PubMed2003

Additional neuromagnetic source activity outside the auditory cortex in duration discrimination correlates with behavioural ability.

In magneto- and electroencephalographic experiments on an oddball paradigm we compared the components of the auditory evoked fields and potentials of "attend" with "nonattend" conditions in 17 subjects. The former consisted of the performance of a duration discrimination task, where we observed augmented activity for the auditory sustained response. A multiple source analysis showed this effect mainly stemming from a third source outside the auditory cortices. The dipole moment of this specific activation was increased by 150% under the attend condition. Having anatomical 3D MRI data sets of 12 subjects the likely location of the third source was shown to be within the area of the precuneus or the posterior cingulate gyrus, which, along with its waveform, suggests it to be a CNV equivalent. Further, the dipole moment is correlated significantly to the subjects' psychometrically derived discriminative abilities.

Acoustic Stimulation↗
PubMed2001

Differences between the N1 waves of the responses to interaural time and intensity disparities: scalp topography and dipole sources.

OBJECTIVES: Being the two complementary cues to directional hearing, interaural time and intensity disparities (ITD and IID, respectively), are known to be separately encoded in the brain stem. We address the question as to whether their codes are collapsed into a single lateralization code subcortically or they reach the cortex via separate channels and are processed there in different areas. METHODS: Two continuous trains of 100/s clicks were dichotically presented. At 2 s intervals either an interaural time delay of 1ms or an interaural level difference of 20 dB (HL) was introduced for 50 ms, shifting the intracranial sound image laterally for this brief period of time. Long-latency responses to these directional stimuli, which had been tested to evoke no potentials under monotic or diotic conditions, as well as to sound pips of 50 ms duration were recorded from 124 scalp electrodes. Scalp potential and current density maps at N1 latency were obtained from thirteen normal subjects. A 4-sphere head model with bilaterally symmetrical dipoles was used for source analysis and a simplex algorithm preceded by a genetic algorithm was employed for solving the inverse problem. RESULTS: Inter- and intra-subject comparisons showed that the N1 responses evoked by IID and ITD as well as by sound pip stimuli had significantly different scalp topographies and interhemispheric dominance patterns. Significant location and orientation differences between their estimated dipole sources were also noted. CONCLUSIONS: We conclude that interaural time and intensity disparities (thus the lateral shifts of a sound image caused by these two cues) are processed in different ways and/or in different areas in auditory cortex.

Adolescent↗
PubMed2002

Involuntary attention in children as a function of sound source location: evidence from event-related potentials.

OBJECTIVES: The present study addressed the question of whether location of the auditory stimulation source affects an involuntary attention triggering to the deviant sounds in a passive oddball paradigm in 8-10-year-old children. METHODS: Using free-field stimulation two late event-related potentials components were examined: the mismatch negativity (MMN), indexing preconscious sound change detection and the P3a, indexing involuntary attention switch. Data were registered to frequency changes in sounds of different complexities in two experimental conditions. In the 'in-front' condition, the sound sequences were presented through the loudspeakers situated in front of a participant on both sides of the video display. In the 'on-sides' condition, the sources of auditory and visual stimuli were separated by moving the loudspeakers to the sides of the participant. RESULTS: The MMN amplitude or the MMN and P3a latencies varied in neither stimulus class significantly as a function of sound location. However, significantly larger P3 amplitude was found in the 'in-front', as compared to the 'on-sides' condition. CONCLUSIONS: The present results indicate enhanced involuntary attention switching in children when unattended auditory events occur within the space attended actively for visual modality. Such study design favouring cross-modal integration can be advantageous when studying involuntary auditory attention and its impairment in children.

Acoustic Stimulation↗
PubMed2002

Sound motion evoked magnetic fields.

OBJECTIVE: The aim of present study was to determine which brain regions are involved in the conscious perception of sound motion in humans. METHODS: Six kinds of sound stimuli were studied. Two static sound stimuli with durations of 100 or 1000 ms remained at a fixed position during the stimulation period. Four moving sound stimuli with duration of 100 or 1000 ms were moving from left to right, or right to left, during the stimulation period. Evoked magnetic fields were recorded using a 151-channel whole cortex magnetoencephalographic system. RESULTS: The response identified in all sound stimuli was M100. Responses identified only in moving sound stimuli were M180, M280 and M680. Contour maps and dipoles overlapped on magnetic resonance imaging indicated that both the M100 and M680 responses were generated in the superior temporal cortex (left and right), while M180 and M280 were generated in the parietal cortex (right). CONCLUSIONS: The results of this MEG study indicated that the right parietal cortex was involved in sound motion processing. We hypothesize that the right parietal cortex, in association with the left and right superior temporal cortex, forms a network to process sound motion information.

Acoustic Stimulation↗
PubMed2003

The electrophysiological net response ('F-complex') to spatial fusion of speech elements forming an auditory object.

OBJECTIVE: The purpose of this study was to define and analyze the brain activity associated with fusion of speech elements to form an auditory object and to study the effects of presenting the elements at different spatial locations (duplex stimulus). METHODS: Stimuli were formant transitions (presented to the front, left or right of the subject) and base (presented to the front), that fused to result in V-C-V sequences /aga/ and /ada/. Ten right-handed, adult, native Hebrew speakers discriminated each fused stimulus, and the brain potentials associated with performance of the task were recorded from 21 electrodes. The net-fusion response, the 'F(fusion)-complex', was extracted by subtracting the sum of potentials to the base and formant transitions from the potentials to the fused sound. Low resolution electromagnetic tomography analysis (LORETA) was performed to assess the timing and brain location of the fusion process. RESULTS: The 'F-complex', comprising of the difference N(1), P(2), N(2b) (FN(1), FP(2), FN(2b)) components could be identified for each of the stimuli and reflected a process indicating inhibition, occlusion or both, with right ear advantage in fusion. LORETA analyses indicate sequential processing of speech fusion in the temporal lobes, beginning with right prominence in FN(1) and FP(2) shifting to a more symmetrical pattern in FN(2). CONCLUSIONS: The electrophysiological correlates of speech fusion highlight the uniqueness of speech perception and the brain areas involved in its analysis.

Acoustic Stimulation↗
PubMed2003

Evoked potentials to auditory movement sensation in duplex perception.

OBJECTIVE: The purpose of this study was to examine the processing of auditory movement sensation accompanying duplex perception in binaural hearing. METHODS: Stimuli were formant transitions (presented to the front, left or right of the subject) and base (presented to the front), that fused to result in vowel-consonant-vowel (V-C-V) sequences /aga/ and /ada/. An illusion of auditory movement (duplex sensation) accompanied the fusion of these V-C-V sequences when the spatial locations of the formant transitions and base were different. Ten right-handed, adult, native Hebrew speakers discriminated each fused stimulus, and the brain potentials associated with performance of the task were recorded from 21 electrodes. The processing of auditory movement was studied by a factorial design (ANOVA) and statistical non-parametric mapping (SnPM) of low resolution electromagnetic tomography (LORETA) images of the net-fusion response. Brain regions implicated in auditory movement processing were expected to be associated with the lateralized formant location, which gave rise to duplex perception. In addition, the time-course of significant activation in brain areas that differentiated between fusion conditions was determined. RESULTS: The posterior parietal, anterior cingulate and premotor cortices were found to be implicated in duplex processing. Auditory cortex involvement was also evident, and together with the latter two brain regions was affected by right-ear advantage. CONCLUSIONS: Duplex perception resulting from fusion of spatially separate sounds forming an auditory object results in activation of a network of brain regions reflecting enhanced allocation of attention and the effect of language processing.

Acoustic Stimulation↗