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R Hari

Publications and source records attributed to R Hari.

At least 55 records · Page 3Linked to original sources

Cognitive response profile of the human fusiform face area as determined by MEG.

Activation in or near the fusiform gyrus was estimated to faces and control stimuli. Activation peaked at 165 ms and was strongest to digitized photographs of human faces, regardless of whether they were presented in color or grayscale, suggesting that face- and color-specific areas are functionally separate. Schematic sketche evoked approximately 30% less activation than did face photographs. Scrambling the locations of facial features reduced the response by approximately 25% in either hemisphere, suggesting that configurational versus analytic processing is not lateralized at this latency. Animal faces evoked approximately 50% less activity, and common objects, animal bodies or sensory controls evoked approximately 80% less activity than human faces. The (small) responses evoked by meaningless control images were stronger when they included surfaces and shading, suggesting that the fusiform gyrus may use these features in constructing its face-specific response. Putative fusiform activation was not significantly related to stimulus repetition, gender or emotional expression. A midline occipital source significantly distinguished between faces and control images as early as 110 ms, but was more sensitive to sensory qualities. This source significantly distinguished happy and sad faces from those with neutral expressions. We conclude that the fusiform gyrus may selectively encode faces at 165 ms, transforming sensory input for further processing.

Adult↗

Normal movement reading in Asperger subjects.

Patients with autism and Asperger syndrome (AS) are impaired in mindreading and imitation skills. One possibility would be that their 'mirror neuron' system, which matches action execution and observation, does not function properly. To test this hypothesis we compared action-viewing related motor cortex functions in an AS group (one autistic and four AS subjects) and eight control subjects. In both groups viewing hand actions modified the neuromagnetic approximately 20 Hz oscillatory activity in the primary motor cortex to the same extent. Thus impaired mindreading and imitation skills found in AS and autism do not seem to result from dysfunction of the motor cortex part of the action execution/observation system.

Adult↗

Left-hemisphere dominance for processing of vowels: a whole-scalp neuromagnetic study.

Brain activation of 11 healthy right-handed subjects was studied with magnetoencephalography to estimate individual hemispheric dominance for speech sounds. The auditory stimuli comprised binaurally presented Finnish vowels, tones, and piano notes in groups of two or four stimuli. The subjects were required to detect whether the first and the last item in a group were the same. In the left hemisphere, vowels evoked significantly stronger (37-79%) responses than notes and tones, whereas in the right hemisphere the responses to different stimuli did not differ significantly. Specifically, in the two-stimulus task, all 11 subjects showed left-hemisphere dominance in the vowel vs tone comparison. This simple paradigm may be helpful in non-invasive evaluation of language lateralization.

Acoustic Stimulation↗

Prolonged attentional dwell time in dyslexic adults.

Dyslexic adults have been shown to be slow in processing rapid sequences of stimuli in all sensory modalities. We now demonstrate, by means of an attentional blink task, that the attentional dwell time is prolonged by approximately 30% in dyslexic adults compared with normal readers. Thus a target captures attentional resources for considerably longer time in dyslexics than control subjects. The observed prolongation could significantly contribute to the sluggish temporal processing of dyslexic adults.

Adult↗

Non-impaired auditory phase locking in dyslexic adults.

Dyslexic adults have profound difficulties in discriminating rapidly presented sound sequences. To test whether these deficits might be caused by impaired neuronal phase locking to the envelopes of the sound stimuli, 20 normal-reading and 13 dyslexic adults discriminated pitches of pure tones at approximately 1 kHz (producing spectral pitch due to place coding in the cochlea) and of approximately 80 Hz amplitude modulations of white noise (producing periodicity pitch based on temporal information only). We proposed that a specific deficit in phase locking would result in a worse ability to discriminate periodicity than spectral pitch. The dyslexics were significantly less accurate than the control subjects in discriminating both spectral and periodicity pitch stimuli but their performance was not disproportionally worse in the periodicity pitch task. Thus it seems that impaired neuronal phase-locking cannot explain the problems dyslexics face in processing of rapid sound sequences.

Acoustic Stimulation↗

Magnetoencephalography in the study of human somatosensory cortical processing.

Magnetoencephalography (MEG) is a totally non-invasive research method which provides information about cortical dynamics on a millisecond time-scale. Whole-scalp magnetic field patterns following stimulation of different peripheral nerves indicate activation of an extensive cortical network. At the SI cortex, the responses reflect mainly the activity of area 3b, with clearly somatotopical representations of different body parts. The SII cortex is activated bilaterally and it also receives, besides tactile input, nociceptive afference. Somatically evoked MEG signals may also be detected from the posterior parietal cortex, central mesial cortex and the frontal lobe. The serial versus parallel processing in the cortical somatosensory network is still under debate.

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Human parieto-occipital visual cortex: lack of retinotopy and foveal magnification.

We studied visual representation in the parietal cortex by recording whole-scalp neuromagnetic responses to luminance stimuli of varying eccentricities. The stimuli were semicircles (5.5 degrees in radius) presented at horizontal eccentricities from 0 degree to 16 degrees, separately in the right and left hemifields. All stimuli evoked responses in the contralateral occipital and medial parietal areas. The waveforms and distributions of the occipital responses varied with stimulus side (left, right) and eccentricity, whereas the parietal responses were remarkably similar to all stimuli. The equivalent sources of the parietal signals clustered within 1 cm3 in the medial parieto-occipital sulcus and did not differ significantly between the stimuli. The strength of the parietal activation remained practically constant with increasing stimulus eccentricity, suggesting that the visual areas in the parieto-occipital sulcus lack the enhanced foveal representation typical of most other visual areas. This result strengthens our previous suggestion that the medial parieto-occipital sulcus is the human homologue of the monkey V6 complex, characterized by, for example, lack of retinotopy and the absence of relative foveal magnification.

Adult↗

Subject's own speech reduces reactivity of the human auditory cortex.

Previous studies on monkeys have shown that uttering-related cortical areas exert an inhibitory effect on the auditory cortex, and cerebral blood-flow analyses on humans have revealed modulation of the activity of the auditory cortex during own speech. To study this modulation on a millisecond time scale, we recorded neuromagnetic evoked responses to short 1-kHz tones while the subjects were reading silently and aloud. The 100-ms response (M100) of the auditory cortex was delayed by 10-21 ms and its amplitude was dampened by 44-71% during reading aloud compared with reading silently. This effect was more prominent in responses to ipsilateral than contralateral tones, possibly due to a sum effect of diminished ipsilateral input to the cortex and decreased transcallosal excitation.

Acoustic Stimulation↗

Task-dependent modulation of 15-30 Hz coherence between rectified EMGs from human hand and forearm muscles.

1. Recent reports have shown task-related changes in oscillatory activity in the 15-30 Hz range in the sensorimotor cortex of human subjects and monkeys during skilled hand movements. In the monkey these oscillations have been shown to be coherent with oscillatory activity in the electromyographic activity of hand and forearm muscles. 2. In this study we investigated the modulation of oscillations in the electromyogram (EMG) of human volunteers during tasks requiring precision grip of two spring-loaded levers. 3. Two tasks were investigated: in the 'hold' task, subjects were required to maintain a steady grip force (ca 2.1 N or 2.6 N) for 8 s. In the 'ramp' task, there was an initial hold period for 3 s (force ca 2.1 N) followed by a linear increase in grip force over a 2 s period. The task ended with a further steady hold for 3 s at the higher force level (ca 2.6 N). 4. Surface EMGs were recorded from five hand and forearm muscles in 12 subjects. The coherence of oscillatory activity was calculated between each muscle pair. Frequencies between 1 and 100 Hz were analysed. 5. Each subject showed a peak in the coherence spectra in the 15-30 Hz bandwidth during the hold task. This coherence was absent during the initial movement of the levers. During the ramp task the coherence in the 15-30 Hz range was also significantly reduced during the movement phase, and significantly increased during the second hold period, relative to the initial hold. 6. There was coherence between the simultaneously recorded magnetoencephalogram (MEG) and EMG during steady grip in the hold task; this coherence disappeared during the initial lever movement. Using a single equivalent current dipole source model, the coherent cortical activity was localized to the hand region of the contralateral motor cortex. This suggests that the EMG-EMG coherence was, therefore, at least in part, of cortical origin. 7. The results are discussed in terms of a possible role for synchrony in the efficient recruitment of motor units during maintained grip.

Adult↗

Cortical visuomotor integration during eye pursuit and eye-finger pursuit.

To elucidate cortical mechanisms of visuomotor integration, we recorded whole-scalp neuromagnetic signals from six normal volunteers while they were viewing a black dot moving linearly at the speed of 4 degrees /sec within a virtual rectangle. The dot changed its direction randomly once every 0.3-2 sec. The subject either (1) fixated a cross in the center of the screen (eye fixation task), (2) followed the moving dot with the eyes (eye pursuit task), or (3) followed the dot with both the eyes and the right index finger (eye-finger pursuit task). Prominent magnetic signals, triggered by the changes of the direction of the dot, were seen in all conditions, but they were clearly enhanced by the tasks and were strongest during the eye-finger pursuit task and over the anterior inferior parietal lobule (aIPL). Source modeling indicated activation of aIPL [Brodmann's area (BA) 40], the posterosuperior parietal lobule (SPL; BA 7), the dorsolateral frontal cortex (DLF; BA 6), and the occipital cortex (BA 18/19). The activation first peaked in the occipital areas, then in the aIPL and DLF, and some 50 msec later in the SPL. Our results suggest that all these areas are involved in visuomotor transformation, with aIPL playing a crucial role in this process.

Adult↗

Rhythmical corticomotor communication.

Recent non-invasive human studies show that rhythmic oscillatory activity of the motor cortex and the firing of motor units of the muscle are coherent during isometric contraction, with peak frequencies around 20 Hz or 40 Hz, depending on the contraction strength. The cortical signals precede the motor unit firing and appear to reflect modulation of the common central drive to the spinal motoneuron pool. The rhythmic modulation may form a tool for efficient driving of motor units but we express some reservations about the assumed binding and attention-related roles of the rolandic brain rhythms. The cortex-muscle coherence is of interest for understanding of cortical control of voluntary movements and the pathophysiology of various motor disorders, as well as for unravelling the functional significance of cortical rhythms.

Animals↗

Relationship between responses to contra- and ipsilateral stimuli in the human second somatosensory cortex SII.

We studied the interaction between responses to contra- and ipsilateral stimuli in the human second somatosensory cortex SII by recording somatosensory evoked magnetic fields (SEFs) from 8 healthy subjects with a 122-channel whole-scalp SQUID magnetometer. Right (R) and left (L) median nerves were electrically stimulated at the wrists at intensities exceeding the motor threshold. In each stimulus sequence, the four equiprobable pairs (L-L, R-R, L-R, R-L) were presented in a random order once every 2 s, with a 300-ms interstimulus interval within the pair. The responses were modelled with a four-dipole model, with current dipoles located in the SI and SII cortices of both hemispheres. The SII responses peaked around 85-120 ms and responses to the 1st (2nd) stimulus on the pair were on average 2 (12) ms earlier and about 3 (2.5) times stronger for contralateral than ipsilateral stimuli. Independently of the condition, the 2nd response always peaked later than the 1st; the mean delay was 16 ms. The responses to the 2nd stimulus depended only slightly on the type of the 1st: the latency increased more and the amplitude decreased less after different than identical 1st stimuli. These results suggest that neuronal activations due to contra- and ipsilateral stimuli overlap strongly in the human SII cortex.

Adult↗

Ipsilateral movement-evoked fields reconsidered.

The generation mechanism of movement-evoked fields (MEFs) is poorly known and the existence of ipsilateral MEFs is still in dispute. We recorded whole-scalp neuromagnetic activity from eight subjects who were pressing response keys alternately with the right 2nd and 4th digits, while keeping the left palm on the table containing the keys. Clear ipsilateral MEFs peaked 58 +/- 2 ms after the key touch, with sources in the hand area of the right primary somatosensory cortex. The ipsilateral MEFs decreased to half size when the resting left hand was palm up on the table. However, very similar responses were obtained when another person operated the response keys and the subjects just kept their left palm on the table. No signals were elicited when the subjects only viewed these actions with no hand contact to the table. The results indicate that the MEFs receive a strong contribution from tactile input. In our experiment the ipsilateral sensorimotor activation was triggered by the movement-related vibrations transmitted to the resting hand.

Adult↗

Stronger occipital cortical activation to lower than upper visual field stimuli. Neuromagnetic recordings.

We recorded whole-scalp magnetoencephalographic (MEG) responses to black-and-white checkerboards to study whether the human cortical responses are quantitatively similar to stimulation of the lower and upper visual field at small, 0-6 degrees, eccentricities. All stimuli evoked strong occipital responses peaking at 50-100 ms (mean 75 ms). The activation was modeled with a single equivalent current dipole in the contralateral occipital cortex, close to the calcarine fissure, agreeing with an activation of the V1/V2 cortex. The dipole was, on average, twice as strong to lower than to upper field stimuli. Responses to hemifield stimuli that extended to both lower and upper fields resembled the responses to lower field stimuli in source current direction and strength. These results agree with psychophysical data, which indicate lower visual field advantage in complex visual processing. Parieto-occipital responses in the putative V6 complex were similar to lower and upper field stimuli.

Adult↗

Effects of voluntary hyperventilation on cortical sensory responses. Electroencephalographic and magnetoencephalographic studies.

It is well established that voluntary hyperventilation (HV) slows down electroencephalographic (EEG) rhythms. Little information is available, however, on the effects of HV on cortical responses elicited by sensory stimulation. In the present study, we recorded auditory evoked potentials (AEPs) and magnetic fields (AEFs), and somatosensory evoked magnetic fields (SEFs) from healthy subjects before, during, and after a 3- to 5-min period of voluntary HV. The effectiveness of HV was verified by measuring the end-tidal CO2 levels. Long-latency (100-200 ms) AEPs and long-latency AEFs originating at the supratemporal auditory cortex, as well as long-latency SEFs from the primary somatosensory cortex (SI) and from the opercular somatosensory cortex (OC), were all reduced during HV. The short-latency SEFs from SI were clearly less modified, there being, however, a slight reduction of the earliest cortical excitatory response, the N20m deflection. A middle-latency SEF deflection from SI at about 60 ms (P60 m) was slightly increased. For AEFs and SEFs, the center-of-gravity locations of the activated neuronal populations were not changed during HV. All amplitude changes returned to baseline levels within 10 min after the end of HV. The AEPs were not altered when the subjects breathed 5% CO2 in air in a hyperventilation-like manner, which prevented the development of hypocapnia. We conclude that moderate HV suppresses long-latency evoked responses from the primary projection cortices, while the early responses are less reduced. The reduction of long-latency responses is probably mediated by hypocapnia rather than by other nonspecific effects of HV. It is suggested that increased neuronal excitability caused by HV-induced hypocapnia leads to spontaneous and/or asynchronous firing of cortical neurones, which in turn reduces stimulus-locked synaptic events.

Adult↗

Where the abstract feature maps of the brain might come from.

Three types of neuronal organization can be called 'brain maps': sets of feature-sensitive cells, ordered projections between neuronal layers and ordered maps of abstract features. The latter are most intriguing as they reflect the central properties of an organism's experiences and environment. It is proposed that such feature maps are learned in a process that involves parallel input to neurons in a brain area and adaptation of neurons in the neighborhood of the cells that respond most strongly to this input. This article presents a new mathematical formulation for such adaptation and relates it to physiological functions.

Algorithms↗

Mu rhythm modulation during changes of visual percepts.

Cooperation between vision and somatomotor behavior, such as manual exploration of objects, suggests close functional coupling between the visual and sensorimotor systems. We observed this type of interaction in human volunteers during binocular rivalry while following the level of sensorimotor mu rhythm with a whole-scalp neuromagnetometer. The observers viewed a weak vertical grating in the lower visual field of one eye and a strong horizontal grating in the same spatial window of the other eye. When stationary, the weak grating was permanently invisible because of its low contrast and spatial frequency. A sudden brief drifting movement of the weak grating wiped out the dominant grating, and the weak grating became visible for less than the 3-s interval between the movements. The postcentral 8- to 15-Hz mu rhythm was found in six of nine observers, and its level increased transiently by 10-15%, starting about 450 ms after the beginning of the movement. The mu level was also enhanced by the actual disappearance of the stronger stimulus, when it occurred in random order with the rivalry stimuli. Identical visual motion, when not accompanied by a perceptual dominance change, produced only minor effects on the mu rhythm. Our results show that a change in visual percept, even with no real or imagined motor response, is associated with modified activity of the postcentral gyrus. This modification may reflect visuohaptic interactions and/or activity of the distributed cortical network implementing visually guided movements.

Adult↗

Somatosensory evoked fields to large-area vibrotactile stimuli.

We describe a method to apply large-area vibrotactile stimuli, based on a vibrating balloon, on the palms of both hands during evoked response studies. Magnetoencephalographic (MEG) signals were recorded with a whole-scalp neuromagnetometer from six healthy subjects while they held their hands on a balloon which was made to vibrate by delivering tones to it through a loudspeaker and a tube. The 200 Hz stimuli, presented once every 1 or 2 s in separate sessions, elicited prominent and replicable somatosensory evoked fields (SEFs) and also auditory evoked fields (AEFs) due to the concomitant sound. Source modelling allowed reliable differentiation between bilateral activation of the primary somatosensory (SI) cortices (peaks at 46-61 ms after the stimulus onset) and of the supratemporal auditory cortices (peaks at 104-126 ms). These simple vibrotactile stimuli could be useful for rapid and reliable identification of the somatosensory and auditory cortices, for example in presurgical evaluation of children.

Acoustic Stimulation↗