Cortical activity elicited by changes in auditory stimuli: different sources for the magnetic N100m and mismatch responses.

Magnetic responses to frequent and infrequent auditory stimuli, all presented in the same stimulus block in randomized order, were recorded. The standard stimuli, comprising 90% of all the stimuli, were 100-ms, 1000 Hz, 90dB sinusoidal tone bursts. There were three deviant tones, each presented at a probability of 3.3%, which differed from the standard tone on one dimension only: frequency deviant (1500 Hz), intensity deviant (67dB SPL), or duration deviant (50 ms). All mismatch fields, i.e., responses elicited by different deviants, as well as N100m to the standards and deviants, could be explained by neural activity in the supratemporal auditory cortex. The source of N100m to standards and deviants was significantly posterior to the sources for the three different mismatch fields. The mean locations of the equivalent dipoles for the different mismatch fields did not differ significantly from each other, but some differences were found for individual subjects.

Reactions of human auditory cortex to a change in tone duration.

Auditory evoked magnetic fields were measured using a stimulation sequence where repetitive identical tone bursts were randomly and infrequently replaced by shorter tones. The deviation in the stimulus duration evoked a specific response, the mismatch field, peaking about 130 ms after the end of the shorter stimulus. The response can be explained by neural activity at the supratemporal auditory cortex. The results suggest the existence of a neural mechanism specific to changes in sound duration.

Nociceptive responses of trigeminal neurons in SII-7b cortex of awake monkeys.

A cluster of trigeminal nociceptive neurons was located in the lateral sulcus on the upper bank of the frontoparietal operculum in a region bordering between cortical areas SII and 7b. These neurons were isolated in cortical cell layers IV and V-VI. All nociceptive neurons responded exclusively to noxious mechanical stimulation of cutaneous receptive fields on the face/head or intraoral tissue. Sustained noxious mechanical stimulation elicited slowly adapting responses that accurately encoded the duration of the stimulation. Prolonged discharges following removal of noxious stimulation were not observed. These nociceptive specific neurons poorly encoded graded noxious stimuli. Trigeminal somatosensory neurons within and surrounding the SII-7b cluster were not topographically organized according to divisions of the trigeminal nerve, laterality of receptive fields, or division of face/head and intraoral receptive fields. The thalamocortical, corticocortical and indirect corticolimbic connectivities of SII and area 7b and the possible role of SII-7b nociceptive neurons in learning, memory and avoidance behaviors are discussed.

Selective listening modifies activity of the human auditory cortex.

We have studied the effect of selective listening on the neuromagnetic evoked activity of the human auditory cortex. In the word categorization experiment the stimuli were 5-letter words, each beginning with (k). Half of them were targets, i.e., names of animals or plants, and half other meaningful Finnish words. In the duration discrimination experiment equiprobable tones of 425 ms (targets) or 600 ms duration were presented. In both experiments the interstimulus interval (ISI) was 2.3 s and the stimuli of the two classes were presented randomly. Subjects either ignored the stimuli (reading condition) or counted the number of targets (listening condition). The magnetic field over the head was measured with a 7-channel 1st-order SQUID-gradiometer. The stimuli evoked a transient response followed by a sustained field. The transient response did not differ between the two conditions but the sustained field was significantly larger in the listening than reading condition; the increase began 120-200 ms after stimulus onset and continued for several hundred milliseconds. The equivalent source locations of both transient and sustained responses agreed with activation of the supratemporal auditory cortex. In the dichotic listening experiment 25-ms square-wave stimuli were presented randomly and equiprobably either to the left or to the right ear at an ISI of 0.8-1 s, either alone or in presence of a speech masker. Counting the stimuli of either ear resulted in differences between responses to relevant and irrelevant sounds. The difference began 140-150 ms after stimulus onset and peaked at 200-240 ms. During monaural speech masking, N100m was larger for attended than ignored stimuli.(ABSTRACT TRUNCATED AT 250 WORDS)

Interaural interaction in the human auditory cortex.

We studied the effect of binaural, contralateral and ipsilateral stimulation on middle- and long-latency auditory-evoked magnetic fields using trains of 40-Hz clicks. The stimuli evoked both a transient response (N100m) and a 40-Hz response, which presumably reflects coalescence of middle-latency responses. Binaural stimuli elicited significantly larger 40-Hz responses and sustained fields than contralateral stimuli. N100m amplitudes did not differ between binaural and contralateral stimulation; the dipole moments were even smaller to binaural than contralateral stimuli. Responses to the ipsilateral stimuli were always the smallest.

Cerebral magnetic responses to stimulation of tibial and sural nerves.

We report somatosensory evoked magnetic fields (SEFs) to stimulation of the mixed posterior tibial nerve (PTN) and the sensory sural nerve (SN) in 6 healthy subjects. The first peak of the responses occurred at 39-50 ms (P40m), with a 2-3 ms longer latency for SN than PTN stimulation. Within 200 ms several other deflections followed, with interindividually varying waveforms and latencies. Magnetic field mappings indicated that the source of P40m for PTN can be modelled by a single equivalent current dipole at the primary sensorimotor cortex; for the smaller responses to SN stimulation the single dipole model was less applicable. Field patterns for later deflections differed from those of P40m, indicating that several current sources within or near the primary foot projection area are sequentially activated after stimulation of both a mixed and a sensory lower limb nerve. These late deflections could not always be satisfactorily explained by single current dipoles, suggesting more complex geometries for the underlying neural activity.

Cortical activity evoked by a multichannel cochlear prosthesis.

We have recorded electric potentials and neuromagnetic fields evoked by electric stimulation of the auditory nerve in a totally deaf patient with an implanted multichannel prosthesis. The evoked electric responses were a vertex-negative deflection at about 70 ms after stimulus onset and a vertex-positive deflection at about 180 ms. Evoked magnetic responses coinciding with the vertex potential were found in the right hemisphere, ipsilateral to the stimulated ear. The equivalent source of these responses corresponds to activation of the right auditory cortex. In the left hemisphere, the magnetic responses were considerably smaller and less reliable. These results suggest an abnormality of the central auditory pathways in this patient. In the future, neuromagnetic recordings might be used preoperatively to forecast the effectiveness of the possible implantation.

Responses of the human auditory cortex to vowel onset after fricative consonants.

Neuromagnetic responses to different auditory stimuli (noise bursts and short speech stimuli) were mapped over both hemispheres of seven healthy subjects. The results indicate that a particular acoustic feature of speech, vowel onset after voiceless fricative consonants, evokes a prominent response in the human supratemporal auditory cortex. Although the observed response seems to be specific to acoustic rather than phonetic characteristics of the stimuli, it might reflect feature detection essential for further speech processing.

Cortical responses to painful CO2 stimulation of nasal mucosa; a magnetoencephalographic study in man.

Magnetic and electrical responses to CO2 stimulation of the nasal mucosa were recorded in 4 subjects. The magnetic responses peaked at 350-400 msec, coinciding with the negative vertex potential. The field pattern suggested neural activation in the upper bank of the sylvian fissure near the lateral end of the central sulcus, i.e., at or near SII. The results also suggest that this area contributes to the generation of the electrical vertex potential.

Activation of the auditory cortex by cochlear stimulation in a deaf patient.

We have recorded cerebral electric and magnetic responses to electric stimulation of the auditory nerve in a deaf patient with multichannel cochlear prosthesis. The electric response peaked with a vertex-negative deflection at 65 ms. Clear magnetic responses, coinciding with the vertex potential, were obtained only over the hemisphere ipsilateral to the stimulation; the field pattern indicated activation of the auditory cortex within the Sylvian fissure. The results suggest modification of the central auditory pathways in this patient deaf from early childhood.

Mixed and sensory nerve stimulations activate different cytoarchitectonic areas in the human primary somatosensory cortex SI. Neuromagnetic recordings and statistical considerations.

Magnetic responses evoked by stimulation of the mixed median nerve at the wrist and its cutaneous branches on the glabrous skin of the index and middle fingers were studied. The first responses to mixed nerve stimulation peaked at 19-24 ms, and those to cutaneous nerve stimulation about 4 ms later. The responses, up to a latency of 150 ms, reversed in polarity between the upper and lower parts of the rolandic fissure. Equivalent dipoles for the mixed nerve stimulation were stronger and they lay statistically significantly deeper from the scalp than those activated by the cutaneous nerve stimulation. It is suggested that mixed nerve stimulation activates areas 3a and 3b whereas cutaneous stimulation activates mainly area 3b at the human primary somatosensory cortex. Statistical procedures were developed for comparison of different field patterns and for determining confidence limits of source model parameters. For these purposes the quality and quantity of the noise were studied. The error caused by inaccuracies in the positioning of the magnetometer was found to be minimal in comparison with the signal noise which was estimated from the standard deviation of the averaged response.

Cerebral magnetic fields evoked by peroneal nerve stimulation.

We measured evoked magnetic fields and evoked potentials to peroneal nerve stimulation in healthy humans. The results were consistent with activation of the primary sensorimotor foot area on the mesial surface of the hemisphere during several deflections between 40 and 200 msec. A cortical origin is suggested for the electrical P40. Distinct magnetic field patterns were observed over the primary and secondary somatosensory cortices (SI and SII). At SII, responses to ipsilateral stimulation were weaker and had longer latencies than those to contralateral stimulation. Simulations were used to clarify the differences between electrical and magnetic patterns when SI and SII were simultaneously active.

Cerebral neuromagnetic responses evoked by short auditory stimuli.

We presented 30 msec sinusoidal tone bursts to the subject's left ear once every 1300 msec. The number of standard tones (1000 Hz) between deviants (1030 Hz) varied randomly from 3 to 15 (even distribution) so that the probability of the standards was 0.9 and that of the deviants 0.1. During stimulation the subject was reading a book. Magnetic responses to the standards and deviants were measured at the estimated ends of the sylvian fissure and electrical responses at Fpz, Fz and Cz. In addition, extensive field maps over the right hemisphere were made from 60 to 75 points in 3 subjects. A least-squares fit was performed to find out the parameters of the equivalent current dipole in a spherically symmetrical head model. Field maps suggested that the source of magnetic response at 100 msec (N100m) can be approximated by a current dipole at the supratemporal plane, possibly at the primary auditory cortex. In two subjects the location and/or the orientation of the equivalent dipole changed during N100m, possibly due to change in the size of the activated cortical area. The deviant stimuli elicited in addition to N100m a second deflection, MMNm, peaking at about 200 msec. This response was regarded as specific to stimulus change. On the basis of field maps it was also concluded that MMNm got a contribution from activity at the supratemporal plane.

Neuromagnetic studies of somatosensory system: principles and examples.

A review is given about the basic principles of neuromagnetic recordings and somatically evoked magnetic fields with examples from the authors' own work. MEG provides good spatial resolution for activity in the fissural cortex. It has, for example, allowed differentiation of current sources in the primary and secondary somatosensory cortices. Some cortical areas activated by painful stimuli have also been localized by means of MEG.

Responses of the primary auditory cortex to pitch changes in a sequence of tone pips: neuromagnetic recordings in man.

Auditory evoked magnetic fields of the human brain were recorded with a four-channel 1st order gradiometer. Pitch deviance in a sequence of repetitive tone pips elicited magnetic evoked-response changes with a topography suggesting that a neuronal mismatch process to the deviant tones activates the primary auditory cortex.

Somatosensory evoked cerebral magnetic fields from SI and SII in man.

We have recorded cerebral magnetic fields elicited by electrical stimulation of median and peroneal nerves. Field mapping indicates that the deflections at 30-80 and 150-180 msec are due to activity at SI. Additional activity at 90-125 msec is generated at SII, on the superior bank of the sylvian fissure. At SI, the source locations are in agreement with the known somatotopy. Only contralateral stimuli evoke responses at SI, whereas both ipsi- and contralateral stimuli elicit responses at SII.

Neuromagnetic localization of cortical activity evoked by painful dental stimulation in man.

We have recorded cerebral magnetic fields evoked by painful dental stimulation. The field pattern indicates a current source at the upper bank of the anterior Sylvian Fissure, corresponding to the anterior end of the secondary somatosensory cortex. This finding suggests cortical representation of tooth pulp in man. The neuromagnetic technique, allowing the investigation of this cortical area, thus provides a new non-invasive tool for pain research.

Neuromagnetic responses from the second somatosensory cortex in man.

Cerebral magnetic fields elicited by electric stimulation of peripheral nerves were studied in man. Responses were found over the Sylvian fissure at latencies of 95-125 ms for both contra- and ipsilateral stimuli. The field distribution indicated that the responses are generated in the second somatosensory cortex SII at the upper bank of the Sylvian fissure. These responses seem to provide the first non-invasive tool to study the function of SII in man.

[Rhythmic activity of central portions of the cat visual analyzer during different forms of behavior]. / Ritmicheskaia aktivnost' tsentral'nykh otdelov zritel'nogo analizatora koshki pri nekotorykh formakh povedeniia.

Synchronized EEG activity of visual cortex and some other parts of the brain was recorded in cats during milk licking. The frequency range, cortico-subcortical topography and some conditions of its appearance and blockade were analyzed. It was found, that this activity consisted of two rhythms with frequencies of 6--9 and 9--15 c/s and was strongly influenced by visual conditions. By come parameters it also differed from EEG of drowsiness and light sleep. Possible mechanisms and localization of pacemakers of this activity was discussed as well as its similarity to human alpha rhythm.