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Biomedical subjects

Ryusuke Kakigi

Publications and source records attributed to Ryusuke Kakigi.

At least 73 records · Page 4Linked to original sources

Cognitive processes in two-point discrimination: an ERP study.

OBJECTIVE: To elucidate the temporal features of the cognitive process in two-point discrimination (TPD). METHODS: We measured somatosensory event-related potentials (ERPs) in 9 subjects during the TPD task, in which we provided a pair of electrical pulses simultaneously, altering the distance between the electrodes. We analyzed the TPD-related ERPs and investigated the relationship between the potentials and the subjects' judgments. RESULTS: During the TPD task, a negative potential approximately 140 ms after the stimulation (N140) was enhanced as compared to a stimulus counting task. Two late positive components, LPC-1 and LPC-2, whose peak latencies were 300 and 500 ms, respectively, were identified only in the TPD task. The LPC-1 was recorded dominantly in the fronto-central area, while the LPC-2 was detected dominantly in the centro-parietal area. The amplitude of the LPC-2 was significantly modulated by the degree of consistency in the subjects' judgment. On the other hand, these ERP components did not show significant difference between the alternate judgments, i.e. 'one-point' or 'two-point' judgment. CONCLUSIONS: Our results suggest that the N140 is related to the attention toward the stimulation. The LPC-1 and LPC-2 are likely to correspond to the processes represented by P3a and P3b, based on their temporal and spatial behavior.

Adult↗

Temporal structure of the apparent motion perception: a magnetoencephalographic study.

Humans perceive motion when numerous small dots pattern is followed by one of the same pattern but with all the dots shifted a little in one direction. When the amount of shift exceeds a level humans no more perceive motion even though physical visual information does not change. Using this stimulus, we addressed to elucidate the temporal structure of the neural activity related to this apparent motion perception. The magnetic responses to the random-dot patterns with various amounts of shift were measured while the subjects were performing a direction discrimination task. A significant magnetic response amplitude change occurred with three distinct peaks when the response inducing apparent motion was compared with those inducing no motion without change in the response latencies. The major difference occurred at about 110, 140, 210 ms after the stimulus onset. The response origin was always within the occipitotemporal area. The results indicate that the neural activity for the perception of apparent motion can be measured by MEG that occur at least 110 ms after the stimulus onset possibly in the human MT+. Three distinct peaks in the response difference may represent the sequential multiple neural process proposed theoretically though further study is necessary to prove.

Adult↗

Face representation in the human primary somatosensory cortex.

To investigate the representation of facial skin areas in the primary somatosensory cortex (SI), we recorded magnetic fields evoked by air pressure-induced tactile stimulation applied to six points on the face, lower lip and thumb. The thumb area in the SI was located more medial and superior to the lip area, which was consistent with Penfield's homunculus. However, the representations of all skin-covered areas including forehead, cheek, nose and chin in the SI were located between the thumb and lower lip area. There was no significant difference in location among the six facial points. Our results imply that lips occupy a large area of the face representation in the SI, whereas only a small area located between the thumb and lip areas is devoted to skin-covered surfaces. This is the first study showing that the facial skin areas in the human SI are located between the thumb and lower lip areas and close together.

Adult↗

Movements modulate cortical activities evoked by noxious stimulation.

To evaluate the effects of movement on cortical activities evoked by noxious stimulation, we recorded magnetoencephalography following noxious YAG laser stimulation applied to the dorsum of the left hand in normal volunteers. Results of the present study can be summarized as follows: (1) active movement of the hand ipsilateral to the side of noxious stimulation resulted in significant attenuation of both primary and secondary somatosensory cortices (SI and SII) in the hemisphere contralateral to the stimulated hand (cSI and cSII). Activity in the hemisphere ipsilateral to the side of stimulation (iSII) was not affected. (2) Active movement of the hand contralateral to the side of noxious stimulation resulted in significant attenuation of cSII. Activity in cSI and iSII was not affected. (3) Passive movement of the hand ipsilateral to the side of noxious stimulation resulted in significant attenuation of cSI. Activity in cSII and iSII was not affected. (4) Visual analogue scale (VAS) changes showed a similar pattern to the amplitude changes of cSII. These results suggest that activities in three regions are modulated by movements differently. Inhibition in cSI was considered to be mainly due to an interaction in SI by the signals ascending from the stimulated and movement hand. Inhibition in cSII was considered to be mainly due to particular brain activities relating to motor execution and/or movement execution associated with a specific attention effect. In addition, since VAS changes showed a similar relationship with the amplitude changes of cSII, cSII may play a role in pain perception.

Adult↗

The effect of phonological repetition on cortical magnetic responses evoked by visually presented words.

Neuroimaging studies have reported that the left superior temporal cortical area is activated by visually presented words. In the present study, we recorded cortical magnetic responses evoked by visual words and examined the effect of phonological repetition (e.g., hair-hare) on left superior temporal cortical activity, using pairs of homophonic Japanese words as stimuli. Unlike English, Japanese has a large number of homophone pairs with a totally different orthography. By taking advantage of this feature of the Japanese writing system, the effect of phonological repetition can be solely examined without being confounded by the effect of orthographic similarity. Magnetic responses were recorded over the bilateral temporal sites of the brain while subjects silently read words. The words were presented one by one; a quarter of them was immediately followed by a homophonic word. Clear magnetic responses in the latency range of 300-600 msec were observed in the left hemisphere, and the responses to the homophones were smaller than those to the first presented words. In the right hemisphere, clear responses were not consistently recorded in the same latency range, and no effect of phonological repetition was observed. The sources of the responses recorded over the left hemisphere were estimated to be in the left superior temporal cortical area adjacent to the auditory cortex and the source strength as well as the magnetic responses showed a reduction by phonological repetition. This result suggests that the activity in the left superior temporal cortical area is associated with access to the phonological representation of words.

Adult↗

Human brain processing and central mechanisms of pain as observed by electro- and magneto-encephalography.

We review the recent progress of electroencephalography (EEG) and magnetoencephalography (MEG) to elucidate pain perception mechanisms in humans, since EEG and MEG have an excellent temporal resolution in order of msec. MEG is more useful to detect activated areas following painful stimulation, because the spatial resolution of EEG is not very high. For recording activities following Adelta fiber stimulation relating to the first pain, painful CO2 laser stimulation is now widely used, but our new method, epidermal stimulation (ES), is also very useful. The primary small activity was recorded from the primary somatosensory cortex (SI), probably in area 1, in the hemisphere contralateral to the stimulation. Then, secondary somatosensory cortex (SII) and insula were activated with the second activity in SI. These 3 regions were activated in parallel with almost the same time period. This is a very characteristic finding in pain perception. Then, the cingulate cortex and medial temporal area (MT) around the amygdala and hippocampus were activated. In the hemisphere ipsilateral to the stimulation as well, the above regions were activated, except for SI. Therefore, we speculated that SI plays a main role in localization of the stimulus point, the SII and insula are important sites for pain perception, and the cingulate and MT are mainly responsible for cognitive or emotional aspects of pain perception. For recording activities following C fiber stimulation relating to the second pain, we recently developed a new method, that is, applying weaker CO2 laser stimuli to tiny areas of the skin. MEG findings following C fiber stimulation were also similar to those following Adelta fiber stimulation. However, the effects of sleep and attention on MEG following C fiber stimulation was much larger than that following Adelta fiber stimulation. This finding may suggest greater effects of cognitive or emotional functions on second pain than the first pain.

Brain↗

Microneurographic study of C fiber discharges induced by CO2 laser stimulation in humans.

We investigated C-fiber discharges and cerebral potentials evoked by weak CO(2) laser beams applied to a tiny skin area in five healthy subjects. Microneurography was performed from the peroneal nerve in the right popliteal area. Cerebral potentials were recorded from the Cz electrode referred to linked earlobes. The mean conduction velocity of five stable single units was 1.1+/-0.3 m/s. The mean latency of the positive peak of cerebral potentials was 1327.4+/-46.2 ms. These findings indicated that this new stimulation method selectively activated C-fiber nociceptors of the skin.

Adult↗

Magnetoencephalographic study of the cortical activity elicited by human voice.

In an attempt to identify voice-specific neural activities in auditory cortex in humans, we recorded cortical magnetic responses. Volunteers were instructed to listen to vocal and instrumental sounds matched in fundamental-frequency, duration, temporal envelope and average root mean square power. The stimuli were sounds produced by four singers and four musical instruments at each of two fundamental frequencies: 220 Hz (musical note A3) and 261.9 Hz (C3). Two components of the evoked responses were analyzed, one at approximately 100 ms (N1m) and the other 400 ms after the stimulus onset (sustained field, SF). The source locations of equivalent current dipoles for both components were estimated around the Heschl's gyrus in both hemispheres. Compared with the instrumental sound, the source strength of the SF component for the voice was significantly larger.

Acoustic Stimulation↗

Human cortical response to incoherent motion on a background of coherent motion.

To investigate whether humans achieve a high sensitivity to coherent motion by excluding the response to incoherent motion, we measured the magnetoencephalographic response to the motion of randomly located dots one half of which moved coherently while the other half moved incoherently. The response was related to the faster motion of either coherent or incoherent motion though the observers saw both. All the estimated response sources were within the extrastriate area. The results indicate that incoherent motion is represented in the neural activity of the human extrastriate area even when the coherent motion is perceived at the same time. The fact that the neural activity for the slower coherent motion is not represented in the magnetic response suggests the existence of interaction between the neural activities for the two motions.

Adult↗

Central mechanisms for two-point discrimination in humans.

We studied the cognitive mechanisms for two-point discrimination (TPD) in 11 normal subjects, using electrical pulses. We used six ball-shaped electrodes placed in line on the dorsal surface of the left hand, and two-point was stimulated by two electrodes randomly selected. We measured the reaction time for TPD and calculated the percentage of correct responses for each two-point stimulation. The subjects' response was significantly affected by the preceding stimuli as well as the distance of the stimuli: for a two-point stimulus condition, subjects tended to feel the stimuli as two-point when the distance between the stimuli was longer than that of preceding stimuli, whereas they felt the stimuli as one-point when the distance was shorter than that of the preceding stimuli. The present results indicate that the TPD process involved evaluation of the distance between the stimuli relatively to that of the preceding stimuli, as well as evaluation of absolute distance between the stimuli.

Adult↗

Physiological evidence of interaction of first- and second-order motion processes in the human visual system: a magnetoencephalographic study.

Humans have several mechanisms for the visual perception of motion, including one that is luminance-based (first-order) and another that is luminance-independent (second-order). Recent psychophysical studies have suggested that significant interaction occurs between these two neural processes. We investigated whether such interactions are represented as neural activity measured by magnetoencephalography (MEG). The second-order motion of a drifting sinusoidal grating, which is defined by the speed of the dot motion, did not generate a response. Apparent motion (AM) of the square area, defined by the speed of randomly moving dots, evoked a magnetic response whose latency and amplitude changed with the distance that the area moved (a second-order characteristic), though the response properties were significantly different from those for the first-order AM. AM, defined by both first- and second-order attributes, evoked an MEG response and the latencies and the amplitudes were distributed between those for the first- and second-order motions. The cortical source of the response was estimated to be around MT+. The results show a distinct difference in the neural processing of the second-order motion that cannot be explained by the difference in visibility, and they indicate that the interaction of the neural processes underlying first- and second-order motion detection occurs before the MEG response. Our study provides the first physiological evidence of a neural interaction between the two types of early motion detection.

Adult↗

Effects of sleep on pain-related somatosensory evoked potentials in humans.

We investigated effects of sleep on pain-related somatosensory evoked potentials (SEP) following painful electrical stimulation of the left index finger. The biggest advantage of this method is that signals ascending through both A-beta fibers relating to touch and A-delta fibers relating to pain can be recorded simultaneously. While the subject was awake, non-painful stimulation evoked early- and middle latency components, N20, P30 and N60, at the C4 electrode, and painful stimulation evoked not only early- and middle latency components at the C4 but also later pain-specific components, N130 and P240, at the Cz electrode. During sleep, N20 and P30 did not show a significant change in amplitude, N60 showed a slight but significant amplitude reduction, and N130 and P240 significantly decreased in amplitude or disappeared, as compared with those while awake. Therefore, we speculate on the mechanisms generating each component as follows; (1) N20 and P30 are the primary components generated in SI ascending through A-beta fibers. (2) N60 is the secondary component generated in SI involving cognitive function to some degree. (3) N130-P240 are the pain-specific components ascending through A-delta fibers, and closely related to cognitive function, because they were much affected by consciousness, different from the components ascending through A-beta fibers.

Adult↗

Cerebral responses following stimulation of unmyelinated C-fibers in humans: electro- and magneto-encephalographic study.

There are two kinds of pain, a sharp pain ascending through Adelta fibers (first pain) and a second burning pain ascending though C fibers (second pain). By using a novel method, the application of a low intensity CO(2) laser beam to a tiny area of skin using a very thin aluminum plate with numerous tiny holes as a spatial filter, we succeeded in selectively stimulating unmyelinated C fibers of the skin in humans, and could record consistent and clear brain responses using electroencephalography (EEG) and magnetoencephalography (MEG). The conduction velocity (CV) of the C fibers of the peripheral nerve and spinal cord, probably spinothalamic tract (STT), is approximately 1-4 m/s, which is significantly slower than that of Adelta (approximately 10-15 m/s) and Abeta fibers (approximately 50-70 m/s). This method should be very useful for clinical application. Following C fiber stimulation, primary and secondary somatosensory cortices (SI and SII) are simultaneously activated in the cerebral hemisphere contralateral to the stimulation, and then, SII in the hemisphere ipsilateral to the stimulation is activated. These early responses are easily detected by MEG. Then, probably limbic systems such as insula and cingulate cortex are activated, and those activities reflected in EEG components. Investigations of the cortical processing in pain perception including both first and second pain should provide a better understanding of pain perception and, therefore, contribute to pain relief in clinical medicine.

Animals↗

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.

Adult↗

Spatiotemporal separability in the human cortical response to visual motion speed: a magnetoencephalography study.

Humans can estimate the speed of an object's motion independently of other visual information. Although speed-related neural activity is known to exist in the primate brain, there has been no physiological study that investigated where and how the speed of motion is represented in the human brain. Nine different combinations of spatial and temporal frequencies were used to make drifting sinusoidal grating of five different speeds (from 1.5 to 24 deg/s). Using the stimuli, we evaluated whether the magnetoencephalographic response property changes were due to a speed-tuned mechanism or to separable spatial and temporal frequency detection mechanisms. The latency change was caused mainly by an inseparable speed-tuned mechanism. In contrast, the amplitude was inversely related to the spatial frequency and was also affected by the temporal frequency differently depending on the frequency. Our results support the view that the human visual system has three sets of mechanisms tuned to spatial frequency, temporal frequency, and speed.

Adult↗

Effects of sleep on pain-related somatosensory evoked magnetic fields in humans.

We investigated the effects of sleep on pain-related somatosensory evoked magnetic fields (SEFs) following painful electrical stimulation to identify the mechanisms generating them in both fast A-beta fibers relating to touch and slow A-delta fibers relating to pain. While the subjects were awake, non-painful and painful electrical stimulations were applied, and while asleep, painful stimulation was applied to the left index finger. During awake, five components (1M-5M) were identified following both non-painful and painful stimulation, but the 4M and 5M at around 70-100 ms and 140-180 ms, respectively, were significantly enhanced following painful stimulation. During sleep, 1M and 2M generated in the primary somatosensory cortex (SI) did not show a significant change, 3M in SI showed a slight but significant amplitude reduction, and 4M and 5M generated in both SI and the secondary somatosensory cortex (SII) were significantly decreased in amplitude or disappeared. The 4M and 5M are complicated components generated in SI and SII ascending through both A-beta fibers and A-delta fibers. They are specifically enhanced by painful stimulation due to an increase of signals ascending through A-delta fibers, and are markedly decreased during sleep, because they much involve cognitive function.

Adult↗

Cortical activities relating to modulation of sound frequency: how to vocalize?

This is the first report to clarify the underlying mechanisms of processing in the modulation of frequencies (tones) in humans using magnetoencephalography (MEG). Volunteers were instructed to vocalize a simple vowel sound (/u/) after receiving a cue (S2) for either one of three (low, middle, or high fundamental frequencies) (F0s). Three tasks, (1) the modulated vocalization task in which the subjects were asked to modulate vocalization tones according to S2, (2) the non-modulated vocalization task in which the subjects were asked to vocalize the same sound (/u/) with a fixed F0, and (3) the image task in which the subjects had to modulate according to S2 and imagine the vowel (/u/) sound, but not vocalize it. In all tasks, two clear components, 1M and 2M, were recorded at approximately 190 and 290 ms after the S2. Since both were identified even in the Image task, they appear to be specifically related to activity for modulation. The equivalent current dipoles of both 1M and 2M were estimated to lie mainly in the inferior frontal lobe or insula in both hemispheres. Therefore, the activity relating to modulation mainly took place in the inferior frontal lobe or insula in both hemispheres starting about 200 ms after the viewing of a cue.

Acoustic Stimulation↗

Cortical evidence of the perceptual backward masking effect on /l/ and /r/ sounds from a following vowel in Japanese speakers.

We examined the influence of stimulus duration of foreign consonant vowel stimuli on the MMNm (magnetic counter part of mismatch negativity). In Experiment 1, /ra/ and /la/ stimuli were synthesized and subjects were native Japanese speakers who are known to have difficulty discriminating the stimuli. "Short" duration stimuli were terminated in the middle of the consonant-to-vowel transition (110 ms). They were nevertheless clearly identifiable by English speakers. A clear MMNm was observed only for short-duration stimuli but not for untruncated long-duration (150-ms) stimuli. We suggest that the diminished MMNm for longer duration stimuli result from more effective masking by the longer vowel part. In Experiment 2 we examined this hypothesis by presenting only the third formant (F3) component of the original stimuli, since the acoustic difference between /la/ and /ra/ is most evident in the third formant, whereas F1 and F2 play a major role in vowel perception. If the MMNm effect depends on the acoustic property of F3, a stimulus duration effect comparable to that found with the original /la/ and /ra/ stimuli might be expected. However, if the effect is attributable to the masking effect from the vowel, no influence of stimulus duration would be expected, since neither stimulus contains F1 and F2 components. In fact, the results showed that the "F3 only" stimuli did not show a duration effect; MMNm was always elicited independent of stimulus duration. The MMN stimulus duration effect is thus suggested to come from the backward masking of foreign consonants by subsequent vowels.

Acoustic Stimulation↗