Sabrina Pitzalis

Cortical sources of the early components of the visual evoked potential

This study aimed to characterize the neural generators of the early components of the visual evoked potential (VEP) to isoluminant checkerboard stimuli. Multichannel scalp recordings, retinotopic mapping and dipole modeling techniques were used to estimate the locations of the cortical sources giving rise to the early C1, P1, and N1 components. Dipole locations were matched to anatomical brain regions visualized in structural magnetic resonance imaging (MRI) and to functional MRI (fMRI) activations elicited by the same stimuli. These converging methods confirmed previous reports that the C1 component (onset latency 55 msec; peak latency 90–92 msec) was generated in the primary visual area (striate cortex; area 17). The early phase of the P1 component (onset latency 72–80 msec; peak latency 98–110 msec) was localized to sources in dorsal extrastriate cortex of the middle occipital gyrus, while the late phase of the P1 component (onset latency 110–120 msec; peak latency 136–146 msec) was localized to ventral extrastriate cortex of the fusiform gyrus. Among the N1 subcomponents, the posterior N150 could be accounted for by the same dipolar source as the early P1, while the anterior N155 was localized to a deep source in the parietal lobe. These findings clarify the anatomical origin of these VEP components, which have been studied extensively in relation to visual‐perceptual processes. Hum. Brain Mapping 15:95–111, 2001.

Wide-Field Retinotopy Defines Human Cortical Visual Area V6

The retinotopic organization of a newly identified visual area near the midline in the dorsalmost part of the human parieto-occipital sulcus was mapped using high-field functional magnetic resonance imaging, cortical surface-based analysis, and wide-field retinotopic stimulation. This area was found in all 34 subjects that were mapped. It represents the contralateral visual hemifield in both hemispheres of all subjects, with upper fields located anterior and medial to areas V2/V3, and lower fields medial and slightly anterior to areas V3/V3A. It contains a representation of the center of gaze distinct from V3A, a large representation of the visual periphery, and a mirror-image representation of the visual field. Based on similarity in position, visuotopic organization, and relationship with the neighboring extrastriate visual areas, we suggest it might be the human homolog of macaque area V6, and perhaps of area M (medial) or DM (dorsomedial) of New World primates.

Identification of the neural sources of the pattern-reversal VEP

This study aimed to characterize the neural generators of the early components of the visual-evoked potential (VEP) to pattern-reversal gratings. Multichannel scalp recordings of VEPs and dipole modeling techniques were combined with functional magnetic resonance imaging (fMRI) and retinotopic mapping in order to estimate the locations of the cortical sources giving rise to VEP components in the first 200 ms poststimulus. Dipole locations were seeded to visual cortical areas in which fMRI activations were elicited by the same stimuli. The results provide strong evidence that the first major component of the VEP elicited by a pattern-reversal stimulus (N75/P85) arises from surface-negative activity in the primary visual cortex (area V1). Subsequent waveform components could be accounted for by dipoles that were in close proximity to fMRI activations in the following cortical areas: P95 (area MT/V5), P125/N135 (area V1), N150 (transverse parietal sulcus, TPS), N160 (ventral occipital areas VP, V4v, and V4/V8), and N180 (dorsal occipital areas V3A/V7). These results provide a detailed spatiotemporal profile of the cortical origins of the pattern-reversal VEP, which should enhance its utility in both clinical and basic studies of visual-perceptual processing.

Spatiotemporal analysis of the cortical sources of the steady-state visual evoked potential

This study aimed to characterize the neural generators of the steady‐state visual evoked potential (SSVEP) to repetitive, 6 Hz pattern‐reversal stimulation. Multichannel scalp recordings of SSVEPs and dipole modeling techniques were combined with functional magnetic resonance imaging (fMRI) and retinotopic mapping in order to estimate the locations of the cortical sources giving rise to the SSVEP elicited by pattern reversal. The time‐varying SSVEP scalp topography indicated contributions from two major cortical sources, which were localized in the medial occipital and mid‐temporal regions of the contralateral hemisphere. Colocalization of dipole locations with fMRI activation sites indicated that these two major sources of the SSVEP were located in primary visual cortex (V1) and in the motion sensitive (MT/V5) areas, respectively. Minor contributions from mid‐occipital (V3A) and ventral occipital (V4/V8) areas were also considered. Comparison of SSVEP phase information with timing information collected in a previous transient VEP study (Di Russo et al. [ 2005 ] Neuroimage 24:874–886) suggested that the sequence of cortical activation is similar for steady‐state and transient stimulation. These results provide a detailed spatiotemporal profile of the cortical origins of the SSVEP, which should enhance its use as an efficient clinical tool for evaluating visual‐cortical dysfunction as well as an investigative probe of the cortical mechanisms of visual‐perceptual processing. Hum. Brain Mapp, 2007.

Human V6: The Medial Motion Area

Cortical-surface-based functional Magnetic Resonance Imaging mapping techniques and wide-field retinotopic stimulation were used to verify the presence of pattern motion sensitivity in human area V6. Area V6 is highly selective for coherently moving fields of dots, both at individual and group levels and even with a visual stimulus of standard size. This stimulus is a functional localizer for V6. The wide retinotopic stimuli used here also revealed a retinotopic map in the middle temporal cortex (area MT/V5) surrounded by several polar-angle maps that resemble the mosaic of small areas found around macaque MT/V5. Our results suggest that the MT complex (MT+) may be specialized for the analysis of motion signals, whereas area V6 may be more involved in distinguishing object and self-motion.

Separate neural systems for processing action- or non-action-related sounds

The finding of a multisensory representation of actions in a premotor area of the monkey brain suggests that similar multimodal action-matching mechanisms may also be present in humans. Based on the existence of an audiovisual mirror system, we investigated whether sounds referring to actions that can be performed by the perceiver underlie different processing in the human brain. We recorded multichannel ERPs in a visuoauditory version of the repetition suppression paradigm to study the time course and the locus of the semantic processing of action-related sounds. Results show that the left posterior superior temporal and premotor areas are selectively modulated by action-related sounds; in contrast, the temporal pole is bilaterally modulated by non-action-related sounds. The present data, which support the hypothesis of distinctive action sound processing, may contribute to recent theories about the evolution of human language from a mirror system precursor.

The appreciation of wine by sommeliers: a functional magnetic resonance study of sensory integration

We set out to investigate how the expertise of a sommelier is embodied in neural circuitry by comparing brain activity elicited by wine tasting with that found in naive drinkers of wine. We used fMRI to study 7 sommeliers and 7 age- and sex-matched control subjects to test the hypothesis that any difference in brain activity would reflect a learned ability to integrate information from gustatory and olfactory senses with past experience. A group analysis showed activation of a cerebral network involving the left insula and adjoining orbito-frontal cortex in sommeliers. Both these areas have been implicated in gustatory/olfactory integration in primates. In addition, activation was found bilaterally in the dorsolateral prefrontal cortex, which is implicated in high-level cognitive processes such as working memory and selection of behavioral strategies. Naive individuals activated the primary gustatory cortex and brain areas, including the amygdala, implicated in emotional processing.

Fixation stability and saccadic latency in élite shooters

This study tested the hypothesis that elementary visuo-motor functions involved in visual scanning, as measured by fixation and saccadic tasks, are better in a group of high-level clay target shooters (N=7) than in a control group (N=8). In the fixation task, subject were told to keep fixation as still as possible on a target for 1 min, both in the presence and absence of distracters. For shooters, time did not have an effect on fixation stability, and they had more stable fixation than controls in the distracters condition. Results indicate a difference between groups on both the temporal span of attention and selective attention. In the saccadic task, subjects were asked to saccade, as fast as possible, towards a peripherally displayed target. Two conditions were used: simple reaction to target onset and discrimination between targets and distracters. Shooters had faster saccadic latency to targets than controls in both conditions. Finally, to evaluate the effect of exercise on saccadic latency, we trained one control subject to saccade to a target displayed at a constant spatial position. At the end of the training, saccadic latency reached a value comparable to that recorded in shooters. Learning was largely retinotopic, not showing transfer to untrained spatial positions.

What is Involved and What is Necessary for Complex Linguistic and Nonlinguistic Auditory Processing: Evidence from Functional Magnetic Resonance Imaging and Lesion Data

We used functional magnetic resonance imaging (fMRI) in conjunction with a voxel-based approach to lesion symptom mapping to quantitatively evaluate the similarities and differences between brain areas involved in language and environmental sound comprehension. In general, we found that language and environmental sounds recruit highly overlapping cortical regions, with cross-domain differences being graded rather than absolute. Within language-based regions of interest, we found that in the left hemisphere, language and environmental sound stimuli evoked very similar volumes of activation, whereas in the right hemisphere, there was greater activation for environmental sound stimuli. Finally, lesion symptom maps of aphasic patients based on environmental sounds or linguistic deficits [Saygin, A. P., Dick, F., Wilson, S. W., Dronkers, N. F., & Bates, E. Shared neural resources for processing language and environmental sounds: Evidence from aphasia. Brain, 126, 928945, 2003] were generally predictive of the extent of blood oxygenation level dependent fMRI activation across these regions for sounds and linguistic stimuli in young healthy subjects.

Influence of the radial and vertical dimensions on lateral neglect

Abstract. The influence of radial (near-far) and vertical (upper-lower) dimensions on lateral visuo-spatial neglect was studied using two horizontal line-bisection tasks (one motor and one perceptual). A group of 15 patients with neglect and a group of 14 right-brain damaged patients without neglect were examined. This latter group was used to define the range of variability in line-bisection performance that was independent of neglect. For the radial dimension, some neglect patients showed greater errors in far space than in near space (for both stimuli presented in the upper and lower space). Fewer patients showed the opposite pattern (i.e., greater errors for near-space stimuli). These near-far asymmetries were present for both the motor and perceptual conditions and showed a good degree of intra-individual consistency. This finding contradicts the hypothesis that the motor component is critical for yielding such asymmetry. For the vertical dimension, the results indicated that neglect patients make more bisection errors for lower-space stimuli than for upper-space stimuli. This vertical asymmetry was nearly always confined to stimuli in near space. Asymmetries along the vertical dimension were present for both perceptual and motor conditions, although intra-individual consistency was low. When perceptual and motor conditions were directly compared, several neglect patients showed greater errors in the perceptual than in the motor task.