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1.
Neuroimage ; 63(3): 1585-600, 2012 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-22917988

RESUMO

Presentation of a face stimulus for several seconds at a periodic frequency rate leads to a right occipito-temporal evoked steady-state visual potential (SSVEP) confined to the stimulation frequency band. According to recent evidence (Rossion and Boremanse, 2011), this face-related SSVEP is largely reduced in amplitude when the exact same face is repeated at every stimulation cycle as compared to the presentation of different individual faces. Here this SSVEP individual face repetition effect was tested in 20 participants stimulated with faces at a 4 Hz rate for 84 s, in 4 conditions: faces upright or inverted, normal or contrast-reversed (2×2 design). To study the temporal dynamics of this effect, all stimulation sequences started with 15s of identical faces, after which, in half of the sequences, different faces were introduced. A larger response to different than identical faces at the fundamental (4 Hz) and second harmonic (8 Hz) components was observed for upright faces over the right occipito-temporal cortex. Weaker effects were found for inverted and contrast-reversed faces, two stimulus manipulations that are known to greatly affect the perception of facial identity. Addition of the two manipulations further decreased the effect. The phase of the fundamental frequency SSVEP response was delayed for inverted and contrast-reversed faces, to the same extent as the latency delay observed at the peak of the face-sensitive N170 component observed at stimulation sequence onset. Time-course analysis of the entire sequence of stimulation showed an immediate increase of 4Hz amplitude at the onset (16th second) of different face presentation, indicating a fast, large and frequency-specific release to individual face adaptation in the human brain. Altogether, these observations increase our understanding of the characteristics of the human steady-state face potential response and provide further support for the interest of this approach in the study of the neurofunctional mechanisms of face perception.


Assuntos
Mapeamento Encefálico , Encéfalo/fisiologia , Potenciais Evocados Visuais/fisiologia , Reconhecimento Visual de Modelos/fisiologia , Adolescente , Adulto , Eletroencefalografia , Face , Feminino , Humanos , Masculino , Estimulação Luminosa , Adulto Jovem
2.
Brain Cogn ; 74(3): 225-38, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20851511

RESUMO

When the bottom halves of two faces differ, people's behavioral judgment of the identical top halves of those faces is impaired: they report that the top halves are different, and/or take more time than usual to provide a response. This behavioral measure is known as the composite face effect (CFE) and has traditionally been taken as evidence that faces are perceived holistically. Recently, however, it has been claimed that this effect is driven almost entirely by decisional, rather than perceptual, factors (Richler, Gauthier, Wenger, & Palmeri, 2008). To disentangle the contribution of perceptual and decisional brain processes, we aimed to obtain an event-related potential (ERP) measure of the CFE at a stage of face encoding (Jacques & Rossion, 2009) in the absence of a behavioral CFE effect. Sixteen participants performed a go/no-go task in an oddball paradigm, lifting a finger of their right or left hand when the top half of a face changed identity. This change of identity of the top of the face was associated with an increased ERP signal on occipito-temporal electrode sites at the N170 face-sensitive component (∼160 ms), the later decisional P3b component, and the lateralized readiness potential (LRP) starting at ∼350 ms. The N170 effect was observed equally early when only the unattended bottom part of the face changed, indicating that an identity change was perceived across the whole face in this condition. Importantly, there was no behavioral response bias for the bottom change trials, and no evidence of decisional biases from electrophysiological data (no P3b and LRP deflection in no-go trials). These data show that an early CFE can be measured in ERPs in the absence of any decisional response bias, indicating that the CFE reflects primarily the visual perception of the whole face.


Assuntos
Variação Contingente Negativa/fisiologia , Eletroencefalografia , Potenciais Evocados Visuais/fisiologia , Face , Lobo Occipital/fisiologia , Ilusões Ópticas/fisiologia , Lobo Temporal/fisiologia , Adulto , Tomada de Decisões , Feminino , Humanos , Masculino , Testes Neuropsicológicos , Reconhecimento Visual de Modelos/fisiologia , Estimulação Luminosa/métodos , Tempo de Reação , Percepção Espacial
3.
Front Hum Neurosci ; 5: 138, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-22275889

RESUMO

Compared to objects, pictures of faces elicit a larger early electromagnetic response at occipito-temporal sites on the human scalp, with an onset of 130 ms and a peak at about 170 ms. This N170 face effect is larger in the right than the left hemisphere and has been associated with the early categorization of the stimulus as a face. Here we tested whether this effect can be observed in the absence of some of the visual areas showing a preferential response to faces as typically identified in neuroimaging. Event-related potentials were recorded in response to faces, cars, and their phase-scrambled versions in a well-known brain-damaged case of prosopagnosia (PS). Despite the patient's right inferior occipital gyrus lesion encompassing the most posterior cortical area showing preferential response to faces ("occipital face area"), we identified an early face-sensitive component over the right occipito-temporal hemisphere of the patient that was identified as the N170. A second experiment supported this conclusion, showing the typical N170 increase of latency and amplitude in response to inverted faces. In contrast, there was no N170 in the left hemisphere, where PS has a lesion to the middle fusiform gyrus and shows no evidence of face-preferential response in neuroimaging (no left "fusiform face area"). These results were replicated by a magnetoencephalographic investigation of the patient, disclosing a M170 component only in the right hemisphere. These observations indicate that face-preferential activation in the inferior occipital cortex is not necessary to elicit early visual responses associated with face perception (N170/M170) on the human scalp. These results further suggest that when the right inferior occipital cortex is damaged, the integrity of the middle fusiform gyrus and/or the superior temporal sulcus - two areas showing face-preferential responses in the patient's right hemisphere - might be necessary to generate the N170 effect.

4.
J Psychiatry Neurosci ; 33(2): 111-22, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18330457

RESUMO

OBJECTIVES: Chronic alcoholism leads to impaired visual and auditory processing of emotions, but the cross-modal (auditory-visual) processing of emotional stimuli has not yet been explored. Our objectives were to describe the electrophysiological correlates of unimodal (visual and auditory) impairments in emotion processing in people suffering from alcoholism, to determine whether this deficit is general or emotion-specific, and to explore potential deterioration in the specific cross-modal integration processes in alcoholism. METHODS: We used an emotion-detection task, with recording of event-related potentials (ERPs), in which 15 patients suffering from alcoholism and 15 matched healthy control subjects were asked to detect the emotion (angry, happy or neutral) displayed by auditory, visual or auditory-visual stimuli. Behavioural performance and ERP data recorded between June 2005 and April 2006 were analyzed. RESULTS: ERPs demonstrated that the deficit in alcoholism originates earlier in the cognitive stream than has previously been described (mainly P300), namely, at the level of specific face (N170) and voice (N2) perceptive processing. Moreover, while patients with alcoholism did not show impaired processing of happy and neutral audio-visual stimuli, they did have a specific impairment in the cross-modal processing of anger. A source location analysis was used to confirm and illustrate the results. CONCLUSION: These results suggest that the specific deficit that people with alcoholism demonstrate in processing anger stimuli, widely described in clinical situations but not clearly identified in earlier studies (using unimodal stimuli), is particularly obvious during cross-modal processing, which is more common than unimodal processing in everyday life.


Assuntos
Alcoolismo , Ira , Transtornos da Percepção Auditiva/epidemiologia , Potenciais Evocados Auditivos/fisiologia , Potenciais Evocados Visuais/fisiologia , Percepção Visual/fisiologia , Adulto , Alcoolismo/epidemiologia , Alcoolismo/fisiopatologia , Alcoolismo/psicologia , Atrofia/epidemiologia , Atrofia/patologia , Atrofia/fisiopatologia , Encéfalo/patologia , Encéfalo/fisiopatologia , Doença Crônica , Eletroencefalografia , Feminino , Felicidade , Humanos , Masculino , Pessoa de Meia-Idade , Tempo de Reação
5.
Neuroimage ; 37(4): 1384-95, 2007 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-17689986

RESUMO

In order to study the temporal activation course of visual areas V1 and V5 in response to a motion stimulus, a random dots kinematogram paradigm was applied to eight subjects while magnetic fields were recorded using magnetoencephalography (MEG). Sources generating the registered magnetic fields were localized with Magnetic Field Tomography (MFT). Anatomical identification of cytoarchitectonically defined areas V1/V2 and V5 was achieved by means of probabilistic cytoarchitectonic maps. We found that the areas V1/V2 and V5+ (V5 and other adjacent motion sensitive areas) exhibited two main activations peaks at 100-130 ms and at 140-200 ms after motion onset. The first peak found for V1/V2, which corresponds to the visual evoked field (VEF) M1, always preceded the peak found in V5+. Additionally, the V5+ peak was correlated significantly and positively with the second V1/V2 peak. This result supports the idea that the M1 component is generated not only by the visual area V1/V2 (as it is usually proposed), but also by V5+. It reflects a forward connection between both structures, and a feedback projection to V1/V2, which provokes a second activation in V1/V2 around 200 ms. This second V1/V2 activation (corresponding to motion VEF M2) appeared earlier than the second V5+ activation but both peaked simultaneously. This result supports the hypothesis that both areas also generate the M2 component, which reflects a feedback input from V5+ to V1/V2 and a crosstalk between both structures. Our study indicates that during visual motion analysis, V1/V2 and V5+ are activated repeatedly through forward and feedback connections and both contribute to m-VEFs M1 and M2.


Assuntos
Percepção de Movimento/fisiologia , Córtex Visual/fisiologia , Adulto , Idoso , Algoritmos , Mapeamento Encefálico , Cadáver , Potenciais Evocados Visuais/fisiologia , Humanos , Processamento de Imagem Assistida por Computador , Magnetoencefalografia , Masculino , Pessoa de Meia-Idade , Modelos Estatísticos , Distribuição Normal , Estimulação Luminosa , Córtex Visual/anatomia & histologia
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