Implicit response-irrelevant number information triggers the SNARC effect : Evidence using a neural overlap paradigm

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Human brain activity related to the perception of spatial features of objects.

International audienceThe role of the parietal cortex in visuospatial analysis of object was investigated by cerebral blood flow measurements in seven objects using positron emission tomography. Data were acquired while subjects performed a matching task requiring the discrimination of simultaneously presented objects based on one of their spatial properties. Three properties were studied separately during three scanning conditions repeated twice:surface orientation, principal axis orientation, and size. Scans were also obtained during a sensorimotor control task (similar visual stimulation, same motor action, voluntary saccades toward each object) as well as during rest (no stimulation, eyes closed). Compared to rest, the three property matching tasks showed the same pattern of activation: the whole occipital lobe, the right intraparietal sulcus (IPS), and the right occipitotemporal (OT) junction. Compared to the control condition, only right IPS and OT junction were significantly activated during discrimination of the spatial properties. The IPS focus was located between the superior parietal lobule and the angular gyrus, and the OT activation overlapped the posterior part of the inferior temporal gyrus and the middle occipital gyrus. These results indicate that discrimination of spatial attributes requires the activation of both the parietal and the temporal cortices of the right hemisphere and provide further evidence that the IPS plays a critical role in visuospatial analysis of objects

Visual pathways for object-oriented action and object recognition: functional anatomy with PET.

International audienceThe purpose of this study was to identify the functional anatomy of the mechanisms involved in visually guided prehension and in object recognition in humans. The cerebral blood flow of seven subjects was investigated by positron emission tomography. Three conditions were performed using the same set of stimuli. In the 'grasping' condition, subjects were instructed to accurately grasp the objects. In the 'matching' condition, subjects were requested to compare the shape of the presented object with that of the previous one. In the 'pointing' condition (control), subjects pointed towards the objects. The comparison between grasping and pointing showed a regional cerebral blood flow (rCBF) increase in the anterior part of the inferior parietal cortex and part of the posterior parietal cortex. The comparison between grasping and matching showed an rCBF increase in the cerebellum, the left frontal cortex around the central sulcus, the mesial frontal cortex and the left inferior parietal cortex. Finally, the comparison between matching and pointing showed an rCBF increase in the right temporal cortex and the right posterior parietal cortex. Thus object-oriented action and object recognition activate a common posterior parietal area, suggesting that some kind of within-object spatial analysis was processed by this area whatever the goal of the task

Visual working memory for shape and 3D-orientation: a PET study.

International audienceIn order to determine the neural substrate of working memory for shape and 3D-orientation, regional cerebral blood flow (rCBF) changes were estimated using positron emission tomography (PET). Subjects were scanned during the performance of two delayed-matching-to-sample tasks using flat polydedrical objects of different shapes and 3D-orientations presented in a virtual environment. The shape matching task was associated with activation in the occipito-temporal junction, occipito-parietal cortex and mesial frontal pole of the right hemisphere. During the orientation matching task, rCBF increased in the mesial occipito-temporal cortex, superior temporal gyrus and middle frontal gyrus of the left hemisphere. The right supramarginal gyrus was also activated. These results suggest that both visual pathways are engaged in the processing of objects presented in different orientations. The dorsal stream is involved mainly in working memory of 3D-orientation, while the ventral stream is involved especially in shape working memory

How the pain of others enhances our pain: Searching the cerebral correlates of ‘compassional hyperalgesia’

International audienceObserving other people's pain increases our own reports to painful stimuli, a phenomenon that can be defined as 'compassional hyperalgesia' (CH). This functional magnetic resonance imaging study examined the neural correlates of CH, and whether CH could emerge when exposure to the driving stimulus was subliminal. Subjects received electric somatosensory stimuli while observing images of people undergoing painful or enjoyable somatic sensations, presented during a period allowing or not allowing conscious perception. The intensity attributed to painful stimuli increased significantly when these were delivered close to images showing human pain, but only when such images were consciously perceived. The basic core of the Pain Matrix (SI, SII, insula, mid-anterior cingulate) was activated by painful stimuli, but its activation magnitude did not increase during CH. Compassional hyperalgesia was associated with increased activity in polymodal areas involved in emotional tuning (anterior prefrontal, pregenual cingulated) and areas involved in multisensory integration and short-term memory (dorsolateral prefrontal, temporo-parieto-occipital junction). CH appears as a high-order phenomenon needing conscious appraisal of the eliciting visual stimulus, and supported by polymodal areas distinct from the basic Pain Matrix. This suggests that compassion to pain does not result from a mere 'sensory resonance' in pain networks, but rather from an interaction between the output of a first-line processing in the Pain Matrix, and the activity of a high-order network involving multisensory integration (temporo-parietal), encoding of internal states (mid-prefrontal) and short-time memory encoding (dorsolateral prefrontal). The Pain Matrix cannot be considered as an 'objective' correlate of the pain experience in all situations

Brain activity sustaining the modulation of pain by empathetic comments

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Does an observer's empathy influence my pain? Effect of perceived empathetic or unempathetic support on a pain test

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