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2004 Towards Studies of The Social Brain
2004 Towards Studies of The Social Brain
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Abstracts
brain area in which the mirror neurons were rst discovered. Somatosensory cortices seem to be closely connected to the MNS, possibly contributing to dierentiation between brain activations associated with the subjects own movements and those elicited by observation of other persons actions. Our MEG recordings suggest that the human MNS is activated in a well-dened temporal sequence within about 250 ms: visual cortices STS inferior parietal cortex Brocas area motor cortex. Brocas area is activated signicantly stronger during on-line imitation than during execution or observation of nger and mouth movements, emphasizing its role in imitation. The characterization of the human MNS arises some intriguing speculations about the evolutionary and functional relationship between human speech and orofacial/hand gestures. Future studies should address the generality of the MNS in humans and also determine to which extent the MNS functions can be trained. Moreover, it would be important to evaluate whether impaired mind reading and imitation skills, observed in some neurological and psychiatric diseases, could be related to dysfunctional MNS.
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4. Processing of music and speech by the human auditory cortex: Neuroimaging evidence
Robert J. Zatorre Cognitive Neuroscientist, Montreal Neurological Institute, McGill University, Montreal, Que., Canada The human auditory cortex has evolved specialized mechanisms for processing the information contained in our acoustic environment. Among the more complex and interesting of these signals are speech sounds and musical patterns. I shall present data bearing on the organization of the human auditory cortices as they pertain to the processing of these types of sounds using functional neuroimaging techniques. In particular, I will argue that studying musical processes oers useful insights into the functional dierences between auditory cortical regions within and between the cerebral hemispheres and how these dierences may relate to higher-order processing of music and speech. Second, I will present data pertaining to anatomical organization, which may help explain hemispheric functional dierences. In particular, I will discuss recent data indicating that individual dierences in white-matter distribution predict speed of learning of novel speech sounds. Together, the data contribute towards a better model of how auditory cortical organization underlies auditory cognitive processes.
proprioception and can be used in order to rene existing skills. The recognized discrepancy pathway relates to a specic perceptual quality and cues in one modality can help to process information in another one. Furthermore, the information from dierent modalities can interact and add new quality of perception that conveys information not inherent in each single modality. In general, it seems that the perception of cross-modal cues, involving cross-modal plasticity mechanisms, is important for playing an instrument and primary cortices that have been classically thought to be unimodal might actually by multifold.
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Rotman Research Institute Abstracts / Brain and Cognition 54 (2004) 128132 patients but lack of available immediate positive reinforcers necessary for rapid learning. Supported by the Deutsche Forschungsgemeinschaft (DFG) and National Institute of Health (NIH).
auditory objects along the horizontal (time) and vertical (frequency) axes recruit distinct neural networks. A neurophysiological model of auditory scene analysis will be outlined at the end of this presentation.
10. Understanding the present and plotting the future: Structural and functional brain mapping in stroke and dementia
Sandra E. Black Head, Division of Neurology, Sunnybrook and Womens College Health Sciences Centre; Professor of Medicine (Neurology), University of Toronto, Ont., Canada The advent of Computerized Tomography (CT) in the mid 1970s followed shortly thereafter by magnetic resonance imaging (MRI) in the early 1980s revolutionized clinical Cognitive Neuroscience providing the opportunity for in vivo brainbehaviour correlations as never resting-state patterns of dysfunction in dierent disorders, and activation techniques using the subtraction method with oxygen-15 in the late 1980s took this to another level. Technical advances in the 1990s brought computerized methods for quantitative tissue volumetry of MRI images and functional MRI, which because of the lack of
Rotman Research Institute Abstracts / Brain and Cognition 54 (2004) 128132 radiation and the wider availability, opened the doors to activation studies across the human lifespan and in many structural techniques, which go beyond static cerebral localization to the study of dynamic abilities, at dierent ages and in dierent emerging methodologies for studying brainbehaviour relationships as exemplied by applications in dementia and stroke recovery, using group theoretical modeling. The potential for quantitative structural imaging to serve as surrogate markers of disease progression or retardation will also be considered, as well as the role in dierential diagnosis of topographic patterns of tissue atrophy, which reect the regional selectivity of the common neurodegenerative processes. The possibility of early detection of predementia states using PET, fMRI, and MR spectroscopy will also be discussed. Finally, the ability of fMRI to help to map brain reorganization at dierent stages post stroke, and possibly in response to new interventions will be highlighted. Neuroimaging advances continue to open unparalleled opportunities, but must be disciplined by carefully planned experiments, both functional and structural, with conscientious attention to methodological limitations and quality control, if we are to properly exploit these powerful new methods.
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granted in adults are acquired (an enormous range of perceptual and motor skills, of social skills, expressive and written language(s), understanding and producing music, to name a few). The second is to better understand the neural substrates of these abilities in adults (why are certain regions of the brain most often used for certain types of processing, such as language? What are the correlates predicting poor skill acquisition (i.e., dyslexia), for example). The third is to better understand the full developmental spectrum; learning how, when and in what order brain regions and their associated skills develop, may help in determining the decline in some abilities with aging. In this talk I will review developmental neuroimaging studies that touch on several aspects of cognition, studies which try to disentangle the various processes implicated in tasks, to determine which processes develop when. The studies are largely neurophysiological (event-related potential (ERP) studies), as this is the most readily applied technique with children. I will focus on two areas of research: Visual attention/search paradigms and face processing paradigms. The rst series of studies measured short-latency ERPs and demonstrated the early presence of top-down processing and binding of features in serial presentation tasks. Facilitation of processing with conjunction search is also seen in children, although it continues to develop until teenage years. In more traditional visual search tasks, children show evidence of automatic strategy shifts as a function of task demands, similar to adults, despite the ubiquitous latency and amplitude decreases with age. The results of these studies have important ramications for current models of attentional processing. The second series of studies investigated both early and later stages of face processing in childrenunder conditions of non-directed attention (non-faces were targets), explicit memory tasks and implicit processing of facial emotional expressions. Early stages of processing appear to follow a more protracted developmental course for faces than the simple stimuli in visual search tasks, but the salience of faces is evident at the youngest ages tested. These developmental data make signicant contributions to our understanding of the brain areas involved in perceptual, featural, and emotional processing of faces. Finally, I will present preliminary neuroimaging data from 10 to 12-year-olds in three modalities: functional and structural MRI, and magnetoencephalography (MEG) using a facial expression task, to discuss the convergence of the resultant data and the feasibility of these studies in children.
13. Learning about attentional processes by observing neural activity in extrastriate cortex
Kathleen OCraven fMRI Scientist, The Rotman Research Institute, Baycrest Centre for Geriatric Care, Ont., Canada; Assistant Professor, Department of Psychology, University of Toronto, Ont., Canada Visual attention allows a viewer to select the subset of visual information in a complex scene that is relevant to a particular task or goal and to devote more extensive processing to that information. How does this selection occur? How does it aect visual processing? How can we measure those eects? I will discuss results from one technique: observing the eects of attentional processes on neural activity in extrastriate regions of visual cortex. Certain posterior brain regions are specialized for processing particular aspects of visual stimuli. For example, Area MT/MST responds to visual motion, the fusiform face area (FFA) to faces, the Parahippocampal Place Area (PPA) to spatial layout, and the lateral occipital complex (LOC) to objects. By functionally dening these regions in individual subjects, and then measuring the magnitude of activity in each area during experimental tasks, we can infer the degree of processing for the dierent task conditions (for each attribute). If the same stimulus produces more activity in area MT/MST in one
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Rotman Research Institute Abstracts / Brain and Cognition 54 (2004) 128132 cortical region that responds to that attribute (e.g., MT/MST) shows enhanced activity (basic attentional modulation). Additionally, however, the regions which respond to other attributes of the object, which possesses the attended attribute, also show increased activity. While the subject is attending to motion, FFA is more active if the moving item happens to be a face than if a face is the overlapping stationary item. Similarly, PPA is more active if the moving item is a house and the face is the stationary distractor. In each condition, a face, a house, and motion are all present. But the levels of activity within the three corresponding cortical areas depend on what attribute is being attended, and on how the attributes are bound together into objects. Thus, it is possible to determine that attention directed to one attribute of a complex visual stimulus can spread to other attributes of the object, reecting a non-spatial deployment of attention. Current studies are exploring how this object-based attention interacts with spatial attention.
condition than another, for example, this implies motion is being processed to a greater extent in the rst condition. Our group and researchers in other laboratories have used this approach with fMRI data to further our understanding of visual processing. Twenty years ago it was widely believed that the occipital visual areas process visual input veridically, with little top-down inuence. It is now well-established that attention can modulate neural activity in mostif not allsensory areas. Furthermore, we have shown that visual imagery of a particular stimulus recruits the same specialized neural machinery that is recruited to process an actual visual stimulus with the same content. That is, FFA is more active when a subject imagines seeing a face than when she imagines seeing a place, and PPA shows exactly the opposite pattern of results. We can learn more about how attention operates by extending this approach. When two objects overlap in a single location, and subjects attend to one attribute of one of those objects (e.g., motion), the