Although generally studied in isolation, language and action often co-occur in everyday life. Here we investigated one particular form of simultaneous language and action, namely speech and gestures that speakers use in everyday communication. In a functional magnetic resonance imaging study, we identified the neural networks involved in the integration of semantic information from speech and gestures. Verbal and/or gestural content could be integrated easily or less easily with the content of the preceding part of speech. Premotor areas involved in action observation (Brodmann area [BA] 6) were found to be specifically modulated by action information "mismatching" to a language context. Importantly, an increase in integration load of both verbal and gestural information into prior speech context activated Broca’s area and adjacent cortex (BA 45/47). A classical language area, Broca’s area, is not only recruited for language-internal processing but also when action observation is integrated with speech. These findings provide direct evidence that action and language processing share a high-level neural integration system.

Motor disorders are a frequent consequence of stroke and much effort is invested in the re-acquisition of motor control. Although patients often regain some of their lost function after therapy, most remain chronically disabled. Functional recovery is achieved largely through reorganization processes in the damaged brain. Neural reorganization depends on the information provided by sensorimotor efferent-afferent feedback loops. it has, however, been shown that the motor system can also be activated "offline" by imagining (motor imagery) or observing movements. the discovery of mirror neurones, which fire not only when an action is executed, but also when one observes another person performing the same action, also show that our action system can be used "online" as well as offline. It is an intriguing question as to whether the information provided by motor imagery or motor observation can lead to functional recovery and plastic changes in patients after stroke. this article reviews the evidence for motor imagery or observation as novel methods in stroke rehabilitation.

■ According to embodied theories of language, people under-stand a verb like throw, at least in part, by mentally simulating throwing. This implicit simulation is often assumed to be similar or identical tomotor imagery. Here we used fMRI to test whether implicit simulations of actions during language understanding in-volve the same cortical motor regions as explicit motor imagery. Healthy participants were presented with verbs related to hand actions (e.g., to throw) and nonmanual actions (e.g., to kneel). They either read these verbs (lexical decision task) or actively imagined performing the actions named by the verbs (imagery task). Primary motor cortex showed effector-specific activation during imagery, but not during lexical decision. Parts of premotor cortex distinguished manual from nonmanual actions during both lexical decision and imagery, but there was no overlap or correlation between regions activated during the two tasks. These dissociations suggest that implicit simulation and explicit imagery cued by action verbs may involve different types of mo-tor representations and that the construct of “mental simulation” should be distinguished from “mental imagery ” in embodied theories of language. ■

& Mental rotation is a hypothesized imagery process that has inspired controversy regarding the substrate of human spatial reasoning. Two central questions about mental rotation remain: Does mental rotation depend on analog spatial representations, and does mental rotation depend on motor simulation? A re-view and meta-analysis of neuroimaging studies help answer these questions. Mental rotation is accompanied by increased activity in the intraparietal sulcus and adjacent regions. These areas contain spatially mapped representations, and activity in these areas is modulated by parametric manipulations of mental rotation tasks, supporting the view that mental rotation de-pends on analog representations. Mental rotation also is ac-companied by activity in the medial superior precentral cortex, particularly under conditions that favor motor simulation, sup-porting the view that mental rotation depends on motor sim-ulation in some situations. The relationship between mental rotation and motor simulation can be understood in terms of how these two processes update spatial reference frames. &

Motor imagery is widely used to study cognitive aspects of the neural control of action. However, what is exactly simulated during motor imagery is still a matter of debate. On the one hand, it is conceivable that motor imagery is an embodied cognitive process, involving a simulation of movements of one's own body. The alternative possibility is that, although motor imagery relies on knowledge of the motor processes, it does not entail an actual motor simulation that is influenced by the physical configuration of one's own body. Here we discriminate between these two hypotheses, in the context of an established motor imagery task: laterality judgments of rotated hand drawings. We found that reaction times of hand laterality judgments followed the biomechanical constraints of left or right hand movements. Crucially, the position of subjects' own left and right arm influenced laterality judgments of left and right hands. In neural terms, hand laterality judgments activated a parieto-frontal network. The activity within this network increased with increasing biomechanical complexity of the imagined hand movements, even when the amount of stimulus rotation was identical. Moreover, activity in the intraparietal sulcus was modulated by subjects' own hand position: a larger incongruence in orientation between the subjects' hand and the stimulus hand led to a selective increase in intraparietal activity. Our results indicate that motor imagery generates motor plans that depend on the current configuration of the limbs. This motor plan is calculated by a parieto-frontal network. Within this network, the posterior parietal cortex appears to incorporate proprioceptive information related to the current position of the body into the motor plan.

hand dystonia

& Mental images of number lines, Galton’s ‘‘number forms’’ (NF), are a useful way of investigating the relation between number and space. Here we report the first neuroimaging study of number-form synesthesia, investigating 10 synesthetes with NFs going from left to right compared with matched controls. Neuroimaging with functional magnetic resonance imaging re-vealed no difference in brain activation during a task focused on number magnitude but, in a comparable task on number order, synesthetes showed additional activations in the left and right posterior intraparietal sulci, suggesting that NFs are essen-tially ordinal in nature. Our results suggest that there are sepa-rate but partially overlapping neural circuits for the processing of ordinal and cardinal numbers, irrespective of the presence of an NF, but a core region in the anterior intraparietal sulcus representing (cardinal) number meaning appears to be activated autonomously, irrespective of task. This article provides an im-portant extension beyond previous studies that have focused on word–color or grapheme–color synesthesia. &

An observation that neurons in the motor cortex of the monkey are active both when the monkey performs a specific action and when he watches an actor executing the same action led to the mirror-system hypothesis. This hypothesis suggests that primates perceive and interpret others ’ actions by generating an internal motor representation (e.g., simulation). Recent evidence suggests that humans have a similar mirror system. In this review, we focus on the essential congruence between the motor and visual properties of an action. We summarize behavioral and imaging studies in humans that show that observing others ’ actions can interfere with our own motor execution. We discuss a framework for understanding such an internal representation and suggest that the activity in the parietal cortex during observation of others ’ actions is based on the sensory-to-motor remapping properties of this region, which are necessary for fine control of our own actions.

Recent functional imaging studies of working memory (WM) have suggested a relationship between the requirement for response selection and activity in dorsolateral prefrontal (DLPFC) and parietal regions. Although a number of WM operations are likely to occur during response selection, the current study was particularly interested in the contribution of this neural network to WM-based response selection when compared to the selection of an item from a list being maintained in memory, during a verbal learning task. The design manipulated stimulus–response mappings so that selecting an item from memory was not always accompanied with selecting a motor response. Functional activation during selection supported previous findings of fronto-parietal involvement, although in contrast to previous findings left, rather than right, DLPFC activity was significantly more active for selecting a memory-guided motor response, when compared to selecting an item currently maintained in memory or executing a memory-guided response. Our results contribute to the debate over the role of fronto-parietal activity during WM tasks, suggesting that this activity appears particularly related to response selection, potentially supporting the hypothesized role of prefrontal activity in biasing attention toward task-relevant material in more posterior regions. © 2006 Elsevier Inc. All rights reserved.

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