Function Of Posterior Parietal Cortex Research Articles

The Visuospatial and Sensorimotor Functions of Posterior Parietal Cortex in Drawing Tasks: A Review.

Drawing is a comprehensive skill that primarily involves visuospatial processing, eye-hand coordination, and other higher-order cognitive functions. Various drawing tasks are widely used to assess brain function. The neuropsychological basis of drawing is extremely sophisticated. Previous work has addressed the critical role of the posterior parietal cortex (PPC) in drawing, but the specific functions of the PPC in drawing remain unclear. Functional magnetic resonance imaging and electrophysiological studies found that drawing activates the PPC. Lesion-symptom mapping studies have shown an association between PPC injury and drawing deficits in patients with global and focal cerebral pathology. These findings depicted a core framework of the fronto-parietal network in drawing tasks. Here, we review neuroimaging and electrophysiological studies applying drawing paradigms and discuss the specific functions of the PPC in visuospatial and sensorimotor aspects. Ultimately, we proposed a hypothetical model based on the dorsal stream. It demonstrates the organization of a PPC-centered network for drawing and provides systematic insights into drawing for future neuropsychological research.

Electrical microstimulation evokes saccades in posterior parietal cortex of common marmosets.

The common marmoset (Callithrix jacchus) is a small-bodied New World primate increasing in prominence as a model animal for neuroscience research. The lissencephalic cortex of this primate species provides substantial advantages for the application of electrophysiological techniques such as high-density and laminar recordings, which have the capacity to advance our understanding of local and laminar cortical circuits and their roles in cognitive and motor functions. This is particularly the case with respect to the oculomotor system, as critical cortical areas of this network such as the frontal eye fields (FEF) and lateral intraparietal area (LIP) lie deep within sulci in macaques. Studies of cytoarchitecture and connectivity have established putative homologies between cortical oculomotor fields in marmoset and macaque, but physiological investigations of these areas, particularly in awake marmosets, have yet to be carried out. Here we addressed this gap by probing the function of posterior parietal cortex of the common marmoset with electrical microstimulation. We implanted two animals with 32-channel Utah arrays at the location of the putative area LIP and applied microstimulation while they viewed a video display and made untrained eye movements. Similar to previous studies in macaques, stimulation evoked fixed-vector and goal-directed saccades, staircase saccades, and eyeblinks. These data demonstrate that area LIP of the marmoset plays a role in the regulation of eye movements, provide additional evidence that this area is homologous with that of the macaque, and further establish the marmoset as a valuable model for neurophysiological investigations of oculomotor and cognitive control.NEW & NOTEWORTHY The macaque monkey has been the preeminent model for investigations of oculomotor control, but studies of cortical areas are limited, as many of these areas are buried within sulci in this species. Here we applied electrical microstimulation to the putative area LIP of the lissencephalic cortex of awake marmosets. Similar to the macaque, microstimulation evoked contralateral saccades from this area, supporting the marmoset as a valuable model for studies of oculomotor control.

Phase Synchronization Between Motor Cortices During Gait Movement in Patients With Spinal Cord Injury.

Spinal cord injury (SCI) frequently leads to generalized locomotor disability and gait disturbances which cause serious discomfort among patients. Human gait is a complex process in the central nervous system that results from the integration of various mechanisms which remain unclear. Therefore, it is of great theoretical and practical significance to investigate the cortical activity patterns during gait movement in SCI. In this study, brain activity was recorded by electroencephalogram (EEG) during two kinds of gait-like movements. Phase synchronization between motor cortices was investigated through source analysis and phase locking. Results revealed that diverse neural networks with different resonance-like frequencies exist in the brain. Further, we found that the premotor cortex played an important role in the control of passive gait-like movement. In attempted/active movement, spatial function and multimodal integration with somatosensory information are crucial aspects of posterior parietal cortex function which need to be considered separately in different EEG bands. Our results further confirmed that neural system control patterns in passive gait-like movement differ from those in attempted or active gait-like movement. Novel insights into human gait will provide a basis for improvements in future neurorehabilitation applications.

Meta-analysis: how does posterior parietal cortex contribute to reasoning?

Reasoning depends on the contribution of posterior parietal cortex (PPC). But PPC is involved in many basic operations—including spatial attention, mathematical cognition, working memory, long-term memory, and language—and the nature of its contribution to reasoning is unclear. Psychological theories of the processes underlying reasoning make divergent claims about the neural systems that are likely to be involved, and better understanding the specific contribution of PPC can help to inform these theories. We set out to address several competing hypotheses, concerning the role of PPC in reasoning: (1) reasoning involves application of formal logic and is dependent on language, with PPC activation for reasoning mainly reflective of linguistic processing; (2) reasoning involves probabilistic computation and is thus dependent on numerical processing mechanisms in PPC; and (3) reasoning is built upon the representation and processing of spatial relations, and PPC activation associated with reasoning reflects spatial processing. We conducted two separate meta-analyses. First, we pooled data from our own studies of reasoning in adults, and examined activation in PPC regions of interest (ROI). Second, we conducted an automated meta-analysis using Neurosynth, in which we examined overlap between activation maps associated with reasoning and maps associated with other key functions of PPC. In both analyses, we observed reasoning-related activation concentrated in the left Inferior Parietal Lobe (IPL). Reasoning maps demonstrated the greatest overlap with mathematical cognition. Maintenance, visuospatial, and phonological processing also demonstrated some overlap with reasoning, but a large portion of the reasoning map did not overlap with the map for any other function. This evidence suggests that the PPC’s contribution to reasoning may be most closely related to its role in mathematical cognition, but that a core component of this contribution may be specific to reasoning.

On the time course of attentional focusing in older adults

Many sensory and cognitive changes accompany normal ageing, including changes to visual attention. Several studies have investigated age-related changes in the control of attention to specific locations (spatial orienting), but it is unknown whether control over the distribution or breadth of attention (spatial focus) also changes with age. In the present study, we employed a dual-stream attentional blink task and assessed changes to the spatial distribution of attention through the joint consequences of temporal lag and spatial separation on second-target accuracy. Experiment 1 compared the rate at which attention narrows in younger (mean age 22.6, SD 4.25) and older (mean age 66.8, SD 4.36) adults. The results showed that whereas young adults can narrow attention to one stream within 133ms, older adults were unable to do the same within this time period. Experiment 2 showed that older adults can narrow their attention to one stream when given more time (266ms). Experiment 3 confirmed that age-related changes in retinal illuminance did not account for delayed attentional narrowing in older adults. Considered together, these experiments demonstrate that older adults can narrow their attentional focus, but that they are delayed in initiating this process compared to younger adults. This finding adds to previously reported reductions in attentional dynamics, deficits in inhibitory processes, and reductions in posterior parietal cortex function that accompany normal ageing.

Cognitive functions of the posterior parietal cortex

The posterior parietal cortex has traditionally been associated with visuo-spatial perception and spatial attention, however, accumulating evidence indicates that it is involved in a much wider range of cognitive functions. The articles included in the E-book review experimental data and theoretical considerations, as well as reviews of recent work supporting this idea. Anatomical, lesion, neurophysiological, and functional imaging data are discussed. Animal models (rodent and primate) as well as human studies are covered. Finally, the unique and shared functions of the posterior parietal cortex are compared to other brain areas. These contributions provide a primer of the current state of knowledge, identify unresolved questions, highlight recent conceptual and methodological advances, and, we hope, will stimulate future research. In the first part of the E-book, evidence from rodent model systems is presented. Articles examine the contribution of animal models to long-term memory (Myskiw and Izquierdo, 2012), illusory conjunctions (Kesner, 2012), ranking of topographic signals (Broussard, 2012), and relational learning (Robinson and Bucci, 2012). A common theme across these topics is the intersection of attentional functions of posterior parietal cortex with learning/memory-related processes. Data are presented from studies that combine experimental lesion techniques and electrophysiological methods with sophisticated behavioral assays that attempt to elucidate the precise contributions of posterior parietal cortex. A series of experiments in non-human primate models similarly reveal activation of the posterior parietal cortex in a variety of cognitive functions, such as numerosity (Roitman et al., 2012), categorization (Fitzgerald et al., 2012), and decision-making (Huk and Meister, 2012). Spatial signals are present and shape peri-personal shape and limb movements (Hadjidimitrakis et al., 2012), however, spatial information also forms an abstract spatial representation that can be decoupled from sensorimotor control (Chafee and Crowe, 2012). Neurophysiological experiments provide insights on the nature of differences between the posterior parietal cortex and other cortical areas, such as the prefrontal cortex, in the context of visual search (Wardak et al., 2012) and other tasks (Katsuki and Constantinidis, 2012). The conclusion that emerges from these studies is that the posterior parietal cortex is activated in a wide range of tasks, and individual parietal neurons exhibit neural correlates of complex cognitive functions. In the last part of the E-book, evidence from human studies is considered. Imaging studies routinely reveal BOLD activation during episodic memory tasks (Berryhill, 2012; Levy, 2012). In recent years, nuanced memory deficits following parietal lesions have also been recognized (Berryhill, 2012). EEG and MEG studies have yielded consistent evidence about the time course of parietal mnemonic activation (Levy, 2012). Both process- and content-based models have been proposed to account for the nature of this activation (Berryhill, 2012; Levy, 2012). Finally, the posterior parietal cortex has been implicated in cognitive control, with different subdivisions proposed to be specialized for bottom-up and top-down control (Shomstein, 2012). Collectively, these studies illustrate our current understanding of the posterior parietal cortex with regard to cognitive operations. While the nature and extent of its involvement continues to be investigated, it is now clear that its role goes beyond the functions traditionally ascribed to it, spatial representation and attention—a major development of the past few years.

Choice-specific sequences in parietal cortex during a virtual-navigation decision task

The posterior parietal cortex (PPC) plays an important role in many cognitive behaviors; however, the neural circuit dynamics underlying PPC function are not well understood. Here we optically imaged the spatial and temporal activity patterns of neuronal populations in mice performing a PPC-dependent task that combined a perceptual decision and memory-guided navigation in a virtual environment. Individual neurons had transient activation staggered relative to one another in time, forming a sequence of neuronal activation spanning the entire length of a task trial. Distinct sequences of neurons were triggered on trials with opposite behavioral choices and defined divergent, choice-specific trajectories through a state space of neuronal population activity. Cells participating in the different sequences and at distinct time points in the task were anatomically intermixed over microcircuit length scales (< 100 micrometers). During working memory decision tasks the PPC may therefore perform computations through sequence-based circuit dynamics, rather than long-lived stable states, implemented using anatomically intermingled microcircuits.

Insights from neuropsychology: pinpointing the role of the posterior parietal cortex in episodic and working memory

The role of posterior parietal cortex (PPC) in various forms of memory is a current topic of interest in the broader field of cognitive neuroscience. This large cortical region has been linked with a wide range of mnemonic functions affecting each stage of memory processing: encoding, maintenance, and retrieval. Yet, the precise role of the PPC in memory remains mysterious and controversial. Progress in understanding PPC function will require researchers to incorporate findings in a convergent manner from multiple experimental techniques rather than emphasizing a particular type of data. To facilitate this process, here, we review findings from the human neuropsychological research and examine the consequences to memory following PPC damage. Recent patient-based research findings have investigated two typically disconnected fields: working memory (WM) and episodic memory. The findings from patient participants with unilateral and bilateral PPC lesions performing diverse experimental paradigms are summarized. These findings are then related to findings from other techniques including neurostimulation (TMS and tDCS) and the influential and more abundant functional neuroimaging literature. We then review the strengths and weaknesses of hypotheses proposed to account for PPC function in these forms of memory. Finally, we address what missing evidence is needed to clarify the role(s) of the PPC in memory.

Contributions of human parietal and frontal cortices to attentional control during conflict resolution: a 1-Hz offline rTMS study

Various brain regions contribute to aspects of attentional control in conflict resolution. Here, we used transcranial magnetic stimulation (TMS) to examine the functions of posterior parietal cortex (PPC) and dorsal medial frontal cortex (dMFC) in a visual flanker task. Participants responded to a central target that was flanked by congruent, neutral or incongruent stimuli on the left or right. Offline low-frequency repetitive TMS (1 Hz, 110% motor threshold, 20 min) was applied to right PPC or dMFC. Performance, as measured by reaction times and accuracy, was established at baseline, after rTMS, and sham stimulation before or after active rTMS. After rTMS to right PPC, the interference of flankers presented in the left visual hemispace diminished selectively. By contrast, after rTMS over the right dMFC, flanker effects in both visual fields remained. Our results suggest that right PPC specifically contributes to the assignment of spatial attention during stimulus encoding.

Multiple cognitive control mechanisms associated with the nature of conflict

Cognitive control is required to regulate conflict. The conflict monitoring theory suggests that the dorsal anterior cingulate cortex (dACC) is involved in detecting response conflict and the dorsolateral prefrontal cortex (DLPFC) plays a critical role in regulating conflict. Recent studies, however, have suggested that rostral dACC (rdACC) responds to response conflict whereas caudal dACC (cdACC) is associated with perceptual conflict. Moreover, DLPFC has been engaged only in regulation of response conflict. A neural network involved in perceptual conflict, however, remains unclear. In this study, we used functional magnetic resonance imaging (fMRI) in an attempt to reveal monitor–controller networks corresponding to either perceptual conflict or response conflict. A version of the Stroop color matching task was used to manipulate perceptual conflict, response conflict was manipulated by an arrow. The results demonstrated that rdACC and DLPFC were engaged in response conflict whereas cdACC and the dorsal portion of premotor cortex (pre-PMd) were involved in perceptual conflict. Interestingly, the posterior parietal cortex (PPC) was activated by both types of conflict. Correlation analyses between behavioral conflict effects and neural responses demonstrated that rdACC and DLPFC were associated with response conflict whereas cdACC and pre-PMd were associated with perceptual conflict. PPC was not correlated with either perceptual conflict or response conflict. We suggest that cdACC and pre-PMd play critical roles in perceptual conflict processing, and this network is independent from the rdACC/DLPFC network for response conflict processing. We also discussed the function of PPC in conflict processing.

Sensory-motor and cognitive functions of the human posterior parietal cortex involved in manual actions

The posterior parietal cortex (PPC) is considered the dominant structure in the dorsal stream of visual processing, defined in the context of systems for perception and action. It is well-established that the human PPC is critical to sensory-motor transformations involved in online manual actions. A related body of literature identifies the PPC as important to cognitive aspects of action representation such as imagery, tool use, and gestures. The goal of the present paper is to review and compare the PPC contribution to representations of both motor control and motor cognition. Relating the sensory-motor and cognitive components of PPC function is important for an understanding of integrative representations of manual actions and the relation between perception, action, and cognition. Proposed theories of multiple dorsal stream systems supporting different action-relevant goals are discussed.

Seeing the brain through the architect's eyes: A rejoinder to Gevers and Notebaert

We welcome Gevers and Notebaert’s note, whichshows how converging efforts are being made byindependent laboratories and from different per-spectives, in the attempt to reach a better under-standing of the relation between Simon andSNARC (spatial-numerical association ofresponse codes) effects. We would like to drawattention to a crucial distinction between numberand space processing on the one hand andbetween the processes that are involved in theSimon and SNARC effects on the other.Space and number magnitude possess intri-guing similarities and give rise to analogous signa-tures when processed in the context of structurallysimilar tasks (e.g., Hubbard, Piazza, Pinel, D Walsh, 2003; but see alsoRusconi, Umilta`, & Galfano, 2006). In addition,both the core representation of number and thevisuo-motor representation of space are knownto rest massively on parietal networks (e.g.,Andersen & Buneo, 2003; Nieder, 2004). Onelogical possibility is that the mental representationof numbers is intrinsically spatial (Dehaene, 1997).Alternatively, the connection between numbersand space might be a cultural achievement. Infact, these possibilities do not exclude each other,since an original neural overlap may be joint byculture-specific representations, which build onlearnt symbolic tools such as the Cartesian system.It is generally claimed that the mental numberline is a specialized function of posterior parietalcortex, where also the processing of physicalspace takes place (see Hubbard et al., 2005; andRusconi & Umilta`, in press, for reviews). In fact,its behavioural effects could originate from aninteraction between the core representation ofnumber magnitude in the horizontal intraparietalsulcus (e.g., Castelli, Glaser, & Butterworth,

Topographic Organization for Delayed Saccades in Human Posterior Parietal Cortex

Posterior parietal cortex (PPC) is thought to play a critical role in decision making, sensory attention, motor intention, and/or working memory. Research on the PPC in non-human primates has focused on the lateral intraparietal area (LIP) in the intraparietal sulcus (IPS). Neurons in LIP respond after the onset of visual targets, just before saccades to those targets, and during the delay period in between. To study the function of posterior parietal cortex in humans, it will be crucial to have a routine and reliable method for localizing specific parietal areas in individual subjects. Here, we show that human PPC contains at least two topographically organized regions, which are candidates for the human homologue of LIP. We mapped the topographic organization of human PPC for delayed (memory guided) saccades using fMRI. Subjects were instructed to fixate centrally while a peripheral target was briefly presented. After a further 3-s delay, subjects made a saccade to the remembered target location followed by a saccade back to fixation and a 1-s inter-trial interval. Targets appeared at successive locations "around the clock" (same eccentricity, approximately 30 degrees angular steps), to produce a traveling wave of activity in areas that are topographically organized. PPC exhibited topographic organization for delayed saccades. We defined two areas in each hemisphere that contained topographic maps of the contra-lateral visual field. These two areas were immediately rostral to V7 as defined by standard retinotopic mapping. The two areas were separated from each other and from V7 by reversals in visual field orientation. However, we leave open the possibility that these two areas will be further subdivided in future studies. Our results demonstrate that topographic maps tile the cortex continuously from V1 well into PPC.

Functional-Anatomic Correlates of Memory Retrieval That Suggest Nontraditional Processing Roles for Multiple Distinct Regions within Posterior Parietal Cortex

Current theories of posterior parietal cortex (PPC) function emphasize space-based attention and motor intention. Imaging studies of long-term memory have demonstrated PPC activation during successful memory retrieval. Here, we explored the relationship between memory processes and classical notions of PPC function. Study 1 investigated old-new recognition using picture and sound stimuli to test whether PPC memory effects were dependent on visuospatial attention. A region lateral to the intraparietal sulcus [inferior parietal lobule complex (IPLC)] and two regions in the medial PPC [precuneus complex (PCC) and posterior cingulate/retrosplenial cortex (pC/Rsp)] showed strong retrieval success effects for both picture and sound stimuli. Study 2 explored a recognition task with varied response contingencies to investigate whether these retrieval success effects are dependent on motor intentions. In one condition, subjects responded to both old and new items. In two other conditions, subjects responded only to old or only to new items. IPLC, PCC, and pC/Rsp continued to show retrieval success effects with similar magnitudes for all response contingencies, including a condition in which no responses were made to old items. In a third study, IPLC and PCC activity was modulated at retrieval based on levels of processing at study, suggesting sensitivity to memory demands. These studies demonstrate that retrieval success effects in lateral and medial PPC regions are not affected by manipulations predicted by classical theories of PPC function but can be modulated by memory-related manipulations. PPC regions thus have prominent response properties associated with memory, which may arise through interactions with medial temporal cortex.