Disruption of synaesthesia following TMS of the right posterior parietal cortex

This study examines the role of four regions of the parietal lobe in grapheme-colour synaesthesia. TMS applied over a right parieto-occipital region disrupts performance on a synaesthetic priming task. TMS over the left parietal or a more anterior right parietal site did not have a reliable effect on synaesthesia even though one of the sites had been implicated in synaesthesia by previous fMRI studies. The same disruption is found for synaesthetes who experience colours in their "mind's eye" as well as those who project colours onto the inducing grapheme. This region may be important for binding graphemes and colours to different spatial reference frames.     

Differential effects of transcranial magnetic stimulation of left and right posterior parietal cortex on mental rotation tasks

A recently published study used the interference strategy of transcranial magnetic stimulation (TMS) to demonstrate the role of the right posterior parietal cortex (PPC) in the mental rotation of alphanumeric stimuli. We used similar stimulation parameters over the same left and right PPC regions, and examined the ability to rotate more complex 3D Shepard and Metzler (1971) images. There was reduced accuracy of performance with both right and left PPC stimulation for different angles of rotation of the visual stimuli. Right PPC stimulation led to reduced accuracy to rotate stimuli by 1200, whereas left PPC stimulation affected 180 degrees C rotation. We hypothesise that the two hemispheres make different contributions to the processing underlying visuospatial mental imagery: the right PPC is important for spatial rotations through smaller angles; the left hemisphere has a unique role when the stimuli to be compared are rotated through 180 degrees C, a task that engages verbal strategies due to the well-documented special nature of enantiomorphs.     

Paired pulse TMS over the right posterior parietal cortex modulates visuospatial perception

OBJECTIVE: We previously observed a relative contralateral neglect by right parietal single-pulse TMS given 150 ms after visual stimulus presentation. Here we investigated the effects of parietal paired TMS in normal subjects performing a visuospatial task. METHODS: Thirteen right-handed healthy subjects underwent a line-length judgement task during single-pulse and paired (1, 3, 5, 10 ms ISIs) TMS, delivered on the right parietal cortex 150 ms after visual stimulus. RESULTS: Single pulse TMS over the right parietal cortex induced a significant rightward bias compared to the baseline condition. At 1 and 3 ms ISIs, paired-pulse TMS did not show any effect in comparison with single pulse TMS. More importantly, 5 ms ISI was able to restore baseline levels, thus inducing a significant improvement of the performance compared to single-pulse TMS and 1-3 ms ISIs. CONCLUSIONS: Paired TMS seems able to modulate activity of the right posterior parietal cortex in healthy subjects performing a cognitive visuospatial task.     

Event-related TMS over the right posterior parietal cortex induces ipsilateral visuo-spatial interference

The right posterior parietal cortex (PPC) is implicated in visuo-spatial processing, as illustrated by patients with visuo-spatial neglect, but the precise time-course of its contribution is still an open question. In the present study we assessed whether single-pulse transcranial magnetic stimulation (TMS) can interfere with the performance of normal subjects in a standard visuo-spatial task. Participants had to perform a landmark task while TMS was applied over the right PPC, the homologue region in the left hemisphere or the right primary motor cortex. Stimulation was time-locked to the stimulus presentation with a stimulus onset asynchrony (SOA) varying between 50 and 200 ms. Our results indicate that TMS interfered mainly with the visuo-spatial task when applied over the right PPC at an early stage (50 ms post-stimulus). The interference effect of single-pulse TMS in the present visuo-spatial processing is revealed by a processing cost for ipsilateral targets. These results are in agreement with neuropsychological and brain imaging studies showing a right hemispheric dominance in visuo-spatial processing but add crucial information about the time-course of visuo-spatial processing within the right PPC.     

Stimulus-driven incidental episodic retrieval involves activation of the left posterior parietal cortex

Recent reviews have highlighted the important role that the posterior parietal cortex (PPC) serves during episodic memory retrieval. A handful of studies have also noted that the PPC is active when old information is present on tasks that do not require overt episodic retrieval. Based on this observation, we examined whether incidental study-phase retrieval, cued by the repeated presence of stimuli, was sufficient to activate the PPC and whether this activation would be modulated by the lag between the initial and repeated presentation of those stimuli. Blood flow was measured with positron emission tomography (PET) while subjects classified pictures that were either new, repeated following a short lag, or repeated following a long lag. Activity in the left inferior parietal lobule (IPL, BA 40), amongst other regions, was greater for repeated than new pictures, and was greater following a long lag than a short lag, even though intentional retrieval was not required. These results suggest that the presence of repeated stimuli is sufficient to initiate left PPC mediated episodic retrieval.     

Working memory retrieval: contributions of the left prefrontal cortex, the left posterior parietal cortex, and the hippocampus

Functional magnetic resonance was used to identify regions involved in the working memory (WM) retrieval. Neural activation was examined in two WM tasks: an item recognition task, which can be mediated by a direct- access retrieval process, and a judgement of recency task that require a serial search. Dissociations were found in the activation patterns in the hippocampus and in the left inferior frontal gyrus (LIFG) when the probe contained the most recently studied serial position (where a test probe can be matched to the contents of focal attention)compared to when it contained all other positions (where retrieval is required). The data implicate the hippocampus and the LIFG in retrieval from WM, complementing their established role in long-term memory. Results further suggest that the left posterior parietal cortex (LPPC) support serial retrieval processes that are often required to recover temporal order information. Together this data suggest that the LPPC, the LIFG, and the hippocampus collectively support WM retrieval. Critically, the reported findings support accounts that posit a distinction between representations maintained in and outside of focal attention, but are at odds with traditional dual-store models that assume distinct mechanisms for short- and long-term memory representation.     

The role of right and left posterior parietal cortex in the modulation of spatial attentional biases by self and non-self face stimuli

In the present research we investigated whether the direction of the attentional bias in line bisection judgment displayed by healthy subjects is influenced by the evaluation of the social distance between self and other. We used inhibitory repetitive transcranial magnetic stimulation (rTMS) trains over the right and left parietal cortex to investigate the role of these regions in the task. Following right parietal rTMS, the self face is perceived as closer when it is located at the right line endpoint; following left parietal rTMS, the self face is perceived as closer when it is located at the left line endpoint. In both cases, the side of space ipsilateral to the rTMS is underestimated from an attentional point of view, while it is overestimated from a social point of view. These results are a projection of how an individual perceives himself in the social relational space.     

Positive emotions and the right parietal cortex

The achievement of a state of solace is a developmental necessity to the unfolding of the capacity for positive emotions. In addition, solace is a significant subjective component of noninstinctual feelings such as love, joy, gratitude, and rapture. Pure solace is experienced primarily in relation to the sense of self, whereas the solace derivatives connect, in varying degrees, with objects external to the self. Psychiatrists see many patients who are unsolaceable and who, because of this, cannot experience sustained positive emotion of any kind. Those diagnosed as personality, conduct, and behaviorally disordered, as well as those with alexithymia, are particularly likely to exhibit a basic unsolaceability. The psychiatrist should also be alert to a deficiency of positive emotion in those with attention deficit disorder and the so-called learning disability syndrome. The coexistence of unsolaceability with features of right parietal cortex dysfunction suggests a directionality of positive emotional experience and parietal neocortical activity. The tertiary zones of the right parietal cortex appear to be the structural system most likely to subserve complex positive affects.     

Visuomotor functions of the posterior parietal cortex

In this special issue of Neuropsychologia leading experts in the field discuss controversies and advances in the role of the posterior parietal cortex (PPC) in visuomotor control. The papers are wide-ranging in their scope, covering monkey physiology and anatomy, functional imaging in humans and monkeys as well as transcranial magnetic stimulation and lesion studies in humans. The collection provides an important overview of the current state-of the-art in this area of research, including discussions on homologies between monkey and human parietal regions, the role of co-ordinate transformations and intermediate representations from vision to action, and reviews of controversial hot topics in this field.     

TMS over right posterior parietal cortex induces neglect in a scene-based frame of reference

Although damage to right posterior parietal cortex (RPPC) produces bias in line bisection, Karnath et al. [Karnath, H.-O., Berger, M. F., Küker, W., & Rorden, C. (2004). The anatomy of spatial neglect based on voxelwise statistical analysis: A study of 140 patients. Cerebral Cortex, 14, 1164-1172] claim that it plays little role in spatial neglect, which is better measured by target cancellation. We used a detection task (approximating cancellation in requiring detection) to investigate this claim by compromising the parietal cortex with transcranial magnetic stimulation (TMS). Two outline shapes, one on each side of fixation, were briefly displayed before a mask. The target was a discontinuity in the left or right of the outline of one of these perceptual objects. Subjects indicated position or absence of target as fast as possible. Stimulus-mask onset asynchrony was adjusted individually to yield 75% detection. TMS was delivered over left posterior parietal cortex (LPPC), RPPC and Vertex, with Sham TMS over RPPC as a baseline control. Target detection was near ceiling and fastest at central positions and worst and slowest at the far right. Detection was significantly reduced at the far left position by TMS over RPPC. No other effects were obtained and latency was not affected by TMS. Disruption of RPPC by TMS does produce left neglect as measured by detection. Given the pattern of performance and since it was disrupted on one side of the display rather than on one side of each shape, attention and neglect were in a scene-based rather than object-based reference frame.     

Both left and right posterior parietal activations contribute to compensatory processes in normal aging

Older adults often exhibit greater brain activation in prefrontal cortex compared to younger adults, and there is some evidence that this increased activation compensates for age-related neural degradation that would otherwise adversely affect cognitive performance. Less is known about aging and compensatory recruitment in the parietal cortex. In this event-related functional magnetic resonance imaging study, we presented healthy young and old participants with two Stroop-like tasks (number magnitude and physical size). In young, the number magnitude task activated right parietal cortex and the physical size task activated left parietal cortex. In older adults, we observed contralateral parietal recruitment that depended on the task: in the number magnitude task older participants recruited left posterior parietal cortex (in addition to the right parietal activity observed in young) while in the physical size task they recruited right (in addition to left) posterior parietal cortex. In both cases, the additional parietal activity was associated with better performance suggesting that it played a compensatory role. Older adults also recruited left prefrontal cortex during both tasks and this common activation was also associated with better performance. The results provide evidence for task-specific compensatory recruitment in parietal cortex as well as task-independent compensatory recruitment in prefrontal cortex in normal aging.     

Visual vector inversion in the posterior parietal cortex

In the antisaccade task, a saccade must be triggered towards the mirror location of a visual target. The neural basis required for this visual vector inversion remains unclear, although neuronal activities reflecting this process have been recorded in the monkey lateral intraparietal area. We examined a patient with a small, right-sided, posterior parietal stroke who complained of difficulty in manipulating visual information. Antisaccades were markedly hypometric rightwards but normal leftwards. Largely unaffected performances in other saccade tasks revealed that visual and motor processing were not significantly affected. Antisaccade inaccuracy could therefore be ascribed to the impairment of visual vector inversion, a processing specifically required in this task. These findings provide the first evidence in humans that visual vector inversion could be an intrinsic property of the posterior parietal cortex.     

Temporal feature integration in the right parietal cortex

When searching for a target presented among distractors by means of Rapid Serial Visual Presentation (RSVP), participants often report the stimulus that is preceding or following the target as being the target. These so-called temporal binding errors are accompanied by high levels of confidence so that participants are bemused with the mismatch between their perceptual experience and the actual presented stimulus. By contrast with spatial binding the neural basis for temporal binding errors remains unexplored. Previous neuropsychology studies using non-spatial selective attention tasks have shown that right temporo-parietal cortex is involved in the temporal deployment of attention. Here we investigated the neural basis of temporal binding in five patients with visual extinction whose lesions involved different cortical areas in the right hemisphere, including the temporo-parietal cortex. Patients made significantly more binding errors for contralesional than ipsilesional stimuli and more binding errors than healthy controls. Incorrect binding from distractors near to the target was the most common for both patients and controls. Eye movements did not contribute to the pattern of results. These results show that right hemisphere cortical areas contribute to the accurate temporal coding of visual features.     

Correlates of stimulus-response congruence in the posterior parietal cortex

Primate behavior is flexible: The response to a stimulus often depends on the task in which it occurs. Here we study how single neurons in the posterior parietal cortex (PPC) respond to stimuli which are associated with different responses in different tasks. Two rhesus monkeys performed a task-switching paradigm. Each trial started with a task cue instructing which of two tasks to perform, followed by a stimulus requiring a left or right button press. For half the stimuli, the associated responses were different in the two tasks, meaning that the task context was necessary to disambiguate the incongruent stimuli. The other half of stimuli required the same response irrespective of task context (congruent). Using this paradigm, we previously showed that behavioral responses to incongruent stimuli are significantly slower than to congruent stimuli. We now demonstrate a neural correlate in the PPC of the additional processing time required for incongruent stimuli. Furthermore, we previously found that 29% of parietal neurons encode the task being performed (task-selective cells). We now report differences in neuronal timing related to congruency in task-selective versus task nonselective cells. These differences in timing suggest that the activity in task nonselective cells reflects a motor command, whereas activity in task-selective cells reflects a decision process.     

Disorders of visual attention and the posterior parietal cortex

Traditionally, both the monkey and human posterior parietal cortex (PPC) have been considered to have a privileged role in spatial perception or action. Lesions to this region of the human brain, particularly of the right hemisphere, undoubtedly lead to spatially lateralised deficits such as visual extinction or neglect. However, although studies in monkeys have revealed much about the spatial functions of the parietal lobe, the monkey PPC may not be a good model system with which to understand fully the disorders of attention that follow damage to the human parietal cortex. Several lines of evidence, from functional imaging as well as investigations of patients with parietal damage, demonstrate that parts of the human inferior parietal lobe (IPL) have non-spatial functions. Here, we argue that it is important to distinguish spatially lateralised from spatial deficits. Both spatial and non-spatial impairments might, in principle, contribute to a spatially lateralised behavioural syndrome such as neglect. In this review, we discuss the evidence for such a proposal and suggest that a better understanding of human parietal syndromes may emerge from considering both the spatial and non-spatial functions of this region.     

Eye position encoding in the macaque posterior parietal cortex

In two previous studies, we had demonstrated the influence of eye position on neuronal discharges in the middle temporal area, medial superior temporal area, lateral intraparietal area and area 7A of the awake monkey ( Bremmer et al. 1997a , b). Eye position effects also have been found in visual cortical areas V3A and V6 and even in the premotor cortex and the supplementary eye field. These effects are generally discussed in light of a coordinate transformation of visual signals into a non-retinocentric frame of reference. Neural network studies dealing with the eye position effect succeeded in constructing such non-retinocentric representations by using model neurones whose response characteristics resembled those of ‘real’ neurones. However, to our knowledge, response properties of real neurones never acted as input into these neural networks. In the present study, we thus investigated whether, theoretically, eye position could be estimated from the population discharge of the (previously) recorded neurones and, if so, we intended to develop an encoding algorithm for the position of the eyes in the orbit. The optimal linear estimator proved the capability of the ensemble activity for determining correctly eye position. We then developed the so-called subpopulation encoding of eye position. This algorithm is based on the partition of the ensemble of neurones into two pairs of subpopulations. Eye position is represented by the differences of activity levels within each pair of subpopulations. Considering this result, encoding of the location of an object relative to the head could easily be accomplished by combining eye position information with the intrinsic knowledge about the retinal location of a visual stimulus. Taken together, these results show that throughout the monkey’s visual cortical system information is available which can be used in a fairly simple manner in order to generate a non-retinocentric representation of visual information.     

Neglect-like visual exploration behaviour after theta burst transcranial magnetic stimulation of the right posterior parietal cortex

The right posterior parietal cortex (PPC) is critically involved in visual exploration behaviour, and damage to this area may lead to neglect of the left hemispace. We investigated whether neglect-like visual exploration behaviour could be induced in healthy subjects using theta burst repetitive transcranial magnetic stimulation (rTMS). To this end, one continuous train of theta burst rTMS was applied over the right PPC in 12 healthy subjects prior to a visual exploration task where colour photographs of real-life scenes were presented on a computer screen. In a control experiment, stimulation was also applied over the vertex. Eye movements were measured, and the distribution of visual fixations in the left and right halves of the screen was analysed. In comparison to the performance of 28 control subjects without stimulation, theta burst rTMS over the right PPC, but not the vertex, significantly decreased cumulative fixation duration in the left screen-half and significantly increased cumulative fixation duration in the right screen-half for a time period of 30 min. These results suggest that theta burst rTMS is a reliable method of inducing transient neglect-like visual exploration behaviour.     

Visual enhancing of tactile perception in the posterior parietal cortex

The visual modality typically dominates over our other senses. Here we show that after inducing an extreme conflict in the left hand between vision of touch (present) and the feeling of touch (absent), sensitivity to touch increases for several minutes after the conflict. Transcranial magnetic stimulation of the posterior parietal cortex after this conflict not only eliminated the enduring visual enhancement of touch, but also impaired normal tactile perception. This latter finding demonstrates a direct role of the parietal lobe in modulating tactile perception as a result of the conflict between these senses. These results provide evidence for visual-to-tactile perceptual modulation and demonstrate effects of illusory vision of touch on touch perception through a long-lasting modulatory process in the posterior parietal cortex.     

Maintenance of visual stability in the human posterior parietal cortex

Visual stability refers to our stable visuospatial perceptions despite the unstable visual input caused by saccades. Functional neuroimaging results, studies on patients with posterior parietal cortex (PPC) lesions, and single-unit recordings in the lateral intraparietal sulcus of primates indirectly suggest that the PPC might be a potential locus of visual stability through its involvement with spatial remapping. Here we directly explored the role of the PPC in visual stability by applying transcranial magnetic stimulation (TMS) while participants performed a perisaccadic displacement detection task. We show that TMS over the PPC but not a frontal control site alters sensitivity to displacement detection when administered just before contralateral saccades and that a general impairment in attention or in the perception of apparent motion cannot account for the decreased sensitivity. The specific relationship between the timing of TMS and saccade direction demonstrates that saccadic suppression of displacement (SSD) is likely a consequence of noisy contralateral spatial representations in the PPC around the time of a saccade. The same mechanism may keep the unstable visual world in the temporal proximity of saccades from reaching our consciousness.