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Biomedical subjects

Arash Sahraie

Publications and source records attributed to Arash Sahraie.

12 recordsLinked to original sources

Increased sensitivity after repeated stimulation of residual spatial channels in blindsight.

Lesions of the occipital cortex result in areas of cortical blindness affecting the corresponding regions of the patient's visual field. The traditional view is that, aside from some spontaneous recovery in the first few months after the damage, when acute effects have subsided the areas of blindness are absolute and permanent. It has been found, however, that within such field defects some residual visual capacities may persist in the absence of acknowledged awareness by the subject (blindsight type 1) or impaired awareness (type 2). Neuronal pathways mediating blindsight have a specific and narrow spatial and temporal bandwidth. A group of cortically blind patients (n = 12) carried out a daily detection "training" task over a 3-month period, discriminating grating visual stimuli optimally configured for blindsight from homogeneous luminance-matched stimuli. No feedback was given during the training. Assessment of training was by psychophysical measurements carried out before and after training and included detection of a range of spatial frequencies (0.5-7 cycles per degree), contrast detection at 1 cycle per degree, clinical perimetry, and subjective estimates of visual field defect. The results show that repeated stimulation by appropriate visual stimuli can result in improvements in visual sensitivities in the very depths of the field defect.

Adult↗

Can blindsight be superior to 'sighted-sight'?

DB, the first blindsight case to be tested extensively (Weiskrantz, 1986) has demonstrated the ability to detect and discriminate a range of visual stimuli presented within his perimetrically blind visual field defect. In a temporal two alternative forced choice (2AFC) detection experiment we have investigated the limits of DB's detection ability within his field defect. Blind field performance was compared to his sighted field performance and to an age-matched control group (n=6). DB reliably detected the presence of a small (2 degrees ), low contrast (7%), 4.6c/ degrees Gabor patch with the same space-averaged luminance as the background presented within his blind field but performed at chance levels at the same eccentricity (11.3 degrees ) within his sighted field. Investigation of detection as a function of stimulus contrast revealed DB's ability to detect the presence of an 8% contrast stimulus within his blind field, compared to 12% in his sighted field. No significant difference in detection performance between DB's sighted field and the performance of six age-matched control participants suggests poor sighted field performance does not account for the results. Monocular testing also rules out differences between the eyes as an explanation, suggesting that DB demonstrates superior detection for certain stimuli within his visual field defect compared to normal vision.

Choice Behavior↗

ERPs predict the appearance of visual stimuli in a temporal selection task.

In contrast to the visual spatial domain, the effect of attention on sensory processing and stimulus appearance in temporal selection tasks is still controversial. Using a rapid serial visual presentation (RSVP) procedure, we examined whether the stimulus onset asynchrony (SOA) between a color cue and a motion target affects the appearance of the latter. Event-related brain potentials (ERPs) recorded simultaneously allowed us to test whether a change in the targets' appearance is associated with a modulation of the sensory ERP components. In the experimental condition 'SOA', the temporal interval between the cue and the target was varied between 0 and 300 ms. In a control condition, the physical appearance of the motion target was varied (level of coherence: 25-100%) while holding the cue-target SOA constant (300 ms). In trials when the participant detected the target motion, his/her task was to report the strength of the perceived motion on a 5-point scale. In both conditions, the mean rating of the target's appearance increased monotonically with increasing SOA and the level of coherence, respectively. The psychophysical ratings were associated with an increase of a negative deflection about 200 ms (N200) related to the sensory processing of visual motion. The physical variation of motion coherence and the variation of the cue-target SOA affected the N200 response in similar fashion. These results indicate that sensory processing is also modulated by attentional resources in temporal selection tasks which - in turn - affect the appearance of the relevant target stimulus.

Adult↗

The effect of perceptual load on attention-induced motion blindness: the efficiency of selective inhibition.

Recent visual marking studies have shown that the carry-over of distractor inhibition can impair the ability of singletons to capture attention if the singleton and distractors share features. The current study extends this finding to first-order motion targets and distractors, clearly separated in time by a visual cue (the letter X). Target motion discrimination was significantly impaired, a result attributed to the carry-over of distractor inhibition. Increasing the difficulty of cue detection increased the motion target impairment, as distractor inhibition is thought to increase under demanding (high load) conditions in order to maximize selection efficiency. The apparent conflict with studies reporting reduced distractor inhibition under high load conditions was resolved by distinguishing between the effects of "cognitive" and "perceptual" load.

Adolescent↗

Awareness of faces is modulated by their emotional meaning.

A central question in perception is how stimuli are selected for access to awareness. This study investigated the impact of emotional meaning on detection of faces using the attention blink paradigm. Experiment 1 showed that fearful faces were detected more frequently than neutral faces, and Experiment 2 revealed preferential detection of fearful faces compared with happy faces. To rule out image artifacts as a cause for these results, Experiment 3 manipulated the emotional meaning of neutral faces through fear conditioning and showed a selective increase in detection of conditioned faces. These results extend previous reports of preferential detection of emotional words or schematic objects and suggest that fear conditioning can modulate detection of formerly neutral stimuli.

Adult↗

Specifying the distractor inhibition account of attention-induced motion blindness.

There is growing evidence that motion perception is modulated by visual selective attention. In the 'attention-induced motion blindness' paradigm the detection of coherent motion in a random dot kinematogram (RDK) is impaired in a rapid serial presentation task [Sahraie, A., Milders, M., & Niedeggen, M. (2001). Attention induced motion blindness. Vision Research, 41, 1613-1617]. The effect depends on irrelevant motion episodes (distractors) prior to the target. In this study, we show that both the number and timing of distractors affect detection performance, allowing for implications on the build-up and release of inhibition. Furthermore, we rule out the possibility that subjects falsely classify targets as distractors due to uncertainty of temporal order.

Adult↗

Central inhibition ability modulates attention-induced motion blindness.

Impaired motion perception can be induced in normal observers in a rapid serial visual presentation task. Essential for this effect is the presence of motion distractors prior to the motion target, and we proposed that this attention-induced motion blindness results from high-level inhibition produced by the distractors. To investigate this, we compared the extent of the attention-induced motion blindness effect with performance on central inhibition tasks: Stroop colour naming and negative priming. A negative correlation between Stroop interference and motion performance reflected that low Stroop scores, indicative of strong inhibition ability, was associated with more severe impairments in motion perception. This association could not be explained by individual differences in fluid intelligence, task switching or response speed. Negative priming was not specifically associated with attention-induced motion blindness. The results confirm that attention can modulate motion perception and suggest that the processes involved may be shared with high-level cognitive abilities.

Adult↗

Probing the prerequisites for motion blindness.

Neurobiological studies of visual awareness usually focus on the neural events elicited by perceived or nonperceived stimuli but neglect the preexisting conditions that allow (or prevent) conscious perception. We have examined the conditions that lead to temporary motion blindness in a rapid serial visual presentation paradigm, in which subjects have to detect coherent motion in the peripheral stream after a cue (a red fixation point) in the central stream. The failure of awareness depends critically on the occurrence of similar coherent motion events (probes) before the cue. Event-related brain potentials (ERPs) were recorded to track the processing of motion distractors, which determine the prerequisites for this transient deficit. Analysis of motion-evoked responses revealed that there is no progressive reduction in sensitivity in early visual processing. There is, however, a progressive increase in amplitude of a negative wave over the frontal cortex at approximately 250 msec after motion onset and a corresponding reduction of a centro-parietal positivity at approximately 350 msec with an increasing number of distractors. We propose that these nonsensory ERP components reflect a postperceptual frontal gating mechanism that controls the access of visual stimuli to higher order evaluation and conscious detection.

Adult↗

Spatial and temporal processing in a subject with cortical blindness following occipital surgery.

Blindsight subjects are typically better at discriminating rapid, transient visual events than those with gradual on/off-sets. Surprisingly, the detailed investigation of temporal characteristics of mechanisms mediating blindsight is only reported in one subject (GY). It is of interest to establish whether these characteristics are similar to those in other cases of blindsight. Here, we report on a systematic study of spatio-temporal properties of mechanisms mediating blindsight in a subject VN. VN has a lower right quadranopia following surgical removal of the left occipital cortex above the calcarine sulcus, therefore, there are no remaining islands of intact visual cortex within this area. Similar to GY, the blindsight mechanisms in VN have narrowly tuned band-pass temporal characteristics with a peak sensitivity at 20Hz and above chance performance at temporal frequencies >/=10 and </=33Hz. The spatial channel in VN has low-pass characteristics with an upper cut-off <3.5c/ degrees. There is extensive spatial summation in the blindfield whereas no temporal summation was found in the time range tested (50-1600ms). In agreement with our previous reports, pupillary responses can predict the existence of residual vision within the field defect and show similar spatial characteristics to those obtained psychophysically. The spatio-temporal characteristics of blindsight in VN reported here are similar to those reported in subjects with ischaemic lesions, suggesting that such visual capacities need not necessarily be attributed to spared areas of visual cortex.

Adult↗

Spatial channels of visual processing in cortical blindness.

Blindsight is the ability of some cortically blind patients to discriminate visual events presented within their field defect. We have examined a fundamental aspect of visual processing, namely the detection of spatial structures presented within the field defect of 10 cortically blind patients. The method outlined is based on the detection of high-contrast stimuli and is effective in flagging a 'window of detection' in the spatial frequency spectrum, should it exist. Here we report on the presence of a narrowly tuned psychophysical spatial channel optimally responding to frequencies less than 4 cycles/ degrees in eight out of 10 patients tested. The two patients who did not show any evidence of blindsight appear to have intact midbrain structures, but have lesions that extend from the occipital cortex to the thalamus. In addition, we have recorded subjective reports of awareness of the visual events in each trial. Detection scores of eight blindsight patients were subsequently subdivided based on the subjective reports of awareness. It appears that the psychophysical spatial channel-mediating responses in the absence of any awareness of the visual event have a narrower frequency response than those involved when the patients report some awareness of the visual event. The findings are discussed in relation to previous reports on the incidence of blindsight and performance on tasks involving spatial processing.

Adult↗

Oculomotor control and the maintenance of spatially and temporally distributed events in visuo-spatial working memory.

Previous studies have demonstrated that working memory for spatial location can be significantly disrupted by concurrent eye or limb movement (Baddeley, 1986; Smyth, Pearson, & Pendleton, 1988). Shifts in attention alone can also interfere with spatial span (Smyth & Scholey, 1994), even with no corresponding movement of the eyes or limbs (Smyth, 1996). What is not clear from these studies is how comparable is the magnitude of effect caused by different forms of spatial disrupter. Recently, it has been demonstrated that limb movements produce as much interference with spatial span as do reflexive saccades (Lawrence, Myerson, Oonk, & Abrams, 2001). In turn this has led to the hypothesis that all spatially directed movement can produce similar effects in visuo-spatial working memory. This paper reports the results of five experiments that have contrasted the effect of concurrent eye movement, limb movement, and covert attention shifts on participants' working memory for sequences of locations. All conditions involving concurrent eye movement produced significantly greater reduction in span than equivalent limb movement or covert attention shifts with eyes fixated. It is argued that these results demonstrate a crucial role for oculomotor control processes during the rehearsal of location-specific representations in working memory.

Adult↗

Is experimental motion blindness due to sensory suppression? An ERP approach.

Recent psychophysical studies have revealed attentional modulation of visual motion perception and interest now focuses on the locus of this interaction. Using event-related brain potentials (ERPs) we examined whether transient motion blindness evoked in a dual task [Vision Res. 41 (2001) 1613-1617] is related to a selection process occurring at the stage of sensory processing or at a higher level. In our paradigm, a particular change of colour of the fixation point cued the subject to detect a brief episode of coherent random dot motion embedded in a succession of episodes of incoherent motion. Detection of the coherent motion was significantly impaired when it occurred simultaneously with the colour cue, and recovered over the subsequent 300 ms. This functional relationship was reflected in the amplitude of a sensory, motion-evoked component (N200), and in a late positive complex (P300). However, a direct comparison of ERPs produced by stimuli that were detected or missed revealed differences only in the P300 component. These results indicate that attenuation of sensory motion processing does not account for this transient, attention-induced deficit in visual motion perception.

Adult↗