Visual illusion susceptibility in autism: A neural model.

While atypical sensory perception is reported among individuals with autism spectrum disorder (ASD), the underlying neural mechanisms of autism that give rise to disruptions in sensory perception remain unclear. We developed a neural model with key physiological, functional and neuroanatomical parameters to investigate mechanisms underlying the range of representations of visual illusions related to orientation perception in typically developed subjects compared to individuals with ASD. Our results showed that two theorized autistic traits, excitation/inhibition imbalance and weakening of top-down modulation, could be potential candidates for reduced susceptibility to some visual illusions. Parametric correlation between cortical suppression, balance of excitation/inhibition, feedback from higher visual areas on one hand and susceptibility to a class of visual illusions related to orientation perception on the other hand provide the opportunity to investigate the contribution and complex interactions of distinct sensory processing mechanisms in ASD. The novel approach used in this study can be used to link behavioural, functional and neuropathological studies; estimate and predict perceptual and cognitive heterogeneity in ASD; and form a basis for the development of novel diagnostics and therapeutics.

Effect of visual cues on the resolution of perceptual ambiguity in Parkinson's disease and normal aging.

Parkinson's disease (PD) and normal aging have been associated with changes in visual perception, including reliance on external cues to guide behavior. This raises the question of the extent to which these groups use visual cues when disambiguating information. Twenty-seven individuals with PD, 23 normal control adults (NC), and 20 younger adults (YA) were presented a Necker cube in which one face was highlighted by thickening the lines defining the face. The hypothesis was that the visual cues would help PD and NC to exert better control over bistable perception. There were three conditions, including passive viewing and two volitional-control conditions (hold one percept in front; and switch: speed up the alternation between the two). In the Hold condition, the cue was either consistent or inconsistent with task instructions. Mean dominance durations (time spent on each percept) under passive viewing were comparable in PD and NC, and shorter in YA. PD and YA increased dominance durations in the Hold cue-consistent condition relative to NC, meaning that appropriate cues helped PD but not NC hold one perceptual interpretation. By contrast, in the Switch condition, NC and YA decreased dominance durations relative to PD, meaning that the use of cues helped NC but not PD in expediting the switch between percepts. Provision of low-level cues has effects on volitional control in PD that are different from in normal aging, and only under task-specific conditions does the use of such cues facilitate the resolution of perceptual ambiguity.

Perceived temporal asynchrony between sinusoidally modulated luminance and depth.

Simultaneously presented visual events lead to temporally asynchronous percepts. This has led some researchers to conclude that the asynchronous experience is a manifestation of differences in neural processing time for different visual attributes. Others, however, have suggested that the asynchronous experience is due to differences in temporal markers for changes of different visual attributes. Here, two sets of bars were presented, one to each eye. Either the bars were moving or their luminance was gradually changing. Bars moved horizontally in counterphase at low frequencies along short trajectories and were presented stereoscopically, such that the horizontal movements were perceived as back-and-forth motion on a sagittal plane, or monocularly to a dominant eye, preserving a perception of the horizontal movements on a frontal plane. In a control condition, bars were stationary and their luminance was modulated. The changes in stimulus speed or luminance occurred sinusoidally. When asked to adjust the phase of one stimulus to the other to achieve synchronous perception, participants showed a constant phase offset at the lowest frequencies used. Given the absence of abrupt transitions and the presence of similar gradual turning points in our stimuli to control for attentional effects, it can be concluded that asynchronous percepts in multimodal stimuli may at least in part be a manifestation of difference in neural processing time of visual attributes rather than solely a difference in the temporal markers (transitions versus turning points).

Hypovolemic shock following induced abortion and spontaneous heterotopic pregnancy.

Spontaneous heterotopic pregnancy is a rare clinical condition in which intrauterine and extrauterine pregnancies occur at the same time. It is rare, estimated to occur in 1 in 30,000 pregnancies. The case was a 38-year-old woman with spontaneously conceived heterotopic pregnancy. She was admitted to our center with hypovolemic shock. Focused assessment sonography for trauma examination in emergency department showed large amount of free fluid in peritoneal cavity. She was managed surgical laparotomy. Considering spontaneous pregnancies, physician should be aware of the possibility of heterotopic pregnancy in all reproductive age women, especially those with history of recent abortion. It can occur without any predisposing risk factors. Patients should be informed about possible side effects of nonprescription medicines, and also the health care centers must be safe peaceful environment for them without severe legal consequences.

Object-centered reference frames in depth as revealed by induced motion.

An object-centric reference frame is a spatial representation in which objects or their parts are coded relative to others. The existence of object-centric representations is supported by the phenomenon of induced motion, in which the motion of an inducer frame in a particular direction induces motion in the opposite direction in a target dot. We report on an experiment made with an induced motion display where a degree of slant is imparted to the inducer frame using either perspective or binocular disparity depth cues. Critically, the inducer frame oscillates perpendicularly to the line of sight, rather than moving in depth. Participants matched the perceived induced motion of the target dot in depth using a 3D rotatable rod. Although the frame did not move in depth, we found that subjects perceived the dot as moving in depth, either along the slanted frame or against it, when depth was given by perspective and disparity, respectively. The presence of induced motion is thus not only due to the competition among populations of planar motion filters, but rather incorporates 3D scene constraints. We also discuss this finding in the context of the uncertainty related to various depth cues, and to the locality of representation of reference frames.

A neural modeling approach to study mechanisms underlying the heterogeneity of visual spatial frequency sensitivity in schizophrenia.

Patients with schizophrenia exhibit abnormalities in spatial frequency sensitivity, and it is believed that these abnormalities indicate more widespread dysfunction and dysregulation of bottom-up processing. The early visual system, including the first-order Lateral Geniculate Nucleus of the thalamus (LGN) and the primary visual cortex (V1), are key contributors to spatial frequency sensitivity. Medicated and unmedicated patients with schizophrenia exhibit contrasting changes in spatial frequency sensitivity, thus making it a useful probe for examining potential effects of the disorder and antipsychotic medications in neural processing. We constructed a parameterized, rate-based neural model of on-center/off-surround neurons in the early visual system to investigate the impacts of changes to the excitatory and inhibitory receptive field subfields. By incorporating changes in both the excitatory and inhibitory subfields that are associated with pathophysiological findings in schizophrenia, the model successfully replicated perceptual data from behavioral/functional studies involving medicated and unmedicated patients. Among several plausible mechanisms, our results highlight the dampening of excitation and/or increase in the spread and strength of the inhibitory subfield in medicated patients and the contrasting decreased spread and strength of inhibition in unmedicated patients. Given that the model was successful at replicating results from perceptual data under a variety of conditions, these elements of the receptive field may be useful markers for the imbalances seen in patients with schizophrenia.

Multiscale sampling model for motion integration.

Biologically plausible strategies for visual scene integration across spatial and temporal domains continues to be a challenging topic. The fundamental question we address is whether classical problems in motion integration, such as the aperture problem, can be solved in a model that samples the visual scene at multiple spatial and temporal scales in parallel. We hypothesize that fast interareal connections that allow feedback of information between cortical layers are the key processes that disambiguate motion direction. We developed a neural model showing how the aperture problem can be solved using different spatial sampling scales between LGN, V1 layer 4, V1 layer 6, and area MT. Our results suggest that multiscale sampling, rather than feedback explicitly, is the key process that gives rise to end-stopped cells in V1 and enables area MT to solve the aperture problem without the need for calculating intersecting constraints or crafting intricate patterns of spatiotemporal receptive fields. Furthermore, the model explains why end-stopped cells no longer emerge in the absence of V1 layer 6 activity (Bolz & Gilbert, 1986), why V1 layer 4 cells are significantly more end-stopped than V1 layer 6 cells (Pack, Livingstone, Duffy, & Born, 2003), and how it is possible to have a solution to the aperture problem in area MT with no solution in V1 in the presence of driving feedback. In summary, while much research in the field focuses on how a laminar architecture can give rise to complicated spatiotemporal receptive fields to solve problems in the motion domain, we show that one can reframe motion integration as an emergent property of multiscale sampling achieved concurrently within lamina and across multiple visual areas.

Modeling a space-variant cortical representation for apparent motion.

Receptive field sizes of neurons in early primate visual areas increase with eccentricity, as does temporal processing speed. The fovea is evidently specialized for slow, fine movements while the periphery is suited for fast, coarse movements. In either the fovea or periphery discrete flashes can produce motion percepts. Grossberg and Rudd (1989) used traveling Gaussian activity profiles to model long-range apparent motion percepts. We propose a neural model constrained by physiological data to explain how signals from retinal ganglion cells to V1 affect the perception of motion as a function of eccentricity. Our model incorporates cortical magnification, receptive field overlap and scatter, and spatial and temporal response characteristics of retinal ganglion cells for cortical processing of motion. Consistent with the finding of Baker and Braddick (1985), in our model the maximum flash distance that is perceived as an apparent motion (Dmax) increases linearly as a function of eccentricity. Baker and Braddick (1985) made qualitative predictions about the functional significance of both stimulus and visual system parameters that constrain motion perception, such as an increase in the range of detectable motions as a function of eccentricity and the likely role of higher visual processes in determining Dmax. We generate corresponding quantitative predictions for those functional dependencies for individual aspects of motion processing. Simulation results indicate that the early visual pathway can explain the qualitative linear increase of Dmax data without reliance on extrastriate areas, but that those higher visual areas may serve as a modulatory influence on the exact Dmax increase.

A neural model of modified excitation/inhibition and feedback levels in schizophrenia.

Introduction: The strength of certain visual illusions, including contrast-contrast and apparent motion, is weakened in individuals with schizophrenia. Such phenomena have been interpreted as the impaired integration of inhibitory and excitatory neural responses, and impaired top-down feedback mechanisms. Methods: To investigate whether and how these factors influence the perceived contrast-contrast and apparent motion illusions in individuals with schizophrenia, we propose a two-layer network, with top-down feedback from layer 2 to layer 1 that can model visual receptive fields (RFs) and their inhibitory and excitatory subfields. Results: Our neural model suggests that illusion perception changes in individuals with schizophrenia can be influenced by altered top-down mechanisms and the organization of the on-center off-surround receptive fields. Alteration of the RF inhibitory surround and/or the excitatory center can replicate the difference of illusion precepts between individuals with schizophrenia within certain clinical states and normal controls. The results show that the simulated top-down feedback modulation enlarges the difference of the model illusion representations, replicating the difference between the two groups. Discussion: We propose that the heterogeneity of visual and in general sensory processing in certain clinical states of schizophrenia can be largely explained by the degree of top-down feedback reduction, emphasizing the critical role of top-down feedback in illusion perception, and to a lesser extent on the imbalance of excitation/inhibition. Our neural model provides a mechanistic explanation for the modulated visual percepts of contrast-contrast and apparent motion in schizophrenia with findings that can explain a broad range of visual perceptual observations in previous studies. The two-layer motif of the current model provides a general framework that can be tailored to investigate subcortico-cortical (such as thalamocortical) and cortico-cortical networks, bridging neurobiological changes in schizophrenia and perceptual processing.

A neural modeling approach to study mechanisms underlying the heterogeneity of visual spatial frequency sensitivity in schizophrenia.

Patients with schizophrenia exhibit abnormalities in spatial frequency sensitivity, and it is believed that these abnormalities indicate more widespread dysfunction and dysregulation of bottom-up processing. The early visual system, including the first-order Lateral Geniculate Nucleus of the thalamus (LGN) and the primary visual cortex (V1), are key contributors to spatial frequency sensitivity. Medicated and unmedicated patients with schizophrenia exhibit contrasting changes in spatial frequency sensitivity, thus making it a useful probe for examining potential effects of the disorder and antipsychotic medications in neural processing. We constructed a parameterized, rate-based neural model of on-center/off-surround neurons in the early visual system to investigate the impacts of changes to the excitatory and inhibitory receptive field subfields. By incorporating changes in both the excitatory and inhibitory subfields that are associated with pathophysiological findings in schizophrenia, the model successfully replicated perceptual data from behavioral/functional studies involving medicated and unmedicated patients. Among several plausible mechanisms, our results highlight the dampening of excitation and/or increase in the spread and strength of the inhibitory subfield in medicated patients and the contrasting decreased spread and strength of inhibition in unmedicated patients. Given that the model was successful at replicating results from perceptual data under a variety of conditions, these elements of the receptive field may be useful markers for the imbalances seen in patients with schizophrenia.

Sleep spindles in primates: Modeling the effects of distinct laminar thalamocortical connectivity in core, matrix, and reticular thalamic circuits.

Sleep spindles are associated with the beginning of deep sleep and memory consolidation and are disrupted in schizophrenia and autism. In primates, distinct core and matrix thalamocortical (TC) circuits regulate sleep spindle activity through communications that are filtered by the inhibitory thalamic reticular nucleus (TRN); however, little is known about typical TC network interactions and the mechanisms that are disrupted in brain disorders. We developed a primate-specific, circuit-based TC computational model with distinct core and matrix loops that can simulate sleep spindles. We implemented novel multilevel cortical and thalamic mixing, and included local thalamic inhibitory interneurons, and direct layer 5 projections of variable density to TRN and thalamus to investigate the functional consequences of different ratios of core and matrix node connectivity contribution to spindle dynamics. Our simulations showed that spindle power in primates can be modulated based on the level of cortical feedback, thalamic inhibition, and engagement of model core versus matrix, with the latter having a greater role in spindle dynamics. The study of the distinct spatial and temporal dynamics of core-, matrix-, and mix-generated sleep spindles establishes a framework to study disruption of TC circuit balance underlying deficits in sleep and attentional gating seen in autism and schizophrenia.

A neural model of modified excitation/inhibition and feedback levels in schizophrenia.

The strength of certain visual illusions is weakened in individuals with schizophrenia. Such phenomena have been interpreted as the impaired integration of inhibitory and excitatory neural responses, and impaired top-down feedback mechanisms. To investigate whether and how these factors influence the perceived illusions in individuals with schizophrenia, we propose a two-layer network that can model visual receptive fields (RFs), their inhibitory and excitatory subfields, and the top-down feedback. Our neural model suggests that illusion perception changes in individuals with schizophrenia can be influenced by altered top-down mechanisms and the organization of the on-center off-surround receptive fields. Alteration of the RF inhibitory surround and/or the excitatory center can replicate the difference of illusion precepts between individuals with schizophrenia and normal controls. The results show that the simulated top-down feedback modulation enlarges the difference of the model illusion representations, replicating the difference between the two groups. We propose that the heterogeneity of visual and in general sensory processing in schizophrenia can be largely explained by the degree of top-down feedback reduction, emphasizing the critical role of top-down feedback in illusion perception, and to a lesser extent on the imbalance of excitation/inhibition. Our neural model provides a mechanistic explanation for the modulated visual percepts in schizophrenia with findings that can explain a broad range of visual perceptual observations in previous studies. The two-layer motif of the current model provides a general framework that can be tailored to investigate subcortico-cortical (such as thalamocortical) and cortico-cortical networks, bridging neurobiological changes in schizophrenia and perceptual processing.

Perception of rigidity in three- and four-dimensional spaces.

Our brain employs mechanisms to adapt to changing visual conditions. In addition to natural changes in our physiology and those in the environment, our brain is also capable of adapting to "unnatural" changes, such as inverted visual-inputs generated by inverting prisms. In this study, we examined the brain's capability to adapt to hyperspaces. We generated four spatial-dimensional stimuli in virtual reality and tested the ability to distinguish between rigid and non-rigid motion. We found that observers are able to differentiate rigid and non-rigid motion of hypercubes (4D) with a performance comparable to that obtained using cubes (3D). Moreover, observers' performance improved when they were provided with more immersive 3D experience but remained robust against increasing shape variations. At this juncture, we characterize our findings as "3 1/2 D perception" since, while we show the ability to extract and use 4D information, we do not have yet evidence of a complete phenomenal 4D experience.

Dynamic coding of border-ownership in visual cortex.

Humans are capable of rapidly determining whether regions in a visual scene appear as figures in the foreground or as background, yet how figure-ground segregation occurs in the primate visual system is unknown. Figures in the environment are perceived to own their borders, and recent neurophysiology has demonstrated that certain cells in primate visual area V2 have border-ownership selectivity. We present a dynamic model based on physiological data that indicates areas V1, V2, and V4 act as an interareal network to determine border-ownership. Our model predicts that competition between curvature- sensitive cells in V4 that have on-surround receptive fields of different sizes can determine likely figure locations and rapidly propagate the information interareally to V2 border-ownership cells that receive contrast information from V1. In the model border-ownership is an emergent property produced by the dynamic interactions between V1, V2, and V4, one which could not be determined by any single cortical area alone.

Impact of optogenetic pulse design on CA3 learning and replay: A neural model.

Optogenetic manipulation of hippocampal circuitry is an important tool for investigating learning in vivo. Numerous approaches to pulse design have been employed to elicit desirable circuit and behavioral outcomes. Here, we systematically test the outcome of different single-pulse waveforms in a rate-based model of hippocampal memory function at the level of mnemonic replay extension and de novo synaptic weight formation in CA3 and CA1. Lower-power waveforms with long forward or forward and backward ramps yield more natural sequence replay dynamics and induce synaptic plasticity that allows for more natural memory replay timing, in contrast to square or backward ramps. These differences between waveform shape and amplitude are preserved with the addition of noise in membrane potential, light scattering, and protein expression, improving the potential validity of predictions for in vivo work. These results inform future optogenetic experimental design choices in the field of learning and memory.

The effect of contrast intensity and polarity in the achromatic watercolor effect.

The watercolor effect (WCE) is a filling-in phenomenon in a region demarcated by two thin abutting lines. The perceived chromaticity of the region is similar to that of the interior line. We develop a series of achromatic WCE stimuli to induce lightness changes analogous to the induced chromaticity in the chromatic version of the WCE. We use a variation of the paired-comparison paradigm to quantify the induced lightness of the filled-in regions to regions with real luminance variations. The luminance of the inner line is fixed, while the luminance of the outer line varies across stimuli. Data from seven subjects (five naive) confirm that an achromatic WCE exists. Moreover, outer lines with both high and low luminances can generate a WCE with an inner line of a moderate luminance. All subjects show a single peak of the effect strength for both polarity conditions, which is never at the extreme luminance levels. Most subjects show an inverted U curve for effect strength as a function of the contrast of the outer lines against the background. Results suggest that the contrast difference between the outer line and the inner line affects the existence and the strength of the achromatic WCE in a nonlinear way.

Speed, more than depth, determines the strength of induced motion.

Motion of an inducer in a given direction can cause illusory motion in the opposite direction in a neighboring target object, a phenomenon called induced motion. Induced motion may be due to inducer-target interactions that are local in visual space. Accordingly, increasing the depth between inducer and target should weaken induced motion. Alternatively, separation in depth may not determine whether one object can affect the motion of another. Either viewpoint is supported by separate studies. We show that this contradiction is due to a methodological artifact related to target velocity. Our results support the suggestion that induced motion is not affected by depth separation. Participants rated the effect of an inducer on a target dot presented at different disparities. When target velocity varied with depth, induced motion decreased with depth separation. When target velocity was constant across depth, induced motion was also constant across depth. Thus, target velocity, more than depth, influence motion induction.

End stopping in V1 is sensitive to contrast.

Common situations that result in different perceptions of grouping and border ownership, such as shadows and occlusion, have distinct sign-of-contrast relationships at their edge-crossing junctions. Here we report a property of end stopping in V1 that distinguishes among different sign-of-contrast situations, thereby obviating the need for explicit junction detectors. We show that the inhibitory effect of the end zones in end-stopped cells is highly selective for the relative sign of contrast between the central activating stimulus and stimuli presented at the end zones. Conversely, the facilitatory effect of end zones in length-summing cells is not selective for the relative sign of contrast between the central activating stimulus and stimuli presented at the end zones. This finding indicates that end stopping belongs in the category of cortical computations that are selective for sign of contrast, such as direction selectivity and disparity selectivity, but length summation does not.

Lightness induction enhancements and limitations at low frequency modulations across a variety of stimulus contexts.

Lightness illusions are often studied under static viewing conditions with figures varying in geometric design, containing different types of perceptual grouping and figure-ground cues. A few studies have explored the perception of lightness induction while modulating lightness illusions continuously in time, where changes in perceived lightness are often linked to the temporal modulation frequency, up to around 2-4 Hz. These findings support the concept of a cut-off frequency for lightness induction. However, another critical change (enhancement) in the magnitude of perceived lightness during slower temporal modulation conditions has not been addressed in previous temporal modulation studies. Moreover, it remains unclear whether this critical change applies to a variety of lightness illusion stimuli, and the degree to which different stimulus configurations can demonstrate enhanced lightness induction in low modulation frequencies. Therefore, we measured lightness induction strength by having participants cancel out any perceived modulation in lightness detected over time within a central target region, while the surrounding context, which ultimately drives the lightness illusion, was viewed in a static state or modulated continuously in time over a low frequency range (0.25-2 Hz). In general, lightness induction decreased as temporal modulation frequency was increased, with the strongest perceived lightness induction occurring at lower modulation frequencies for visual illusions with strong grouping and figure-ground cues. When compared to static viewing conditions, we found that slow continuous surround modulation induces a strong and significant increase in perceived lightness for multiple types of lightness induction stimuli. Stimuli with perceptually ambiguous grouping and figure-ground cues showed weaker effects of slow modulation lightness enhancement. Our results demonstrate that, in addition to the existence of a cut-off frequency, an additional critical temporal modulation frequency of lightness induction exists (0.25-0.5 Hz), which instead maximally enhances lightness induction and seems to be contingent upon the prevalence of figure-ground and grouping organization.

Perception, Cognition, and Action in Hyperspaces: Implications on Brain Plasticity, Learning, and Cognition.

We live in a three-dimensional (3D) spatial world; however, our retinas receive a pair of 2D projections of the 3D environment. By using multiple cues, such as disparity, motion parallax, perspective, our brains can construct 3D representations of the world from the 2D projections on our retinas. These 3D representations underlie our 3D perceptions of the world and are mapped into our motor systems to generate accurate sensorimotor behaviors. Three-dimensional perceptual and sensorimotor capabilities emerge during development: the physiology of the growing baby changes hence necessitating an ongoing re-adaptation of the mapping between 3D sensory representations and the motor coordinates. This adaptation continues in adulthood and is quite general to successfully deal with joint-space changes (longer arms due to growth), skull and eye size changes (and still being able of accurate eye movements), etc. A fundamental question is whether our brains are inherently limited to 3D representations of the environment because we are living in a 3D world, or alternatively, our brains may have the inherent capability and plasticity of representing arbitrary dimensions; however, 3D representations emerge from the fact that our development and learning take place in a 3D world. Here, we review research related to inherent capabilities and limitations of brain plasticity in terms of its spatial representations and discuss whether with appropriate training, humans can build perceptual and sensorimotor representations of spatial 4D environments, and how the presence or lack of ability of a solid and direct 4D representation can reveal underlying neural representations of space.