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The effect of stimulus blanking on the detection of intrasaccadic displacements of translating objects.

In a display with a stationary and a translating object, subjects made a saccade towards one of the objects and had to detect intrasaccadic changes in the position of either the saccade target or the saccade flanker. Sensitivity for displacements of the stationary and moving objects was measured in conditions with (60 and 220 ms) and without blanking. In the conditions without blanking, displacement detection for translating objects was better than detection for stationary objects, which confirmed previous results (Vis. Res. 42 (2002) 379). This pattern was reversed in the blanking conditions: Sensitivity for intrasaccadic displacements of the translating object decreased drastically in comparison to conditions without a blank and was even lower than sensitivity for the stationary object. The results suggest differences in the transsaccadic spatial representation of translating and stationary objects. While a change in the spatial position of a stationary object can be detected after a blank period of 60 and 220 ms, this seems impossible for a translating object, indicating timing differences in postsaccadic spatial localization processes. Accounts in terms of a fast and accurate motion processing mechanism that possibly makes use of gain control are discussed.

Analysis of Variance↗

Fusion of competing features is not serial.

How features of an object are bound into a unique percept is one of the puzzling problems in the cognitive and neuro-sciences. In order to investigate the spatio-temporal mechanisms of feature binding, we serially present two verniers with opposite offset directions for very short durations. Only one vernier is perceived with its offset dominated by the vernier presented second. This dominance reverses if the two verniers are followed by masking gratings, i.e. the first presented vernier dominates performance. Therefore, feature fusion can neither be explained completely by spatially local mechanisms nor by the temporal order of appearance of elements.

Adult↗

Spatio-temporal dynamics of depth propagation on uniform region.

The depth of each point on a binocularly presented untextured horizontal bar is physically ambiguous except for the two vertical edges at both ends, since the correspondence between left and right images is not unique on such a uniform region. These depths, however, are unambiguously perceived, and this suggests the existence of some mechanism that interpolates the depth information from the two ends toward the center. Temporal properties of this integration process were examined by a phase-matching task, which allowed us to measure the phase of the perceived depth at the center of a horizontal bar when disparities at the ends were sinusoidally oscillated. We found that the perceived depth at the center of the bar was slightly temporally delayed for 7-60 ms relative to the physical depth at the ends. The difference increased with the length of the bar, decreased as the vertical position of the bar became farther from the fixation point, and increased in the presence of occluders. This finding indicates that depth information is propagated over an object to solve this ambiguity by using a time-consuming process. Accordingly, we suggest that depth propagation is accomplished by spatially local diffusion-like interactions of locally represented depth information.

Analysis of Variance↗

Isolation and interaction of ON and OFF pathways in human vision: contrast discrimination at pattern offset.

Pattern contrast discrimination is typically studied with simultaneous onset of the base contrast (C) and added contrast (delta C) patterns. I measured contrast discrimination functions at pattern offset. A brief (30 msec) localized, spatially narrow-band D6 test stimulus was delta C. The onset of delta C was simultaneous with the offset of a large, 500 msec cosine pattern (the base contrast C). The D6 was either positive or negative contrast, and was masked by either positive or negative contrast, i.e., a light or dark bar of the cosine pattern. Stimuli were 3 cpd. Discrimination of negative delta C at the offset of positive contrast followed a "dipper" function, as if the OFF pathway were isolated. A dipper function was also obtained for a positive delta C at the offset of negative contrast (ON pathway isolation). But same-polarity delta C and C yield a monotonic discrimination function ("bumper" function) at the offset of C, suggesting inhibitory interaction. These discrimination functions for same-and opposite-polarity delta C and C are the reverse of functions obtained at pattern onset. Manipulations of temporal asynchrony between patterns and manipulations of pattern polarity are thus functionally equivalent in determining the form of the contrast discrimination function. In a second experiment, I determined delta C at times before and after the offset of a high-contrast C and manipulated pattern polarity. The time course of threshold change is different for same vs opposite-polarity test and mask. The results suggest that interaction between ON and OFF pathways is delayed relative to the masking process within a pathway. Interaction between pathways may function to improve temporal resolution by suppressing persistence of neural response in the complementary pathway. The present pattern polarity and temporal asynchrony effects on the contrast discrimination function also decisively falsify the "uncertainty" hypothesis for low-contrast threshold facilitation (the dipper).

Contrast Sensitivity↗

Spatial interactions with real and gap-induced illusory lines in vernier acuity.

Vernier acuity for illusory line targets induced by gaps in a horizontal grating was measured in the presence of real and illusory flanks. In a 500 msec presentation forced choice task, observers judged the position of a comparison illusory line positioned 3 min arc below the target. The results show that illusory lines are capable of interacting with real lines in spatial localization. Thus, they provide psychophysical evidence for a common localization mechanism that supports real and illusory contour definitions. The results further show a sensitivity of the visual system to the contrast polarity of real lines. This sensitivity was absent for illusory lines. The present findings are discussed in terms of their relationship to physiological findings, and in terms of their potential to constrain computational models that account for illusory contour brightness.

Humans↗

Dishevelled: a mobile scaffold catalyzing development.

Wnt proteins are secreted glycoprotein ligands that regulate critical aspects of development, including cell proliferation, apoptosis, and cell fate. For those pathways downstream from the "canonical" Wnt/beta-catenin signaling, from the "non-canonical" or planar cell polarity (PCP), and from the Wnt-Ca(2+)/cyclic guanosine monophosphate (cGMP) pathway, Wnt activation of its cellular receptor, a member of the superfamily of G-protein-coupled receptor Frizzled family, requires both heterotrimeric G proteins and the phosphoprotein Dishevelled. Our understanding of the roles of Dishevelled proteins in development is evolving and most recent observations suggest that Dishevelled proteins act as scaffolds essential for Wnt signaling, providing docking sites for a diverse and interesting set of protein kinases, phosphatases, adaptor proteins, G proteins, and other scaffolds such as Axin. The protein-protein interactions of Dishevelled are dynamic, as is the spatial localization of this "toolbox" of signaling molecules involved in development. Much excitement awaits the elucidation of the complete set of tools in the toolbox and of the dynamic regulation of Dishevelled proteins and their interacting proteins.

Adaptor Proteins, Signal Transducing↗

High-frequency gamma oscillations and human brain mapping with electrocorticography.

Invasive EEG recordings with depth and/or subdural electrodes are occasionally necessary for the surgical management of patients with epilepsy refractory to medications. In addition to their vital clinical utility, electrocorticographic (ECoG) recordings provide an unprecedented opportunity to study the electrophysiological correlates of functional brain activation in greater detail than non-invasive recordings. The proximity of ECoG electrodes to the cortical sources of EEG activity enhances their spatial resolution, as well as their sensitivity and signal-to-noise ratio, particularly for high-frequency EEG activity. ECoG recordings have, therefore, been used to study the event-related dynamics of brain oscillations in a variety of frequency ranges, and in a variety of functional-neuroanatomic systems, including somatosensory and somatomotor systems, visual and auditory perceptual systems, and cortical networks responsible for language. These ECoG studies have confirmed and extended the original non-invasive observations of ERD/ERS phenomena in lower frequencies, and have discovered novel event-related responses in gamma frequencies higher than those previously observed in non-invasive recordings. In particular, broadband event-related gamma responses greater than 60 Hz, extending up to approximately 200 Hz, have been observed in a variety of functional brain systems. The observation of these "high gamma" responses requires a recording system with an adequate sampling rate and dynamic range (we use 1000 Hz at 16-bit A/D resolution) and is facilitated by event-related time-frequency analyses of the recorded signals. The functional response properties of high-gamma activity are distinct from those of ERD/ERS phenomena in lower frequencies. In particular, the timing and spatial localization of high-gamma ERS often appear to be more specific to the putative timing and localization of functional brain activation than alpha or beta ERD/ERS. These findings are consistent with the proposed role of synchronized gamma oscillations in models of neural computation, which have in turn been inspired by observations of gamma activity in animal preparations, albeit at somewhat lower frequencies. Although ECoG recordings cannot directly measure the synchronization of action potentials among assemblies of neurons, they may demonstrate event-related interactions between gamma oscillations in macroscopic local field potentials (LFP) generated by different large-scale populations of neurons engaged by the same functional task. Indeed, preliminary studies suggest that such interactions do occur in gamma frequencies, including high-gamma frequencies, at latencies consistent with the timing of task performance. The neuronal mechanisms underlying high-gamma activity and its unique response properties in humans are still largely unknown, but their investigation through invasive methods is expected to facilitate and expand their potential clinical and research applications, including functional brain mapping, brain-computer interfaces, and neurophysiological studies of human cognition.

Animals↗

The vestibulo-ocular reflex: an outdated concept?

Traditionally, the vestibulo-ocular reflex (VOR) is described as a distinct, phylogenetically old oculomotor subsystem, which serves to stabilize gaze direction. It is supposed to act as a stereotyped reflex with definite input-output relations, which can be measured by rotating a subject passively in darkness, and which are kept at an ideal level by adaptive, parametric adjustments. This paper argues that such a view is not realistic: (1) the VOR in darkness does not have an ideal, or even well defined, gain; (2) a fixed, automatic VOR is not appropriate in most behavioural situations, and would need continuous conditioning by other subsystems. As there is no compelling phylogenetic, physiological or anatomical evidence for an independent VOR subsystem, a more fruitful hypothesis may be that vestibular signals are just one of many inputs to a spatial localization process, which computes the relative position (and motion) between the subject and a target of his choice. The VOR in darkness may represent no more than a default operation, based on incomplete information, of this larger, multiple input gaze control system. Likewise, adaptation phenomena of the VOR in darkness may be merely an epiphenomenon of adaptation of gaze control with vision active.

Animals↗

Molecular mimicry in the decoding of translational stop signals.

Molecular mimicry was a concept that was revived as we understood more about the ligands that bound to the active center of the ribosome, and the characteristics of the active center itself. It has been particularly useful for the termination phase of protein synthesis, because for many years this major process seemed not only to be out of step) with the initiation and elongation phases but also there were no common features of the process between eubacteria and eukaryotes. As the facts that supported molecular mimicry emerged, it was seen that the protein factors that facilitated polypeptide chain release when the decoding of an mRNA was complete had common features with the ligands involved in the other phases. Moreover, now common features and mechanisms began to emerge between the eubacterial and eukaryotic RFs and suddenly there seemed to be remarkable synergy between the external ligands and commonality in at least some features of the mechanistic prnciples. Almost 10 years after molecular mimicry took hold as a framework concept, we can now see that this idea is probably too simple. For example, structural mimicry can be apparent if there are extensive conformational changes either in the ribosome active center or in the ligand itself or, most likely, both. Early indications are that the bacterial RF may indeed undergo extensive conformational changes from its solution structure to achieve this accommodation. Thus, as important if not more important than structural and functional mimicry among the ligands, might be their accomodation of a common single active center made up of at least three parts to carry out a complex series of reactions. One part of the ribosomal active center is committed to decoding, a second is committed to the chemistry of putting the protein together and releasing it, and a third part, perhaps residing in the subdomains, is committed to binding ligands so that they can perform their respective single or multiple functions. It might be more accurate to regard the decoding RF as the cuckoo taking over the nest that was crafted and honed through evolution by another, the tRNA. A somewhat ungainly RF, perhaps bigger in dimensions than the tRNA, is able, nevertheless, like the cuckoo, to maneuvre into the nest. Perhaps it pushes the nest a little out of shape, but is still able to use the site for its own functions of stop signal decoding and for facilitating the release of the polypeptide. The term molecular mimicry has been dominant in the literature for a period of important advances in the understanding of protein synthesis. When the first structures of the ribosome appeared, the concept survived and was seen to be valid still. Now, we are at the stage of understanding the more detailed molecular interactions between ligands and the rRNA in particular, and how subtle changes in localized spatial orientations of atoms occur within these interactions. The simplicity of the original concept of mimicry will inevitably be blurred by this more detailed analysis. Nevertheless, it has provided a significant set of principles that allowed development of experimental programs to enhance our understanding of the dynamic events at this remarkable active site at the interface between the two subunits of this fascinating cell organelle, the ribosome.

Amino Acid Sequence↗

Intrauterine growth retardation does not alter the distribution of tyrosine hydroxylase-immunoreactive neurons of A8, A9 and A10 groups in the rat: a three-dimensional reconstruction study.

The purpose of the present investigation was to evaluate possible effects of severe prenatal hypotrophy on the number and spatial distribution of tyrosine hydroxylase-immunoreactive neurons of the A8, A9 and A10 cell groups in the rat brain. Prenatal hypotrophy was induced in rat pups by ligaturing one uterine artery in pregnant rats on the 17th day of gestation. This procedure induces a severe growth retardation, which is never caught up with, even at adulthood. In both control and growth-retarded adult rats, serial coronal sections were cut through the retrorubral field, the substantia nigra, and the ventral tegmental area (A8, A9 and A10 cell groups, respectively). The number of tyrosine hydroxylase-immunoreactive neurons was determined, and their spatial localization was recorded by means of a 3-dimensional reconstruction software developed in our laboratory. Our 3-dimensional models provide a visual illustration of the heterogeneous continuum formed by the dopaminergic neurons. They illustrate the difficulty in demarcating the A8, A9 and A10 cell groups. Finally, our results show that intrauterine growth retardation did not affect either the number or the 3-dimensional organization of tyrosine hydroxylase-immunoreactive neurons in the adult rat brain.

Animals↗

Xwnt-2 (Xwnt-2b) is maternally expressed in Xenopus oocytes and embryos.

Xwnt-2 (formerly Xwnt-2b) is a member of the Xwnt-8 class of axis-inducing Wnts. Its zygotic expression is at the prosencephalic-mesencephalic border of the early tadpole brain and above the heart primordium [Mech. Dev. 63 (1997) 199]. Here, we report that Xwnt-2 has an earlier, maternal pattern of expression. It is detected in the oocyte, egg and the developing embryo. Studies of the spatial localization of maternal Xwnt-2 show transcripts in both vegetal and animal blastomeres with enrichment in the animal hemisphere. The identification of maternal Xwnt-2 raises questions about possible roles of dorsalizing Xwnts in axial patterning of the Xenopus embryo.

Animals↗

Light quenching of pyridine2 fluorescence with time-delayed pulses.

We describe the effects of time-delayed long-wavelength pulses on the intensity and anisotropy decays of pyridine2. The sample was exposed to a continuous train of 360 nm excitation pulses and time-delayed 720 nm pulses. The long-wavelength pulses, which overlapped the emission spectrum of pyridine2, resulted in a spatially localized decrease in intensity at the point of beam overlap. The time-delayed quenching pulses caused a stepwise decrease in the intensity and anisotropy decays, as seen by oscillations in the frequency-domain data. The time-resolved anisotropy was shown to decrease below zero (-0.2) following the vertically polarized quenching pulse. The extent of light quenching depended on the time delay between the excitation and quenching pulses, and can be used to measure the decay time. Light quenching and/or multipulse methods may provide a new class of experiments for fluorescence spectroscopy and imaging.

Fluorescence Polarization↗

Infrared spectroscopy: a new frontier in medicine.

As we enter the second half of the nineties, one of the major challenges for biological infrared spectroscopists is to transfer the knowledge we have gained from studies on isolated molecules to the complex world of medicine. That it is possible to meet this challenge is suggested by comparison with the development of other biophysical techniques, such as magnetic resonance spectroscopy and imaging, which have already found their place in medical research and practice. The Spectroscopy Group in Winnipeg is developing and evaluating a variety of new IR techniques for the analysis of body fluids and tissues, both in vitro and in vivo. Herein, we review these methodologies, which comprise both instrumental (imaging and spatially localized IR spectroscopy) and interpretational procedures aimed at optimizing the measurements and their conversion to biodiagnostic information.

Diagnostic Imaging↗

Can natural strain and strain rate quantify regional myocardial deformation? A study in healthy subjects.

Strain rate (SR) and strain (epsilon) have been proposed as new ultrasound (US) indices for quantifying regional wall deformation, and can be measured from color Doppler myocardial data by determining the local spatial velocity gradient. The aim of this study was to define normal regional SR/epsilon values for both radial and longitudinal myocardial deformation. SR/epsilon profiles were obtained from 40 healthy volunteers. For radial deformation, posterior left ventricular (LV) wall SR/epsilon were calculated. For longitudinal, they were determined for basal, mid- and apical segments of the 1. septum; 2. lateral, 3. posterior and 4. anterior LV walls and for the 5. right ventricular (RV) lateral wall. SR/epsilon values describing radial deformation were higher than the corresponding SR/epsilon values obtained for longitudinal deformation. Longitudinal SR/epsilon were homogeneous throughout the septum and all LV walls. This was in contrast to the normal base-apex velocity gradient. The RV segmental SR/epsilon values were higher than those obtained from the corresponding LV wall and inhomogeneous (higher in the apical segments). SR/epsilon imaging appears to be a robust technique for quantifying regional myocardial deformation.

Adult↗

Effects of random jumps on a very simple neuronal diffusion model.

The effects of taking into account in a perfect integrate and fire model of neuronal activity the spatial localization of the synapses are studied by superposing to the diffusion a simple discrete jump component. Different criteria are employed to assess the role of excitatory and inhibitory discrete contributions. Comparisons are performed with respect to the case where contributions coming from synapses more distal from the trigger zone are summed up in a continuous model. A systematic study of the output frequency and of the inter spike interval coefficient of variation (CV) is performed by means of examples as the model parameters are varied.

Models, Neurological↗

Active Brownian particles with energy depots modeling animal mobility.

In the model of active motion studied here, Brownian particles have the ability to take up energy from the environment to store it in an internal depot and to convert internal energy into kinetic energy. Considering also internal dissipation, we derive a simplified model of active biological motion. For the take-up of energy two different examples are discussed: (i) a spatially homogeneous supply of energy, and (ii) the supply of energy at spatially localized sources (food centers). The motion of the particles is described by a Langevin equation which includes an acceleration term resulting from the conversion of energy. Dependent on the energy sources, we found different forms of periodic motion (limit cycles), i.e. periodic motion between 'nest' and 'food'. An analytic approximation allows the description of the stationary motion and the calculation of critical parameters for the take-up of energy. Finally, we derive an analytic expression for the efficiency ratio of energy conversion, which considers the take-up of energy, compared to (internal and external) dissipation.

Animals↗

Steady-state visual evoked potentials reveal frontally-mediated working memory activity in humans.

Steady-state visual evoked potentials (SSVEPs) reflect power changes at the stimulus driving frequency and have been used to assess brain activity reflecting cognitive processing. Only one study has demonstrated SSVEP modulation associated with working memory (WM), and none have compared the spatial localization of SSVEP modulations during WM performance with other brain imaging methods. Here we examined WM-related activity recorded with dense-array SSVEPs, analyzed using low resolution electromagnetic tomography, and compared the results to our previous findings using functional magnetic resonance imaging (fMRI). WM was associated with increased SSVEP activity over the right dorsolateral prefrontal cortex, paralleling our previous fMRI findings. Frontal WM-related SSVEP power correlated selectively with task performance. These results demonstrate the utility of SSVEPs for studying representational aspects of cognition.

Adolescent↗

Biophysical shunt theory for neuropsychopathology. Part II: Neuronal network miswiring.

Neuronal networks have become recognized in neuroscience as the backbone of information-processing by virtue of their dynamics and their relationship to biocommunication to defined targets. Their patterns of activity and regulation derive from the final architecture of the associated neurons, each with its distinct network and working regimen. These networks are spatially localized in the brain, adhere to temporal, fixed bonds and have a definite unit specification. This article focuses primarily on the vast amount of data concerning normal neuronal networks which can produce collateral pathways to compensate for the loss of innervation of adjacent cells. It is suggested that, under abnormal conditions such mechanisms may cause 'miswiring' leading to a fundamental bypass in neuroconduction, misguided biosignal orientation, direction and distribution, and culminating in misinformation. This re-establishment of complementary neuronal networks is manifested in recognizable neuropsychopathological states.

Animals↗