Brief Flashes Of Light Research Articles

Response of the Human Circadian System to Millisecond Flashes of Light

Ocular light sensitivity is the primary mechanism by which the central circadian clock, located in the suprachiasmatic nucleus (SCN), remains synchronized with the external geophysical day. This process is dependent on both the intensity and timing of the light exposure. Little is known about the impact of the duration of light exposure on the synchronization process in humans. In vitro and behavioral data, however, indicate the circadian clock in rodents can respond to sequences of millisecond light flashes. In a cross-over design, we tested the capacity of humans (n = 7) to respond to a sequence of 60 2-msec pulses of moderately bright light (473 lux) given over an hour during the night. Compared to a control dark exposure, after which there was a 3.5±7.3 min circadian phase delay, the millisecond light flashes delayed the circadian clock by 45±13 min (p<0.01). These light flashes also concomitantly increased subjective and objective alertness while suppressing delta and sigma activity (p<0.05) in the electroencephalogram (EEG). Our data indicate that phase shifting of the human circadian clock and immediate alerting effects can be observed in response to brief flashes of light. These data are consistent with the hypothesis that the circadian system can temporally integrate extraordinarily brief light exposures.

Interactions of numerical and temporal stimulus characteristics on the control of response location by brief flashes of light

Pigeons pecked on three keys, responses to one of which could be reinforced after 3 flashes of the houselight, to a second key after 6, and to a third key after 12. The flashes were arranged according to variable-interval schedules. Response allocation among the keys was a function of the number of flashes. When flashes were omitted, transitions occurred very late. Increasing flash duration produced a leftward shift in the transitions along a number axis. Increasing reinforcement probability produced a leftward shift, and decreasing reinforcement probability produced a rightward shift. Intermixing different flash rates within sessions separated allocations: Faster flash rates shifted the functions sooner in real time, but later in terms of flash count, and conversely for slower flash rates. A model of control by fading memories of number and time was proposed.

The phase of ongoing EEG oscillations predicts visual perception

Oscillations are ubiquitous in electrical recordings of brain activity. While the amplitude of ongoing oscillatory activity is known to correlate with various aspects of perception, the influence of oscillatory phase on perception remains unknown. In particular, since phase varies on a much faster timescale than the more sluggish amplitude fluctuations, phase effects could reveal the fine-grained neural mechanisms underlying perception. We presented brief flashes of light at the individual luminance threshold while EEG was recorded. Although the stimulus on each trial was identical, subjects detected approximately half of the flashes (hits) and entirely missed the other half (misses). Phase distributions across trials were compared between hits and misses. We found that shortly before stimulus onset, each of the two distributions exhibited significant phase concentration, but at different phase angles. This effect was strongest in the theta and alpha frequency bands. In this time-frequency range, oscillatory phase accounted for at least 16% of variability in detection performance and allowed the prediction of performance on the single-trial level. This finding indicates that the visual detection threshold fluctuates over time along with the phase of ongoing EEG activity. The results support the notion that ongoing oscillations shape our perception, possibly by providing a temporal reference frame for neural codes that rely on precise spike timing.

Retinal Ganglion Cell Adaptation to Small Luminance Fluctuations

To accommodate the wide input range over which the visual system operates within the narrow output range of spiking neurons, the retina adjusts its sensitivity to the mean light level so that retinal ganglion cells can faithfully signal contrast, or relative deviations from the mean luminance. Given the large operating range of the visual system, the majority of work on luminance adaptation has involved logarithmic changes in light level. We report that luminance gain controls are recruited for remarkably small fluctuations in luminance as well. Using spike recordings from the rat optic tract, we show that ganglion cell responses to a brief flash of light are modulated in amplitude by local background fluctuations as little as 15% contrast. The time scale of the gain control is rapid (<125 ms), at least for on cells. The retinal locus of adaptation precedes the ganglion cell spike generator because response gain changes of on cells were uncorrelated with firing rate. The mechanism seems to reside within the inner retinal network and not in the photoreceptors, because the adaptation profiles of on and off cells differed markedly. The response gain changes follow Weber's law, suggesting that network mechanisms of luminance adaptation described in previous work modulates retinal ganglion cell sensitivity, not just when we move between different lighting environments, but also as our eyes scan a visual scene. Finally, we show that response amplitude is uniformly reduced for flashes on a modulated background that has spatial contrast, indicating that another gain control that integrates luminance signals nonlinearly over space operates within the receptive field center of rat ganglion cells.

The Phase of Ongoing EEG Oscillations Predicts Visual Perception

Oscillations are ubiquitous in electrical recordings of brain activity. While the amplitude of ongoing oscillatory activity is known to correlate with various aspects of perception, the influence of oscillatory phase on perception remains unknown. In particular, since phase varies on a much faster timescale than the more sluggish amplitude fluctuations, phase effects could reveal the fine-grained neural mechanisms underlying perception. We presented brief flashes of light at the individual luminance threshold while EEG was recorded. Although the stimulus on each trial was identical, subjects detected approximately half of the flashes (hits) and entirely missed the other half (misses). Phase distributions across trials were compared between hits and misses. We found that shortly before stimulus onset, each of the two distributions exhibited significant phase concentration, but at different phase angles. This effect was strongest in the theta and alpha frequency bands. In this time-frequency range, oscillatory phase accounted for at least 16% of variability in detection performance and allowed the prediction of performance on the single-trial level. This finding indicates that the visual detection threshold fluctuates over time along with the phase of ongoing EEG activity. The results support the notion that ongoing oscillations shape our perception, possibly by providing a temporal reference frame for neural codes that rely on precise spike timing.

Frequency response characteristics of isolated retinas from hatchling leatherback (Dermochelys coriacea L.) and loggerhead (Caretta caretta L.) sea turtles

Electroretinographic recordings were made from hatchling loggerhead and leatherback sea turtle eyecup preparations during presentation of sinusoidally modulated lights of different frequencies, mean intensities and colors. Cross-correlation analysis was performed to determine the extent to which the responses followed the intensity modulated light sources. For both species mean light intensity had no significant effect on the frequency modulated responses over a 1.5log unit range of intensities. Both species showed the best following to blue light and the poorest tracking to red light. Leatherback retinas did not follow frequencies above 10Hz, while loggerhead responses extended out to 15Hz. These visual low pass filter characteristics are consistent with attributes of the visual ecology of each species, as well as with the latencies and slow rise times exhibited by these retinas to brief flashes of light.

Brief intermittent light stimulation disrupts saccadic oculomotor control

This study sought to determine the effect of very brief, single and multiple pulses of light on spatial and temporal aspects of saccadic eye movements. Twelve visually normal, young adult subjects participated in the experiments. Horizontal eye position was monitored as subjects attempted to track target step displacements in the presence of either single or multiple brief flashes of light in the visual field. Three primary findings were observed: (1) increased saccadic latency, (2) increased time for target acquisition and (3) increased initial saccadic error. The present findings suggest the influence of attentional processes and/or visual masking effects on saccadic eye movement control.

The application of the 5-choice serial reaction time task for the assessment of visual attentional processes and impulse control in rats

One popular way of measuring visual attentional processes in the rat is using 5-choice serial reaction time task (5-CSRTT). This paradigm requires subjects to detect brief flashes of light presented in a pseudorandom order in one of five spatial locations over a large number of trials. For this task, the animals are trained for approximately 30-40 daily sessions during which they gradually learn to respond in the appropriate aperture within a certain amount of time. If they fail to respond, respond in the wrong hole or at an inappropriate time, a short period of darkness (time-out) is presented as punishment and no reward is delivered. The 5-CSRTT provides the possibility to test the effects of various neural, pharmacological and behavioral manipulations on discrete and somewhat independent measures of behavioral control, including accuracy of discrimination, impulsivity, perseverative responses and response latencies.

Unconscious inference and conscious representation: Why primary visual cortex (V1) is directly involved in visual awareness

AbstractThe extent to which visual processing can proceed in the visual hierarchy without awareness determines the magnitude of perceptual delay. Increasing data demonstrate that primary visual cortex (V1) is involved in consciousness, constraining the magnitude of visual delay. This makes it possible that visual delay is actually within the optimal lengths to allow sufficient computation; thus it might be unnecessary to compensate for visual delay.The time delay problem – that perception lives slightly in the past as a result of neural conduction – has recently attracted a considerate amount of attention in the context of the flash-lag effect. The effect refers to a visual illusion wherein a brief flash of light and a continuously moving object that physically align in space and time are perceived to be displaced from one another – the flashed stimulus appears to lag behind the moving object (Krekelberg &amp; Lappe 2001). In the target article, Nijhawan compellingly argues that delay compensation could be undertaken by a predictive process in the feedforward pathways in the vision system. Before jumping into the quest for the mechanism of delay compensation, however, I would like to argue that the magnitude of delay has been overestimated, and that it might even be unnecessary to compensate for such a delay.

Phases of ongoing EEG oscillations are coupled with visual detection performance

Event Abstract Back to Event Phases of ongoing EEG oscillations are coupled with visual detection performance Niko Busch1* and R. VanRullen1 1 Centre de Recherche Cerveau & Cognition, CNRS-Université Paul Sabatier, France The current state of the cortex at the moment when information about a particular stimulus reaches it can affect how this information will be processed. In particular, neuronal oscillations which induce large variations in local electrical fields could influence certain aspects of the neuronal response. In the extreme case, a stimulus appearing at a particular phase of the ongoing oscillation would be optimally processed and detected, while at another phase it might be entirely missed. To test this possibility, we presented brief flashes of light at the individual contrast threshold while EEG was recorded. Even though the stimuli in each trial were identical, subjects detected approximately half of the flashes (hits) while they entirely missed the other half (misses). Phase distributions across trials were compared between hits and misses. We found that around stimulus onset, the two distributions each exhibited significant phase concentration, but at different phase angles. This effect was strongest in the theta and alpha frequency bands. This finding indicates that the detection threshold fluctuates over time along with the phase of ongoing EEG activity. In sum, the results support the notion that ongoing oscillations shape our perceptions, possibly by providing a temporal reference frame for neural codes that rely on precise spike timing. Conference: 10th International Conference on Cognitive Neuroscience, Bodrum, Türkiye, 1 Sep - 5 Sep, 2008. Presentation Type: Oral Presentation Topic: Brain Electrical Oscillations in Cognition Citation: Busch N and VanRullen R (2008). Phases of ongoing EEG oscillations are coupled with visual detection performance. Conference Abstract: 10th International Conference on Cognitive Neuroscience. doi: 10.3389/conf.neuro.09.2009.01.111 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 03 Dec 2008; Published Online: 03 Dec 2008. * Correspondence: Niko Busch, Centre de Recherche Cerveau & Cognition, CNRS-Université Paul Sabatier, Toulouse, France, busch@cerco.ups-tlse.fr Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Niko Busch R. VanRullen Google Niko Busch R. VanRullen Google Scholar Niko Busch R. VanRullen PubMed Niko Busch R. VanRullen Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page.

Chromophore switch from 11‐cis‐dehydroretinal (A2) to 11‐cis‐retinal (A1) decreases dark noise in salamander red rods

Dark noise, light-induced noise and responses to brief flashes of light were recorded in the membrane current of isolated rods from larval tiger salamander retina before and after bleaching most of the native visual pigment, which mainly has the 11-cis-3,4-dehydroretinal (A2) chromophore, and regenerating with the 11-cis-retinal (A1) chromophore in the same isolated rods. The purpose was to test the hypothesis that blue-shifting the pigment by switching from A2 to A1 will decrease the rate of spontaneous thermal activations and thus intrinsic light-like noise in the rod. Complete recordings were obtained in five cells (21 degrees C). Based on the wavelength of maximum absorbance, lambda max,A1 = 502 nm and lambda max,A2 = 528 nm, the average A2 : A1 ratio determined from rod spectral sensitivities and absorbances was approximately 0.74 : 0.26 in the native state and approximately 0.09 : 0.91 in the final state. In the native (A2) state, the single-quantum response (SQR) had an amplitude of 0.41 +/- 0.03 pA and an integration time of 3.16 +/- 0.15 s (mean +/- s.e.m.). The low-frequency branch of the dark noise power spectrum was consistent with discrete SQR-like events occurring at a rate of 0.238 +/- 0.026 rod(-1) s(-1). The corresponding values in the final state were 0.57 +/- 0.07 pA (SQR amplitude), 3.47 +/- 0.26 s (SQR integration time), and 0.030 +/- 0.006 rod(-1) s(-1) (rate of dark events). Thus the rate of dark events per rod and the fraction of A2 pigment both changed by ca 8-fold between the native and final states, indicating that the dark events originated mainly in A2 molecules even in the final state. By extrapolating the linear relation between event rates and A2 fraction to 0% A2 (100% A1) and 100% A2 (0% A1), we estimated that the A1 pigment is at least 36 times more stable than the A2 pigment. The noise component attributed to discrete dark events accounted for 73% of the total dark current variance in the native (A2) state and 46% in the final state. The power spectrum of the remaining 'continuous' noise component did not differ between the two states. The smaller and faster SQR in the native (A2) state is consistent with the idea that the rod behaves as if light-adapted by dark events that occur at a rate of nearly one per integration time. Both the decreased level of dark noise and the increased SQR amplitude must significantly improve the reliability of photon detection in dim light in the presence of the A1 chromophore compared to the native (A2) state in salamander rods.

Lights can reverse illusory directional hearing

Adding brief flashes of light to a train of auditory clicks [R. Hari, Illusory directional hearing in humans, Neurosci. Lett. 189 (1995) 29–30] can alter the sounds perceived location within the head. In an experimental procedure adopted from Hari [R. Hari, Illusory directional hearing in humans, Neurosci. Lett. 189 (1995) 29–30], 16 observers listened over headphones to 8 binaural clicks (i.e., 4 left-ear leading followed by 4 right-ear leading) separated by one of three ISIs (8, 64 and 120 ms), then reported the perceived location of each click-pair within the head. Flashing a light rightward across a CRT screen during temporally coincident click-pairs made observers report the location of the sounds in roughly equally spaced steps from left-to-right through the head. In contrast, light flashes originating on the right of the CRT and moving leftward reversed the perceived location of the clicks, so that the sound appeared to originate on the right side of the head and shift leftward. These effects were diminished when the first four lights were all presented on one side of the CRT and the last four lights were all presented on the other side of the CRT. This multimodal phenomenon occurs although the light was perceived external to the head while the sounds presented over headphones were perceived within the head.

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6

We report three unrelated patients with mutations in the GRM6 gene that normally encodes the glutamate receptor mGluR6. This neurotransmitter receptor has been shown previously to be present only in the synapses of the ON bipolar cell dendrites, and it mediates synaptic transmission from rod and cone photoreceptors to this type of second-order neuron. Despite the synaptic defect, best visual acuities were normal or only moderately reduced (20/15 to 20/40). The patients were night blind from an early age, and when maximally dark-adapted, they could perceive lights only with an intensity equal to or slightly dimmer than that normally detected by the cone system (i.e., 2-3 log units above normal). Electroretinograms (ERGs) in response to single brief flashes of light had clearly detectable a-waves, which are derived from photoreceptors, and greatly reduced b-waves, which are derived from the second-order inner retinal neurons. ERGs in response to sawtooth flickering light indicated a markedly reduced ON response and a nearly normal OFF response. There was no subjective delay in the perception of suddenly appearing white vs. black objects on a gray background. These patients exemplify a previously unrecognized, autosomal recessive form of congenital night blindness associated with a negative ERG waveform.

Postsynaptic calcium feedback between rods and rod bipolar cells in the mouse retina

Light-evoked currents were recorded from rod bipolar cells in a dark-adapted mouse retinal slice preparation. Low-intensity light steps evoked a sustained inward current. Saturating light steps evoked an inward current with an initial peak that inactivated, with a time constant of about 60-70 ms, to a steady plateau level that was maintained for the duration of the step. The inactivation was strongest at hyperpolarized potentials, and absent at positive potentials. Inactivation was mediated by an increase in the intracellular calcium concentration, as it was abolished in cells dialyzed with 10 mM BAPTA, but was present in cells dialyzed with 1 mM EGTA. Moreover, responses to brief flashes of light were broader in the presence of intracellular BAPTA indicating that the calcium feedback actively shapes the time course of the light responses. Recovery from inactivation observed for paired-pulse stimuli occurred with a time constant of about 375 ms. Calcium feedback could act to increase the dynamic range of the bipolar cells, and to reduce variability in the amplitude and duration of the single-photon signal. This may be important for nonlinear processing at downstream sites of convergence from rod bipolar cells to AII amacrine cells. A model in which intracellular calcium rapidly binds to the light-gated channel and reduces the conductance can account for the results.

Deficits in a sustained attention task following nicotine withdrawal in rats.

Behavioural consequences of spontaneous and antagonist-precipitated withdrawal from nicotine upon performance of rats were compared alongside non-nicotinic antagonists in the 5-choice serial reaction time task (5-CSRTT). Male hooded Lister rats were trained to detect and respond to brief flashes of light presented every 15 s in one of five holes until a stable level of performance was achieved. Surgical removal of osmotic minipumps from rats having received nicotine (3.16 mg/kg per day base SC) chronically for 7 days produced marked deficits in performance. Compared to saline-treated controls, deficits were apparent 10 h and 16 h following nicotine abstinence; the percentage of omission errors increased concomitantly with modest decreases in response accuracy. Tests conducted 34 h and 106 h post-withdrawal indicated a progressive and complete recovery in attention performance, respectively. In another experiment, following the exposure to the same nicotine regime, administration of the competitive nicotine receptor antagonist dihydro-beta-erythroidine precipitated immediate deficits in performance that were greater than those observed in saline-treated subjects. Methyllycaconitine, an alpha(7) nicotinic receptor antagonist failed to precipitate attention deficits in nicotine-treated rats. Tests with SCH23390 and raclopride produced impairments that were similar in profile to nicotine withdrawal contrasting with non-specific effects of dizocilpine. These results provide evidence of a cognitive impairment resulting from nicotine deprivation in rodents. Specifically, blockade of D(1) receptors by SCH23390 produced decrements in performance that were qualitatively similar but greater in magnitude to the alterations observed following nicotine withdrawal. Overall, assessing nicotine withdrawal in the 5-CSRTT presents an animal model that exhibits robust construct and face validity.

Reversible modulation of GABA(A) receptor-mediated currents by light is dependent on the redox state of the receptor.

Light has recently been shown to be a physical modulator of GABAA receptor activity. Here, we further characterize the effects of light on a native cortical and retinal population of GABAA receptors, and identify a possible mechanism for light induced potentiation using recombinant receptors. GABA-induced currents in cortical neurons were observed to be rapidly and reversibly potentiated following exposure to a brief flash of light (0.5-2 s; > 280 nm) directed via an optical fibre (50 micro m i.d.). GABAA receptor-mediated responses in retinal ganglion cells were also enhanced by light, while glycine-induced currents in these cells were unaffected by the same stimulus. We also determined that physiological levels of light, that is, those that would normally reach the retina, also enhanced GABA-induced currents. Finally, we observed that chemical reduction of recombinant alpha1beta2 and alpha1beta2gamma2S GABAA receptors by dithiothreitol substantially attenuated the effects of light. These results suggest that GABAA receptors can be reversibly modified by a brief pulse of light via an allosteric mechanism that is intimately linked to redox modulation.

Protein kinases and light: unlikely partners in a receptor localization puzzle

Brief flashes of light directed at neuronal cell bodies and proximal dendrites of neurons in culture can enhance whole-cell electrophysiological responses mediated by NMDA and GABA A receptors. In experiments aimed at identifying the molecular moieties responsible for mediating this phenomenon, we observed that broad-spectrum protein kinase inhibitors substantially amplified the actions of light. Kinase inhibitors, however, were surprisingly ineffective in altering light-induced potentiation of recombinant NMDA receptors expressed in Chinese hamster ovary (CHO) cells. Furthermore, receptors assembled from truncated NMDA receptor subunits, previously shown to be relatively insensitive to modulation via phosphorylation, remained light sensitive. Phosphatase inhibitors had no effects of light-induced NMDA receptor potentiation in neurons, and nucleated patches excised from neuronal somata behaved similarly to CHO cells. Taken together, these data suggests that the effects of kinase inhibitors were unrelated to the molecular mechanism of light-induced potentiation. We propose a model whereby kinase inhibition promotes an enrichment of NMDA receptors in the neuronal cell body vs. the distal dendrites. Under these conditions, NMDA receptor redistribution elicited by kinase inhibitors would increase the number of receptors exposed to light and, as a consequence, the whole cell response. These observations support a critical role for protein kinases in the rapid redistribution of neurotransmitter receptors, with profound physiological significance.

Identification of Diagnostic Evoked Response Potential Segments in Alzheimer's Disease

Evoked response potentials (ERPs) to brief flashes of light were analyzed for constituent features that could be used to distinguish individuals with Alzheimer's disease (AD, n = 15) from matched control subjects (n = 17). Statistical k nearest-neighbor methods distinguished AD from control with a maximum sensitivity of 29% and false alarm rate of 12%. The comparable sensitivity/false-alarm values for a statistical projection pursuit method and an extended projection pursuit method, which selectively identify discriminative features for classification, were 75%/18% and 100%/6%, respectively. The results demonstrate that combinations of selected ERP time segments across different electrodes contain signal features that discriminate AD from control subjects with high sensitivity and specificity.

Argon rectification and the cause of light emission in single-bubble sonoluminescence.

In single-bubble sonoluminescence, repeated brief flashes of light are produced in a gas bubble strongly driven by a periodic acoustic field. A startling hypothesis has been made by Lohse and co-workers [Phys. Rev. Lett. 78, 1359 (1997)] that the non-noble gases in an air bubble undergo chemical reaction into soluble products, leaving only argon. In the present work, this dissociation hypothesis is supported by simulations, although the associated temperatures of about 7000 K seem too low for bremsstrahlung, which has been proposed as the dominant light emission mechanism. This suggests that emission from water vapor and its reaction products, heretofore not included, may play an important role.

Acoustical vision of neglected stimuli: interaction among spatially converging audiovisual inputs in neglect patients.

Cross-modal spatial integration between auditory and visual stimuli is a common phenomenon in space perception. The principles underlying such integration have been outlined by neurophysiological and behavioral studies in animals (Stein & Meredith, 1993), but little evidence exists proving that similar principles occur also in humans. In the present study, we explored such possibility in patients with visual neglect, namely, patients with visuospatial impairment. To test this hypothesis, neglect patients were required to detect brief flash of light presented in one of six spatial positions, either in a unimodal condition (i.e., only visual stimuli were presented) or in a cross-modal condition (i.e., a sound was presented simultaneously to the visual target, either at the same spatial position or at one of the remaining five possible positions). The results showed an improvement of visual detection when visual and auditory stimuli were originating from the same position in space or at close spatial disparity (16 degrees ). In contrast, no improvement was found when the spatial separation of visual and auditory stimuli was larger than 16 degrees. Moreover, the improvement was larger for visual positions that were more affected by the spatial impairment, i.e., the most peripheral positions in the left visual field (LVF). In conclusion, the results of the present study considerably extend our knowledge about the multisensory integration, by showing in humans the existence of an integrated visuoauditory system with functional properties similar to those found in animals.