scholarly journals fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep

2021 ◽  
Vol 11 (11) ◽  
pp. 1528
Author(s):  
Charles Chong-Hwa Hong ◽  
James H. Fallon ◽  
Karl J. Friston

System-specific brain responses—time-locked to rapid eye movements (REMs) in sleep—are characteristically widespread, with robust and clear activation in the primary visual cortex and other structures involved in multisensory integration. This pattern suggests that REMs underwrite hierarchical processing of visual information in a time-locked manner, where REMs index the generation and scanning of virtual-world models, through multisensory integration in dreaming—as in awake states. Default mode network (DMN) activity increases during rest and reduces during various tasks including visual perception. The implicit anticorrelation between the DMN and task-positive network (TPN)—that persists in REM sleep—prompted us to focus on DMN responses to temporally-precise REM events. We timed REMs during sleep from the video recordings and quantified the neural correlates of REMs—using functional MRI (fMRI)—in 24 independent studies of 11 healthy participants. A reanalysis of these data revealed that the cortical areas exempt from widespread REM-locked brain activation were restricted to the DMN. Furthermore, our analysis revealed a modest temporally-precise REM-locked decrease—phasic deactivation—in key DMN nodes, in a subset of independent studies. These results are consistent with hierarchical predictive coding; namely, permissive deactivation of DMN at the top of the hierarchy (leading to the widespread cortical activation at lower levels; especially the primary visual cortex). Additional findings indicate REM-locked cerebral vasodilation and suggest putative mechanisms for dream forgetting.

2018 ◽  
Author(s):  
Adam P. Morris ◽  
Bart Krekelberg

SummaryHumans and other primates rely on eye movements to explore visual scenes and to track moving objects. As a result, the image that is projected onto the retina – and propagated throughout the visual cortical hierarchy – is almost constantly changing and makes little sense without taking into account the momentary direction of gaze. How is this achieved in the visual system? Here we show that in primary visual cortex (V1), the earliest stage of cortical vision, neural representations carry an embedded “eye tracker” that signals the direction of gaze associated with each image. Using chronically implanted multi-electrode arrays, we recorded the activity of neurons in V1 during tasks requiring fast (exploratory) and slow (pursuit) eye movements. Neurons were stimulated with flickering, full-field luminance noise at all times. As in previous studies 1-4, we observed neurons that were sensitive to gaze direction during fixation, despite comparable stimulation of their receptive fields. We trained a decoder to translate neural activity into metric estimates of (stationary) gaze direction. This decoded signal not only tracked the eye accurately during fixation, but also during fast and slow eye movements, even though the decoder had not been exposed to data from these behavioural states. Moreover, this signal lagged the real eye by approximately the time it took for new visual information to travel from the retina to cortex. Using simulations, we show that this V1 eye position signal could be used to take into account the sensory consequences of eye movements and map the fleeting positions of objects on the retina onto their stable position in the world.


2018 ◽  
Vol 120 (3) ◽  
pp. 926-941 ◽  
Author(s):  
Dzmitry A. Kaliukhovich ◽  
Hans Op de Beeck

Similar to primates, visual cortex in rodents appears to be organized in two distinct hierarchical streams. However, there is still little known about how visual information is processed along those streams in rodents. In this study, we examined how repetition suppression and position and clutter tolerance of the neuronal representations evolve along the putative ventral visual stream in rats. To address this question, we recorded multiunit spiking activity in primary visual cortex (V1) and the more downstream visual laterointermediate (LI) area of head-restrained Long-Evans rats. We employed a paradigm reminiscent of the continuous carry-over design used in human neuroimaging. In both areas, stimulus repetition attenuated the early phase of the neuronal response to the repeated stimulus, with this response suppression being greater in area LI. Furthermore, stimulus preferences were more similar across positions (position tolerance) in area LI than in V1, even though the absolute responses in both areas were very sensitive to changes in position. In contrast, the neuronal representations in both areas were equally good at tolerating the presence of limited visual clutter, as modeled by the presentation of a single flank stimulus. When probing tolerance of the neuronal representations with stimulus-specific adaptation, we detected no position tolerance in either examined brain area, whereas, on the contrary, we revealed clutter tolerance in both areas. Overall, our data demonstrate similarities and discrepancies in processing of visual information along the ventral visual stream of rodents and primates. Moreover, our results stress caution in using neuronal adaptation to probe tolerance of the neuronal representations. NEW & NOTEWORTHY Rodents are emerging as a popular animal model that complement primates for studying higher level visual functions. Similar to findings in primates, we demonstrate a greater repetition suppression and position tolerance of the neuronal representations in the downstream laterointermediate area of Long-Evans rats compared with primary visual cortex. However, we report no difference in the degree of clutter tolerance between the areas. These findings provide additional evidence for hierarchical processing of visual stimuli in rodents.


1998 ◽  
Vol 78 (2) ◽  
pp. 467-485 ◽  
Author(s):  
CHARLES D. GILBERT

Gilbert, Charles D. Adult Cortical Dynamics. Physiol. Rev. 78: 467–485, 1998. — There are many influences on our perception of local features. What we see is not strictly a reflection of the physical characteristics of a scene but instead is highly dependent on the processes by which our brain attempts to interpret the scene. As a result, our percepts are shaped by the context within which local features are presented, by our previous visual experiences, operating over a wide range of time scales, and by our expectation of what is before us. The substrate for these influences is likely to be found in the lateral interactions operating within individual areas of the cerebral cortex and in the feedback from higher to lower order cortical areas. Even at early stages in the visual pathway, cells are far more flexible in their functional properties than previously thought. It had long been assumed that cells in primary visual cortex had fixed properties, passing along the product of a stereotyped operation to the next stage in the visual pathway. Any plasticity dependent on visual experience was thought to be restricted to a period early in the life of the animal, the critical period. Furthermore, the assembly of contours and surfaces into unified percepts was assumed to take place at high levels in the visual pathway, whereas the receptive fields of cells in primary visual cortex represented very small windows on the visual scene. These concepts of spatial integration and plasticity have been radically modified in the past few years. The emerging view is that even at the earliest stages in the cortical processing of visual information, cells are highly mutable in their functional properties and are capable of integrating information over a much larger part of visual space than originally believed.


2020 ◽  
Author(s):  
Nicolò Meneghetti ◽  
Chiara Cerri ◽  
Elena Tantillo ◽  
Eleonora Vannini ◽  
Matteo Caleo ◽  
...  

AbstractGamma band is known to be involved in the encoding of visual features in the primary visual cortex (V1). Recent results in rodents V1 highlighted the presence, within a broad gamma band (BB) increasing with contrast, of a narrow gamma band (NB) peaking at ∼60 Hz suppressed by contrast and enhanced by luminance. However, the processing of visual information by the two channels still lacks a proper characterization. Here, by combining experimental analysis and modeling, we prove that the two bands are sensitive to specific thalamic inputs associated with complementary contrast ranges. We recorded local field potentials from V1 of awake mice during the presentation of gratings and observed that NB power progressively decreased from low to intermediate levels of contrast. Conversely, BB power was insensitive to low levels of contrast but it progressively increased going from intermediate to high levels of contrast. Moreover, BB response was stronger immediately after contrast reversal, while the opposite held for NB. All the aforementioned dynamics were accurately reproduced by a recurrent excitatory-inhibitory leaky integrate-and-fire network, mimicking layer IV of mouse V1, provided that the sustained and periodic component of the thalamic input were modulated over complementary contrast ranges. These results shed new light on the origin and function of the two V1 gamma bands. In addition, here we propose a simple and effective model of response to visual contrast that might help in reconstructing network dysfunction underlying pathological alterations of visual information processing.Significance StatementGamma band is a ubiquitous hallmark of cortical processing of sensory stimuli. Experimental evidence shows that in the mouse visual cortex two types of gamma activity are differentially modulated by contrast: a narrow band (NB), that seems to be rodent specific, and a standard broad band (BB), observed also in other animal models.We found that narrow band correlates and broad band anticorrelates with visual contrast in two complementary contrast ranges (low and high respectively). Moreover, BB displayed an earlier response than NB. A thalamocortical spiking neuron network model reproduced the aforementioned results, suggesting they might be due to the presence of two complementary but distinct components of the thalamic input into visual cortical circuitry.


2019 ◽  
Author(s):  
Ahmad Yousef

We had learnt from cognitive vision that involuntarily visual awareness should be generated by exogenous stimuli; but not indigenous! Given the complexity of understanding the reasons behind the rapid eye movements during vivid dreams; dreams that carry highly bizarre information; dreams that disallow the human subjects to have control over what they see; these types of dreams should be therefore reside under the umbrella of the “involuntary human awareness”. We therefore suggest possibilities of physical particles that could carry the visual information of these extraordinary exogenous stimuli; particles that should be able to invade the human’s eyes while they are closed; particles that have the ability to move the eye rapidly aiming for perfect transformation of the visual information. The present research aims to talk about these particles, proposes scenarios of how human eye & retina deal with them.


2008 ◽  
Vol 100 (3) ◽  
pp. 1476-1487 ◽  
Author(s):  
Bin Zhang ◽  
Earl L. Smith ◽  
Yuzo M. Chino

Vision of newborn infants is limited by immaturities in their visual brain. In adult primates, the transient onset discharges of visual cortical neurons are thought to be intimately involved with capturing the rapid succession of brief images in visual scenes. Here we sought to determine the responsiveness and quality of transient responses in individual neurons of the primary visual cortex (V1) and visual area 2 (V2) of infant monkeys. We show that the transient component of neuronal firing to 640-ms stationary gratings was as robust and as reliable as in adults only 2 wk after birth, whereas the sustained component was more sluggish in infants than in adults. Thus the cortical circuitry supporting onset transient responses is functionally mature near birth, and our findings predict that neonates, known for their “impoverished vision,” are capable of initiating relatively mature fixating eye movements and of performing in detection of simple objects far better than traditionally thought.


2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Emiliano Santarnecchi ◽  
Chiara Del Bianco ◽  
Isabella Sicilia ◽  
Davide Momi ◽  
Giorgio Di Lorenzo ◽  
...  

Insomnia might occur as result of increased cognitive and physiological arousal caused by acute or long acting stressors and associated cognitive rumination. This might lead to alterations in brain connectivity patterns as those captured by functional connectivity fMRI analysis, leading to potential insight about primary insomnia (PI) pathophysiology as well as the impact of long-term exposure to sleep deprivation. We investigated changes of voxel-wise connectivity patterns in a sample of 17 drug-naïve PI patients and 17 age-gender matched healthy controls, as well as the relationship between brain connectivity and age of onset, illness duration, and severity. Results showed a significant increase in resting-state functional connectivity of the bilateral visual cortex in PI patients, associated with decreased connectivity between the visual cortex and bilateral temporal pole. Regression with clinical scores originally unveiled a pattern of increased local connectivity as measured by intrinsic connectivity contrast (ICC), specifically resembling the default mode network (DMN). Additionally, age of onset was found to be correlated with the connectivity of supplementary motor area (SMA), and the strength of DMN←→SMA connectivity was significantly correlated with both age of onset (R2 = 41%) and disease duration (R2 = 21%). Chronic sleep deprivation, but most importantly early insomnia onset, seems to have a significant disruptive effect over the physiological negative correlation between DMN and SMA, a well-known fMRI marker of attention performance in humans. This suggests the need for more in-depth investigations on the prevention and treatment of connectivity changes and associated cognitive and psychological deficits in PI patients.


Science ◽  
2019 ◽  
Vol 363 (6422) ◽  
pp. 64-69 ◽  
Author(s):  
Riccardo Beltramo ◽  
Massimo Scanziani

Visual responses in the cerebral cortex are believed to rely on the geniculate input to the primary visual cortex (V1). Indeed, V1 lesions substantially reduce visual responses throughout the cortex. Visual information enters the cortex also through the superior colliculus (SC), but the function of this input on visual responses in the cortex is less clear. SC lesions affect cortical visual responses less than V1 lesions, and no visual cortical area appears to entirely rely on SC inputs. We show that visual responses in a mouse lateral visual cortical area called the postrhinal cortex are independent of V1 and are abolished upon silencing of the SC. This area outperforms V1 in discriminating moving objects. We thus identify a collicular primary visual cortex that is independent of the geniculo-cortical pathway and is capable of motion discrimination.


2016 ◽  
Vol 23 (5) ◽  
pp. 529-541 ◽  
Author(s):  
Sara Ajina ◽  
Holly Bridge

Damage to the primary visual cortex removes the major input from the eyes to the brain, causing significant visual loss as patients are unable to perceive the side of the world contralateral to the damage. Some patients, however, retain the ability to detect visual information within this blind region; this is known as blindsight. By studying the visual pathways that underlie this residual vision in patients, we can uncover additional aspects of the human visual system that likely contribute to normal visual function but cannot be revealed under physiological conditions. In this review, we discuss the residual abilities and neural activity that have been described in blindsight and the implications of these findings for understanding the intact system.


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