Orientation specificity of contrast adaptation in mouse primary visual cortex

2012 ◽  
Vol 108 (5) ◽  
pp. 1381-1391 ◽  
Author(s):  
Aaron C. Stroud ◽  
Emily E. LeDue ◽  
Nathan A. Crowder

Contrast adaptation is a commonly studied phenomenon in vision, where prolonged exposure to spatial contrast alters perceived stimulus contrast and produces characteristic shifts in the contrast response functions of primary visual cortex neurons in cats and primates. In this study we investigated contrast adaptation in mouse primary visual cortex with two goals in mind. First, we sought to establish a quantitative description of contrast adaptation in an animal model, where genetic tools are more readily applicable to this phenomenon. Second, the orientation specificity of contrast adaptation was studied to comparatively assess the possible role of local cortical networks in contrast adaptation. In cats and primates, predictable differences in visual processing across the cortical surface are thought to be caused by inhomogeneous local network membership that arises from the pinwheel organization of orientation columns. Because mice lack this pinwheel organization, we predicted that local cortical networks would have access to a broad spectrum of orientation signals, and contrast adaptation in mice would not be specific to the recorded cell's preferred orientation. We found that most mouse V1 neurons showed contrast adaptation that was robust regardless of whether the adapting stimulus matched the cell's preferred orientation or was orthogonal to it.

2016 ◽  
Author(s):  
Dylan R Muir ◽  
Patricia Molina-Luna ◽  
Morgane M Roth ◽  
Fritjof Helmchen ◽  
Björn M Kampa

AbstractLocal excitatory connections in mouse primary visual cortex (V1) are stronger and more prevalent between neurons that share similar functional response features. However, the details of how functional rules for local connectivity shape neuronal responses in V1 remain unknown. We hypothesised that complex responses to visual stimuli may arise as a consequence of rules for selective excitatory connectivity within the local network in the superficial layers of mouse V1. In mouse V1 many neurons respond to overlapping grating stimuli (plaid stimuli) with highly selective and facilitatory responses, which are not simply predicted by responses to single gratings presented alone. This complexity is surprising, since excitatory neurons in V1 are considered to be mainly tuned to single preferred orientations. Here we examined the consequences for visual processing of two alternative connectivity schemes: in the first case, local connections are aligned with visual properties inherited from feedforward input (a ‘like-to-like’ scheme specifically connecting neurons that share similar preferred orientations); in the second case, local connections group neurons into excitatory subnetworks that combine and amplify multiple feedforward visual properties (a ‘feature binding’ scheme). By comparing predictions from large scale computational models with in vivo recordings of visual representations in mouse V1, we found that responses to plaid stimuli were best explained by a assuming ‘feature binding’ connectivity. Unlike under the ‘like-to-like’ scheme, selective amplification within feature-binding excitatory subnetworks replicated experimentally observed facilitatory responses to plaid stimuli; explained selective plaid responses not predicted by grating selectivity; and was consistent with broad anatomical selectivity observed in mouse V1. Our results show that visual feature binding can occur through local recurrent mechanisms without requiring feedforward convergence, and that such a mechanism is consistent with visual responses and cortical anatomy in mouse V1.Author summaryThe brain is a highly complex structure, with abundant connectivity between nearby neurons in the neocortex, the outermost and evolutionarily most recent part of the brain. Although the network architecture of the neocortex can appear disordered, connections between neurons seem to follow certain rules. These rules most likely determine how information flows through the neural circuits of the brain, but the relationship between particular connectivity rules and the function of the cortical network is not known. We built models of visual cortex in the mouse, assuming distinct rules for connectivity, and examined how the various rules changed the way the models responded to visual stimuli. We also recorded responses to visual stimuli of populations of neurons in anaesthetised mice, and compared these responses with our model predictions. We found that connections in neocortex probably follow a connectivity rule that groups together neurons that differ in simple visual properties, to build more complex representations of visual stimuli. This finding is surprising because primary visual cortex is assumed to support mainly simple visual representations. We show that including specific rules for non-random connectivity in cortical models, and precisely measuring those rules in cortical tissue, is essential to understanding how information is processed by the brain.


2007 ◽  
Vol 24 (5) ◽  
pp. 679-690 ◽  
Author(s):  
SÉVERINE DURAND ◽  
TOBE C.B. FREEMAN ◽  
MATTEO CARANDINI

The responses of neurons in primary visual cortex (V1) are suppressed by stimuli presented in the region surrounding the receptive field. There is debate as to whether this surround suppression is due to intracortical inhibition, is inherited from lateral geniculate nucleus (LGN), or is due to a combination of these factors. The mechanisms involved in surround suppression may differ from those involved in suppression within the receptive field, which is called cross-orientation suppression. To compare surround suppression to cross-orientation suppression, and to help elucidate its underlying mechanisms, we studied its temporal properties in anesthetized and paralyzed cats. We first measured the temporal resolution of suppression. While cat LGN neurons respond vigorously to drift rates up to 30 Hz, most cat V1 neurons stop responding above 10–15 Hz. If suppression originated in cortical responses, therefore, it should disappear above such drift rates. In a majority of cells, surround suppression decreased substantially when surround drift rate was above ∼15 Hz, but some neurons demonstrated suppression with surround drift rates as high as 21 Hz. We then measured the susceptibility of suppression to contrast adaptation. Contrast adaptation reduces responses of cortical neurons much more than those of LGN neurons. If suppression originated in cortical responses, therefore, it should be reduced by adaptation. Consistent with this hypothesis, we found that prolonged exposure to the surround stimulus decreased the strength of surround suppression. The results of both experiments differ markedly from those previously obtained in a study of cross-orientation suppression, whose temporal properties were found to resemble those of LGN neurons. Our results provide further evidence that these two forms of suppression are due to different mechanisms. Surround suppression can be explained by a mixture of thalamic and cortical influences. It could also arise entirely from intracortical inhibition, but only if inhibitory neurons respond to somewhat higher drift rates than most cortical cells.


NeuroImage ◽  
2012 ◽  
Vol 63 (3) ◽  
pp. 1464-1477 ◽  
Author(s):  
Andreas A. Ioannides ◽  
Vahe Poghosyan ◽  
Lichan Liu ◽  
George A. Saridis ◽  
Marco Tamietto ◽  
...  

2021 ◽  
Vol 15 ◽  
Author(s):  
Yun Lin ◽  
Xi Zhou ◽  
Yuji Naya ◽  
Justin L. Gardner ◽  
Pei Sun

The linearity of BOLD responses is a fundamental presumption in most analysis procedures for BOLD fMRI studies. Previous studies have examined the linearity of BOLD signal increments, but less is known about the linearity of BOLD signal decrements. The present study assessed the linearity of both BOLD signal increments and decrements in the human primary visual cortex using a contrast adaptation paradigm. Results showed that both BOLD signal increments and decrements kept linearity to long stimuli (e.g., 3 s, 6 s), yet, deviated from linearity to transient stimuli (e.g., 1 s). Furthermore, a voxel-wise analysis showed that the deviation patterns were different for BOLD signal increments and decrements: while the BOLD signal increments demonstrated a consistent overestimation pattern, the patterns for BOLD signal decrements varied from overestimation to underestimation. Our results suggested that corrections to deviations from linearity of transient responses should consider the different effects of BOLD signal increments and decrements.


2018 ◽  
Author(s):  
Andreea Lazar ◽  
Chris Lewis ◽  
Pascal Fries ◽  
Wolf Singer ◽  
Danko Nikolić

SummarySensory exposure alters the response properties of individual neurons in primary sensory cortices. However, it remains unclear how these changes affect stimulus encoding by populations of sensory cells. Here, recording from populations of neurons in cat primary visual cortex, we demonstrate that visual exposure enhances stimulus encoding and discrimination. We find that repeated presentation of brief, high-contrast shapes results in a stereotyped, biphasic population response consisting of a short-latency transient, followed by a late and extended period of reverberatory activity. Visual exposure selectively improves the stimulus specificity of the reverberatory activity, by increasing the magnitude and decreasing the trial-to-trial variability of the neuronal response. Critically, this improved stimulus encoding is distributed across the population and depends on precise temporal coordination. Our findings provide evidence for the existence of an exposure-driven optimization process that enhances the encoding power of neuronal populations in early visual cortex, thus potentially benefiting simple readouts at higher stages of visual processing.


2018 ◽  
Author(s):  
Petr Znamenskiy ◽  
Mean-Hwan Kim ◽  
Dylan R. Muir ◽  
Maria Florencia Iacaruso ◽  
Sonja B. Hofer ◽  
...  

In the cerebral cortex, the interaction of excitatory and inhibitory synaptic inputs shapes the responses of neurons to sensory stimuli, stabilizes network dynamics1 and improves the efficiency and robustness of the neural code2–4. Excitatory neurons receive inhibitory inputs that track excitation5–8. However, how this co-tuning of excitation and inhibition is achieved by cortical circuits is unclear, since inhibitory interneurons are thought to pool the inputs of nearby excitatory cells and provide them with non-specific inhibition proportional to the activity of the local network9–13. Here we show that although parvalbumin-expressing (PV) inhibitory cells in mouse primary visual cortex make connections with the majority of nearby pyramidal cells, the strength of their synaptic connections is structured according to the similarity of the cells’ responses. Individual PV cells strongly inhibit those pyramidal cells that provide them with strong excitation and share their visual selectivity. This fine-tuning of synaptic weights supports co-tuning of inhibitory and excitatory inputs onto individual pyramidal cells despite dense connectivity between inhibitory and excitatory neurons. Our results indicate that individual PV cells are preferentially integrated into subnetworks of inter-connected, co-tuned pyramidal cells, stabilising their recurrent dynamics. Conversely, weak but dense inhibitory connectivity between subnetworks is sufficient to support competition between them, de-correlating their output. We suggest that the history and structure of correlated firing adjusts the weights of both inhibitory and excitatory connections, supporting stable amplification and selective recruitment of cortical subnetworks.


1997 ◽  
Vol 17 (20) ◽  
pp. 7926-7940 ◽  
Author(s):  
Juan A. Varela ◽  
Kamal Sen ◽  
Jay Gibson ◽  
Joshua Fost ◽  
L. F. Abbott ◽  
...  

1996 ◽  
Vol 13 (3) ◽  
pp. 509-516 ◽  
Author(s):  
Pedro E. Maldonado ◽  
Charles M. Gray

AbstractWe have employed the tetrode technique, which allows accurate discrimination of individual neuronal spike trains from multiunit recordings, in order to examine the variation of orientation selectivity among local groups of neurons. We recorded a total of 321 cells from 62 sites in area 17 of halothane-anesthetized cats; each site contained between three to ten neurons that were estimated to be less than 65 μm away from the tetrode tip. For each cell, we determined the orientation tuning in response to moving bars. Of the cells tested, 8.4% were unresponsive, 22.7% had no preferential response to any particular orientation, while 68.8% were tuned. The average difference in preferred orientation between cell pairs recorded at the same site was 10.7 deg, but the variance in preferred orientation differences differed significantly among sites. Some clusters of cells exhibited the same or nearly the same orientation preference, while others had orientation preferences that differed by as much as 90 deg. Our data demonstrate that the tuning for orientation is more heterogeneously distributed at a local level than previous studies have suggested.


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