Cited by 201Visual perception and processing mechanismsNeuroscience and Neuropharmacology ResearchNeural dynamics and brain function

The DOI matches its Crossref record; 67 of the 67 references it cites were found in a registry or an index.

GABAAInhibition Controls Response Gain in Visual Cortex

Open access

Katzner, Steffen, Busse, Laura, Carandini, Matteo·2011·The Journal of Neuroscience

DOI 10.1523/jneurosci.5753-10.2011PMC PMC3083851

Open this paper in CoChat — free account

Abstract

GABA A inhibition is thought to play multiple roles in sensory cortex, such as controlling responsiveness and sensitivity, sharpening selectivity, and mediating competitive interactions. To test these proposals, we recorded in cat primary visual cortex (V1) after local iontophoresis of gabazine, the selective GABA A antagonist. Gabazine increased responsiveness by as much as 300%. It slightly decreased selectivity for stimulus orientation and direction, often by raising responses to all orientations. Strikingly, gabazine affected neither contrast sensitivity nor cross-orientation suppression, the competition seen when stimuli of different orientation are superimposed. These results were captured by a simple model in which GABA A inhibition has the same selectivity as excitation and keeps responses to unwanted stimuli below threshold. We conclude that GABA A inhibition in V1 helps enhance stimulus selectivity but is not responsible for competition among superimposed stimuli. It controls the sensitivity of V1 neurons by adjusting their response gain, without affecting their input gain.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1523/jneurosci.5753-10.2011

Cites

67 of 67 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

An Introduction to the Bootstrap
Efron, B., & Tibshirani, R. J. (1994) · doi:10.1201/9780429246593 · Cited by 40,500
An Introduction to the Bootstrap
Efron, B., & Tibshirani, R. J. (1993) · doi:10.1007/978-1-4899-4541-9 · Cited by 21,230
What's new in Psychtoolbox-3?
Kleiner, M., Brainard, D. H., & Pelli, D. G. (2007) · MPG.PuRe (Max Planck Society) · Cited by 3,602
Interneurons of the neocortical inhibitory system
Markram, H., Toledo-Rodriguez, M., Wang, Y., Gupta, A., Silberberg, G., & Wu, C. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1519 · Cited by 2,954
Normalization of cell responses in cat striate cortex
Heeger, D. J. (1992) · Visual Neuroscience · doi:10.1017/s0952523800009640 · Cited by 1,835
Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex
The Petilla Interneuron Nomenclature Group (PING) (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2402 · Cited by 1,491
Balanced inhibition underlies tuning and sharpens spike timing in auditory cortex
Wehr, M., & Zador, A. M. (2003) · Nature · doi:10.1038/nature02116 · Cited by 1,413
Neocortical Network Activity In Vivo Is Generated through a Dynamic Balance of Excitation and Inhibition
Haider, B., Duque, A., Hasenstaub, A. R., & McCormick, D. A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.5297-05.2006 · Cited by 962
Striate cortex of monkey and cat: contrast response function.
Albrecht, D. G., & Hamilton, D. B. (1982) · Journal of Neurophysiology · doi:10.1152/jn.1982.48.1.217 · Cited by 953
Linearity and Normalization in Simple Cells of the Macaque Primary Visual Cortex
Carandini, M., Heeger, D. J., & Movshon, J. A. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-21-08621.1997 · Cited by 926
Self-citation

Show all 67 references

Sorted by citations

GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits
Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033
Normalization as a canonical neural computation
Carandini, M., & Heeger, D. J. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3136 · Cited by 1,906
Self-citation
How Inhibition Shapes Cortical Activity
Isaacson, J. S., & Scanziani, M. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.027 · Cited by 1,678
Parvalbumin-expressing interneurons linearly transform cortical responses to visual stimuli
Atallah, B. V., Bruns, W., Carandini, M., & Scanziani, M. (2012) · Neuron · doi:10.1016/j.neuron.2011.12.013 · Cited by 612
Self-citation
Division and subtraction by distinct cortical inhibitory networks in vivo
Wilson, N. R., Runyan, C. A., Wang, F. L., & Sur, M. (2012) · Nature · doi:10.1038/nature11347 · Cited by 568
Central gain control in tinnitus and hyperacusis
Auerbach, B. D., Rodrigues, P. V., & Salvi, R. J. (2014) · Frontiers in Neurology · doi:10.3389/fneur.2014.00206 · Cited by 439
Disinhibition, a Circuit Mechanism for Associative Learning and Memory
Letzkus, J. J., Wolff, S. B. E., & Lüthi, A. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.024 · Cited by 430
Mechanisms underlying gain modulation in the cortex
Ferguson, K. A., & Cardin, J. A. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0253-y · Cited by 327
The mediodorsal thalamus drives feedforward inhibition in the anterior cingulate cortex via parvalbumin interneurons
Delevich, K., Tucciarone, J., Huang, Z. J., & Li, B. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4565-14.2015 · Cited by 226
Short-Term Monocular Deprivation Alters GABA in the Adult Human Visual Cortex
Lunghi, C., Emir, U. E., Morrone, M. C., & Bridge, H. (2015) · Current Biology · doi:10.1016/j.cub.2015.04.021 · Cited by 224
Mechanisms of Neuronal Computation in Mammalian Visual Cortex
Priebe, N. J., & Ferster, D. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.011 · Cited by 209
Broad Inhibition Sharpens Orientation Selectivity by Expanding Input Dynamic Range in Mouse Simple Cells
Liu, B.-H., Li, Y.-T., Ma, W.-P., Pan, C.-J., Zhang, L. I., & Tao, H. W. (2011) · Neuron · doi:10.1016/j.neuron.2011.06.017 · Cited by 173
Linear transformation of thalamocortical input by intracortical excitation
Li, Y.-T., Ibrahim, L. A., Liu, B., Zhang, L. I., & Tao, H. W. (2013) · Nature Neuroscience · doi:10.1038/nn.3494 · Cited by 165
The cortical modulation of stimulus-specific adaptation in the auditory midbrain and thalamus: a potential neuronal correlate for predictive coding
Malmierca, M. S., Anderson, L. A., & Antunes, F. M. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00019 · Cited by 162
A computational perspective on autism
Rosenberg, A., Patterson, J. S., & Angelaki, D. E. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510583112 · Cited by 156
A Substantial and Unexpected Enhancement of Motion Perception in Autism
Foss‐Feig, J. H., Tadin, D., Schauder, K. B., & Cascio, C. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1608-12.2013 · Cited by 152
Measuring neural excitation and inhibition in autism: Different approaches, different findings and different interpretations
Dickinson, A. H., Jones, M., & Milne, E. (2016) · Brain Research · doi:10.1016/j.brainres.2016.07.011 · Cited by 136
Interneuron subtypes and orientation tuning
Lee, S., Kwan, A. C., & Dan, Y. (2014) · Nature · doi:10.1038/nature13128 · Cited by 134
Layer-Specific Refinement of Visual Cortex Function after Eye Opening in the Awake Mouse
Hoy, J. L., & Niell, C. M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3174-14.2015 · Cited by 117
The effect of auditory cortex deactivation on stimulus‐specific adaptation in the inferior colliculus of the rat
Anderson, L. A., & Malmierca, M. S. (2012) · European Journal of Neuroscience · doi:10.1111/ejn.12018 · Cited by 115
GABAA-Mediated Inhibition Modulates Stimulus-Specific Adaptation in the Inferior Colliculus
Pérez‐González, D., Hernández, O., Covey, E., & Malmierca, M. S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034297 · Cited by 96
An excitatory basis for divisive normalization in visual cortex
Sato, T. K., Haider, B., Häusser, M., & Carandini, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4249 · Cited by 91
Self-citation
Active Dendritic Properties and Local Inhibitory Input Enable Selectivity for Object Motion in Mouse Superior Colliculus Neurons
Gale, S. D., & Murphy, G. J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0645-16.2016 · Cited by 97
Mouse dLGN Receives Functional Input from a Diverse Population of Retinal Ganglion Cells with Limited Convergence
Rosón, M. R., Bauer, Y., Kotkat, A. H., Berens, P., Euler, T., & Busse, L. (2019) · Neuron · doi:10.1016/j.neuron.2019.01.040 · Cited by 88
Self-citation
Opposite Dynamics of GABA and Glutamate Levels in the Occipital Cortex during Visual Processing
Kurcyus, K., Birtwistle, E., Hanning, N. M., Harris, A. D., Oeltzschner, G., Edden, R. A. E., & Riedl, V. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1214-18.2018 · Cited by 84
Neural Hyperexcitability in Autism Spectrum Disorders
Takarae, Y., & Sweeney, J. (2017) · Brain Sciences · doi:10.3390/brainsci7100129 · Cited by 82
A Comprehensive Optogenetic Pharmacology Toolkit for In Vivo Control of GABA A Receptors and Synaptic Inhibition
Lin, W.-C., Tsai, M., Davenport, C. M., Smith, C. M., Veit, J., Wilson, N. M., Adesnik, H., & Krämer, R. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.026 · Cited by 83
Differential tuning of excitation and inhibition shapes direction selectivity in ferret visual cortex
Wilson, D. E., Scholl, B., & Fitzpatrick, D. (2018) · Nature · doi:10.1038/s41586-018-0354-1 · Cited by 82
Functional modulation of primary visual cortex by the superior colliculus in the mouse
Ahmadlou, M., Zweifel, L. S., & Heimel, J. A. (2018) · Nature Communications · doi:10.1038/s41467-018-06389-6 · Cited by 81
Suppression and facilitation of human neural responses
Schallmo, M., Kale, A. M., Millin, R., Flevaris, A. V., Brkanac, Z., Edden, R. A. E., Bernier, R., & Murray, S. O. (2018) · eLife · doi:10.7554/elife.30334 · Cited by 78
Variability in visual cortex size reflects tradeoff between local orientation sensitivity and global orientation modulation
Song, C., Schwarzkopf, D. S., & Rees, G. E. (2013) · Nature Communications · doi:10.1038/ncomms3201 · Cited by 74
Control of response reliability by parvalbumin-expressing interneurons in visual cortex
Zhu, Y., Qiao, W., Liu, K., Zhong, H., & Yao, H. (2015) · Nature Communications · doi:10.1038/ncomms7802 · Cited by 72
Modulation of stimulus‐specific adaptation by GABA A receptor activation or blockade in the medial geniculate body of the anaesthetized rat
Duque, D., Malmierca, M. S., & Caspary, D. M. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.261941 · Cited by 75
Contribution of the GABAergic System to Non-Motor Manifestations in Premotor and Early Stages of Parkinson’s Disease
Murueta‐Goyena, A., Andikoetxea, A., Gómez‐Esteban, J. C., & Gabilondo, I. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01294 · Cited by 72
Spectrotemporal Contrast Kernels for Neurons in Primary Auditory Cortex
Rabinowitz, N. C., Willmore, B. D. B., Schnupp, J. W. H., & King, A. J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1715-12.2012 · Cited by 67
GABAergic synapses: their plasticity and role in sensory cortex - See more at: http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00091/abstract#sthash.l5jGe6MC.dpuf
Griffen, T. C. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00091 · Cited by 64
The cannabinoid system and visual processing: A review on experimental findings and clinical presumptions
Schwitzer, T., Schwan, R., Angioï-Duprez, K., Ingster-Moati, I., Lalanne, L., Giersch, A., & Laprévote, V. (2014) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2014.11.002 · Cited by 66
Response-dependent dynamics of cell-specific inhibition in cortical networks in vivo
El-Boustani, S., & Sur, M. (2014) · Nature Communications · doi:10.1038/ncomms6689 · Cited by 61
Neurochemistry of Visual Attention
Lockhofen, D. E. L., & Mulert, C. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.643597 · Cited by 66
Corticothalamic feedback sculpts visual spatial integration in mouse thalamus
Born, G., Schneider-Soupiadis, F. A., Erisken, S., Vaičeliūnaitė, A., Lao, C. L., Mobarhan, M. H., Spacek, M. A., Einevoll, G. T., & Busse, L. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00943-0 · Cited by 62
Self-citation
Staring us in the face? An embodied theory of innate face preference
Wilkinson, N., Paikan, A., Gredebäck, G., Rea, F., & Giorgio Metta, B. (2014) · Developmental Science · doi:10.1111/desc.12159 · Cited by 62
Windows to the soul: vision science as a tool for studying biological mechanisms of information processing deficits in schizophrenia
Yoon, J. H., Sheremata, S., Rokem, A., & Silver, M. A. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00681 · Cited by 61
Cholinergic suppression of visual responses in primate V1 is mediated by GABAergic inhibition
Disney, A. A., Aoki, C., & Hawken, M. J. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00188.2012 · Cited by 57
Contribution of Cholinergic and GABAergic Mechanisms to Direction Tuning, Discriminability, Response Reliability, and Neuronal Rate Correlations in Macaque Middle Temporal Area
Thiele, A., Herrero, J. L., Distler, C., & Hoffmann, K. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0554-12.2012 · Cited by 60
Stimulus-specific adaptation in the inferior colliculus: The role of excitatory, inhibitory and modulatory inputs
Ayala, Y. A., Pérez‐González, D., & Malmierca, M. S. (2015) · Biological Psychology · doi:10.1016/j.biopsycho.2015.06.016 · Cited by 56
Anodal Transcranial Direct Current Stimulation Reduces Psychophysically Measured Surround Suppression in the Human Visual Cortex
Spiegel, D. P., Hansen, B. C., Byblow, W. D., & Thompson, B. S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036220 · Cited by 55
High‐dose Vitamin B6 supplementation reduces anxiety and strengthens visual surround suppression
Field, D. T., Cracknell, R., Eastwood, J., Scarfe, P., Williams, C. M., Zheng, Y., & Tavassoli, T. (2022) · Human Psychopharmacology Clinical and Experimental · doi:10.1002/hup.2852 · Cited by 55
Cortical Inhibition Reduces Information Redundancy at Presentation of Communication Sounds in the Primary Auditory Cortex
Gaucher, Q., Huetz, C., Gourévitch, B., & Edeline, J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0079-13.2013 · Cited by 54
The neurogenesis of P1 and N1: A concurrent EEG/LFP study
Bruyns‐Haylett, M., Luo, J., Kennerley, A. J., Harris, S., Boorman, L. W., Milne, E., Vautrelle, N., Hayashi, Y., Whalley, B. J., Jones, M., et al. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.09.034 · Cited by 55
Assessing the kaleidoscope of monocular deprivation effects
Ramamurthy, M., & Blaser, E. (2018) · Journal of Vision · doi:10.1167/18.13.14 · Cited by 51
Broader visual orientation tuning in patients with schizophrenia
Rokem, A., Yoon, J. H., Ooms, R. E., Maddock, R. J., Minzenberg, M. J., & Silver, M. A. (2011) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00127 · Cited by 50
Cortical Control of Spatial Resolution by VIP+Interneurons
Ayzenshtat, I., Karnani, M. M., Jackson, J., & Yuste, R. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.1920-16.2016 · Cited by 50
Basal forebrain activation controls contrast sensitivity in primary visual cortex
Bhattacharyya, A., Veit, J., Kretz, R., Bondar, I. V., & Rainer, G. (2013) · BMC Neuroscience · doi:10.1186/1471-2202-14-55 · Cited by 50
Sublinear binocular integration preserves orientation selectivity in mouse visual cortex
Zhao, X., Liu, M., & Cang, J. (2013) · Nature Communications · doi:10.1038/ncomms3088 · Cited by 49
Inhibition in the auditory brainstem enhances signal representation and regulates gain in complex acoustic environments
Keine, C., Rübsamen, R., & Englitz, B. (2016) · eLife · doi:10.7554/elife.19295 · Cited by 41
Expression of m1‐type muscarinic acetylcholine receptors by parvalbumin‐immunoreactive neurons in the primary visual cortex: A comparative study of rat, guinea pig, ferret, macaque, and human
Disney, A. A., & Reynolds, J. H. (2014) · Journal of Comparative Neurology · doi:10.1002/cne.23456 · Cited by 40
“…2011; Hasselmo and McGaughy, 2004; Herrero et al., 2008; Himmelheber et al., 2000; McGaughy and Sarter, 1998; Sarter et al., 2005), and it has also been argued that changes in GABAergic inhibition could account for response gain changes seen in V1 during attention tasks (Katzner et al., 2011).”
Background
Hearing in Complex Environments: Auditory Gain Control, Attention, and Hearing Loss
Auerbach, B. D., & Gritton, H. J. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.799787 · Cited by 42
Elevating Endogenous GABA Levels with GAT-1 Blockade Modulates Evoked but Not Induced Responses in Human Visual Cortex
Muthukumaraswamy, S. D., Myers, J., Wilson, S. J., Nutt, D., Hamandi, K., Lingford-Hughes, A. R., & Singh, K. D. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.9 · Cited by 40
Interrogating the mouse thalamus to correct human neurodevelopmental disorders
Schmitt, L. I., & Halassa, M. M. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.183 · Cited by 41
Human Occipital and Parietal GABA Selectively Influence Visual Perception of Orientation and Size
Song, C., Sandberg, K., Andersen, L. M., Blicher, J. U., & Rees, G. E. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3945-16.2017 · Cited by 42
Differential classical conditioning selectively heightens response gain of neural population activity in human visual cortex
Song, I., & Keil, A. (2014) · Psychophysiology · doi:10.1111/psyp.12260 · Cited by 38
Enhanced Awareness Followed Reversible Inhibition of Human Visual Cortex: A Combined TMS, MRS and MEG Study
Allen, C. P. G., Dunkley, B. T., Muthukumaraswamy, S. D., Edden, R. A. E., Evans, J., Sumner, P., Singh, K. D., & Chambers, C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0100350 · Cited by 41
Reduced crowding and poor contour detection in schizophrenia are consistent with weak surround inhibition
Robol, V., Tibber, M. S., Anderson, E. J., Bobin, T., Carlin, P., Shergill, S. S., & Dakin, S. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060951 · Cited by 37
Superior orientation discrimination and increased peak gamma frequency in autism spectrum conditions.
Dickinson, A. H., Bruyns‐Haylett, M., Smith, R. S., Jones, M., & Milne, E. (2016) · Journal of Abnormal Psychology · doi:10.1037/abn0000148 · Cited by 38
Neurochemical changes within human early blind occipital cortex
Weaver, K. E., Richards, T. L., Sàenz, M., Petropoulos, H., & Fine, I. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.004 · Cited by 39
GABAA receptors in epilepsy: Elucidating phenotypic divergence through functional analysis of genetic variants
Absalom, N. L., Lin, S. X. N., Liao, V. W. Y., Chua, H. C., Møller, R. S., Chebib, M., & Ahring, P. K. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15932 · Cited by 35
Spatial Clustering of Inhibition in Mouse Primary Visual Cortex
D’Souza, R. D., Bista, P., Meier, A. M., Ji, W., & Burkhalter, A. (2019) · Neuron · doi:10.1016/j.neuron.2019.09.020 · Cited by 35
A Unifying Motif for Spatial and Directional Surround Suppression
Liu, L. D., Miller, K. D., & Pack, C. C. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2386-17.2017 · Cited by 33
Integration of cortical population signals for visual perception
Andrei, A. R., Pojoga, S., Janz, R., & Dragoi, V. (2019) · Nature Communications · doi:10.1038/s41467-019-11736-2 · Cited by 34
Strengthening of Direction Selectivity by Broadly Tuned and Spatiotemporally Slightly Offset Inhibition in Mouse Visual Cortex
Li, Y.-T., Liu, B., Chou, X.-L., Zhang, L. I., & Tao, H. W. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu049 · Cited by 33
Vision as a Beachhead
Heeger, D. J., Behrmann, M., & Dinstein, I. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.09.019 · Cited by 32
Short-Term Plasticity Combines with Excitation–Inhibition Balance to Expand Cerebellar Purkinje Cell Dynamic Range
Vilmint, A. G., Valera, A. M., Kumar, A., & Isope, P. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3270-17.2018 · Cited by 32
Cellular neuroanatomy of rat presubiculum
Simonnet, J., Eugène, E., Cohen, I., Miles, R., & Fricker, D. (2012) · European Journal of Neuroscience · doi:10.1111/ejn.12065 · Cited by 33
Oblique Orientation Discrimination Thresholds Are Superior in Those with a High Level of Autistic Traits
Dickinson, A. H., Jones, M., & Milne, E. (2014) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-014-2147-1 · Cited by 31
Increased peak gamma frequency in individuals with higher levels of autistic traits
Dickinson, A. H., Bruyns‐Haylett, M., Jones, M., & Milne, E. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12881 · Cited by 32
Modulation of cardiopulmonary depressor reflex in nucleus ambiguus by electroacupuncture: roles of opioids and γ-aminobutyric acid
Tjen‐A‐Looi, S. C., Li, P., Li, M., & Longhurst, J. C. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00440.2011 · Cited by 30
Parvalbumin-expressing interneurons can act solo while somatostatin-expressing interneurons act in chorus in most cases on cortical pyramidal cells
Safari, M.-S., Mirnajafi‐Zadeh, J., Hioki, H., & Tsumoto, T. (2017) · Scientific Reports · doi:10.1038/s41598-017-12958-4 · Cited by 29
Changes in GABAergic markers accompany degradation of neuronal function in the primary visual cortex of senescent rats
Ding, Y., Zheng, Y., Liu, T., Chen, T., Wang, C., Sun, Q., Hua, M., & Hua, T. (2017) · Scientific Reports · doi:10.1038/s41598-017-15006-3 · Cited by 29
Simultaneous intrinsic signal imaging of auditory and visual cortex reveals profound effects of acute hearing loss on visual processing
Teichert, M., & Bolz, J. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.07.037 · Cited by 31
Supplementation of gamma-aminobutyric acid (GABA) affects temporal, but not spatial visual attention
Leonte, A., Colzato, L. S., Steenbergen, L., Hommel, B., & Akyürek, E. G. (2017) · Brain and Cognition · doi:10.1016/j.bandc.2017.11.004 · Cited by 28
Untangling stability and gain modulation in cortical circuits with multiple interneuron classesPreprint
Bos, H., Miehl, C., Oswald, A.-M. M., & Doiron, B. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.15.148114 · Cited by 25
Larger Receptive Field Size as a Mechanism Underlying Atypical Motion Perception in Autism Spectrum Disorder
Schauder, K. B., Park, W. J., Tadin, D., & Bennetto, L. (2017) · Clinical Psychological Science · doi:10.1177/2167702617707733 · Cited by 31
fMRI evidence of aberrant neural adaptation for objects in schizophrenia and bipolar disorder
Lee, J., Reavis, E. A., Engel, S. A., Altshuler, L. L., Cohen, M. S., Glahn, D. C., Nuechterlein, K. H., Wynn, J. K., & Green, M. F. (2018) · Human Brain Mapping · doi:10.1002/hbm.24472 · Cited by 28
Computational Modeling of Contrast Sensitivity and Orientation Tuning in First-Episode and Chronic Schizophrenia
Silverstein, S. M., Demmin, D. L., & Bednar, J. A. (2017) · Computational Psychiatry · doi:10.1162/cpsy_a_00005 · Cited by 26
Synaptic inhibition in the neocortex: Orchestration and computation through canonical circuits and variations on the theme
Lourenço, J., Koukouli, F., & Bacci, A. (2020) · Cortex · doi:10.1016/j.cortex.2020.08.015 · Cited by 25
Language Tasks and the Network Control Role of the Left Inferior Frontal Gyrus
Medaglia, J. D., Harvey, D. Y., Kelkar, A. S., Zimmerman, J. P., Mass, J. A., Bassett, D. S., & Hamilton, R. H. (2021) · eNeuro · doi:10.1523/eneuro.0382-20.2021 · Cited by 25
Inhibition shapes response selectivity in the inferior colliculus by gain modulation
Gittelman, J. X., Wang, L., Colburn, H. S., & Pollak, G. D. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00067 · Cited by 23
Stronger Neural Modulation by Visual Motion Intensity in Autism Spectrum Disorders
Peiker, I., Schneider, T. R., Milne, E., Schöttle, D., Vogeley, K. T., Münchau, A. M., Schunke, O., Siegel, M., Engel, A. K., & David, N. (2015) · PLoS ONE · doi:10.1371/journal.pone.0132531 · Cited by 25
Local inhibition modulates learning-dependent song encoding in the songbird auditory cortex
Thompson, J. V., Jeanne, J. M., & Gentner, T. Q. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00262.2012 · Cited by 23
3D Clustering of GABAergic Neurons Enhances Inhibitory Actions on Excitatory Neurons in the Mouse Visual Cortex
Ebina, T., Sohya, K., Imayoshi, I., Yin, S., Kimura, R., Yanagawa, Y., Kameda, H., Hioki, H., Kaneko, T., & Tsumoto, T. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.10.057 · Cited by 20
Inhibition for gain modulation in the motor system
Greenhouse, I. (2022) · Experimental Brain Research · doi:10.1007/s00221-022-06351-5 · Cited by 18
The Effects of tDCS Across the Spatial Frequencies and Orientations that Comprise the Contrast Sensitivity Function
Richard, B., Johnson, A. P., Thompson, B. S., & Hansen, B. C. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01784 · Cited by 18
Effects of ketamine on orientation selectivity and variability of neuronal responses in primary visual cortex
Ouelhazi, A., Bharmauria, V., Chanauria, N., Bachatene, L., Lussiez, R., & Molotchnikoff, S. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146462 · Cited by 16
Laminar circuit organization and response modulation in mouse visual cortex
Olivas, N. D., Quintanar-Zilinskas, V., Nenadic, Z., & Xu, X. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00070 · Cited by 17
Hippocampal Feedforward Inhibition Focuses Excitatory Synaptic Signals into Distinct Dendritic Compartments
Willadt, S., Nenniger, M., & Vogt, K. E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080984 · Cited by 17
Reduced Oblique Effect in Children with Autism Spectrum Disorders (ASD)
Sysoeva, O., Davletshina, M. A., Orekhova, E. V., Galuta, I. A., & Stroganova, T. A. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00512 · Cited by 19
Dietary modulation of cortical excitation and inhibition
Smith, A. K., Wade, A. R., Penkman, K. E. H., & Baker, D. H. (2017) · Journal of Psychopharmacology · doi:10.1177/0269881117699613 · Cited by 17
Mechanisms of Spatiotemporal Selectivity in Cortical Area MT
Pawar, A. S., Gepshtein, S., Savel'ev, S. E., & Albright, T. D. (2018) · Neuron · doi:10.1016/j.neuron.2018.12.002 · Cited by 17
Fast Recruitment of Recurrent Inhibition in the Cat Visual Cortex
Ohana, O., Portner, H., & Martin, K. A. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040601 · Cited by 17
Investigating the Effects of tDCS on Visual Orientation Discrimination Task Performance: “the Possible Influence of Placebo”
Dawood, A. B., Dickinson, A. H., Aytemür, A., Howarth, C., Milne, E., & Jones, M. (2019) · Journal of Cognitive Enhancement · doi:10.1007/s41465-019-00154-3 · Cited by 17

Authors: Katzner, S., Busse, L., & Carandini, M.
Affiliations: University College London (GB)
Smith-Kettlewell Eye Research Institute (US)
Corresponding author: Katzner, Steffen
ORCID: Katzner, Steffen
Busse, Laura
Carandini, Matteo
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 2011-04-20
Volume: 31
Issue: 16
Pages: 5931-5941
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.5753-10.2011
PMC: PMC3083851
OpenAlex: W2022734184
Cited by: 201
References: 67
Citations by year: 2026: 6 · 2025: 11 · 2024: 11 · 2023: 8 · 2022: 11 · 2021: 14 · 2020: 6 · 2019: 9 · 2018: 18 · 2017: 13 · 2016: 17 · 2015: 16 · 2014: 16 · 2013: 19 · 2012: 19
FWCI: 9.74
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-sa
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 183 d)
Locations: Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
UCL Discovery (University College London) (submittedVersion)
Funders: National Eye Institute (EY17396, R01EY017396)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Keywords: GABAA inhibition, primary visual cortex, gabazine, response gain, stimulus selectivity, orientation selectivity, direction selectivity, cross-orientation suppression, contrast sensitivity, neuronal sensitivity, competitive interactions, cat visual cortex
MeSH terms: Action Potentials, Animals, Cats, Electrophysiology, Female, Microelectrodes, Neurons, Photic Stimulation, Pyridazines, Receptors, GABA-A, Visual Cortex, Visual Fields, Contrast Sensitivity, GABA-A Receptor Antagonists

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

GABAAInhibition Controls Response Gain in Visual Cortex

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks