Gamma frequency feedback inhibition accounts for key aspects of orientation selectivity in V1

References

• Anderson JS, Carandini M, Ferster D. Orientation tuning of input conductance, excitation, and inhibition in cat primary visual cortex. Journal of Neurophysiology 2000; 84: 909–926
   PubMed Web of Science ®Google Scholar
• Bartos M, Vida I, Frotscher M, Geiger JR, Jonas P. Rapid signaling at inhibitory synapses in a dentate gyrus interneuron network. Journal of Neurophysiology 2001; 21: 2687–2698
   Google Scholar
• Burns SP, Xing D, Shapley RM. Comparisons of the dynamics of local field potential and multiunit activity signals in macaque visual cortex. Journal of Neurophysiology 2010; 30: 13739–13749
   Google Scholar
• Buzsaki G, Wang XJ. Mechanisms of gamma oscillations. Annu Rev Neurosci 2012; 35: 203–225
   PubMed Web of Science ®Google Scholar
• Cardin J, Carlen M, Meletis K, Knoblich U, Zhang F, Deisseroth K, Tsai L-H, Moore C. Driving fast-spiking cells induces gamma rhythm and controls sensory responses. Nature 2009; 459: 663–667
   PubMed Web of Science ®Google Scholar
• de Almeida L, Idiart M, Lisman JE. A second function of gamma frequency oscillations: an E%-max winner-take-all mechanism selects which cells fire. Journal of Neurophysiology 2009; 29: 7497–7503
   Google Scholar
• Dragoi G, Buzsaki G. Temporal encoding of place sequences by hippocampal cell assemblies. Neuron 2006; 50: 145–157
   PubMed Web of Science ®Google Scholar
• Engel AK, Konig P, Gray CM, Singer W. Stimulus-Dependent Neuronal Oscillations in Cat Visual Cortex: Inter-Columnar Interaction as Determined by Cross-Correlation Analysis. European Journal Of Neuroscience 1990; 2: 588–606
   PubMed Web of Science ®Google Scholar
• Folias SE, Yu S, Snyder A, Nikolic D, Rubin JE, (2013). “Synchronisation hubs in the visual cortex may arise from strong rhythmic inhibition during gamma oscillations”. European Journal of Neuroscience 38:2864–2883
   Google Scholar
• Galarreta M, Hestrin S. A network of fast-spiking cells in the neocortex connected by electrical synapses. Nature 1999; 402: 72–75
   PubMed Web of Science ®Google Scholar
• Gibson JR, Beierlein M, Connors BW. Two networks of electrically coupled inhibitory neurons in neocortex. Nature 1999; 402: 75–79
   PubMed Web of Science ®Google Scholar
• Hubel DH, Wiesel TN. Receptive fields, binocular interaction and functional architecture in the cat's visual cortex. Journal De Physiologie 1962; 160: 106–154
   Google Scholar
• Isaacson JS, Scanziani M. How inhibition shapes cortical activity. Neuron 2011; 72: 231–243
   PubMed Web of Science ®Google Scholar
• Konig P, Engel AK, Roelfsema PR, Singer W. How precise is neuronal synchronization”?. Neural Computation 1995; 7: 469–485
   PubMed Web of Science ®Google Scholar
• Konig P, Engel AK, Singer W. Integrator or coincidence detector? The role of the cortical neuron revisited. Trends in Neuroscience 1996; 19: 130–137
   PubMed Web of Science ®Google Scholar
• Leger JF, Stern EA, Aertsen A, Heck D. Synaptic integration in rat frontal cortex shaped by network activity. Journal of Neurophysiology 2005; 93: 281–293
   PubMed Web of Science ®Google Scholar
• Lien A, Scanziani M. Tuned thalamic excitation is amplified by visual cortical circuits. Nature Neuroscience 2013; 16: 1315–1323
   PubMed Web of Science ®Google Scholar
• Lisman J, Buzsaki G. A neural coding scheme formed by the combined function of gamma and theta oscillations. Schizophrenia Bulletin 2008; 34: 974–980
   Google Scholar
• Lisman JE, Jensen O. The theta–gamma neural code. Neuron 2013; 77: 1002–1016
   PubMed Web of Science ®Google Scholar
• Mehta MR, Lee AK, Wilson MA. Role of experience and oscillations in transforming a rate code into a temporal code. Nature 2002; 417: 741–746
   PubMed Web of Science ®Google Scholar
• Miles R. Synaptic excitation of inhibitory cells by single CA3 hippocampal pyramidal cells of the guinea-pig in vitro. Journal De Physiologie 1990; 428: 61–77
   Google Scholar
• Nauhaus I, Nielsen KJ, Disney AA, Callaway EM. Orthogonal micro-organization of orientation and spatial frequency in primate primary visual cortex. Nature Neuroscience 2012; 15: 1683–1690
   PubMed Web of Science ®Google Scholar
• Palmer SE, Miller KD. Effects of inhibitory gain and conductance fluctuations in a simple model for contrast-invariant orientation tuning in cat V1. Journal of Neurophysiology 2007; 98: 63–78
   PubMed Web of Science ®Google Scholar
• Priebe NJ, Ferster D. Mechanisms of neuronal computation in mammalian visual cortex. Neuron 2012; 75: 194–208
   PubMed Web of Science ®Google Scholar
• Pugh MC, Ringach DL, Shapley R, Shelley MJ. Computational modeling of orientation tuning dynamics in monkey primary visual cortex. Journal of Computational Neuroscience 2000; 8: 143–159
   PubMed Web of Science ®Google Scholar
• angan AV and Young LS. (2013). “Emergent dynamics in a model of visual cortex”. J Comput Neurosci
   Google Scholar
• Scheffzuk C, Kukushka VI, Vyssotski AL, Draguhn A, Tort AB, Brankack J. Global slowing of network oscillations in mouse neocortex by diazepam. Neuropharmacology 2013; 65: 123–133
   PubMed Web of Science ®Google Scholar
• Schmidt-Hieber C, Jonas P, Bischofberger J. Subthreshold dendritic signal processing and coincidence detection in dentate gyrus granule cells. Journal of Neurophysiology 2007; 27: 8430–8441
   Google Scholar
• Sclar G, Freeman RD. Orientation selectivity in the cat's striate cortex is invariant with stimulus contrast. Experimental Brain Research 1982; 46: 457–461
   PubMed Web of Science ®Google Scholar
• Soltesz I, Deschênes M. Low- and high-frequency membrane potential oscillations during theta activity in CA1 and CA3 pyramidal neurons of the rat hippocampus under ketamine-xylazine anesthesia. Journal of Neurophysiology 1993; 70: 97–116
   PubMed Web of Science ®Google Scholar
• Vinck M, Lima B, Womelsdorf T, Oostenveld R, Singer W, Neuenschwander S, Fries P. Gamma-phase shifting in awake monkey visual cortex. Journal of Neurophysiology 2010; 30: 1250–1257
   Google Scholar
• Volgushev M, Pernberg J, Eysel UT. Gamma-frequency fluctuations of the membrane potential and response selectivity in visual cortical neurons. European Journal of Neuroscience 2003; 17: 1768–1776
   PubMed Web of Science ®Google Scholar
• Waters J, Helmchen F. Background synaptic activity is sparse in neocortex. Journal of Neurophysiology 2006; 26: 8267–8277
   Google Scholar
• Whittington MA, Jefferys JG, Traub RD. Effects of intravenous anaesthetic agents on fast inhibitory oscillations in the rat hippocampus in vitro. British Journal of Pharmocology 1996; 118: 1977–1986
   PubMed Web of Science ®Google Scholar
• Womelsdorf T, Lima B, Vinck M, Oostenveld R, Singer W, Neuenschwander S, Fries P. Orientation selectivity and noise correlation in awake monkey area V1 are modulated by the gamma cycle. Proceedings of the National Academy of Sciences of The United States of America 2012; 109: 4302–4307
   PubMed Web of Science ®Google Scholar
• Yu J, Ferster D. Membrane potential synchrony in primary visual cortex during sensory stimulation. Neuron 2010; 68: 1187–1201
   PubMed Web of Science ®Google Scholar