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  • 1
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 1997-05-09
    Description: The firing rate responses of neurons in the primary visual cortex grow with stimulus contrast, the variation in the luminance of an image relative to the mean luminance. These responses, however, are reduced after a cell is exposed for prolonged periods to high-contrast visual stimuli. This phenomenon, known as contrast adaptation, occurs in the cortex and is not present at earlier stages of visual processing. To investigate the cellular mechanisms underlying cortical adaptation, intracellular recordings were performed in the visual cortex of cats, and the effects of prolonged visual stimulation were studied. Surprisingly, contrast adaptation barely affected the stimulus-driven modulations in the membrane potential of cortical cells. Moreover, it did not produce sizable changes in membrane resistance. The major effect of adaptation, evident both in the presence and in the absence of a visual stimulus, was a tonic hyperpolarization. Adaptation affects a class of synaptic inputs, most likely excitatory in nature, that exert a tonic influence on cortical cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Carandini, M -- Ferster, D -- EY04726/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 1997 May 9;276(5314):949-52.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology and Physiology, Northwestern University, Evanston, IL 60208, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9139658" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Physiological ; Animals ; Cats ; Contrast Sensitivity/*physiology ; Evoked Potentials, Visual ; Membrane Potentials ; Neurons/*physiology ; Patch-Clamp Techniques ; Photic Stimulation ; Visual Cortex/cytology/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2012-04-24
    Description: Cell transplantation is a potential strategy for treating blindness caused by the loss of photoreceptors. Although transplanted rod-precursor cells are able to migrate into the adult retina and differentiate to acquire the specialized morphological features of mature photoreceptor cells, the fundamental question remains whether transplantation of photoreceptor cells can actually improve vision. Here we provide evidence of functional rod-mediated vision after photoreceptor transplantation in adult Gnat1-/- mice, which lack rod function and are a model of congenital stationary night blindness. We show that transplanted rod precursors form classic triad synaptic connections with second-order bipolar and horizontal cells in the recipient retina. The newly integrated photoreceptor cells are light-responsive with dim-flash kinetics similar to adult wild-type photoreceptors. By using intrinsic imaging under scotopic conditions we demonstrate that visual signals generated by transplanted rods are projected to higher visual areas, including V1. Moreover, these cells are capable of driving optokinetic head tracking and visually guided behaviour in the Gnat1-/- mouse under scotopic conditions. Together, these results demonstrate the feasibility of photoreceptor transplantation as a therapeutic strategy for restoring vision after retinal degeneration.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888831/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888831/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pearson, R A -- Barber, A C -- Rizzi, M -- Hippert, C -- Xue, T -- West, E L -- Duran, Y -- Smith, A J -- Chuang, J Z -- Azam, S A -- Luhmann, U F O -- Benucci, A -- Sung, C H -- Bainbridge, J W -- Carandini, M -- Yau, K-W -- Sowden, J C -- Ali, R R -- 082217/Wellcome Trust/United Kingdom -- EY016805/EY/NEI NIH HHS/ -- EY06837/EY/NEI NIH HHS/ -- EY11307/EY/NEI NIH HHS/ -- G03000341/Medical Research Council/United Kingdom -- G0901550/Medical Research Council/United Kingdom -- MR/J004553/1/Medical Research Council/United Kingdom -- NIHR-RP-011-003/Department of Health/United Kingdom -- R01 EY011307/EY/NEI NIH HHS/ -- R01 EY011307-18/EY/NEI NIH HHS/ -- R01 EY016805/EY/NEI NIH HHS/ -- R01 EY016805-07/EY/NEI NIH HHS/ -- Department of Health/United Kingdom -- England -- Nature. 2012 May 3;485(7396):99-103. doi: 10.1038/nature10997.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK. rachael.pearson@ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22522934" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; GTP-Binding Protein alpha Subunits/deficiency/genetics ; Light ; Maze Learning ; Mice ; Retinal Bipolar Cells/ultrastructure ; Retinal Horizontal Cells/ultrastructure ; Retinal Rod Photoreceptor Cells/cytology/*physiology/radiation ; effects/*transplantation ; Transducin/deficiency/genetics ; Vision, Ocular/*physiology/radiation effects ; Visual Cortex/physiology/radiation effects
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2012-11-23
    Description: The activity of the cerebral cortex is thought to depend on the precise relationship between synaptic excitation and inhibition. In the visual cortex, in particular, intracellular measurements have related response selectivity to coordinated increases in excitation and inhibition. These measurements, however, have all been made during anaesthesia, which strongly influences cortical state and therefore sensory processing. The synaptic activity that is evoked by visual stimulation during wakefulness is unknown. Here we measured visually evoked responses--and the underlying synaptic conductances--in the visual cortex of anaesthetized and awake mice. Under anaesthesia, responses could be elicited from a large region of visual space and were prolonged. During wakefulness, responses were more spatially selective and much briefer. Whole-cell patch-clamp recordings of synaptic conductances showed a difference in synaptic inhibition between the two conditions. Under anaesthesia, inhibition tracked excitation in amplitude and spatial selectivity. By contrast, during wakefulness, inhibition was much stronger than excitation and had extremely broad spatial selectivity. We conclude that during wakefulness, cortical responses to visual stimulation are dominated by synaptic inhibition, restricting the spatial spread and temporal persistence of neural activity. These results provide a direct glimpse of synaptic mechanisms that control sensory responses in the awake cortex.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537822/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537822/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Haider, Bilal -- Hausser, Michael -- Carandini, Matteo -- 094077/Wellcome Trust/United Kingdom -- 095669/Wellcome Trust/United Kingdom -- G0800791/Medical Research Council/United Kingdom -- Medical Research Council/United Kingdom -- Wellcome Trust/United Kingdom -- England -- Nature. 2013 Jan 3;493(7430):97-100. doi: 10.1038/nature11665. Epub 2012 Nov 21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London EC1V 9EL, UK. b.haider@ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23172139" target="_blank"〉PubMed〈/a〉
    Keywords: Anesthesia ; Animals ; Female ; Mice ; Mice, Inbred C57BL ; Models, Neurological ; Neural Inhibition/*physiology ; Patch-Clamp Techniques ; Photic Stimulation ; Synapses/metabolism ; Synaptic Transmission ; Time Factors ; Visual Cortex/*physiology ; Wakefulness/*physiology
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2014-04-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Atallah, Bassam V -- Scanziani, Massimo -- Carandini, Matteo -- England -- Nature. 2014 Apr 3;508(7494):E3. doi: 10.1038/nature13129.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Champalimaud Neuroscience Programme, Lisbon 1400-038, Portugal [2] Howard Hughes Medical Institute and Center for Neural Circuits and Behavior and Neurobiology Section, Division of Biology, University of California San Diego, La Jolla, California 92093-0634, USA. ; Howard Hughes Medical Institute and Center for Neural Circuits and Behavior and Neurobiology Section, Division of Biology, University of California San Diego, La Jolla, California 92093-0634, USA. ; UCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24695314" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials/*physiology ; Animals ; Interneurons/*metabolism ; Parvalbumins/*metabolism ; Visual Cortex/*cytology
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 5
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 1994-05-27
    Description: Recordings from monkey primary visual cortex (V1) were used to test a model for the visually driven responses of simple cells. According to the model, simple cells compute a linear sum of the responses of lateral geniculate nucleus (LGN) neurons. In addition, each simple cell's linear response is divided by the pooled activity of a large number of other simple cells. The cell membrane performs both operations; synaptic currents are summed and then divided by the total membrane conductance. Current and conductance are decoupled (by a complementary arrangement of excitation and inhibition) so that current depends only on the LGN inputs and conductance depends only on the cortical inputs. Closed form expressions were derived for fitting and interpreting physiological data. The model accurately predicted responses to drifting grating stimuli of various contrasts, orientations, and spatiotemporal frequencies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Carandini, M -- Heeger, D J -- 1-R29-MH50228-01/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1994 May 27;264(5163):1333-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Neural Science, New York University, New York 10003.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8191289" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Electric Conductivity ; Geniculate Bodies/cytology/*physiology ; Macaca ; Membrane Potentials ; *Models, Neurological ; Neurons/*physiology ; Synapses/*physiology ; Visual Cortex/cytology/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2015-04-08
    Description: A large population of neurons can, in principle, produce an astronomical number of distinct firing patterns. In cortex, however, these patterns lie in a space of lower dimension, as if individual neurons were "obedient members of a huge orchestra". Here we use recordings from the visual cortex of mouse (Mus musculus) and monkey (Macaca mulatta) to investigate the relationship between individual neurons and the population, and to establish the underlying circuit mechanisms. We show that neighbouring neurons can differ in their coupling to the overall firing of the population, ranging from strongly coupled 'choristers' to weakly coupled 'soloists'. Population coupling is largely independent of sensory preferences, and it is a fixed cellular attribute, invariant to stimulus conditions. Neurons with high population coupling are more strongly affected by non-sensory behavioural variables such as motor intention. Population coupling reflects a causal relationship, predicting the response of a neuron to optogenetically driven increases in local activity. Moreover, population coupling indicates synaptic connectivity; the population coupling of a neuron, measured in vivo, predicted subsequent in vitro estimates of the number of synapses received from its neighbours. Finally, population coupling provides a compact summary of population activity; knowledge of the population couplings of n neurons predicts a substantial portion of their n(2) pairwise correlations. Population coupling therefore represents a novel, simple measure that characterizes the relationship of each neuron to a larger population, explaining seemingly complex network firing patterns in terms of basic circuit variables.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449271/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449271/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Okun, Michael -- Steinmetz, Nicholas A -- Cossell, Lee -- Iacaruso, M Florencia -- Ko, Ho -- Bartho, Peter -- Moore, Tirin -- Hofer, Sonja B -- Mrsic-Flogel, Thomas D -- Carandini, Matteo -- Harris, Kenneth D -- 095668/Wellcome Trust/United Kingdom -- 095669/Wellcome Trust/United Kingdom -- 095853/Wellcome Trust/United Kingdom -- EY014924/EY/NEI NIH HHS/ -- R01 EY014924/EY/NEI NIH HHS/ -- T32 MH020016/MH/NIMH NIH HHS/ -- Howard Hughes Medical Institute/ -- Medical Research Council/United Kingdom -- Wellcome Trust/United Kingdom -- England -- Nature. 2015 May 28;521(7553):511-5. doi: 10.1038/nature14273. Epub 2015 Apr 6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] UCL Institute of Neurology, University College London, London WC1N 3BG, UK [2] Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6DE, UK [3] UCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK. ; 1] UCL Institute of Neurology, University College London, London WC1N 3BG, UK [2] Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6DE, UK [3] UCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK [4] Howard Hughes Medical Institute and Department of Neurobiology, Stanford University, Stanford, California 94305-5125, USA. ; 1] Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6DE, UK [2] Biozentrum, University of Basel, Klingelbergstrasse 50/70, CH-4056 Basel, Switzerland. ; Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6DE, UK. ; Center for Molecular and Behavioral Neuroscience, Rutgers University, 197 University Avenue, Newark, New Jersey 07102, USA. ; Howard Hughes Medical Institute and Department of Neurobiology, Stanford University, Stanford, California 94305-5125, USA. ; UCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK. ; 1] UCL Institute of Neurology, University College London, London WC1N 3BG, UK [2] Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6DE, UK [3] Center for Molecular and Behavioral Neuroscience, Rutgers University, 197 University Avenue, Newark, New Jersey 07102, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25849776" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Female ; Macaca mulatta ; Male ; Mice ; Models, Neurological ; Neurons/*cytology/*physiology ; Optogenetics ; Synapses/physiology ; Visual Cortex/*cytology/*physiology
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 7
    Publication Date: 2016-06-22
    Description: When making choices under conditions of perceptual uncertainty, past experience can play a vital role. However, it can also lead to biases that worsen decisions. Consistent with previous observations, we found that human choices are influenced by the success or failure of past choices even in a standard two-alternative detection...
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 8
    Publication Date: 2019
    Description: 〈p〉Neuronal populations in sensory cortex produce variable responses to sensory stimuli and exhibit intricate spontaneous activity even without external sensory input. Cortical variability and spontaneous activity have been variously proposed to represent random noise, recall of prior experience, or encoding of ongoing behavioral and cognitive variables. Recording more than 10,000 neurons in mouse visual cortex, we observed that spontaneous activity reliably encoded a high-dimensional latent state, which was partially related to the mouse’s ongoing behavior and was represented not just in visual cortex but also across the forebrain. Sensory inputs did not interrupt this ongoing signal but added onto it a representation of external stimuli in orthogonal dimensions. Thus, visual cortical population activity, despite its apparently noisy structure, reliably encodes an orthogonal fusion of sensory and multidimensional behavioral information.〈/p〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
    Publication Date: 2013-07-10
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Published by Springer Nature
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  • 10
    Publication Date: 2012-04-18
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Published by Springer Nature
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