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Effects of sleep and arousal on the processing of visual information in the cat
Abstract
Single units in the cat lateral geniculate nucleus and primary visual cortex show changes in both spontaneous and visually evoked firing as a function of the state of wakefulness. On arousal spontaneous firing is smoother and often reduced, whereas evoked responses are usually enhanced; the result is an increase in the signal-to-noise ratio. Single- and double-label 2-deoxyglucose autoradiographs show further that slow-wave sleep differentially depresses visually evoked activity in the deeper layers of the visual cortex.
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“Variations in behavioral state strongly affect the magnitude of evoked cortical activity.”
From Waking state: rapid variations modulate neural and behavioral responses (2015) · cites this paper as Livingstone and Hubel, 1981
In the citing paper
“Gain modulation mechanisms are also robustly engaged by changes in internal state32–35.”
From Mechanisms underlying gain modulation in the cortex (2020) · cites this paper as [35]
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“Other classical studies in primary somatosensory and visual cortices (Gücer, 1979; Livingstone and Hubel, 1981) only considered neurons with robust responses during wakefulness and quantified their response profiles in sleep, leaving out potential responses that could be stronger/exclusively present in sleep.”
BackgroundInfluentialDynamic shifting in thalamocortical processing during different behavioural states
Nicolelis, M. A. L., & Fanselow, E. E. (2002) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1175 · Cited by 32
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Membrane Potential and Action Potential
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“…where the EEG power spectrum is dominated by low frequencies, there is some sustained firing (Coenen & Venderik, 1972; Livingstone & Hubel, 1981; Funke & Eysel, 2000), and this typically consists of single spikes rather than spike bursts (Coenen & Venderik, 1972; Livingstone & Hubel, 1981).”
BackgroundInfluentialFunctions of Local Circuits in Neocortex: Synchrony and Laminae
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“…Funke2 1) Department of Psychology, University of Stirling, Stirling, UK 2) Institut für Physiologie, Ruhr-Universität Bochum, Bochum, Germany 3) Department of Neurology and Program in Neuroscience, Harvard Medical School; and Division of Neuroscience, Children’s Hospital, Boston, MA 02115, USA”
BackgroundMethodInfluentialPossible role of the opioid peptides in sleep
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“Bursts are usually associated with sleep states (Livingstone and Hubel, 1981; Steriade et al., 1993), but have now been shown to be present in the wake state (Swadlow and Gusev, 2001; Bezdudnaya et al., 2006) thereby suggesting a role as an effective reboot function to the previously quiescent…”
BackgroundIn Vivo Approach to the Cellular Mechanisms for Sensory Processing in Sleep and Wakefulness
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“Thus, the auditory (Velluti 1997), somatosensory (Pompeiano 1970; Soja et al., 1998), and visual neurons studied (Gambini et al., 1999; Livingstone and Hubel, 1981; McCarley et al., 1983) exhibit changes in their firing rates in correlation with stages of sleep and wakefulness.”
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BackgroundInfluentialHuman flash-VEP and quantitative EEG are independently affected by acute scopolamine
Sannita, W. G., Balestra, V., Bon, G. D., Marotta, V., & Rosadini, G. (1993) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(93)90109-9 · Cited by 27
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Löwel, S., & Singer, W. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00938.x · Cited by 27
The Missing Link in Early Emotional Processing
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“Classically associated with sleep, when they are abundant (e.g., Livingstone & Hubel, 1981), they may also be detected in the awake state, albeit more sporadically.”
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“, 1998b) and—to an even greater extent—the temporalresponse (Ikeda and Wright, 1974; Livingstone and Hubel, 1981) properties of cortical neurons are significantly different during 7024 • J.”
BackgroundResultInfluentialModulation of Inhibitory Activity by Nitric Oxide in the Thalamus
Yang, S., & Cox, C. L. (2007) · Journal of Neurophysiology · doi:10.1152/jn.01270.2006 · Cited by 26
“…was previously reported to be involved in accurate discrimination of incoming signals and enhancing sensitivity for local contrast information (Berardi and Morrone 1984; Govindaiah and Cox 2004; Holdefer et al. 1989; Livingstone and Hubel 1981; Norton and Godwin 1992; Sillito and Kemp 1983).”
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Redies, C., Dikšić, M., Evans, A. C., GJEDDE, A. H., & Yamamoto, Y. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90357-5 · Cited by 26
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State-dependent olfactory processing in freely behaving mice
Schreck, M. R., Zhuang, L., Janke, E., Moberly, A. H., Bhattarai, J. P., Gottfried, J. A., Wesson, D. W., & Ma, M. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110450 · Cited by 25
“…response attenuation has been widely observed in the primary visual, somatosensory, and auditory cortices (Brugge and Merzenich, 1973; Gucer, 1979; Livingstone and Hubel, 1981; Murata and Kameda, 1963; Sharon and Nir, 2018), more recent work in the auditory system challenges this prevailing view…”
Mechanisms underlying state dependent surface-evoked response patterns
Rector, D. M., Schei, J. L., & Rojas, M. J. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.11.031 · Cited by 24
Dasilva, M., Grieve, K. L., Cudeiro, J., & Rivadulla, C. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.01.049 · Cited by 24
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“Thus, it has been extensively studied for its sensory gating mechanism, including sleep and pain transmission (Livingstone and Hubel, 1981; Steriade et al., 1993; Kim et al., 2003; Huang et al., 2006; Huh et al., 2012).”
BackgroundCortical modulation of neuronal activity in the cat's lateral geniculate and perigeniculate nuclei
Waleszczyk, W. J., Bekisz, M., & Wróbel, A. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2005.07.006 · Cited by 24
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“However, response to sensory stimulation, while reduced during nREM sleep, can be observed within thalamocortical sensory pathways all the way to at least the primary sensory cortex (Livingstone and Hubel, 1981; Sela et al., 2016), suggesting at least some maintained sensory throughput.”
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“In addition, since TC neurons are prone to bursting during sleep or anesthesia [9,11,12], studying pain transmission in the awake state should be more valuable [28].”
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“This prestimulus effect was restricted to V1 and therefore it is unlikely to have resulted from general arousal levels [Livingstone and Hubel, 1981].”
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Subdurally recorded pattern and luminance EPs in the alert rhesus monkey
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Brain-stem modulation of the response properties of cells in the cat's perigeniculate nucleus
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“Nevertheless, this observation is consistent with two changes associated with arousal from slow wave sleep: an increase in perigeniculate cell activity (Mukhametov et al., 1970) , and improved visual selectivity of geniculate cells (Livingstone & Hubel, 1981).”
ResultDiscrete Pattern of Burst Stimulation in the Ventrobasal Thalamus for Anti-Nociception
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Cortical feedback regulation of input to visual cortex: role of intrageniculate interneurons
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“The firing properties of neurons in layer 6 of visual cortex of mice are unknown, but available data on lamina 6 neurons in visual cortex of awake, unanaesthetized cats, showed peak firing rates in responses to visual stimuli of about 75 spikes s−1 (Livingstone & Hubel, 1981).”
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Corticogeniculate Feedback and Visual Processing
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A phenomenological model of visually evoked spike trains in cat geniculate nonlagged X-cells
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“…level for spontaneous activity is very difficult to define since, in the general case, it depends on the visual adaptation level of the retina (Kaplan et al., 1979), on the arousal state of the animal (Sakakura, 1968; Livingstone & Hubel, 1981) and on the anesthetics (Levick & Williams, 1964).”
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Bischof, H., & Herrmann, K. (1988) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(88)90402-5 · Cited by 20
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Cumulative latency advance underlies fast visual processing in desynchronized brain state
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Cellular and Synaptic Effects of General Anesthetics
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“One factor that has been shown to contribute to the nonstationarity of LGN activity is the level of arousal of the animal (for example, Hubel, 1960; Coenen & Vendrik, 1972; Livingstone & Hubel, 1981; Kaplan et al., 1993).”
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Arousal and Locomotion Differently Modulate Activity of Somatostatin Neurons across Cortex
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“Introduction Arousal profoundly impacts brain activity, at both local and global scales (Livingstone and Hubel, 1981; Marrocco et al., 1994; Cantero et al., 1999; Gould et al., 2011; Grent’t-Jong et al., 2011; Stringer et al., 2019), and affects sensory perception by tailoring sensory processing to match behavioral de…”
Background
Metadata
- Authors
- Livingstone, M. S., & Hubel, D. H.
- Affiliations
- Harvard University (US)
- Venue
- Nature
- Published
- 1981-06
- Volume
- 291
- Issue
- 5816
- Pages
- 554-561
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2029325913
- Cited by
- 583
- References
- 41
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 15 · 2023: 9 · 2022: 6 · 2021: 5 · 2020: 6 · 2019: 8 · 2018: 5 · 2017: 12 · 2016: 12 · 2015: 18 · 2014: 9 · 2013: 12 · 2012: 5
- FWCI
- 10.34
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01ns007848-19, 5r01ey000605-43)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- sleep, arousal, visual processing, lateral geniculate nucleus, primary visual cortex, single-unit activity, spontaneous firing, visual evoked potentials, signal-to-noise ratio, slow-wave sleep, 2-deoxyglucose autoradiography, cats
- MeSH terms
- Action Potentials, Animals, Arousal, Autoradiography, Axonal Transport, Carbon Radioisotopes, Cats, Deoxyglucose, Evoked Potentials, Geniculate Bodies, Sleep, Tritium, Vision, Ocular, Visual Cortex, Visual Perception
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