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Cordani, L.; Tagliazucchi, E.; Vetter, C.; Hassemer, C.; Roenneberg, T.; Stehle, J.H.; Kell, C.A. "Endogenous modulation of human visual cortex activity improves perception at twilight" (2018) Nature Communications. 9(1)
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Abstract:

Perception, particularly in the visual domain, is drastically influenced by rhythmic changes in ambient lighting conditions. Anticipation of daylight changes by the circadian system is critical for survival. However, the neural bases of time-of-day-dependent modulation in human perception are not yet understood. We used fMRI to study brain dynamics during resting-state and close-to-threshold visual perception repeatedly at six times of the day. Here we report that resting-state signal variance drops endogenously at times coinciding with dawn and dusk, notably in sensory cortices only. In parallel, perception-related signal variance in visual cortices decreases and correlates negatively with detection performance, identifying an anticipatory mechanism that compensates for the deteriorated visual signal quality at dawn and dusk. Generally, our findings imply that decreases in spontaneous neural activity improve close-to-threshold perception. © 2018 The Author(s).

Registro:

Documento: Artículo
Título:Endogenous modulation of human visual cortex activity improves perception at twilight
Autor:Cordani, L.; Tagliazucchi, E.; Vetter, C.; Hassemer, C.; Roenneberg, T.; Stehle, J.H.; Kell, C.A.
Filiación:Cognitive Neuroscience Group, Brain Imaging Center, Goethe University, Frankfurt am Main, 60528, Germany
Department of Neurology, Goethe University, Frankfurt am Main, 60528, Germany
Brain and Spine Institute, Hôpital Pitié Salpêtrière, Paris, 75013, France
Departamento de Física, Instituto de Física de Buenos Aires, CONICET, Buenos Aires, 1428, Argentina
Department of Integrative Physiology, University of Colorado, Boulder, CO 80310, United States
Institute of Medical Psychology, Ludwig Maximilian University, Munich, 80336, Germany
Institute of Anatomy III, Goethe University, Frankfurt am Main, 60590, Germany
Palabras clave:ambient air; brain; performance assessment; threshold; twilight; visual analysis; article; functional magnetic resonance imaging; human; modulation; rest; sensory cortex; visual cortex; adult; anatomy and histology; brain mapping; diagnostic imaging; male; nuclear magnetic resonance imaging; parietal lobe; photoperiodicity; physiology; somatosensory cortex; temporal lobe; vision; visual cortex; Adult; Brain Mapping; Humans; Magnetic Resonance Imaging; Male; Parietal Lobe; Photoperiod; Somatosensory Cortex; Temporal Lobe; Visual Cortex; Visual Perception
Año:2018
Volumen:9
Número:1
DOI: http://dx.doi.org/10.1038/s41467-018-03660-8
Título revista:Nature Communications
Título revista abreviado:Nat. Commun.
ISSN:20411723
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_20411723_v9_n1_p_Cordani

Referencias:

  • Aschoff, J., (1981) Handbook of Behavioral Neurobiology, Volume 4: Biological Rhythms, , (Plenum Press, New York and London)
  • Mohawk, J.A., Green, C.B., Takahashi, J.S., Central and peripheral circadian clocks in mammals (2012) Annu. Rev. Neurosci., 35, pp. 445-462
  • Hastings, M.H., Reddy, A.B., Maywood, E.S., A clockwork web: Circadian timing in brain and periphery, in health and disease (2003) Nat. Rev. Neurosci., 4, pp. 649-661
  • Brown, T.M., Piggins, H.D., Electrophysiology of the suprachiasmatic circadian clock (2007) Prog. Neurobiol., 82, pp. 229-255
  • Chang, D., Reppert, S., The circadian clocks of mice and men (2001) Neuron, 29, pp. 555-558
  • Saper, C.B., Fuller, P.M., Wake-sleep circuitry: An overview (2017) Curr. Opin. Neurobiol., 44, pp. 186-192
  • Schmidt, C., Collette, F., Cajochen, C., Peigneux, P., A time to think: Circadian rhythms in human cognition (2007) Cogn. Neuropsychol., 24, pp. 755-789
  • Silver, R., Kriegsfeld, L.J., Circadian rhythms have broad implications for understanding brain and behavior (2014) Eur. J. Neurosci., 39, pp. 1866-1880
  • Fox, M.D., Raichle, M.E., Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging (2007) Nat. Rev. Neurosci., 8, pp. 700-711
  • Muto, V., Local modulation of human brain responses by circadian rhythmicity and sleep debt (2016) Science, 353, pp. 687-690
  • Vandewalle, G., Effects of light on cognitive brain responses depend on circadian phase and sleep homeostasis (2011) J. Biol. Rhythms, 26, pp. 249-259
  • Shannon, B.J., Morning-evening variation in human brain metabolism and memory circuits (2013) J. Neurophysiol., 109, pp. 1444-1456
  • Blautzik, J., Classifying fMRI-derived resting-state connectivity patterns according to their daily rhythmicity (2013) Neuroimage, 71, pp. 298-306
  • Garrett, D.D., Moment-to-moment brain signal variability: A next frontier in human brain mapping? (2013) Neurosci. Biobehav. Rev., 37, pp. 610-624
  • Bianciardi, M., Modulation of spontaneous fMRI activity in human visual cortex by behavioral state (2009) Neuroimage, 45, pp. 160-168
  • Biswal, B.B., Van Keylen, J., Hyde, J.S., Simultaneous assessment of flow and BOLD signals in resting-state functional connectivity maps (1997) NMR Biomed., 10, pp. 165-170
  • Cordes, D., Frequencies contributing to functional connectivity in the cerebral cortex in "resting-state" data (2001) Ajnr. Am. J. Neuroradiol., 22, pp. 1326-1333
  • Tagliazucchi, E., Laufs, H., Decoding wakefulness levels from typical fMRI resting-state data reveals reliable drifts between wakefulness and sleep (2014) Neuron, 82, pp. 695-708
  • Picchioni, D., Decreased connectivity between the thalamus and the neocortex during human nonrapid eye movement sleep (2014) Sleep, 37, pp. 387-397
  • Schmidt, C., Homeostatic sleep pressure and responses to sustained attention in the suprachiasmatic area (2009) Science, 324, pp. 516-519
  • Shibata, S., Oomura, Y., Kita, H., Hattori, K., Circadian rhythmic changes of neuronal activity in the suprachiasmatic nucleus of the rat hypothalamic slice (1982) Brain Res., 247, pp. 154-158
  • Meijer, J.H., Schaap, J., Albus, H., Multiunit activity recordings in the suprachiasmatic nuclei: In vivo versus in vitro models (1997) Brain Res., 753, pp. 322-327
  • Aston-Jones, G., Chen, S., Zhu, Y., Oshinsky, M.L., A neural circuit for circadian regulation of arousal (2001) Nat. Neurosci., 4, pp. 723-738
  • Kametani, H., Kawamura, H., Circadian rhythm of cortical acetylcholine release as measured by in vivo microdialysis in freely moving rats (1991) Neurosci. Lett., 132, pp. 263-266
  • Berridge, C.W., Waterhouse, B.D., The locus coeruleus-noradrenergic system: Modulation of behavioral state and state-dependent cognitive processes (2003) Brain Res. Rev., 42, pp. 33-84
  • Sato, H., Hata, Y., Masui, H., Tsumoto, T., A functional role of cholinergic innervation to neurons in the cat visual cortex (1987) J. Neurophysiol., 58, pp. 765-780
  • Ponce-Alvarez, A., He, B.J., Hagmann, P., Deco, G., Task-driven activity reduces the cortical activity space of the brain: Experiment and whole-brain modeling (2015) PLoS Comput. Biol., 11, p. e1004445
  • Sadaghiani, S., Hesselmann, G., Friston, K.J., Kleinschmidt, A., The relation of ongoing brain activity, evoked neural responses, and cognition (2010) Front. Syst. Neurosci., 4, p. 20
  • Amedi, A., Von Kriegstein, K., Van Atteveldt, N.M., Beauchamp, M.S., Naumer, M.J., Functional imaging of human crossmodal identification and object recognition (2005) Exp. Brain Res., 166, pp. 559-571
  • Bulkin, D.A., Groh, J.M., Seeing sounds: Visual and auditory interactions in the brain (2006) Curr. Opin. Neurobiol., 16, pp. 415-419
  • Lotze, M., Wittmann, M., Von Steinbüchel, N., Pöppel, E., Roenneberg, T., Daily rhythm of temporal resolution in the auditory system (1999) Cortex, 35, pp. 89-100
  • Van Gelder, T., The dynamical hypothesis in cognitive science (1998) Behav. Brain Sci., 21, pp. 615-665
  • Deco, G., Jirsa, V.K., McIntosh, A.R., Resting brains never rest: Computational insights into potential cognitive architectures (2013) Trends Neurosci., 36, pp. 268-274
  • Yetish, G., Natural sleep and its seasonal variations in three pre-industrial societies (2015) Curr. Biol., 25, pp. 2862-2868
  • Packer, C., Swanson, A., Ikanda, D., Kushnir, H., Fear of darkness, the full moon and the nocturnal ecology of african lions (2011) PLoS ONE, 6, p. e22285
  • Filippi, M., The organization of intrinsic brain activity differs between genders: A resting-state fMRI study in a large cohort of young healthy subjects (2013) Hum. Brain Mapp., 34, pp. 1330-1343
  • Baker, F.C., Driver, H.S., Circadian rhythms, sleep, and the menstrual cycle (2007) Sleep. Med., 8, pp. 613-622
  • Roenneberg, T., Human activity and rest in situ (2015) Methods Enzymol., 552, pp. 257-283
  • Roenneberg, T., Wirz-Justice, A., Merrow, M., Life between clocks: Daily temporal patterns of human chronotypes (2003) J. Biol. Rhythms, 18, pp. 80-90
  • Roenneberg, T., A marker for the end of adolescence (2004) Curr. Biol., 14, pp. R1038-R1039
  • Roenneberg, T., Epidemiology of the human circadian clock (2007) Sleep. Med. Rev., 11, pp. 429-438
  • Vetter, C., Juda, M., Roenneberg, T., The influence of internal time, time awake, and sleep duration on cognitive performance in shiftworkers (2012) Chronobiol. Int., 29, pp. 1127-1138
  • Cespedes, E.M., Comparison of self-reported sleep duration with actigraphy: Results from the hispanic community health Study/Study of latinos sueno ancillary study (2016) Am. J. Epidemiol., 183, pp. 561-573
  • Johns, M.W., A new method for measuring daytime sleepiness: The epworth sleepiness scale (1991) Sleep, 14, pp. 540-545
  • Friston, K.J., Spatial registration and normalization of images (1995) Hum. Brain Mapp., 3, pp. 165-189
  • Weissenbacher, A., Correlations and anticorrelations in resting-state functional connectivity MRI: A quantitative comparison of preprocessing strategies (2009) Neuroimage, 47, pp. 1408-1416
  • Tzourio-Mazoyer, N., Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI singlesubject brain (2002) Neuroimage, 15, pp. 273-289
  • Zang, Y.F., Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI (2007) Brain Dev., 29, pp. 83-91
  • Zuo, X.N., The oscillating brain: Complex and reliable (2010) Neuroimage, 49, pp. 1432-1445
  • Tagliazucchi, E., Carhart-Harris, R., Leech, R., Nutt, D., Chialvo, D.R., Enhanced repertoire of brain dynamical states during the psychedelic experience (2014) Hum. Brain Mapp., 35, pp. 5442-5456
  • Eickhoff, S.B., A new SPM toolbox for combining probabilistic cytoarchitectonic maps and functional imaging data (2005) Neuroimage, 25, pp. 1325-1335
  • Dunlap, W.P., Cortina, J.M., Vaslow, J.B., Burke, M.J., Meta-analysis of experiments with matched groups or repeated measures designs (1996) Psychol. Methods, 1, pp. 170-177
  • Friston, K.J., Penny, W.D., Glaser, D.E., Conjunction revisited (2005) Neuroimage, 25, pp. 661-667
  • Bland, J.M., Altman, D.G., Correlation, regression, and repeated data (1994) Br. Med. J., 308, p. 896
  • Bland, J.M., Altman, D.G., Calculating correlation coefficients with repeated observations: Part 1-correlation within subjects (1995) Br. Med. J., 310, p. 446
  • Kriegeskorte, N., Simmons, W.K., Bellgowan, P.S., Baker, C.I., Circular analysis in systems neuroscience: The dangers of double dipping (2009) Nat. Neurosci., 12, pp. 535-540

Citas:

---------- APA ----------
Cordani, L., Tagliazucchi, E., Vetter, C., Hassemer, C., Roenneberg, T., Stehle, J.H. & Kell, C.A. (2018) . Endogenous modulation of human visual cortex activity improves perception at twilight. Nature Communications, 9(1).
http://dx.doi.org/10.1038/s41467-018-03660-8
---------- CHICAGO ----------
Cordani, L., Tagliazucchi, E., Vetter, C., Hassemer, C., Roenneberg, T., Stehle, J.H., et al. "Endogenous modulation of human visual cortex activity improves perception at twilight" . Nature Communications 9, no. 1 (2018).
http://dx.doi.org/10.1038/s41467-018-03660-8
---------- MLA ----------
Cordani, L., Tagliazucchi, E., Vetter, C., Hassemer, C., Roenneberg, T., Stehle, J.H., et al. "Endogenous modulation of human visual cortex activity improves perception at twilight" . Nature Communications, vol. 9, no. 1, 2018.
http://dx.doi.org/10.1038/s41467-018-03660-8
---------- VANCOUVER ----------
Cordani, L., Tagliazucchi, E., Vetter, C., Hassemer, C., Roenneberg, T., Stehle, J.H., et al. Endogenous modulation of human visual cortex activity improves perception at twilight. Nat. Commun. 2018;9(1).
http://dx.doi.org/10.1038/s41467-018-03660-8