Cited by 119Circadian rhythm and melatoninNonlinear Dynamics and Pattern FormationSleep and Wakefulness Research

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Daily and seasonal adaptation of the circadian clock requires plasticity of the SCN neuronal network

Meijer, Johanna H., Michel, Stephan, VanderLeest, Henk T., Rohling, Jos H. T.·2010·European Journal of Neuroscience

DOI 10.1111/j.1460-9568.2010.07522.x

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Abstract

Circadian rhythms are an essential property of many living organisms, and arise from an internal pacemaker, or clock. In mammals, this clock resides in the suprachiasmatic nucleus (SCN) of the hypothalamus, and generates an intrinsic circadian rhythm that is transmitted to other parts of the CNS. We will review the evidence that basic adaptive functions of the circadian system rely on functional plasticity in the neuronal network organization, and involve a change in phase relation among oscillatory neurons. We will illustrate this for: (i) photic entrainment of the circadian clock to the light–dark cycle; and (ii) seasonal adaptation of the clock to changes in day length. Molecular studies have shown plasticity in the phase relation between the ventral and dorsal SCN during adjustment to a shifted environmental cycle. Seasonal adaptation relies predominantly on plasticity in the phase relation between the rostral and caudal SCN. Electrical activity is integrated in the SCN, and appears to reflect the sum of the differently phased molecular expression patterns. While both photic entrainment and seasonal adaptation arise from a redistribution of SCN oscillatory activity patterns, different neuronal coupling mechanisms are employed, which are reviewed in the present paper.

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Geometrical Methods in the Theory of Ordinary Differential Equations
Arnold, V. I. (1988) · Grundlehren der mathematischen Wissenschaften · doi:10.1007/978-1-4612-1037-5 · Cited by 2,571
The K+/Cl− co-transporter KCC2 renders GABA hyperpolarizing during neuronal maturation
Rivera, C., Voipio, J., Payne, J. A., Ruusuvuori, E., Lahtinen, H., Lamsa, K., Pirvola, U., Saarma, M., & Kaila, K. (1999) · Nature · doi:10.1038/16697 · Cited by 2,152
Resetting central and peripheral circadian oscillators in transgenic rats
Yamazaki, S., Numano, R., Abe, M., Hida, A., Takahashi, R.-I., Ueda, M., Block, G. D., Sakaki, Y., Menaker, M., & Tei, H. (2000) · Science · doi:10.1126/science.288.5466.682 · Cited by 1,907
The genetics of mammalian circadian order and disorder: implications for physiology and disease
Takahashi, J. S., Hong, H.-K., Ko, C. H., & McDearmon, E. L. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2430 · Cited by 1,611
Individual neurons dissociated from rat suprachiasmatic nucleus express independently phased circadian firing rhythms
Welsh, D. K., Logothetis, D. E., Meister, M., & Reppert, S. M. (1995) · Neuron · doi:10.1016/0896-6273(95)90214-7 · Cited by 1,481
The Geometry of Biological Time
Winfree, A. T. (2001) · Interdisciplinary applied mathematics · doi:10.1007/978-1-4757-3484-3 · Cited by 1,242
Suprachiasmatic Nucleus: Cell Autonomy and Network Properties
Welsh, D. K., Takahashi, J. S., & Kay, S. A. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135919 · Cited by 1,216
GABA: an excitatory transmitter in early postnatal life
Cherubini, E., Gaïarsa, J., & Ben‐Ari, Y. (1991) · Trends in Neurosciences · doi:10.1016/0166-2236(91)90003-d · Cited by 1,108
Synchronization of Cellular Clocks in the Suprachiasmatic Nucleus
Yamaguchi, S., Isejima, H., Matsuo, T., Okura, R., Yagita, K., Kobayashi, M., & Okamura, H. (2003) · Science · doi:10.1126/science.1089287 · Cited by 942
The circadian visual system, 2005
Morin, L. P., & Allen, C. N. (2005) · Brain Research Reviews · doi:10.1016/j.brainresrev.2005.08.003 · Cited by 796
Suprachiasmatic nucleus in the mouse: retinal innervation, intrinsic organization and efferent projections
Abrahamson, E. E., & Moore, R. Y. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02890-6 · Cited by 788
Mammalian Photoperiodic System: Formal Properties and Neuroendocrine Mechanisms of Photoperiodic Time Measurement
Goldman, B. D. (2001) · Journal of Biological Rhythms · doi:10.1177/074873001129001980 · Cited by 771
When inhibition not excitation synchronizes neural firing
van Vreeswijk, C., Abbott, L. F., & Ermentrout, B. (1994) · Journal of Computational Neuroscience · doi:10.1007/bf00961879 · Cited by 771
Vasoactive intestinal polypeptide mediates circadian rhythmicity and synchrony in mammalian clock neurons
Aton, S. J., Colwell, C. S., Harmar, A. J., Waschek, J. A., & Herzog, E. D. (2005) · Nature Neuroscience · doi:10.1038/nn1419 · Cited by 767
Intercellular Coupling Confers Robustness against Mutations in the SCN Circadian Clock Network
Liu, A. C., Welsh, D. K., Ko, C. H., Tran, H. G., Zhang, E. E., Priest, A. A., Buhr, E. D., Singer, O., Meeker, K., Verma, I. M., et al. (2007) · Cell · doi:10.1016/j.cell.2007.02.047 · Cited by 711
Ionic basis of GABAA receptor channel function in the nervous system
Kaila, K. (1994) · Progress in Neurobiology · doi:10.1016/0301-0082(94)90049-3 · Cited by 681
Resetting the Biological Clock: Mediation of Nocturnal Circadian Shifts by Glutamate and NO
Ding, J., Chen, D., Weber, E. T., Faiman, L. E., Rea, M. A., & Gillette, M. U. (1994) · Science · doi:10.1126/science.7527589 · Cited by 563
Circadian Systems: Entrainment
Pittendrigh, C. S. (1981) · Springer eBooks · doi:10.1007/978-1-4615-6552-9_7 · Cited by 556
The VPAC2 Receptor Is Essential for Circadian Function in the Mouse Suprachiasmatic Nuclei
Harmar, A. J., Marston, H. M., Shen, S., Spratt, C., West, K. M., Sheward, W. J., Morrison, C. F., Dorin, J. R., Piggins, H. D., Reubi, J.-C., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)00736-5 · Cited by 549
Suprachiasmatic nucleus organization
Moore, R. Y., Speh, J. C., & Leak, R. K. (2002) · Cell and Tissue Research · doi:10.1007/s00441-002-0575-2 · Cited by 547
Orchestrating time: arrangements of the brain circadian clock
Antle, M. C., & Silver, R. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.01.003 · Cited by 463
Synchronization and Maintenance of Timekeeping in Suprachiasmatic Circadian Clock Cells by Neuropeptidergic Signaling
Maywood, E. S., Reddy, A. B., Wong, G. K. Y., O'Neill, J. S., O'Brien, J. A., McMahon, D. G., Harmar, A. J., Okamura, H., & Hastings, M. H. (2006) · Current Biology · doi:10.1016/j.cub.2006.02.023 · Cited by 438
Chronic jet-lag increases mortality in aged mice
Davidson, A. J., Sellix, M. T., Daniel, J., Yamazaki, S., Menaker, M., & Block, G. D. (2006) · Current Biology · doi:10.1016/j.cub.2006.09.058 · Cited by 427
Disrupted circadian rhythms in VIP- and PHI-deficient mice
Colwell, C. S., Michel, S. H., Itri, J. N., Rodriguez, W. I., Nguyen‐Van‐Tam, J. S., Lelièvre, V., Hu, Z., Liu, X., & Waschek, J. A. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00200.2003 · Cited by 384
Self-citation
GABA in the mammalian suprachiasmatic nucleus and its role in diurnal rhythmicity
Wagner, S., Castel, M., Gainer, H., & Yarom, Y. (1997) · Nature · doi:10.1038/42468 · Cited by 370
GABA Synchronizes Clock Cells within the Suprachiasmatic Circadian Clock
Liu, C., & Reppert, S. M. (2000) · Neuron · doi:10.1016/s0896-6273(00)80876-4 · Cited by 340
A GABAergic Mechanism Is Necessary for Coupling Dissociable Ventral and Dorsal Regional Oscillators within the Circadian Clock
Albus, H., Vansteensel, M. J., Michel, S. H., Block, G. D., & Meijer, J. H. (2005) · Current Biology · doi:10.1016/j.cub.2005.03.051 · Cited by 335
Self-citation
The suprachiasmatic nucleus of the golden hamster: Immunohistochemical analysis of cell and fiber distribution
Card, J. P., & Moore, R. Y. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90240-9 · Cited by 321
Sensitivity and integration in a visual pathway for circadian entrainment in the hamster (Mesocricetus auratus).
Nelson, D. E., & Takahashi, J. S. (1991) · The Journal of Physiology · doi:10.1113/jphysiol.1991.sp018660 · Cited by 316
A functional analysis of circadian pacemakers in nocturnal rodents
Daan, S., & Pittendrigh, C. S. (1976) · Journal of Comparative Physiology A · doi:10.1007/bf01417858 · Cited by 301
An Abrupt Shift in the Day/Night Cycle Causes Desynchrony in the Mammalian Circadian Center
Nagano, M., Adachi, A. A., Nakahama, K., Nakamura, T., Tamada, M., Meyer-Bernstein, E. L., Sehgal, A., & Shigeyoshi, Y. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-14-06141.2003 · Cited by 273
Separate oscillating cell groups in mouse suprachiasmatic nucleus couple photoperiodically to the onset and end of daily activity
Inagaki, N., Honma, S., Ono, D., Tanahashi, Y., & Honma, K. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607713104 · Cited by 271
Seasonal Encoding by the Circadian Pacemaker of the SCN
vanderLeest, H. T., Houben, T., Michel, S. H., Deboer, T., Albus, H., Vansteensel, M. J., Block, G. D., & Meijer, J. H. (2007) · Current Biology · doi:10.1016/j.cub.2007.01.048 · Cited by 253
Self-citation
Morning and evening circadian oscillations in the suprachiasmatic nucleus in vitro
Jagota, A., de la Iglesia, H. O., & Schwartz, W. J. (2000) · Nature Neuroscience · doi:10.1038/73943 · Cited by 246
Clock genes, oscillators, and cellular networks in the suprachiasmatic nuclei
Hastings, M. H., & Herzog, E. D. (2004) · Journal of Biological Rhythms · doi:10.1177/0748730404268786 · Cited by 246
Per1 and Per2 gene expression in the rat suprachiasmatic nucleus: circadian profile and the compartment-specific response to light
Yan, L., Takekida, S., Shigeyoshi, Y., & Okamura, H. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00223-7 · Cited by 237
Forced Desynchronization of Dual Circadian Oscillators within the Rat Suprachiasmatic Nucleus
de la Iglesia, H. O., Cambras, T., Schwartz, W. J., & Dı́ez-Noguera, A. (2004) · Current Biology · doi:10.1016/j.cub.2004.04.034 · Cited by 236
Differential Resynchronisation of Circadian Clock Gene Expression within the Suprachiasmatic Nuclei of Mice Subjected to Experimental Jet Lag
Reddy, A. B., Field, M. D., Maywood, E. S., & Hastings, M. H. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-17-07326.2002 · Cited by 224
Luminance coding in a circadian pacemaker: the suprachiasmatic nucleus of the rat and the hamster
Meijer, J. H., Groos, G. A., & Rusak, B. (1986) · Brain Research · doi:10.1016/0006-8993(86)90117-4 · Cited by 221
Self-citation
Neuropeptides phase shift the mammalian circadian pacemaker
Piggins, H. D., Antle, M. C., & Rusak, B. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-08-05612.1995 · Cited by 219
Heterogeneity of rhythmic suprachiasmatic nucleus neurons: Implications for circadian waveform and photoperiodic encoding
Schaap, J., Albus, H., vanderLeest, H. T., Eilers, P. H. C., Détári, L., & Meijer, J. H. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2436298100 · Cited by 216
Self-citation
Electrical synapses coordinate activity in the suprachiasmatic nucleus
Long, M. A., Jutras, M. J., Connors, B. W., & Burwell, R. D. (2004) · Nature Neuroscience · doi:10.1038/nn1361 · Cited by 194
Vasoactive intestinal peptide and the mammalian circadian system
Vosko, A. M., Schroeder, A., Loh, D. H., & Colwell, C. S. (2007) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2007.04.018 · Cited by 182
Vasoactive intestinal peptide (VIP)-like immunoreactive neurons located in the rat suprachiasmatic nucleus receive a direct retinal projection
Ibata, Y., Takahashi, Y., Okamura, H., Kawakami, F., Terubayashi, H., Kubo, T., & Yanaihara, N. (1989) · Neuroscience Letters · doi:10.1016/0304-3940(89)90129-8 · Cited by 182
Visualizing jet lag in the mouse suprachiasmatic nucleus and peripheral circadian timing system
Davidson, A. J., Castanon‐Cervantes, O., Leise, T. L., Molyneux, P. C., & Harrington, M. E. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06534.x · Cited by 171
Excitatory Actions of GABA in the Suprachiasmatic Nucleus
Choi, H. J., Lee, C. J., Schroeder, A., Kim, Y. S., Jung, S. H., Kim, J. S., Kim, D. Y., Son, E. J., Han, H. C., Hong, S. K., et al. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5750-07.2008 · Cited by 167
GABA and G i/o differentially control circadian rhythms and synchrony in clock neurons
Aton, S. J., Huettner, J. E., Straume, M., & Herzog, E. D. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607466103 · Cited by 156
Electrophysiology of the suprachiasmatic circadian clock
Brown, T. M., & Piggins, H. D. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.05.002 · Cited by 156
The Amplitude of Circadian Oscillations: Temperature Dependence, Latitudinal Clines, and the Photoperiodic Time Measurement
Pittendrigh, C. S., Kyner, W. T., & Takamura, T. (1991) · Journal of Biological Rhythms · doi:10.1177/074873049100600402 · Cited by 155
Phase Resetting Light Pulses InducePer1and Persistent Spike Activity in a Subpopulation of Biological Clock Neurons
Kuhlman, S. J., Silver, R., LeSauter, J., Bult‐Ito, A., & McMahon, D. G. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-04-01441.2003 · Cited by 142
The circadian cycle of mPER clock gene products in the suprachiasmatic nucleus of the Siberian hamster encodes both daily and seasonal time
Nuesslein‐Hildesheim, B., O’Brien, J., Ebling, F. J. P., Maywood, E. S., & Hastings, M. H. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00173.x · Cited by 141
Vasoactive intestinal polypeptide (VIP) phase‐shifts the rat suprachiasmatic nucleus clock in vitro
Reed, H. E., Meyer‐Spasche, A., Cutler, D. J., Coen, C. W., & Piggins, H. D. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2000.01437.x · Cited by 139
The regulation of seasonal changes in food intake and body weight
Ebling, F. J. P., & Barrett, P. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01721.x · Cited by 139
Rhythmic coupling among cells in the suprachiasmatic nucleus
Colwell, C. S. (2000) · Journal of Neurobiology · doi:10.1002/1097-4695(20000615)43:4 · Cited by 139
New Insights into Ancient Seasonal Life Timers
Hazlerigg, D. G., & Loudon, A. S. I. (2008) · Current Biology · doi:10.1016/j.cub.2008.07.040 · Cited by 138
Resetting the brain clock: time course and localization of mPER1 and mPER2 protein expression in suprachiasmatic nuclei during phase shifts
Yan, L., & Silver, R. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03189.x · Cited by 137
Resetting of central and peripheral circadian oscillators in aged rats
Davidson, A. J., Yamazaki, S., Arble, D. M., Menaker, M., & Block, G. D. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.10.018 · Cited by 134
Selective deficits in the circadian light response in mice lacking PACAP
Colwell, C. S., Michel, S. H., Itri, J. N., Rodriguez, W., Tam, J., Lelièvre, V., Hu, Z., & Waschek, J. A. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00268.2004 · Cited by 127
Self-citation
Circadian Timing of REM Sleep Is Coupled to an Oscillator within the Dorsomedial Suprachiasmatic Nucleus
Lee, M. L., Swanson, B. E., & de la Iglesia, H. O. (2009) · Current Biology · doi:10.1016/j.cub.2009.03.051 · Cited by 127
Phenotype Matters: Identification of Light-Responsive Cells in the Mouse Suprachiasmatic Nucleus
Karatsoreos, I. N., Yan, L., LeSauter, J., & Silver, R. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1666-03.2004 · Cited by 124
Differential Response of Period 1 Expression within the Suprachiasmatic Nucleus
Nakamura, W. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0889-05.2005 · Cited by 123
Rhythmic multiunit neural activity in slices of hamster suprachiasmatic nucleus reflect prior photoperiod
Mrugała, M. M., Złomańczuk, P., Jagota, A., & Schwartz, W. J. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.278.4.r987 · Cited by 115
The visual properties of rat and cat suprachiasmatic neurones
Groos, G. A., & Mason, R. J. (1980) · Journal of Comparative Physiology A · doi:10.1007/bf00657651 · Cited by 112
Disrupted Neuronal Activity Rhythms in the Suprachiasmatic Nuclei of Vasoactive Intestinal Polypeptide-Deficient Mice
Brown, T. M., Colwell, C. S., Waschek, J. A., & Piggins, H. D. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01206.2006 · Cited by 109
Neuropeptide Y and glutamate block each other's phase shifts in the suprachiasmatic nucleus in vitro
Biello, S. M., Golombek, D. A., & Harrington, M. E. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00547-7 · Cited by 106
Clock Gene Daily Profiles and Their Phase Relationship in the Rat Suprachiasmatic Nucleus Are Affected by Photoperiod
Sumová, A., Jáč, M., Sládek, M., Šauman, I., & Illnerová, H. (2003) · Journal of Biological Rhythms · doi:10.1177/0748730403251801 · Cited by 104
N-methyl-D-aspartate induces phase shifts in circadian rhythm of neuronal activity of rat SCN in vitro
Shibata, S., Watanabe, A., Hamada, T., et al. (1994) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1994.267.2.r360 · Cited by 103
Phase Shifting Capacity of the Circadian Pacemaker Determined by the SCN Neuronal Network Organization
vanderLeest, H. T., Rohling, J. H. T., Michel, S. H., & Meijer, J. H. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004976 · Cited by 102
Self-citation
Photoperiod differentially regulates gene expression rhythms in the rostral and caudal SCN
Hazlerigg, D. G., Ebling, F. J. P., & Johnston, J. D. (2005) · Current Biology · doi:10.1016/j.cub.2005.06.010 · Cited by 101
Gastrin-Releasing Peptide Phase-Shifts Suprachiasmatic Nuclei Neuronal RhythmsIn Vitro
McArthur, A. J., Coogan, A. N., Ajpru, S., Sugden, D., Biello, S. M., & Piggins, H. D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-14-05496.2000 · Cited by 101
Differential regulation of fos family genes in the ventrolateral and dorsomedial subdivisions of the rat suprachiasmatic nucleus
Schwartz, W. J., Carpino, A., de la Iglesia, H. O., Baler, R., Klein, D. C., Nakabeppu, Y., & D, N. A. M. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00140-8 · Cited by 98
Neuropeptide Y and optic chiasm stimulation of affect suprachiasmatic nucleus circadian function in vitro
Shibata, S., & Moore, R. Y. (1993) · Brain Research · doi:10.1016/0006-8993(93)91118-c · Cited by 98
Reorganization of the Suprachiasmatic Nucleus Coding for Day Length
Naito, E., Watanabe, T., Tei, H., Yoshimura, T., & Ebihara, S. (2008) · Journal of Biological Rhythms · doi:10.1177/0748730408314572 · Cited by 98
Gastrin-Releasing Peptide Mediates Light-Like Resetting of the Suprachiasmatic Nucleus Circadian Pacemaker through cAMP Response Element-Binding Protein andPer1Activation
Gamble, K. L., Allen, G. C., Zhou, T., & McMahon, D. G. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1109-07.2007 · Cited by 96
Circadian Modulation of GABA Function in the Rat Suprachiasmatic Nucleus: Excitatory Effects During the Night Phase
de Jeu, M. T. G., & Pennartz, C. M. A. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00241.2001 · Cited by 95
Photoperiod regulates multiple gene expression in the suprachiasmatic nuclei and pars tuberalis of the Siberian hamster (Phodopus sungorus)
Johnston, J. D., Ebling, F. J. P., & Hazlerigg, D. G. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04148.x · Cited by 95
Heterogeneous expression of γ‐aminobutyric acid and γ‐aminobutyric acid‐associated receptors and transporters in the rat suprachiasmatic nucleus
Belenky, M. A., Yarom, Y., & Pickard, G. E. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21553 · Cited by 94
Spatiotemporal Heterogeneity in the Electrical Activity of Suprachiasmatic Nuclei Neurons and their Response to Photoperiod
Brown, T. M., & Piggins, H. D. (2009) · Journal of Biological Rhythms · doi:10.1177/0748730408327918 · Cited by 92
Per and neuropeptide expression in the rat suprachiasmatic nuclei: compartmentalization and differential cellular induction by light
Dardente, H., Poirel, V., Klosen, P., Pévet, P., & Masson‐Pévet, M. (2002) · Brain Research · doi:10.1016/s0006-8993(02)03563-1 · Cited by 91
Organization of cell and tissue circadian pacemakers: A comparison among species
Vansteensel, M. J., Michel, S. H., & Meijer, J. H. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.10.009 · Cited by 87
Self-citation
Signaling within the Master Clock of the Brain: Localized Activation of Mitogen-Activated Protein Kinase by Gastrin-Releasing Peptide
Antle, M. C., Kriegsfeld, L. J., & Silver, R. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4696-04.2005 · Cited by 85
Connexin36 vs. Connexin32, “miniature” neuronal gap junctions, and limited electrotonic coupling in rodent suprachiasmatic nucleus
Rash, J. E., Olson, C. O., Pouliot, W. A., Davidson, K. G. V., Yasumura, T., Furman, C. S., Royer, S., Kamasawa, N., Nagy, J. I., & Dudek, F. E. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.06.052 · Cited by 82
The relation between light-induced discharge in the suprachiasmatic nucleus and phase shifts of hamster circadian rhythms
Meijer, J. H., Rusak, B., & Gänshirt, G. (1992) · Brain Research · doi:10.1016/0006-8993(92)90191-b · Cited by 81
Self-citation
Regulation of glutamatergic signalling by PACAP in the mammalian suprachiasmatic nucleus
Michel, S. H., Itri, J. N., Han, J. H., Gniotczynski, K., & Colwell, C. S. (2006) · BMC Neuroscience · doi:10.1186/1471-2202-7-15 · Cited by 80
Self-citation
In vitro entrainment of the circadian rhythm of vasopressin-releasing cells in suprachiasmatic nucleus by vasoactive intestinal polypeptide
Watanabe, K., Vaněček, J., & Yamaoka, S. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02724-4 · Cited by 78
GABAergic signaling induces divergent neuronal Ca2+ responses in the suprachiasmatic nucleus network
Irwin, R. P., & Allen, C. N. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06944.x · Cited by 73
Responses of suprachiasmatic nucleus neurons to optic nerve stimulation in rat hypothalamic slice preparation
Shibata, S., Oomura, Y., Hattori, K., & Kita, H. (1984) · Brain Research · doi:10.1016/0006-8993(84)91287-3 · Cited by 71
Dissociation between Circadian Per1 and Neuronal and Behavioral Rhythms Following a Shifted Environmental Cycle
Vansteensel, M. J., Yamazaki, S., Albus, H., Deboer, T., Block, G. D., & Meijer, J. H. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00560-8 · Cited by 67
Self-citation
Crossed and uncrossed retinal projections to the hamster circadian system
Muscat, L., Huberman, A. D., Jordan, C. L., & Morin, L. P. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10894 · Cited by 66
Correlation with Behavioral Activity and Rest Implies Circadian Regulation by SCN Neuronal Activity Levels
Houben, T., Deboer, T., van Oosterhout, F., et al. (2009) · Journal of Biological Rhythms · doi:10.1177/0748730409349895 · Cited by 65
Self-citation
A Reexamination of the Role of GABA in the Mammalian Suprachiasmatic Nucleus
Gribkoff, V. K., Pieschl, R. L., Wisialowski, T. A., et al. (1999) · Journal of Biological Rhythms · doi:10.1177/074873099129000515 · Cited by 60
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Authors: Meijer, J. H., Michel, S., VanderLeest, H. T., & Rohling, J. H. T.
Affiliations: Leiden University Medical Center (NL)
Corresponding author: Meijer, Johanna H.
ORCID: Meijer, Johanna H.
Michel, Stephan
Rohling, Jos H. T.
Venue: European Journal of Neuroscience
Publisher: Wiley
Published: 2010-12
Volume: 32
Issue: 12
Pages: 2143-2151
ISSN: 0953-816X (ISSN-L)
1460-9568
DOI: 10.1111/j.1460-9568.2010.07522.x
OpenAlex: W2157329350
Semantic Scholar: e6ae1ddf69a540699da985faa18f4dd0e558d367
Cited by: 119
References: 106
Citations by year: 2026: 6 · 2025: 2 · 2024: 4 · 2023: 11 · 2022: 8 · 2021: 9 · 2020: 4 · 2019: 8 · 2018: 9 · 2017: 6 · 2016: 11 · 2015: 9 · 2014: 8 · 2013: 6 · 2012: 10
FWCI: 0.77
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 11 d)
Locations: European Journal of Neuroscience (publishedVersion)
PubMed (publishedVersion)
Data Archiving and Networked Services (DANS) (submittedVersion)
Leiden Repository (Leiden University) (submittedVersion)
Funders: European Commission
Topics: Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
Physical Sciences › Physics and Astronomy › Statistical and Nonlinear Physics › Nonlinear Dynamics and Pattern Formation
Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
Keywords: circadian clock, suprachiasmatic nucleus, neuroplasticity, light entrainment, seasonal adaptation, day length, neuronal coupling, circadian rhythm
MeSH terms: Adaptation, Physiological, Animals, Circadian Rhythm, Nerve Net, Neuronal Plasticity, Seasons, Suprachiasmatic Nucleus, Photoperiod, Neurotransmitter Agents, Jet Lag Syndrome, Circadian Clocks

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Daily and seasonal adaptation of the circadian clock requires plasticity of the SCN neuronal network

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