Abstract
Sleep is a common physiological state appearing in the everyday life of humans and other animals. In humans, sleep occupies approximately one third of our whole lifetime. People have thus kept asking the question of why we sleep. Sleep deprivation in rats results in lethality, indicating its essential roles (Rechtschaffen A, Bergmann BM, Sleep 25:18–24, 2002; Rechtschaffen A, Bergmann BM, Everson CA, Kushida CA, Gilliland MA, Sleep 12:68–87, 1989). From the aspect of evolution, sleep or sleep-like states are conserved across diverse animal species, implying an existent function for fulfilling a common purpose that may benefit the survival of animals. Up to now, however, the function and mechanism of sleep are still largely unknown. Recently, simple genetic animal models including fruit flies (Drosophila melanogaster), roundworms (Caenorhabditis elegans), and zebrafish (Danio rerio) have been actively studied to reveal the evolutionarily conserved components of sleep, which may lead to solving the fundamental question about the evolutionary origin of sleep (Hendricks JC, Finn SM, Panckeri KA, Chavkin J, Williams JA, Sehgal A, Pack AI, Neuron 25:129–138, 2000; Raizen DM, Zimmerman JE, Maycock MH, Ta UD, You YJ, Sundaram MV, Pack AI, Nature 451:569–572, 2008; Shaw PJ, Cirelli C, Greenspan RJ, Tononi G, Science 287:1834–1837, 2000; Singh K, Ju JY, Walsh MB, DiIorio MA, Hart AC, Sleep 37:1439–1451, 2014; Zhdanova IV, Wang SY, Leclair OU, Danilova NP, Brain Res 903:263–268, 2001). In addition, with the development of new techniques such as two-photon microscopy, optogenetics, and pharmacogenetics, researchers have obtained more ability to observe and manipulate neurons or their activity. Partly owing to the breakthrough of such new tools, researchers have found some evidence suggesting that sleep serves several functions including memory consolidation, clearance of brain metabolites, spine remodeling, and brain development (Bushey D, Tononi G, Cirelli C, Science 332:1576–1581, 2011; Donlea JM, Thimgan MS, Suzuki Y, Gottschalk L, Shaw PJ, Science 332:1571–1576, 2011; Kayser MS, Yue Z, Sehgal A, Science 344:269–274, 2014; Rasch B, Buchel C, Gais S, Born J, Science 315:1426–1429, 2007; Rechtschaffen A, Bergmann BM, Everson CA, Kushida CA, Gilliland MA, Sleep 12:68–87, 1989; Xie L, Kang H, Xu Q, Chen MJ, Liao Y, Thiyagarajan M, O’Donnell J, Christensen DJ, Nicholson C, Iliff JJ, et al. Science 342:373–377, 2013; Yang G, Lai CS, Cichon J, Ma L, Li W, Gan WB, Science 344:1173–1178, 2014). These studies have shown the relationship between sleep and other biological processes in different animals, and it further brings us to the question of whether the function of sleep is only for one purpose or is for multiple purposes. Up to now, our knowledge about sleep seems to be merely the tip of the iceberg. Further research is needed to understand the general function of sleep across species.
Here, we first introduce general criteria for sleep, which allows its definition in animals other than mammals (Sect. 15.1). Then we introduce REM sleep and non-REM sleep, which are the two major sleep stages of mammalian and avian sleep (Sect. 15.2), and introduce studies and hypotheses related to how they evolved (Sect. 15.3). Next, we briefly introduce sleep in aquatic mammals, which have made a unique change from their ancestral mammals to adapt to their lifestyle (Sect. 15.4). Then we introduce the current progress in studies using simple genetic animal models, namely, zebrafish, fruit flies, and roundworms (Sect. 15.5 and Sect. 15.6). Finally, we compare the suggested functions of sleep between mammals and invertebrate animals (Sect. 15.7).
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References
Adamantidis AR, Zhang F, Aravanis AM, Deisseroth K, de Lecea L (2007) Neural substrates of awakening probed with optogenetic control of hypocretin neurons. Nature 450:420–424
Agosto J, Choi JC, Parisky KM, Stilwell G, Rosbash M, Griffith LC (2008) Modulation of GABAA receptor desensitization uncouples sleep onset and maintenance in Drosophila. Nat Neurosci 11:354–359
Allison T, Van Twyver H, Goff WR (1972) Electrophysiological studies of the echidna, Tachyglossus aculeatus. I. Waking and sleep. Arch Ital Biol 110:145–184
Anaclet C, Ferrari L, Arrigoni E, Bass CE, Saper CB, Lu J, Fuller PM (2014) The GABAergic parafacial zone is a medullary slow wave sleep-promoting center. Nat Neurosci 17:1217–1224
Andretic R, van Swinderen B, Greenspan RJ (2005) Dopaminergic modulation of arousal in Drosophila. Curr Biol 15:1165–1175
Aserinsky E, Kleitman N (1953) Regularly occurring periods of eye motility, and concomitant phenomena, during sleep. Science 118:273–274
Baumgartner A, Dietzel M, Saletu B, Wolf R, Campos-Barros A, Graf KJ, Kurten I, Mannsmann U (1993) Influence of partial sleep deprivation on the secretion of thyrotropin, thyroid hormones, growth hormone, prolactin, luteinizing hormone, follicle stimulating hormone, and estradiol in healthy young women. Psychiatry Res 48:153–178
Boissard R, Gervasoni D, Schmidt MH, Barbagli B, Fort P, Luppi PH (2002) The rat ponto-medullary network responsible for paradoxical sleep onset and maintenance: a combined microinjection and functional neuroanatomical study. Eur J Neurosci 16:1959–1973
Boutrel B, Monaca C, Hen R, Hamon M, Adrien J (2002) Involvement of 5-HT1A receptors in homeostatic and stress-induced adaptive regulations of paradoxical sleep: studies in 5-HT1A knock-out mice. J Neurosci 22:4686–4692
Bushey D, Tononi G, Cirelli C (2011) Sleep and synaptic homeostasis: structural evidence in Drosophila. Science 332:1576–1581
Campbell SS, Tobler I (1984) Animal sleep: a review of sleep duration across phylogeny. Neurosci Biobehav Rev 8:269–300
Carter ME, Yizhar O, Chikahisa S, Nguyen H, Adamantidis A, Nishino S, Deisseroth K, de Lecea L (2010) Tuning arousal with optogenetic modulation of locus coeruleus neurons. Nat Neurosci 13:1526–1533
Chauvette S, Seigneur J, Timofeev I (2012) Sleep oscillations in the thalamocortical system induce long-term neuronal plasticity. Neuron 75:1105–1113
Chemelli RM, Willie JT, Sinton CM, Elmquist JK, Scammell T, Lee C, Richardson JA, Williams SC, Xiong Y, Kisanuki Y et al (1999) Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation. Cell 98:437–451
Choi S, Chatzigeorgiou M, Taylor KP, Schafer WR, Kaplan JM (2013) Analysis of NPR-1 reveals a circuit mechanism for behavioral quiescence in C. elegans. Neuron 78:869–880
Cirelli C, Bushey D, Hill S, Huber R, Kreber R, Ganetzky B, Tononi G (2005) Reduced sleep in Drosophila Shaker mutants. Nature 434:1087–1092
Crochet S, Onoe H, Sakai K (2006) A potent non-monoaminergic paradoxical sleep inhibitory system: a reverse microdialysis and single-unit recording study. Eur J Neurosci 24:1404–1412
Crocker A, Sehgal A (2008) Octopamine regulates sleep in Drosophila through protein kinase A-dependent mechanisms. J Neurosci 28:9377–9385
de Lecea L, Kilduff TS, Peyron C, Gao X, Foye PE, Danielson PE, Fukuhara C, Battenberg EL, Gautvik VT, Bartlett FS 2nd et al (1998) The hypocretins: hypothalamus-specific peptides with neuroexcitatory activity. Proc Natl Acad Sci USA 95:322–327
Dement W (1958) The occurrence of low voltage, fast, electroencephalogram patterns during behavioral sleep in the cat. Electroencephalogr Clin Neurophysiol 10:291–296
Dement W, Kleitman N (1957) Cyclic variations in EEG during sleep and their relation to eye movements, body motility, and dreaming. Electroencephalogr Clin Neurophysiol 9:673–690
Donlea JM, Thimgan MS, Suzuki Y, Gottschalk L, Shaw PJ (2011) Inducing sleep by remote control facilitates memory consolidation in Drosophila. Science 332:1571–1576
Douglas CL, Vyazovskiy V, Southard T, Chiu SY, Messing A, Tononi G, Cirelli C (2007) Sleep in Kcna2 knockout mice. BMC Biol 5:42
Driver RJ, Lamb AL, Wyner AJ, Raizen DM (2013) DAF-16/FOXO regulates homeostasis of essential sleep-like behavior during larval transitions in C. elegans. Curr Biol 23:501–506
Equihua AC, De La Herran-Arita AK, Drucker-Colin R (2013) Orexin receptor antagonists as therapeutic agents for insomnia. Front Pharmacol 4:163
Finlay BL, Hersman MN, Darlington RB (1998) Patterns of vertebrate neurogenesis and the paths of vertebrate evolution. Brain Behav Evol 52:232–242
Foltenyi K, Greenspan RJ, Newport JW (2007) Activation of EGFR and ERK by rhomboid signaling regulates the consolidation and maintenance of sleep in Drosophila. Nat Neurosci 10:1160–1167
Franken P, Thomason R, Heller HC, O’Hara BF (2007) A non-circadian role for clock-genes in sleep homeostasis: a strain comparison. BMC Neurosci 8:87
Graves LA, Hellman K, Veasey S, Blendy JA, Pack AI, Abel T (2003) Genetic evidence for a role of CREB in sustained cortical arousal. J Neurophysiol 90:1152–1159
Haas HL, Sergeeva OA, Selbach O (2008) Histamine in the nervous system. Physiol Rev 88:1183–1241
Hagan JJ, Leslie RA, Patel S, Evans ML, Wattam TA, Holmes S, Benham CD, Taylor SG, Routledge C, Hemmati P et al (1999) Orexin A activates locus coeruleus cell firing and increases arousal in the rat. Proc Natl Acad Sci USA 96:10911–10916
Hallam SJ, Jin Y (1998) lin-14 regulates the timing of synaptic remodelling in Caenorhabditis elegans. Nature 395:78–82
Haller J, Makara GB, Kruk MR (1998) Catecholaminergic involvement in the control of aggression: hormones, the peripheral sympathetic, and central noradrenergic systems. Neurosci Biobehav Rev 22:85–97
Hara J, Beuckmann CT, Nambu T, Willie JT, Chemelli RM, Sinton CM, Sugiyama F, Yagami K, Goto K, Yanagisawa M et al (2001) Genetic ablation of orexin neurons in mice results in narcolepsy, hypophagia, and obesity. Neuron 30:345–354
Harrison NL (2007) Mechanisms of sleep induction by GABA(A) receptor agonists. J Clin Psychiatry 68(suppl 5):6–12
Hartse K (1994) Sleep in insects and nonmammalian vertebrates. Principles and practice of sleep medicine, 2nd edn. Saunders, Philadelphia, pp 95–104
Hassani OK, Lee MG, Jones BE (2009) Melanin-concentrating hormone neurons discharge in a reciprocal manner to orexin neurons across the sleep–wake cycle. Proc Natl Acad Sci USA 106:2418–2422
Hayashi Y, Hirotsu T, Iwata R, Kage-Nakadai E, Kunitomo H, Ishihara T, Iino Y, Kubo T (2009) A trophic role for Wnt-Ror kinase signaling during developmental pruning in Caenorhabditis elegans. Nat Neurosci 12:981–987
Hendricks JC, Finn SM, Panckeri KA, Chavkin J, Williams JA, Sehgal A, Pack AI (2000) Rest in Drosophila is a sleep-like state. Neuron 25:129–138
Hendricks JC, Williams JA, Panckeri K, Kirk D, Tello M, Yin JC, Sehgal A (2001) A non-circadian role for cAMP signaling and CREB activity in Drosophila rest homeostasis. Nat Neurosci 4:1108–1115
Huang ZL, Qu WM, Eguchi N, Chen JF, Schwarzschild MA, Fredholm BB, Urade Y, Hayaishi O (2005) Adenosine A2A, but not A1, receptors mediate the arousal effect of caffeine. Nat Neurosci 8:858–859
Jego S, Glasgow SD, Herrera CG, Ekstrand M, Reed SJ, Boyce R, Friedman J, Burdakov D, Adamantidis AR (2013) Optogenetic identification of a rapid eye movement sleep modulatory circuit in the hypothalamus. Nat Neurosci 16:1637–1643
Jouvet M, Michel F, Courjon J (1959) On a stage of rapid cerebral electrical activity in the course of physiological sleep. CR Seances Soc Biol Fil 153:1024–1028
Kayser MS, Yue Z, Sehgal A (2014) A critical period of sleep for development of courtship circuitry and behavior in Drosophila. Science 344:269–274
Keene AC, Duboue ER, McDonald DM, Dus M, Suh GS, Waddell S, Blau J (2010) Clock and cycle limit starvation-induced sleep loss in Drosophila. Curr Biol 20:1209–1215
Konadhode RR, Pelluru D, Blanco-Centurion C, Zayachkivsky A, Liu M, Uhde T, Glen WB Jr, van den Pol AN, Mulholland PJ, Shiromani PJ (2013) Optogenetic stimulation of MCH neurons increases sleep. J Neurosci 33:10257–10263
Kramer A, Yang FC, Snodgrass P, Li X, Scammell TE, Davis FC, Weitz CJ (2001) Regulation of daily locomotor activity and sleep by hypothalamic EGF receptor signaling. Science 294:2511–2515
Kume K, Kume S, Park SK, Hirsh J, Jackson FR (2005) Dopamine is a regulator of arousal in the fruit fly. J Neurosci 25:7377–7384
Kushikata T, Fang J, Chen Z, Wang Y, Krueger JM (1998) Epidermal growth factor enhances spontaneous sleep in rabbits. Am J Physiol 275:R509–R514
Langmesser S, Franken P, Feil S, Emmenegger Y, Albrecht U, Feil R (2009) cGMP-dependent protein kinase type I is implicated in the regulation of the timing and quality of sleep and wakefulness. PLoS One 4, e4238
Lee MG, Hassani OK, Jones BE (2005) Discharge of identified orexin/hypocretin neurons across the sleep-waking cycle. J Neurosci 25:6716–6720
Libersat F, Pflueger HJ (2004) Monoamines and the orchestration of behavior. Bioscience 54:17–25
Lin L, Faraco J, Li R, Kadotani H, Rogers W, Lin X, Qiu X, de Jong PJ, Nishino S, Mignot E (1999a) The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene. Cell 98:365–376
Lin L, Faraco J, Li R, Kadotani H, Rogers W, Lin XY, Qiu XH, de Jong PJ, Nishino S, Mignot E (1999b) The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene. Cell 98:365–376
Lu J, Jhou TC, Saper CB (2006a) Identification of wake-active dopaminergic neurons in the ventral periaqueductal gray matter. J Neurosci 26:193–202
Lu J, Sherman D, Devor M, Saper CB (2006b) A putative flip-flop switch for control of REM sleep. Nature 441:589–594
Maret S, Faraguna U, Nelson AB, Cirelli C, Tononi G (2011) Sleep and waking modulate spine turnover in the adolescent mouse cortex. Nat Neurosci 14:1418–1420
Marshall L, Helgadottir H, Molle M, Born J (2006) Boosting slow oscillations during sleep potentiates memory. Nature 444:610–613
Mieda M, Hasegawa E, Kisanuki YY, Sinton CM, Yanagisawa M, Sakurai T (2011) Differential roles of orexin receptor-1 and −2 in the regulation of non-REM and REM sleep. J Neurosci 31:6518–6526
Mileykovskiy BY, Kiyashchenko LI, Siegel JM (2005) Behavioral correlates of activity in identified hypocretin/orexin neurons. Neuron 46:787–798
Mochizuki T, Crocker A, McCormack S, Yanagisawa M, Sakurai T, Scammell TE (2004) Behavioral state instability in orexin knock-out mice. J Neurosci 24:6291–6300
Modirrousta M, Mainville L, Jones BE (2005) Orexin and MCH neurons express c-Fos differently after sleep deprivation vs. recovery and bear different adrenergic receptors. Eur J Neurosci 21:2807–2816
Monnier M, Fallert M, Battacharya IC (1967) The waking action of histamine. Experientia 23:21–22
Monsalve GC, Van Buskirk C, Frand AR (2011) LIN-42/PERIOD controls cyclical and developmental progression of C. elegans molts. Curr Biol 21:2033–2045
Morrow JD, Vikraman S, Imeri L, Opp MR (2008) Effects of serotonergic activation by 5-hydroxytryptophan on sleep and body temperature of C57BL/6J and interleukin-6-deficient mice are dose and time related. Sleep 31:21–33
Mukhametov LM, Supin AY, Polyakova IG (1977) Interhemispheric asymmetry of the electroencephalographic sleep patterns in dolphins. Brain Res 134:581–584
Mukhametov LM, Lyamin OI, Polyakova IG (1985) Interhemispheric asynchrony of the sleep EEG in northern fur seals. Experientia 41:1034–1035
Naylor E, Bergmann BM, Krauski K, Zee PC, Takahashi JS, Vitaterna MH, Turek FW (2000) The circadian clock mutation alters sleep homeostasis in the mouse. J Neurosci 20:8138–8143
Nicholson AN, Pascoe PA, Stone BM (1985) Histaminergic systems and sleep. Studies in man with H1 and H2 antagonists. Neuropharmacology 24:245–250
Nicol SC, Andersen NA, Phillips NH, Berger RJ (2000) The echidna manifests typical characteristics of rapid eye movement sleep. Neurosci Lett 283:49–52
Nicolau MC, Akaarir M, Gamundi A, Gonzalez J, Rial RV (2000) Why we sleep: the evolutionary pathway to the mammalian sleep. Prog Neurobiol 62:379–406
Obal F Jr, Alfoldi P, Cady AB, Johannsen L, Sary G, Krueger JM (1988) Growth hormone-releasing factor enhances sleep in rats and rabbits. Am J Physiol 255:R310–R316
Oh Y, Jang D, Sonn JY, Choe J (2013) Histamine-HisCl1 receptor axis regulates wake-promoting signals in Drosophila melanogaster. PLoS One 8, e68269
Parisky KM, Agosto J, Pulver SR, Shang Y, Kuklin E, Hodge JJ, Kang K, Liu X, Garrity PA, Rosbash M et al (2008) PDF cells are a GABA-responsive wake-promoting component of the Drosophila sleep circuit. Neuron 60:672–682
Peyron C, Faraco J, Rogers W, Ripley B, Overeem S, Charnay Y, Nevsimalova S, Aldrich M, Reynolds D, Albin R et al (2000) A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains. Nat Med 6:991–997
Piper DC, Upton N, Smith MI, Hunter AJ (2000) The novel brain neuropeptide, orexin-A, modulates the sleep–wake cycle of rats. Eur J Neurosci 12:726–730
Prober DA, Rihel J, Onah AA, Sung RJ, Schier AF (2006) Hypocretin/orexin overexpression induces an insomnia-like phenotype in zebrafish. J Neurosci 26:13400–13410
Qu DQ, Ludwig DS, Gammeltoft S, Piper M, Pelleymounter MA, Cullen MJ, Mathes WF, Przypek J, Kanarek R, Maratos-Flier E (1996) A role for melanin-concentrating hormone in the central regulation of feeding behaviour. Nature 380:243–247
Raizen DM, Zimmerman JE, Maycock MH, Ta UD, You YJ, Sundaram MV, Pack AI (2008) Lethargus is a Caenorhabditis elegans sleep-like state. Nature 451:569–572
Rasch B, Buchel C, Gais S, Born J (2007) Odor cues during slow-wave sleep prompt declarative memory consolidation. Science 315:1426–1429
Rattenborg NC (2006) Evolution of slow-wave sleep and palliopallial connectivity in mammals and birds: a hypothesis. Brain Res Bull 69:20–29
Rattenborg NC, Martinez-Gonzalez D (2014) Avian versus mammalian sleep: the fruits of comparing apples and oranges. Curr Sleep Med Rep 1:55–63
Rattenborg NC, Lima SL, Amlaner CJ (1999) Facultative control of avian unihemispheric sleep under the risk of predation. Behav Brain Res 105:163–172
Rattenborg NC, Amlaner CJ, Lima SL (2000) Behavioral, neurophysiological and evolutionary perspectives on unihemispheric sleep. Neurosci Biobehav Rev 24:817–842
Rechtschaffen A, Bergmann BM (2002) Sleep deprivation in the rat: an update of the 1989 paper. Sleep 25:18–24
Rechtschaffen A, Bergmann BM, Everson CA, Kushida CA, Gilliland MA (1989) Sleep deprivation in the rat: X. Integration and discussion of the findings. Sleep 12:68–87
Renier C, Faraco JH, Bourgin P, Motley T, Bonaventure P, Rosa F, Mignot E (2007) Genomic and functional conservation of sedative-hypnotic targets in the zebrafish. Pharmacogenet Genomics 17:237–253
Rial RV, Nicolau MC, Gamundi A, Akaarir M, Garau C, Aparicio S, Tejada S, Moranta D, Gene L, Esteban S (2007) Comments on evolution of sleep and the palliopallial connectivity in mammals and birds. Brain Res Bull 72:183–186
Rial RV, Akaarir M, Gamundi A, Garau C, Aparicio S, Tejada S, Gene L, Nicolau MC, Esteban S (2008) Wake and sleep hypothalamic regulation in diurnal and nocturnal chronotypes. J Pineal Res 45:225–226
Rial RV, Akaarir M, Gamundi A, Nicolau C, Garau C, Aparicio S, Tejada S, Gene L, Gonzalez J, De Vera LM et al (2010) Evolution of wakefulness, sleep and hibernation: from reptiles to mammals. Neurosci Biobehav Rev 34:1144–1160
Sakai K, Crochet S, Onoe H (2001) Pontine structures and mechanisms involved in the generation of paradoxical (REM) sleep. Arch Ital Biol 139:93–107
Sakurai T, Amemiya A, Ishii M, Matsuzaki I, Chemelli RM, Tanaka H, Williams SC, Richardson JA, Kozlowski GP, Wilson S et al (1998) Orexins and orexin receptors: a family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behavior. Cell 92:573–585
Saper CB, Fuller PM, Pedersen NP, Lu J, Scammell TE (2010) Sleep state switching. Neuron 68:1023–1042
Shaw PJ, Cirelli C, Greenspan RJ, Tononi G (2000) Correlates of sleep and waking in Drosophila melanogaster. Science 287:1834–1837
Shaw PJ, Tononi G, Greenspan RJ, Robinson DF (2002) Stress response genes protect against lethal effects of sleep deprivation in Drosophila. Nature 417:287–291
Siegel JM, Manger PR, Nienhuis R, Fahringer HM, Pettigrew JD (1996) The echidna Tachyglossus aculeatus combines REM and non-REM aspects in a single sleep state: implications for the evolution of sleep. J Neurosci 16:3500–3506
Singh K, Ju JY, Walsh MB, DiIorio MA, Hart AC (2014) Deep conservation of genes required for both Drosophila melanogaster and Caenorhabditis elegans sleep includes a role for dopaminergic signaling. Sleep 37:1439–1451
Sundvik M, Kudo H, Toivonen P, Rozov S, Chen YC, Panula P (2011) The histaminergic system regulates wakefulness and orexin/hypocretin neuron development via histamine receptor H1 in zebrafish. FASEB J 25:4338–4347
Szentirmai E, Krueger JM (2006) Central administration of neuropeptide Y induces wakefulness in rats. Am J Physiol Regul Integr Comp Physiol 291:R473–R480
Taheri S, Lin L, Austin D, Young T, Mignot E (2004) Short sleep duration is associated with reduced leptin, elevated ghrelin, and increased body mass index. PLoS Med 1, e62
Takahashi Y, Kipnis DM, Daughaday WH (1968) Growth hormone secretion during sleep. J Clin Invest 47:2079–2090
Takahashi K, Lin JS, Sakai K (2008) Neuronal activity of orexin and non-orexin waking-active neurons during wake-sleep states in the mouse. Neuroscience 153:860–870
Thannickal TC, Moore RY, Nienhuis R, Ramanathan L, Gulyani S, Aldrich M, Cornford M, Siegel JM (2000) Reduced number of hypocretin neurons in human narcolepsy. Neuron 27:469–474
Tsunematsu T, Ueno T, Tabuchi S, Inutsuka A, Tanaka KF, Hasuwa H, Kilduff TS, Terao A, Yamanaka A (2014) Optogenetic manipulation of activity and temporally controlled cell-specific ablation reveal a role for MCH neurons in sleep/wake regulation. J Neurosci 34:6896–6909
Van Buskirk C, Sternberg PW (2007) Epidermal growth factor signaling induces behavioral quiescence in Caenorhabditis elegans. Nat Neurosci 10:1300–1307
Van Cauter E, Knutson KL (2008) Sleep and the epidemic of obesity in children and adults. Eur J Endocrinol Eur Fed Endocrine Soc 159(suppl 1):S59–S66
Vanni-Mercier G, Sakai K, Lin JS, Jouvet M (1989) Mapping of cholinoceptive brainstem structures responsible for the generation of paradoxical sleep in the cat. Arch Ital Biol 127:133–164
Verret L, Goutagny R, Fort P, Cagnon L, Salvert D, Leger L, Boissard R, Salin P, Peyron C, Luppi PH (2003) A role of melanin-concentrating hormone producing neurons in the central regulation of paradoxical sleep. BMC Neurosci 4:19
Viola AU, Archer SN, James LM, Groeger JA, Lo JC, Skene DJ, von Schantz M, Dijk DJ (2007) PER3 polymorphism predicts sleep structure and waking performance. Curr Biol 17:613–618
Vyazovskiy VV, Olcese U, Hanlon EC, Nir Y, Cirelli C, Tononi G (2011) Local sleep in awake rats. Nature 472:443–447
White JG, Albertson DG, Anness MA (1978) Connectivity changes in a class of motoneurone during the development of a nematode. Nature 271:764–766
Willie JT, Chemelli RM, Sinton CM, Tokita S, Williams SC, Kisanuki YY, Marcus JN, Lee C, Elmquist JK, Kohlmeier KA et al (2003) Distinct narcolepsy syndromes in Orexin receptor-2 and Orexin null mice: molecular genetic dissection of non-REM and REM sleep regulatory processes. Neuron 38:715–730
Wisor JP, Nishino S, Sora I, Uhl GH, Mignot E, Edgar DM (2001) Dopaminergic role in stimulant-induced wakefulness. J Neurosci 21:1787–1794
Wisor JP, O’Hara BF, Terao A, Selby CP, Kilduff TS, Sancar A, Edgar DM, Franken P (2002) A role for cryptochromes in sleep regulation. BMC Neurosci 3:20
Wu MN, Ho K, Crocker A, Yue Z, Koh K, Sehgal A (2009) The effects of caffeine on sleep in Drosophila require PKA activity, but not the adenosine receptor. J Neurosci 29:11029–11037
Xie L, Kang H, Xu Q, Chen MJ, Liao Y, Thiyagarajan M, O’Donnell J, Christensen DJ, Nicholson C, Iliff JJ et al (2013) Sleep drives metabolite clearance from the adult brain. Science 342:373–377
Yang G, Gan WB (2012) Sleep contributes to dendritic spine formation and elimination in the developing mouse somatosensory cortex. Dev Neurobiol 72:1391–1398
Yang G, Lai CS, Cichon J, Ma L, Li W, Gan WB (2014) Sleep promotes branch-specific formation of dendritic spines after learning. Science 344:1173–1178
Yokogawa T, Marin W, Faraco J, Pezeron G, Appelbaum L, Zhang J, Rosa F, Mourrain P, Mignot E (2007) Characterization of sleep in zebrafish and insomnia in hypocretin receptor mutants. PLoS Biol 5, e277
Young JZ (1981) The life of vertebrates, 3rd edn. Clarendon, Oxford
Yuan Q, Joiner WJ, Sehgal A (2006) A sleep-promoting role for the Drosophila serotonin receptor 1A. Curr Biol 16:1051–1062
Zhang Z, Ferretti V, Guntan I, Moro A, Steinberg EA, Ye Z, Zecharia AY, Yu X, Vyssotski AL, Brickley SG et al (2015) Neuronal ensembles sufficient for recovery sleep and the sedative actions of alpha2 adrenergic agonists. Nat Neurosci 18:553–561
Zhdanova IV, Wang SY, Leclair OU, Danilova NP (2001) Melatonin promotes sleep-like state in zebrafish. Brain Res 903:263–268
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Hayashi, Y., Liu, CY. (2017). The Evolution and Function of Sleep. In: Shigeno, S., Murakami, Y., Nomura, T. (eds) Brain Evolution by Design. Diversity and Commonality in Animals. Springer, Tokyo. https://doi.org/10.1007/978-4-431-56469-0_15
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