Galanin neurons in the ventrolateral preoptic area promote sleep and heat loss in mice
Open accessAbstract
The preoptic area (POA) is necessary for sleep, but the fundamental POA circuits have remained elusive. Previous studies showed that galanin (GAL)- and GABA-producing neurons in the ventrolateral preoptic nucleus (VLPO) express cFos after periods of increased sleep and innervate key wake-promoting regions. Although lesions in this region can produce insomnia, high frequency photostimulation of the POA GAL neurons was shown to paradoxically cause waking, not sleep. Here we report that photostimulation of VLPO GAL neurons in mice promotes sleep with low frequency stimulation (1–4 Hz), but causes conduction block and waking at frequencies above 8 Hz. Further, optogenetic inhibition reduces sleep. Chemogenetic activation of VLPO GAL neurons confirms the increase in sleep, and also reduces body temperature. In addition, chemogenetic activation of VLPO GAL neurons induces short-latency sleep in an animal model of insomnia. Collectively, these findings establish a causal role of VLPO GAL neurons in both sleep induction and heat loss.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
General anesthetics coopt warm-sensing and sleep-active preoptic neurons to produce hypnosis and central body cooling.
“Recent work suggests that general anesthetics coopt such “dual purpose” warm-sensing and sleep-active subsets of neurons both to elicit hypnosis and to drive central cooling of body temperature, which occurs during anesthetics states [99, 103, 110].”
From The Biology of General Anesthesia from Paramecium to Primate (2019) · cites this paper as [110]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859 · see citing works
Rapid, reversible activation of AgRP neurons drives feeding behavior in mice
Krashes, M. J., Koda, S., Ye, C., Rogan, S. C., Adams, A. C., Cusher, D. S., Maratos-Flier, E., Roth, B. L., & Lowell, B. B. (2011) · Journal of Clinical Investigation · doi:10.1172/jci46229 · Cited by 1,578 · see citing works
A putative flip–flop switch for control of REM sleep
Lu, J., Sherman, D. L., Devor, M. G., & Saper, C. B. (2006) · Nature · doi:10.1038/nature04767 · Cited by 1,219 · see citing works
Self-citationActivation of ventrolateral preoptic neurons during sleep
Sherin, J. E., Shiromani, P. J., McCarley, R. W., & Saper, C. B. (1996) · Science · doi:10.1126/science.271.5246.216 · Cited by 1,111 · see citing works
Self-citationChemogenetics revealed: DREADD occupancy and activation via converted clozapine
Gomez, J. L., Bonaventura, J., Lesniak, W., Mathews, W. B., Sysa-Shah, P., Rodriguez, L. A., Ellis, R. J., Richie, C. T., Harvey, B. K., Dannals, R. F., et al. (2017) · Science · doi:10.1126/science.aan2475 · Cited by 980 · see citing works
Sherin, J. E., Elmquist, J. K., Torrealba, F., & Saper, C. B. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-12-04705.1998 · Cited by 746 · see citing works
Self-citationSLEEP AS A PROBLEM OF LOCALIZATION
von Economo, C. (1930) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-193003000-00001 · Cited by 687 · see citing works
HYPOTHALAMIC REGULATION OF SLEEP IN RATS. AN EXPERIMENTAL STUDY
Nauta, W. J. H. (1946) · Journal of Neurophysiology · doi:10.1152/jn.1946.9.4.285 · Cited by 668 · see citing works
Effect of Lesions of the Ventrolateral Preoptic Nucleus on NREM and REM Sleep
Lu, J., Greco, M. A., Shiromani, P. J., & Saper, C. B. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-10-03830.2000 · Cited by 667 · see citing works
Self-citationCentral neural pathways for thermoregulation
Shaun, F. M. (2010) · Frontiers in bioscience · doi:10.2741/3677 · Cited by 658 · see citing works
Sleep–waking discharge patterns of ventrolateral preoptic/anterior hypothalamic neurons in rats
Szymusiak, R. S., Alam, N., Steininger, T. L., & McGinty, D. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00631-3 · Cited by 458 · see citing works
Optogenetic identification of a rapid eye movement sleep modulatory circuit in the hypothalamus
Jego, S., Glasgow, S. D., Herrera, C. G., Ekstrand, M. I., Reed, S. J., Boyce, R., Friedman, J. M., Burdakov, D., & Adamantidis, A. (2013) · Nature Neuroscience · doi:10.1038/nn.3522 · Cited by 454 · see citing works
Warm-Sensitive Neurons that Control Body Temperature
Tan, C. L., Cooke, E. K., Leib, D. E., Lin, Y.-C., Daly, G. E., Zimmerman, C. A., & Knight, Z. A. (2016) · Cell · doi:10.1016/j.cell.2016.08.028 · Cited by 402 · see citing works
Keeping cool: a hypothesis about the mechanisms and functions of slow-wave sleep
McGinty, D., & Szymusiak, R. S. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90081-k · Cited by 390 · see citing works
Sterman, M. B., & Clemente, C. (1962) · Experimental Neurology · doi:10.1016/0014-4886(62)90081-x · Cited by 375 · see citing works
EP3 prostaglandin receptors in the median preoptic nucleus are critical for fever responses
Lazarus, M., Yoshida, K., Coppari, R., Bass, C. E., Mochizuki, T., Lowell, B. B., & Saper, C. B. (2007) · Nature Neuroscience · doi:10.1038/nn1949 · Cited by 367 · see citing works
Self-citationA hypothalamic circuit that controls body temperature
Zhao, Z., Yang, W. Z., Gao, C., Fu, X., Zhang, W., Zhou, Q., Chen, W., Ni, X., Lin, J.-K., Yang, J., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1616255114 · Cited by 352 · see citing works
Identification of preoptic sleep neurons using retrograde labelling and gene profiling
Chung, S., Weber, F., Zhong, P., Tan, C. L., Nguyen, T. N., Beier, K. T., Hörmann, N., Chang, W.-C., Zhang, Z., Do, J. P., et al. (2017) · Nature · doi:10.1038/nature22350 · Cited by 317 · see citing works
The effects of high and low ambient temperatures on human sleep stages
Haskell, E. H., Palca, J. W., Walker, J. M., Berger, R. J., & Heller, H. C. (1981) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(81)90226-1 · Cited by 302 · see citing works
Gaus, S. E., Strecker, R. E., Tate, B. A., Parker, R. A., & Saper, C. B. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00308-1 · Cited by 288 · see citing works
Self-citationNeural circuitry engaged by prostaglandins during the sickness syndrome
Saper, C. B., Romanovsky, A. A., & Scammell, T. E. (2012) · Nature Neuroscience · doi:10.1038/nn.3159 · Cited by 285 · see citing works
Self-citationNeuronal ensembles sufficient for recovery sleep and the sedative actions of α2 adrenergic agonists
Zhang, Z., Ferretti, V., Güntan, İ., Moro, A., Steinberg, E. A., Ye, Z., Zecharia, A. Y., Yu, X., Vyssotski, A. L., Brickley, S. G., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.3957 · Cited by 275 · see citing works
Forebrain inhibitory mechanisms: Cortical synchronization induced by basal forebrain stimulation
Sterman, M. B., & Clemente, C. (1962) · Experimental Neurology · doi:10.1016/0014-4886(62)90080-8 · Cited by 244 · see citing works
Neural Circuitry of Stress-Induced Insomnia in Rats
Cano, G., Mochizuki, T., & Saper, C. B. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1809-08.2008 · Cited by 242 · see citing works
Self-citationSallanon, M. M., Denoyer, M., Kitahama, K., Aubert, C., Gay, N., & Jouvet, M. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90289-3 · Cited by 235 · see citing works
Central neural control of thermoregulation and brown adipose tissue
Morrison, S. F. (2016) · Autonomic Neuroscience · doi:10.1016/j.autneu.2016.02.010 · Cited by 213 · see citing works
Dynamic GABAergic afferent modulation of AgRP neurons
Garfield, A. S., Shah, B. P., Burgess, C. R., Li, M. M., Li, C., Steger, J. S., Madara, J. C., Campbell, J. N., Kroeger, D., Scammell, T. E., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4392 · Cited by 211 · see citing works
Self-citationKroeger, D., Ferrari, L. L., Petit, G., Mahoney, C. E., Fuller, P. M., Arrigoni, E., & Scammell, T. E. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1405-16.2016 · Cited by 198 · see citing works
Self-citationLim, A. S. P., Ellison, B. A., Wang, J., Yu, L., Schneider, J. A., Buchman, A. S., Bennett, D. A., & Saper, C. B. (2014) · Brain · doi:10.1093/brain/awu222 · Cited by 187 · see citing works
Self-citationMaximal REM sleep time defines a narrower thermoneutral zone than does minimal metabolic rate
Szymusiak, R. S., & Satinoff, E. (1981) · Physiology & Behavior · doi:10.1016/0031-9384(81)90145-1 · Cited by 176 · see citing works
Sleep and environmental temperature.
Parmeggiani, P. L., & Rabini, C. (1970) · PubMed · Cited by 168 · see citing works
Parallel preoptic pathways for thermoregulation
Yoshida, K., Li, X., Cano, G., Lazarus, M., & Saper, C. B. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2643-09.2009 · Cited by 160 · see citing works
Self-citationA Genetically Defined Circuit for Arousal from Sleep during Hypercapnia
Kaur, S., Wang, J., Ferrari, L. L., Thankachan, S., Kroeger, D., Venner, A., Lazarus, M., Wellman, A., Arrigoni, E., Fuller, P. M., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.009 · Cited by 158 · see citing works
Self-citationParmeggiani, P. L. (2003) · Frontiers in Bioscience · doi:10.2741/1054 · Cited by 153 · see citing works
Takahashi, K., Lin, J., & Sakai, K. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.02.075 · Cited by 142 · see citing works
Neuronal discharge of preoptic/anterior hypothalamic thermosensitive neurons: relation to NREM sleep
Alam, M. N., McGinty, D., & Szymusiak, R. S. (1995) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1995.269.5.r1240 · Cited by 132 · see citing works
Scammell, T. E., Griffin, J. D., Elmquist, J. K., & Saper, C. B. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.274.3.r783 · Cited by 130 · see citing works
Self-citationSleep and Circadian Rhythms in Mammalian Torpor
Heller, H. C., & Ruby, N. F. (2004) · Annual Review of Physiology · doi:10.1146/annurev.physiol.66.032102.115313 · Cited by 124 · see citing works
More functions of torpor and their roles in a changing world
Nowack, J., Stawski, C., & Geiser, F. (2017) · Journal of Comparative Physiology B · doi:10.1007/s00360-017-1100-y · Cited by 124 · see citing works
Qualls‐Creekmore, E., Yu, S., Francois, M., Hoang, J. G., Huesing, C., Bruce‐Keller, A. J., Burk, D. H., Berthoud, H., Morrison, C. D., & Münzberg, H. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0155-17.2017 · Cited by 121 · see citing works
Self-citationRelaxation and sleep induced by warming of preoptic region and anterior hypothalamus in cats
Roberts, W. W., & Robinson, T. C. (1969) · Experimental Neurology · doi:10.1016/0014-4886(69)90051-x · Cited by 115 · see citing works
Interaction Between Sleep and Thermoregulation: An Aspect of the Control of Behavioral States
Parmeggiani, P. L. (1986) · SLEEP · doi:10.1093/sleep/10.5.426 · Cited by 110 · see citing works
Melanin-concentrating hormone neurons specifically promote rapid eye movement sleep in mice
Vetrivelan, R., Kong, D., Ferrari, L. L., Arrigoni, E., Madara, J. C., Bandaru, S. S., Lowell, B. B., Lu, J., & Saper, C. B. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.08.046 · Cited by 109 · see citing works
Self-citationModirrousta, M., Mainville, L., & Jones, B. E. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.07.028 · Cited by 107 · see citing works
Williams, R. H., Chee, M. J. S., Kroeger, D., Ferrari, L. L., Maratos–Flier, E., Scammell, T. E., & Arrigoni, E. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4838-13.2014 · Cited by 107 · see citing works
Self-citationInfluence of hypothalamic and ambient temperatures on sleep in kangaroo rats
Sakaguchi, S., Glotzbach, S. F., & Heller, H. C. (1979) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1979.237.1.r80 · Cited by 104 · see citing works
Leptin modulates nutrient reward via inhibitory galanin action on orexin neurons
Laque, A., Yu, S., Qualls‐Creekmore, E., Gettys, S., Schwartzenburg, C., Bui, K., Rhodes, C. J., Berthoud, H., Morrison, C. D., Richards, B. K. S., et al. (2015) · Molecular Metabolism · doi:10.1016/j.molmet.2015.07.002 · Cited by 99 · see citing works
Self-citationGABAergic neurons in the preoptic area send direct inhibitory projections to orexin neurons
Saito, Y. C., Tsujino, N., Hasegawa, E., Akashi, K., Abe, M., Mieda, M., Sakimura, K., & Sakurai, T. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00192 · Cited by 97 · see citing works
Berger, R. J. (1984) · Biological Psychology · doi:10.1016/0301-0511(84)90045-0 · Cited by 95 · see citing works
Effect of NMDA Lesion of the Medial Preoptic Neurons on Sleep and Other Functions
John, J., & Kumar, V. M. (1998) · SLEEP · doi:10.1093/sleep/21.6.587 · Cited by 95 · see citing works
Elevated body temperature during sleep in orexin knockout mice
Mochizuki, T., Klerman, E. B., Sakurai, T., & Scammell, T. E. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00887.2005 · Cited by 86 · see citing works
Self-citationComparative aspects of energy metabolism, body temperature and sleep.
Berger, R. J., & Phillips, N. H. (1988) · PubMed · Cited by 80 · see citing works
Abbott, S. B. G., & Saper, C. B. (2017) · The Journal of Physiology · doi:10.1113/jp274667 · Cited by 74 · see citing works
Self-citationEffect of ambient temperature on the sleep-waking cycle in two strains of mice
Roussel, B., Turrillot, P., & Kitahama, K. (1984) · Brain Research · doi:10.1016/0006-8993(84)91310-6 · Cited by 72 · see citing works
Preoptic–Raphé Connections for Thermoregulatory Vasomotor Control
Tanaka, M., McKinley, M. J., & McAllen, R. M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6433-10.2011 · Cited by 71 · see citing works
Metabolic Effects of Chronic Sleep Restriction in Rats
Vetrivelan, R., Fuller, P. M., Yokota, S., Lu, J., & Saper, C. B. (2012) · Sleep · doi:10.5665/sleep.2200 · Cited by 61 · see citing works
Self-citationRoles of two preoptic cell groups in tonic and febrile control of rat tail sympathetic fibers
Tanaka, M., McKinley, M. J., & McAllen, R. M. (2009) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.91010.2008 · Cited by 60 · see citing works
Selective increases in non-rapid eye movement sleep following whole body heating in rats
Morairty, S. R., Szymusiak, R. S., Thomson, D., & McGinty, D. (1993) · Brain Research · doi:10.1016/0006-8993(93)90606-n · Cited by 56 · see citing works
Hypothalamic sleep-promoting mechanisms: coupling to thermoregulation.
McGinty, D., Alam, M. N., Szymusiak, R. S., Nakao, M., & Yamamoto, M. (2001) · PubMed · Cited by 34 · see citing works
Chapter 22 Sleep regulation: relation to photoperiod, sleep duration, waking activity, and torpor
Borbély, A. A., & Tobler, I. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)60417-3 · Cited by 26 · see citing works
Glutamate microinjection at the medial preoptic area enhances slow wave sleep in rats
Kaushik, M. K., Kumar, V. M., & Mallick, H. N. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.11.007 · Cited by 24 · see citing works
Dynorphin inhibits basal forebrain cholinergic neurons by pre‐ and postsynaptic mechanisms
Ferrari, L. L., Agostinelli, L. J., Krashes, M. J., Lowell, B. B., Scammell, T. E., & Arrigoni, E. (2015) · The Journal of Physiology · doi:10.1113/jp271657 · Cited by 24 · see citing works
Self-citationInternal temperature variations during the sleep-wake cycle in the rat.
Roussel, B., Dittmar, A., & Chouvet, G. (1980) · PubMed · Cited by 23 · see citing works
Control of slow wave sleep by thermoregulatory mechanisms.
Szymusiak, R., & McGINTY, D. (1990) · PubMed · Cited by 23 · see citing works
Berger, R. J., & Phillips, N. H. (1990) · PubMed · Cited by 20 · see citing works
Berger, R. J. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90210-c · Cited by 19 · see citing works
Sleep induction and temperature lowering by medial preoptic α1 adrenergic receptors
Vetrivelan, R., Mallick, H. N., & Kumar, V. M. (2006) · Physiology & Behavior · doi:10.1016/j.physbeh.2006.01.015 · Cited by 16 · see citing works
Self-citationArmodafinil-induced wakefulness in animals with ventrolateral preoptic lesions
Fuller, P. M., Vetrivelan, R., & Saper, C. B. (2014) · Nature and Science of Sleep · doi:10.2147/nss.s53132 · Cited by 14 · see citing works
Self-citation[Central temperature is the principal factor of regulation of paradoxical sleep in pontile cats].
Jouvet, M., Buda, C., Debilly, G., Dittmar, A., & Sastre, J. (1988) · PubMed · Cited by 13 · see citing works
Unmasking of α1 adrenoceptor induced hypnogenic response from medial preoptic area
Vetrivelan, R., Mallick, H. N., & Kumar, V. M. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.02.013 · Cited by 9 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Sleep deprivation and stress: a reciprocal relationship
Nollet, M., Wisden, W., & Franks, N. P. (2020) · Interface Focus · doi:10.1098/rsfs.2019.0092 · Cited by 307 · see citing works
Oscillating circuitries in the sleeping brain
Adamantidis, A. R., Gutierrez Herrera, C., & Gent, T. C. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0223-4 · Cited by 281 · see citing works
The Temperature Dependence of Sleep
Harding, E. C., Franks, N. P., & Wisden, W. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00336 · Cited by 261 · see citing works
The emergence and influence of internal states
Flavell, S. W., Gogolla, N., Lovett-Barron, M., & Zelikowsky, M. (2022) · Neuron · doi:10.1016/j.neuron.2022.04.030 · Cited by 234 · see citing works
A common neuroendocrine substrate for diverse general anesthetics and sleep
Jiang-Xie, L.-F., Yin, L., Zhao, S., Prevosto, V., Han, B.-X., Dzirasa, K., & Wang, F. (2019) · Neuron · doi:10.1016/j.neuron.2019.03.033 · Cited by 173 · see citing works
A Vagal-NTS Neural Pathway that Stimulates Feeding
Chen, J. W., Cheng, M., Wang, L. Y., Zhang, L., Xu, D., Cao, P., Wang, F., Herzog, H., Song, S., & Zhan, C. (2020) · Current Biology · doi:10.1016/j.cub.2020.07.084 · Cited by 167 · see citing works
The Biology of General Anesthesia from Paramecium to Primate
Kelz, M. B., & Mashour, G. A. (2019) · Current Biology · doi:10.1016/j.cub.2019.09.071 · Cited by 151 · see citing works
Circadian Rhythms of the Hypothalamus: From Function to Physiology
Drunen, R. V., & Eckel‐Mahan, K. L. (2021) · Clocks & Sleep · doi:10.3390/clockssleep3010012 · Cited by 138 · see citing works
Galanin Neurons Unite Sleep Homeostasis and α2-Adrenergic Sedation
Ma, Y., Miracca, G., Yu, X., Harding, E. C., Miao, A., Yustos, R., Vyssotski, A. L., Franks, N. P., & Wisden, W. (2019) · Current Biology · doi:10.1016/j.cub.2019.07.087 · Cited by 126 · see citing works
Orexin neurons inhibit sleep to promote arousal
De Luca, R., Nardone, S., Grace, K. P., Venner, A., Cristofolini, M., Bandaru, S. S., Sohn, L. T., Kong, D., Mochizuki, T., Viberti, B., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-31591-y · Cited by 130 · see citing works
Self-citationTranscriptional Basis for Rhythmic Control of Hunger and Metabolism within the AgRP Neuron
Cedernaes, J., Huang, W., Ramsey, K. M., Waldeck, N. J., Cheng, L., Marcheva, B., Omura, C., Kobayashi, Y., Peek, C. B., Levine, D. C., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.01.023 · Cited by 126 · see citing works
A hypothalamomedullary network for physiological responses to environmental stresses
Nakamura, K., Nakamura, Y., & Kataoka, N. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00532-x · Cited by 120 · see citing works
Harding, E. C., Franks, N. P., & Wisden, W. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.11.008 · Cited by 113 · see citing works
Role of the Preoptic Area in Sleep and Thermoregulation
Rothhaas, R., & Chung, S. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.664781 · Cited by 98 · see citing works
Vanini, G., Bassana, M., Mast, M., Mondino, A., Cerda, I. H., Phyle, M., Chen, V., Colmenero, A. V., Hambrecht‐Wiedbusch, V. S., & Mashour, G. A. (2020) · Current Biology · doi:10.1016/j.cub.2019.12.063 · Cited by 96 · see citing works
Integrating Hunger with Rival Motivations
Hickey, A. K. S., & Krashes, M. J. (2020) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2020.04.006 · Cited by 95 · see citing works
Tau-driven degeneration of sleep- and wake-regulating neurons in Alzheimer’s disease
Lew, C. H., Petersen, C., Neylan, T. C., & Grinberg, L. T. (2021) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2021.101541 · Cited by 95 · see citing works
Interactions between central nervous system and peripheral metabolic organs
Zeng, W., Yang, F., Shen, W. L., Zhan, C., Zheng, P., & Hu, J. (2022) · Science China Life Sciences · doi:10.1007/s11427-021-2103-5 · Cited by 96 · see citing works
Reichert, S., Arocas, O. P., & Rihel, J. (2019) · Neuron · doi:10.1016/j.neuron.2019.08.010 · Cited by 89 · see citing works
EP3R-Expressing Glutamatergic Preoptic Neurons Mediate Inflammatory Fever
Machado, N., Bandaru, S. S., Abbott, S. B. G., & Saper, C. B. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2887-19.2020 · Cited by 86 · see citing works
Self-citationParabrachial neuron types categorically encode thermoregulation variables during heat defense
Yang, W. Z., Du, X., Zhang, W., Gao, C., Xie, H., Xiao, Y., Jia, X., Liu, J., Xu, J., Fu, X., et al. (2020) · Science Advances · doi:10.1126/sciadv.abb9414 · Cited by 80 · see citing works
Adamantidis, A., & de Lecea, L. (2023) · Science · doi:10.1126/science.adh8285 · Cited by 83 · see citing works
Alzheimer’s disease: Neurotransmitters of the sleep-wake cycle
Erum, J. V., Dam, D. V., & Deyn, P. P. D. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.07.019 · Cited by 81 · see citing works
Tossell, K., Yu, X., Giannos, P., Soto, B. A., Nollet, M., Yustos, R., Miracca, G., Vicente, M., Miao, A., Hsieh, B., et al. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01430-4 · Cited by 82 · see citing works
Yue, L., Wu, S. K., Xiang, A., Hu, D., Wang, L., & Zhang, L. (2021) · Current Biology · doi:10.1016/j.cub.2021.06.031 · Cited by 78 · see citing works
Preoptic BRS3 neurons increase body temperature and heart rate via multiple pathways
Piñol, R. A., Mogul, A. S., Hadley, C. K., Saha, A., Li, C., Škop, V., Province, H. S., Xiao, C., Gavrilova, O., Krashes, M. J., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.05.001 · Cited by 76 · see citing works
A signalling pathway for transcriptional regulation of sleep amount in mice
Zhou, R., Wang, G., Li, Q., Meng, F., Liu, C., Gan, R., Ju, D., Liao, M., Xu, J., Sang, D., et al. (2022) · Nature · doi:10.1038/s41586-022-05510-6 · Cited by 76 · see citing works
The retinal iprgc-preoptic circuit mediates the acute effect of light on sleep
Zhang, Z., Beier, C., Weil, T., & Hattar, S. (2021) · Nature Communications · doi:10.1038/s41467-021-25378-w · Cited by 75 · see citing works
Control of the cardiovascular and respiratory systems during sleep
Benarroch, E. E. (2019) · Autonomic Neuroscience · doi:10.1016/j.autneu.2019.01.007 · Cited by 74 · see citing works
Gene family evolution underlies cell-type diversification in the hypothalamus of teleosts
Shafer, M. E. R., Sawh, A. N., & Schier, A. F. (2021) · Nature Ecology & Evolution · doi:10.1038/s41559-021-01580-3 · Cited by 74 · see citing works
Reassessing the Role of Histaminergic Tuberomammillary Neurons in Arousal Control
Venner, A., Mochizuki, T., De Luca, R., Anaclet, C., Scammell, T. E., Saper, C. B., Arrigoni, E., & Fuller, P. M. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.1032-19.2019 · Cited by 70 · see citing works
Self-citationAn Inhibitory Lateral Hypothalamic-Preoptic Circuit Mediates Rapid Arousals from Sleep
Venner, A., Luca, R. D., Sohn, L. T., Bandaru, S. S., Verstegen, A. M. J., Arrigoni, E., & Fuller, P. M. (2019) · Current Biology · doi:10.1016/j.cub.2019.10.026 · Cited by 66 · see citing works
Self-citationThe Sleep-Promoting Ventrolateral Preoptic Nucleus: What Have We Learned over the Past 25 Years?
Arrigoni, E., & Fuller, P. M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23062905 · Cited by 66 · see citing works
Self-citationBao, W., Jiang, S., Qu, W., Li, W., Miao, C., & Huang, Z. (2023) · Pharmacological Reviews · doi:10.1124/pharmrev.122.000717 · Cited by 68 · see citing works
Komagata, N., Latifi, B., Rusterholz, T., Bassetti, C. L., Adamantidis, A., & Schmidt, M. H. (2019) · Current Biology · doi:10.1016/j.cub.2019.05.009 · Cited by 63 · see citing works
Norris, A. J., Shaker, J. R., Cone, A. L., Ndiokho, I., & Bruchas, M. R. (2021) · eLife · doi:10.7554/elife.60779 · Cited by 61 · see citing works
Nakamura, Y., Yahiro, T., Fukushima, A., Kataoka, N., Hioki, H., & Nakamura, K. (2022) · Science Advances · doi:10.1126/sciadv.add5463 · Cited by 61 · see citing works
Galanin peptide family regulation of glucose metabolism
Fang, P., Yu, M., Shi, M., Bo, P., & Zhang, Z. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100801 · Cited by 58 · see citing works
The aging brain: sleep, the circadian clock and exercise
Panagiotou, M., Michel, S. H., Meijer, J. H., & Deboer, T. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114563 · Cited by 59 · see citing works
Cellular Composition of the Preoptic Area Regulating Sleep, Parental, and Sexual Behavior
Tsuneoka, Y., & Funato, H. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.649159 · Cited by 57 · see citing works
Zhou, Q., Fu, X., Xu, J., Dong, S., Liu, C., Cheng, D., Gao, C., Huang, M., Liu, Z., Ni, X., et al. (2022) · Neuron · doi:10.1016/j.neuron.2022.11.008 · Cited by 56 · see citing works
Roles of Neuropeptides in Sleep–Wake Regulation
Shen, Y.-C., Sun, X., Li, L., Zhang, H.-Y.-L., Huang, Z., & Wang, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094599 · Cited by 54 · see citing works
Relationship Between Sleep Disturbances and Chronic Pain: A Narrative Review
Jain, S. V., Panjeton, G. D., & Martins, Y. C. (2024) · Clinics and Practice · doi:10.3390/clinpract14060209 · Cited by 54 · see citing works
Sensory input, sex and function shape hypothalamic cell type development
Kaplan, H. S., Logeman, B. L., Zhang, K., Yawitz, T. A., Santiago, C., Sohail, N., Talay, M., Seo, C., Naumenko, S., Sui, S. J. H., et al. (2025) · Nature · doi:10.1038/s41586-025-08603-0 · Cited by 51 · see citing works
Mondino, A., Hambrecht‐Wiedbusch, V. S., Li, D., York, A. K., Pal, D., González, J., Torterolo, P., Mashour, G. A., & Vanini, G. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2718-20.2021 · Cited by 52 · see citing works
Neural Substrates for the Regulation of Sleep and General Anesthesia
Yang, Q., Zhou, F., Li, A., & Dong, H. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666211214144639 · Cited by 50 · see citing works
NMDA Receptors in the Lateral Preoptic Hypothalamus Are Essential for Sustaining NREM and REM Sleep
Miracca, G., Soto, B. A., Tossell, K., Yustos, R., Vyssotski, A. L., Franks, N. P., & Wisden, W. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0350-21.2022 · Cited by 54 · see citing works
A parabrachial-hypothalamic parallel circuit governs cold defense in mice
Yang, W. Z., Xie, H., Du, X., Zhou, Q., Xiao, Y., Zhao, Z., Jia, X., Xu, J., Zhang, W., Cai, S., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-40504-6 · Cited by 54 · see citing works
GABAergic modulation of sleep-wake states
Oishi, Y., Saito, Y. C., & Sakurai, T. (2023) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2023.108505 · Cited by 49 · see citing works
Median preoptic GABA and glutamate neurons exert differential control over sleep behavior
Machado, N., Todd, W. D., Kaur, S., & Saper, C. B. (2022) · Current Biology · doi:10.1016/j.cub.2022.03.039 · Cited by 47 · see citing works
Self-citationA common neuronal ensemble in nucleus accumbens regulates pain-like behaviour and sleep
Sun, H., Li, Z., Qiu, Z., Shen, Y., Guo, Q., Hu, S.-W., Ding, H., An, S., & Cao, J. (2023) · Nature Communications · doi:10.1038/s41467-023-40450-3 · Cited by 49 · see citing works
Reitz, S. L., Wasilczuk, A. Z., Beh, G. H., Proekt, A., & Kelz, M. B. (2020) · Current Biology · doi:10.1016/j.cub.2020.10.050 · Cited by 46 · see citing works
Regulation of stress-induced sleep fragmentation by preoptic glutamatergic neurons
Smith, J., Honig-Frand, A., Antila, H., Choi, A., Kim, H., Beier, K. T., Weber, F., & Chung, S. (2023) · Current Biology · doi:10.1016/j.cub.2023.11.035 · Cited by 45 · see citing works
The hypothalamic link between arousal and sleep homeostasis in mice
Yamagata, T., Kahn, M. C., Prius-Mengual, J., Meijer, E. J., Šabanović, M., Guillaumin, M. C. C., van der Vinne, V., Huang, Y., McKillop, L. E., Jagannath, A., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2101580118 · Cited by 45 · see citing works
Widely Distributed Neurotensinergic Neurons in the Brainstem Regulate NREM Sleep in Mice
Kashiwagi, M., Kanuka, M., Tatsuzawa, C., Suzuki, H., Morita, M., Tanaka, K., Kawano, T., Shin, J. W., Suzuki, H., Itohara, S., et al. (2020) · Current Biology · doi:10.1016/j.cub.2020.01.047 · Cited by 44 · see citing works
Genetic identification of preoptic neurons that regulate body temperature in mice
Machado, N., & Saper, C. B. (2021) · Temperature · doi:10.1080/23328940.2021.1993734 · Cited by 42 · see citing works
Self-citationThe stress of losing sleep: Sex-specific neurobiological outcomes
Wright, C. J., Milosavljevic, S., & Pocivavsek, A. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100543 · Cited by 45 · see citing works
Tam, S. K. E., Brown, L. A., Wilson, T. S., Tir, S., Fisk, A. S., Pothecary, C. A., van der Vinne, V., Foster, F., Vyazovskiy, V. V., Bannerman, D. M., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2101591118 · Cited by 40 · see citing works
Kroeger, D., Bandaru, S. S., Madara, J. C., & Vetrivelan, R. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.03.020 · Cited by 40 · see citing works
Self-citationRe, C. J., Batterman, A. I., Gerstner, J. R., Buono, R. J., & Ferraro, T. N. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00520 · Cited by 39 · see citing works
The neuroanatomy and neurochemistry of sleep-wake control
Gompf, H. S., & Anaclet, C. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.12.012 · Cited by 39 · see citing works
Be cool to be far: Exploiting hibernation for space exploration
Cerri, M., Hitrec, T., Luppi, M., & Amici, R. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.03.037 · Cited by 38 · see citing works
QPLOT Neurons—Converging on a Thermoregulatory Preoptic Neuronal Population
Upton, B. A., D’Souza, S. P., & Lang, R. A. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.665762 · Cited by 38 · see citing works
Astrocytes in the Ventrolateral Preoptic Area Promote Sleep
Kim, J., Choi, I., Jeong, J.-Y., Jang, I., Lee, M., & Suk, K. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1486-20.2020 · Cited by 38 · see citing works
Islam, M. T., Rumpf, F., Tsuno, Y., Kodani, S., Sakurai, T., Matsui, A., Maejima, T., & Mieda, M. (2022) · Current Biology · doi:10.1016/j.cub.2022.07.020 · Cited by 40 · see citing works
Newly identified sleep–wake and circadian circuits as potential therapeutic targets
Venner, A., Todd, W. D., Fraigne, J. J., Bowrey, H. E., Eban-Rothschild, A., Kaur, S., & Anaclet, C. (2019) · SLEEP · doi:10.1093/sleep/zsz023 · Cited by 36 · see citing works
Wang, J. W. J. L., Lombardi, F., Zhang, X., Anaclet, C., & Ivanov, P. C. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007268 · Cited by 35 · see citing works
Adult hypothalamic neurogenesis and sleep–wake dysfunction in aging
Kostin, A., Alam, A., McGinty, D., & Alam, M. N. (2020) · SLEEP · doi:10.1093/sleep/zsaa173 · Cited by 35 · see citing works
Divergent Neural Activity in the VLPO During Anesthesia and Sleep
Luo, M., Fei, X., Liu, X., Jin, Z., Wang, Y., & Xu, M. (2022) · Advanced Science · doi:10.1002/advs.202203395 · Cited by 34 · see citing works
Sleep need–dependent plasticity of a thalamic circuit promotes homeostatic recovery sleep
Lee, S., Liu, Q., Cheng, A., Kim, D. W., Boudreau, D. M., Mehta, A., Keleş, M. F., Fejfer, R., Palmer, I., Park, K. H., et al. (2025) · Science · doi:10.1126/science.adm8203 · Cited by 34 · see citing works
Self-citationMitochondrial control of sleep
Hartmann, C., & Kempf, A. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102733 · Cited by 34 · see citing works
Zhang, S., Zhang, X., Zhong, H., Li, X., Wu, Y., Ju, J., Liu, B., Zhang, Z., Yan, H., Wang, Y., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34735-2 · Cited by 35 · see citing works
Vanini, G., & Torterolo, P. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-61663-2_5 · Cited by 30 · see citing works
Lateral hypothalamic galanin neurons are activated by stress and blunt anxiety-like behavior in mice
Owens-French, J., Li, S., Francois, M., Townsend, R. L., Daniel, M., Soulier, H., Turner, A., de Lecea, L., Münzberg, H., Morrison, C. D., et al. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113773 · Cited by 30 · see citing works
Self-citationLi, S., Zhai, J., Chu, W., Geng, X., Wang, D., Jiao, L., Lü, G., Chan, W., Sun, K., Sun, Y. W., et al. (2023) · npj Biofilms and Microbiomes · doi:10.1038/s41522-023-00415-2 · Cited by 30 · see citing works
Cheng, J., Wu, F., Zhang, M., Ding, D., Fan, S., Chen, G., Zhang, J., & Wang, L. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.615854 · Cited by 28 · see citing works
Discrete TrkB-expressing neurons of the dorsomedial hypothalamus regulate feeding and thermogenesis
Houtz, J., Liao, G., An, J. J., & Xu, B. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2017218118 · Cited by 29 · see citing works
Non-rapid eye movement sleep determines resilience to social stress
Bush, B. J., Donnay, C., Andrews, E.-J. A., Lewis-Sanders, D., Gray, C. L., Qiao, Z., Brager, A. J., Johnson, H., Brewer, H. C., Sood, S., et al. (2022) · eLife · doi:10.7554/elife.80206 · Cited by 28 · see citing works
Teng, S., Zhen, F., Wang, L., Schalchli, J. C., Simko, J., Chen, X., Jin, H., Makinson, C. D., & Peng, Y. (2022) · Nature Communications · doi:10.1038/s41467-022-32461-3 · Cited by 26 · see citing works
Sleep disturbances in autism spectrum disorder: Animal models, neural mechanisms, and therapeutics
Maurer, J. J., Choi, A., An, I., Sathi, N., & Chung, S. (2023) · Neurobiology of Sleep and Circadian Rhythms · doi:10.1016/j.nbscr.2023.100095 · Cited by 28 · see citing works
Central Mechanisms of Thermoregulation and Fever in Mammals
Nakamura, K. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-981-97-4584-5_10 · Cited by 25 · see citing works
Chronic circadian disruption on a high-fat diet impairs glucose tolerance
Zitting, K., Vetrivelan, R., Yuan, R. K., Vujović, N., Wang, W., Bandaru, S. S., Quan, S. F., Klerman, E. B., Scheer, F. A. J. L., Buxton, O. M., et al. (2022) · Metabolism · doi:10.1016/j.metabol.2022.155158 · Cited by 27 · see citing works
Self-citationProkofeva, K., Saito, Y. C., Niwa, Y., Mizuno, S., Takahashi, S., Hirano, A., & Sakurai, T. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1913-22.2023 · Cited by 24 · see citing works
To sleep or not to sleep – Effects on memory in normal aging and disease
Kroeger, D., & Vetrivelan, R. (2023) · Aging Brain · doi:10.1016/j.nbas.2023.100068 · Cited by 25 · see citing works
Self-citationTurn it off and on again: characteristics and control of torpor
Ambler, M. T., Hitrec, T., & Pickering, A. E. (2021) · Wellcome Open Research · doi:10.12688/wellcomeopenres.17379.1 · Cited by 22 · see citing works
Chauveau, F., Claverie, D., Lardant, E., Varin, C., Hardy, E., Walter, A., Canini, F., Rouach, N., & Rancillac, A. (2019) · SLEEP · doi:10.1093/sleep/zsz189 · Cited by 22 · see citing works
How Temperature Influences Sleep
Fan, Y., Wang, Y., Gu, P., Han, J., & Tian, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012191 · Cited by 22 · see citing works
Scharbarg, E., Walter, A., Lecoin, L., Gallopin, T., Lemaître, F., Guille‐Collignon, M., Rouach, N., & Rancillac, A. (2023) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.2c00660 · Cited by 21 · see citing works
A whole-brain single-cell atlas of circadian neural activity in mice
Yamashita, K., Kinoshita, F. L., Yoshida, S., Matsumoto, K., Mitani, T. T., Fujishima, H., Minami, Y., Morii, E., Yamada, R. G., Okada, S., et al. (2025) · Science · doi:10.1126/science.aea3381 · Cited by 23 · see citing works
A cluster of neuropeptide S neurons regulates breathing and arousal
Angelakos, C. C., Girven, K. S., Liu, Y., Gonzalez, O. C., Murphy, K. R., Jennings, K. J., Giardino, W. J., Zweifel, L. S., Suko, A. V., Palmiter, R. D., et al. (2023) · Current Biology · doi:10.1016/j.cub.2023.11.018 · Cited by 19 · see citing works
Francois, M., Kaiser, L., He, Y., Xu, Y., Salbaum, J. M., Yu, S., Morrison, C. D., Berthoud, H., & Münzberg, H. (2024) · Metabolism · doi:10.1016/j.metabol.2024.156100 · Cited by 19 · see citing works
Self-citationZhang, D., Liu, J., Zhu, T., & Zhou, C. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210909150200 · Cited by 19 · see citing works
Parental brain through time: The origin and development of the neural circuit of mammalian parenting
Kuroda, K. O., Fukumitsu, K., Kurachi, T., Ohmura, N., Shiraishi, Y., & Yoshihara, C. (2024) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.15111 · Cited by 18 · see citing works
Mota, C. M. D., Branco, L. G. S., Morrison, S. F., & Madden, C. J. (2019) · Acta Physiologica · doi:10.1111/apha.13401 · Cited by 18 · see citing works
Preoptic Area Modulation of Arousal in Natural and Drug Induced Unconscious States
Reitz, S. L., & Kelz, M. B. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.644330 · Cited by 18 · see citing works
Öztürk, Ö., Cebeci, D., Şahin, U., Tülüceoğlu, E. E., Calapoğlu, N. Ş., Gonca, T., & Calapoğlu, M. (2021) · Sleep And Breathing · doi:10.1007/s11325-021-02514-w · Cited by 18 · see citing works
Guo, X., Keenan, B. T., Reiner, B. C., Lian, J., & Pack, A. I. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114192 · Cited by 17 · see citing works
Bai, Z., Han, Y., Zhuang, D., & Sun, C. T. (2024) · Building and Environment · doi:10.1016/j.buildenv.2024.112214 · Cited by 17 · see citing works
Nicotinic acid promotes sleep through prostaglandin synthesis in mice
Szentirmai, É., & Kapás, L. (2019) · Scientific Reports · doi:10.1038/s41598-019-53648-7 · Cited by 17 · see citing works
The Role of the Central Histaminergic System in Behavioral State Control
Arrigoni, E., & Fuller, P. M. (2021) · Current topics in behavioral neurosciences · doi:10.1007/7854_2021_263 · Cited by 17 · see citing works
Self-citation
- Authors
- Kroeger, D., Absi, G., Gagliardi, C., Bandaru, S. S., Madara, J. C., Ferrari, L. L., Arrigoni, E., Münzberg, H., Scammell, T. E., Saper, C. B., & Vetrivelan, R.
- Affiliations
- Beth Israel Deaconess Medical Center (US)
- Pennington Biomedical Research Center (US)
- Corresponding author
- Saper, Clifford B.
- Vetrivelan, Ramalingam
- ORCID
- Venue
- Nature Communications
- Published
- 2018-10-08
- Volume
- 9
- Issue
- 1
- Pages
- 4129-4129
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC6175893
- OpenAlex
- W2895180682
- Cited by
- 276
- References
- 70
- Citations by year
- 2026: 26 · 2025: 29 · 2024: 46 · 2023: 37 · 2022: 32 · 2021: 46 · 2020: 29 · 2019: 31
- FWCI
- 15.78
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Office of Extramural Research, National Institutes of Health (NS091126, NS085477, HL095491, AG009975)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroscience of respiration and sleep
- Keywords
- ventrolateral preoptic area, sleep regulation, heat loss, body temperature, photostimulation, optogenetics, chemogenetics, insomnia, c-fos, wakefulness, neuronal firing rate
- MeSH terms
- Animals, Body Temperature Regulation, Electroencephalography, Electromyography, Sleep Initiation and Maintenance Disorders, Male, Mice, Transgenic, Neurons, Preoptic Area, Sleep, Galanin, Gene Expression Profiling
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review