Hypocretin as a Hub for Arousal and Motivation
Open accessAbstract
The lateral hypothalamus is comprised of a heterogeneous mix of neurons that serve to integrate and regulate sleep, feeding, stress, energy balance, reward, and motivated behavior. Within these populations, the hypocretin/orexin neurons are among the most well studied. Here, we provide an overview on how these neurons act as a central hub integrating sensory and physiological information to tune arousal and motivated behavior accordingly. We give special attention to their role in sleep-wake states and conditions of hyper-arousal, as is the case with stress-induced anxiety. We further discuss their roles in feeding, drug-seeking, and sexual behavior, which are all dependent on the motivational state of the animal. We further emphasize the application of powerful techniques, such as optogenetics, chemogenetics, and fiber photometry, to delineate the role these neurons play in lateral hypothalamic functions.
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?
Orexin maintains wakefulness and arousal and regulates sleep stability.
“orexin maintains wakefulness and arousal, as well as regulates sleep stability.17–21”
From Effects of Traumatic Brain Injury on the Orexin/Hypocretin System (2025) · cites this paper as [20]
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
2 retracted
Wu, X., Gao, J., Yan, J., Owyang, C., & Li, Y. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00791.2003 · Cited by 53 · see citing works
Retractedla Herrán-Arita, A. K. D., Kornum, B. R., Mahlios, J., Jiang, W., Lin, L., Hou, T., Macaubas, C., Einen, M. A., Plazzi, G., Crowe, C., et al. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3009995 · Cited by 31 · see citing works
RetractedPositional cloning of the mouse obese gene and its human homologue
Zhang, Y., Proenca, R., Maffei, M., Barone, M., Leopold, L., & Friedman, J. M. (1994) · Nature · doi:10.1038/372425a0 · Cited by 13,419 · see citing works
Sakurai, T., Amemiya, A., Ishii, M., Matsuzaki, I., Chemelli, R. M., Tanaka, H., Williams, S. C., Richardson, J. A., Kozlowski, G. P., Wilson, S., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)80949-6 · Cited by 5,501 · see citing works
Aston-Jones, G., & Cohen, J. D. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135709 · Cited by 4,472 · see citing works
Brain stem reticular formation and activation of the EEG
Moruzzi, G., & Magoun, H. W. (1949) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(49)90219-9 · Cited by 4,307 · see citing works
Ghrelin induces adiposity in rodents
Tschöp, M., Smiley, D. L., & Heiman, M. L. (2000) · Nature · doi:10.1038/35038090 · Cited by 3,949 · see citing works
The hypocretins: hypothalamus-specific peptides with neuroexcitatory activity
de Lecea, L., Kilduff, T. S., Peyron, C., Gao, X.-B., Foye, P. E., Danielson, P. E., Fukuhara, C., Battenberg, E. L. F., Gautvik, V. T., Bartlett, F. S., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.1.322 · Cited by 3,878 · see citing works
Neurons containing hypocretin (orexin) project to multiple neuronal systems
Peyron, C., Tighe, D. K., van den Pol, A. N., de Lecea, L., Heller, H. C., Sutcliffe, J. G., & Kilduff, T. S. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-23-09996.1998 · Cited by 3,466 · see citing works
A role for ghrelin in the central regulation of feeding
Nakazato, M., Murakami, N., Date, Y., Kojima, M., Matsuo, H., Kangawa, K., & Matsukura, S. (2001) · Nature · doi:10.1038/35051587 · Cited by 3,443 · see citing works
Narcolepsy in orexin Knockout Mice
Chemelli, R. M., Willie, J. T., Sinton, C. M., Elmquist, J. K., Scammell, T., Lee, C., Richardson, J. A., Williams, S. C., Xiong, Y., Kisanuki, Y., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)81973-x · Cited by 3,095 · see citing works
Lin, L., Faraco, J., Li, R., Kadotani, H., Rogers, W., Lin, X., Qiu, X., de Jong, P. J., Nishino, S., & Mignot, E. (1999) · Cell · doi:10.1016/s0092-8674(00)81965-0 · Cited by 2,613 · see citing works
Berridge, C. W., & Waterhouse, B. D. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00143-7 · Cited by 2,529 · see citing works
Abnormal splicing of the leptin receptor in diabetic mice
Lee, G.-H., Proenca, R., Montez, J. M., Carroll, K. M., Darvishzadeh, J. G., Lee, J. I., & Friedman, J. M. (1996) · Nature · doi:10.1038/379632a0 · Cited by 2,327 · see citing works
Chen, H., Charlat, O., Tartaglia, L. A., Woolf, E. A., Weng, X., Ellis, S. J., Lakey, N. D., Culpepper, J., More, K. J., Breitbart, R. E., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)81294-5 · Cited by 2,214 · see citing works
Peyron, C., Faraco, J., Rogers, W., Ripley, B., Overeem, S., Charnay, Y., Nevsimalova, S., Aldrich, M., Reynolds, D., Albin, R., et al. (2000) · Nature Medicine · doi:10.1038/79690 · Cited by 2,118 · see citing works
Hypocretin (orexin) deficiency in human narcolepsy
Nishino, S., Ripley, B., Overeem, S., Lammers, G. J., & Mignot, E. (2000) · The Lancet · doi:10.1016/s0140-6736(99)05582-8 · Cited by 1,776 · see citing works
Adult mouse cortical cell taxonomy revealed by single cell transcriptomics
Tasic, B., Menon, V., Nguyen, T. N., Kim, T. K., Jarsky, T., Yao, Z., Levi, B., Gray, L. T., Sorensen, S. A., Dolbeare, T., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4216 · Cited by 1,714 · see citing works
The Novel Hypothalamic Peptide Ghrelin Stimulates Food Intake and Growth Hormone Secretion
Wren, A. M., Small, C. J., Ward, H. L., Murphy, K. G., Dakin, C. L., Taheri, S., Kennedy, A. R., Roberts, G. H., Morgan, D. G. A., Ghatei, M. A., et al. (2000) · Endocrinology · doi:10.1210/endo.141.11.7873 · Cited by 1,593 · see citing works
Genetic Ablation of Orexin Neurons in Mice Results in Narcolepsy, Hypophagia, and Obesity
Hara, J., Beuckmann, C. T., Nambu, T., Willie, J. T., Chemelli, R. M., Sinton, C. M., Sugiyama, F., Yagami, K.-I., Goto, K., Yanagisawa, M., et al. (2001) · Neuron · doi:10.1016/s0896-6273(01)00293-8 · Cited by 1,401 · see citing works
Neural substrates of awakening probed with optogenetic control of hypocretin neurons
Adamantidis, A. R., Zhang, F., Aravanis, A. M., Deisseroth, K., & de Lecea, L. (2007) · Nature · doi:10.1038/nature06310 · Cited by 1,341 · see citing works
A role for lateral hypothalamic orexin neurons in reward seeking
Harris, G. C., Wimmer, M., & Aston-Jones, G. (2005) · Nature · doi:10.1038/nature04071 · Cited by 1,311 · see citing works
The neural circuit of orexin (hypocretin): maintaining sleep and wakefulness
Sakurai, T. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2092 · Cited by 1,276 · see citing works
Orexin A activates locus coeruleus cell firing and increases arousal in the rat
Hagan, J. J., Leslie, R. A., Patel, S., Evans, M. L., Wattam, T. A., Holmes, S., Benham, C. D., Taylor, S. G., Routledge, C., Hemmati, P., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.19.10911 · Cited by 1,234 · see citing works
Whole-Brain Mapping of Direct Inputs to Midbrain Dopamine Neurons
Watabe‐Uchida, M., Zhu, L., Ogawa, S. K., Vamanrao, A., & Uchida, N. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.017 · Cited by 1,221 · see citing works
Ghrelin causes hyperphagia and obesity in rats.
Wren, A., Small, C., Abbott, C., Dhillo, W., Seal, L., Cohen, M., Batterham, R., Taheri, S., Stanley, S., Ghatei, M., et al. (2001) · Diabetes · doi:10.2337/diabetes.50.11.2540 · Cited by 1,197 · see citing works
Ghrelin is an appetite-stimulatory signal from stomach with structural resemblance to motilin
Asakawa, A., Inui, A., Kaga, O., Yuzuriha, H., Nagata, T., Ueno, N., Makino, S., Fujimiya, M., Niijima, A., Fujino, M., et al. (2001) · Gastroenterology · doi:10.1053/gast.2001.22158 · Cited by 1,175 · see citing works
Phenotypes of Mouse diabetes and Rat fatty Due to Mutations in the OB (Leptin) Receptor
Chua, S. C., Chung, W. K., Wu-Peng, X. S., Zhang, Y., Liu, S.-M., Tartaglia, L. A., & Leibel, R. L. (1996) · Science · doi:10.1126/science.271.5251.994 · Cited by 1,071 · see citing works
Circuit architecture of VTA dopamine neurons revealed by systematic input-output mapping
Beier, K. T., Steinberg, E. E., DeLoach, K. E., Xie, S., Miyamichi, K., Schwarz, L., Gao, X. J., Kremer, E. J., Malenka, R. C., & Luo, L. (2015) · Cell · doi:10.1016/j.cell.2015.07.015 · Cited by 1,068 · see citing works
Nucleus basalis and thalamic control of neocortical activity in the freely moving rat
Buzsáki, G., Bickford, R. G., Ponomareff, G., Thal, L. J., Mandel, R. J., & Gage, F. H. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-11-04007.1988 · Cited by 1,039 · see citing works
Distribution of orexin receptor mRNA in the rat brain
Trivedi, P. G., Yu, H., MacNeil, D. J., der Ploeg, L. H. T. V., & Guan, X.-M. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)01266-6 · Cited by 979 · see citing works
The role of histamine and the tuberomamillary nucleus in the nervous system
Haas, H. L., & Panula, P. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1034 · Cited by 914 · see citing works
Dorsal raphe neurons: depression of firing during sleep in cats
McGinty, D., & Harper, R. M. (1976) · Brain Research · doi:10.1016/0006-8993(76)90480-7 · Cited by 900 · see citing works
Discharge of Identified Orexin/Hypocretin Neurons across the Sleep-Waking Cycle
Lee, M., Hassani, O. K., & Jones, B. E. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1887-05.2005 · Cited by 870 · see citing works
Shintani, M., Ogawa, Y., Ebihara, K., Aizawa‐Abe, M., Miyanaga, F., Takaya, K., Hayashi, T., Inoue, G., Hosoda, K., Kojima, M., et al. (2001) · Diabetes · doi:10.2337/diabetes.50.2.227 · Cited by 849 · see citing works
Behavioral Correlates of Activity in Identified Hypocretin/Orexin Neurons
Mileykovskiy, B. Y., Kiyashchenko, L. I., & Siegel, J. M. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.035 · Cited by 841 · see citing works
Attenuation of the Obesity Syndrome of ob/ob Mice by the Loss of Neuropeptide Y
Erickson, J. C., Hollopeter, G., & Palmiter, R. D. (1996) · Science · doi:10.1126/science.274.5293.1704 · Cited by 794 · see citing works
To Eat or to Sleep? Orexin in the Regulation of Feeding and Wakefulness
Willie, J. T., Chemelli, R. M., Sinton, C. M., & Yanagisawa, M. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.429 · Cited by 768 · see citing works
Borgland, S. L., Taha, S. A., Sarti, F., Fields, H. L., & Bonci, A. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.016 · Cited by 718 · 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
Fos Expression in Orexin Neurons Varies with Behavioral State
Estabrooke, I. V., McCarthy, M. T., Ko, E., Chou, T. C., Chemelli, R. M., Yanagisawa, M., Saper, C. B., & Scammell, T. E. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-05-01656.2001 · Cited by 654 · see citing works
Distinct Narcolepsy Syndromes in Orexin Receptor-2 and Orexin Null Mice
Willie, J. T., Chemelli, R. M., Sinton, C. M., Tokita, S., Williams, S. C., Kisanuki, Y. Y., Marcus, J. N., Lee, C., Elmquist, J. K., Kohlmeier, K. A., et al. (2003) · Neuron · doi:10.1016/s0896-6273(03)00330-1 · Cited by 645 · see citing works
The neurobiology, investigation, and treatment of chronic insomnia
Riemann, D. W., Nissen, C., Palagini, L., Otte, A., Perlis, M. L., & Spiegelhalder, K. (2015) · The Lancet Neurology · doi:10.1016/s1474-4422(15)00021-6 · Cited by 639 · see citing works
Excitation of Ventral Tegmental Area Dopaminergic and Nondopaminergic Neurons by Orexins/Hypocretins
Korotkova, T. M., Sergeeva, O. A., Eriksson, K. S., Haas, H. L., & Brown, R. E. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00007.2003 · Cited by 583 · see citing works
VTA dopaminergic neurons regulate ethologically relevant sleep-wake behaviors
Eban-Rothschild, A., Rothschild, G., Giardino, W. J., Jones, J. R., & de Lecea, L. (2016) · Nature Neuroscience · doi:10.1038/nn.4377 · Cited by 583 · see citing works
Afferents to the orexin neurons of the rat brain
Yoshida-Court, K., McCormack, S. L., España, R. A., Crocker, A. J., & Scammell, T. E. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20859 · Cited by 573 · see citing works
Neural regulation of immunity: molecular mechanisms and clinical translation
Pavlov, V. A., & Tracey, K. J. (2017) · Nature Neuroscience · doi:10.1038/nn.4477 · Cited by 534 · see citing works
Role for hypocretin in mediating stress-induced reinstatement of cocaine-seeking behavior
Boutrel, B., Kenny, P. J., Specio, S. E., Martin-Fardon, R., Markou, A., Koob, G. F., & de Lecea, L. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507480102 · Cited by 520 · see citing works
Orexin/Hypocretin Excites the Histaminergic Neurons of the Tuberomammillary Nucleus
Eriksson, K. S., Sergeeva, O. A., Brown, R. E., & Haas, H. L. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-23-09273.2001 · Cited by 509 · see citing works
Hypocretin/orexin overexpression induces an insomnia-like phenotype in zebrafish
Prober, D. A., Rihel, J., Onah, A. A., Sung, R.-J., & Schier, A. F. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4332-06.2006 · Cited by 508 · see citing works
Fadel, J. R., & Deutch, A. Y. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00017-9 · Cited by 503 · see citing works
Nohynek, H., Jokinen, J., Partinen, M., Vaarala, O., Kirjavainen, T., Sundman, J., Himanen, S., Hublin, C., Julkunen, I., Olsén, P., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033536 · Cited by 498 · see citing works
SCN Outputs and the Hypothalamic Balance of Life
Kalsbeek, A., Palm, I. F., la Fleur, S., Scheer, F., Perreau‐Lenz, S., Ruiter, M., Kreier, F., Cailotto, C., & Buijs, R. (2006) · Journal of Biological Rhythms · doi:10.1177/0748730406293854 · Cited by 492 · see citing works
Li, Y., Gao, X., Sakurai, T., & van den Pol, A. N. (2002) · Neuron · doi:10.1016/s0896-6273(02)01132-7 · Cited by 476 · see citing works
Sleep viewed as a state of adaptive inactivity
Siegel, J. M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2697 · Cited by 468 · see citing works
Input of Orexin/Hypocretin Neurons Revealed by a Genetically Encoded Tracer in Mice
Sakurai, T., Nagata, R., Yamanaka, A., Kawamura, H., Tsujino, N., Muraki, Y., Kageyama, H., Kunita, S., Takahashi, S., Goto, K., et al. (2005) · Neuron · doi:10.1016/j.neuron.2005.03.010 · Cited by 468 · see citing works
Ghrelin-Induced Food Intake Is Mediated via the Orexin Pathway
Toshinai, K., Date, Y., Murakami, N., Shimada, M., Mondal, M. S., Shimbara, T., Guan, J., Wang, Q., Funahashi, H., Sakurai, T., et al. (2003) · Endocrinology · doi:10.1210/en.2002-220788 · Cited by 462 · see citing works
Winsky-Sommerer, R., Yamanaka, A., Diano, S., Borok, E., Roberts, A. J., Sakurai, T., Kilduff, T. S., Horvath, T. L., & de Lecea, L. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.3459-04.2004 · Cited by 462 · see citing works
Verret, L., Goutagny, R., Fort, P., Cagnon, L., Salvert, D., Léger, L., Boissard, R., Salin, P. A., Peyron, C., & Luppi, P. (2003) · BMC Neuroscience · doi:10.1186/1471-2202-4-19 · Cited by 453 · see citing works
Hassani, O. K., Lee, M. G., & Jones, B. E. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811400106 · Cited by 451 · see citing works
Yoshida, Y., Fujiki, N., Nakajima, T., Ripley, B. A., Matsumura, H., Yoneda, H., Mignot, E. J.-M., & Nishino, S. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01725.x · Cited by 449 · see citing works
Cholinergic neurons of the laterodorsal tegmental nucleus: Efferent and afferent connections
Satoh, K., & Fibiger, H. C. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902530302 · Cited by 440 · see citing works
Acute Central Ghrelin and GH Secretagogues Induce Feeding and Activate Brain Appetite Centers
Lawrence, C. B., Snape, A. C., Baudoin, F., & Luckman, S. M. (2002) · Endocrinology · doi:10.1210/endo.143.1.8561 · Cited by 436 · see citing works
The slow (<1 Hz) rhythm of non-REM sleep: a dialogue between three cardinal oscillators
Crunelli, V., & Hughes, S. W. (2010) · Nature Neuroscience · doi:10.1038/nn.2445 · Cited by 435 · see citing works
A key role for orexin in panic anxiety
Johnson, P. L., Truitt, W. A., Fitz, S. D., Minick, P. E., Dietrich, A. D., Sanghani, S. P., Träskman‐Bendz, L., Goddard, A. W., Brundin, L., & Shekhar, A. (2009) · Nature Medicine · doi:10.1038/nm.2075 · Cited by 416 · see citing works
CSF hypocretin/orexin levels in narcolepsy and other neurological conditions
Ripley, B., Overeem, S., Fujiki, N., Nevsimalova, S., Uchino, M., Yesavage, J., Di Monte, D., Dohi, K., Melberg, A., Lammers, G. J., et al. (2001) · Neurology · doi:10.1212/wnl.57.12.2253 · Cited by 415 · see citing works
Leinninger, G. M., Jo, Y.-H., Leshan, R. L., Louis, G. W., Yang, H., Barrera, J. G., Wilson, H., Opland, D. M., Faouzi, M. A., Gong, Y., et al. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.06.011 · Cited by 412 · see citing works
Partinen, M., Saarenpää‐Heikkilä, O., Ilveskoski, I., Hublin, C., Linna, M., Olsén, P., Nokelainen, P. T., Alén, R., Wallden, T., Espo, M., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033723 · Cited by 406 · see citing works
Potential Rhythms of the Cerebral Cortex During Sleep
Loomis, A. L., Harvey, E. N., & Hobart, G. (1935) · Science · doi:10.1126/science.81.2111.597 · Cited by 400 · see citing works
HLA DQB1*0602 is Associated With Cataplexy in 509 Narcoleptic Patients
Mignot, E. J.-M., Hayduk, R., Black, J. E., Grumet, F. C., & Guilleminault, C. (1997) · SLEEP · doi:10.1093/sleep/20.11.1012 · Cited by 394 · see citing works
Liu, R.-J., van den Pol, A. N., & Aghajanian, G. K. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-21-09453.2002 · Cited by 392 · see citing works
Nieh, E. H., Vander Weele, C. M., Matthews, G. A., Presbrey, K. N., Wichmann, R., Leppla, C. A., Izadmehr, E. M., & Tye, K. M. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.035 · Cited by 387 · see citing works
Changes in the composition of brain interstitial ions control the sleep-wake cycle
Ding, F., O’Donnell, J., Xu, Q., Kang, N., Goldman, N., & Nedergaard, M. (2016) · Science · doi:10.1126/science.aad4821 · Cited by 383 · see citing works
Neuronal Activity of Histaminergic Tuberomammillary Neurons During Wake–Sleep States in the Mouse
Takahashi, K., Lin, J., & Sakai, K. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2341-06.2006 · Cited by 379 · see citing works
Webster, H. H., & Jones, B. E. (1988) · Brain Research · doi:10.1016/0006-8993(88)90471-4 · Cited by 350 · see citing works
Brown, R. E., Sergeeva, O. A., Eriksson, K. S., & Haas, H. L. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-20-08850.2002 · Cited by 347 · see citing works
Orexin A/Hypocretin-1 Selectively Promotes Motivation for Positive Reinforcers
Borgland, S. L., Chang, S., Bowers, M. S., Thompson, J. L., Vittoz, N. M., Floresco, S., Chou, J., Chen, B. T., & Bonci, A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6096-08.2009 · Cited by 341 · see citing works
A selective orexin-1 receptor antagonist reduces food consumption in male and female rats
Haynes, A. C., Jackson, B., Chapman, H., Tadayyon, M., Johns, A., Porter, R. A., & Arch, J. R. S. (2000) · Regulatory Peptides · doi:10.1016/s0167-0115(00)00199-3 · Cited by 338 · see citing works
Burdakov, D., Gerasimenko, O. V., & Verkhratsky, A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4925-04.2005 · Cited by 337 · see citing works
Release of Hypocretin (Orexin) during Waking and Sleep States
Kiyashchenko, L. I., Mileykovskiy, B. Y., Maidment, N. T., Lam, H. A., Wu, M., John, J., Peever, J. H., & Siegel, J. M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05282.2002 · Cited by 337 · see citing works
Attenuated defense response and low basal blood pressure in orexin knockout mice
Kayaba, Y., Nakamura, A., Kasuya, Y., Ohuchi, T., Yanagisawa, M., Komuro, I., Fukuda, Y., & Kuwaki, T. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00671.2002 · Cited by 337 · see citing works
Evidence for histaminergic arousal mechanisms in the hypothalamus of cat
Lin, J., Sakai, K., & Jouvet, M. (1988) · Neuropharmacology · doi:10.1016/0028-3908(88)90159-1 · Cited by 330 · see citing works
Havel, P. J. (2000) · Proceedings of The Nutrition Society · doi:10.1017/s0029665100000410 · Cited by 329 · see citing works
Orexin A but Not Orexin B Rapidly Enters Brain from Blood by Simple Diffusion
Kastin, A. J., & Akerstrom, V. L. (1999) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)38126-1 · Cited by 325 · see citing works
Independent Feeding and Metabolic Actions of Orexins in Mice
Lubkin, M., & Stricker‐Krongrad, A. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.9750 · Cited by 325 · see citing works
Hypothalamic orexin expression: modulation by blood glucose and feeding.
Cai, X., Widdowson, P. S., Harrold, J. A., Wilson, S., Buckingham, R. E., Arch, J. R. S., Tadayyon, M., Clapham, J. C., Wilding, J. P. H., & Williams, G. H. (1999) · Diabetes · doi:10.2337/diabetes.48.11.2132 · Cited by 320 · see citing works
Orexins/hypocretins excite basal forebrain cholinergic neurones
Eggermann, E., Serafin, M., Bayer, L., Machard, D., Saint-Mleux, B., Jones, B. E., & Mühlethaler, M. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00512-7 · Cited by 316 · see citing works
Wake-promoting and sleep-suppressing actions of hypocretin (orexin): basal forebrain sites of action
España, R. A., Baldo, B. A., Kelley, A. E., & Berridge, C. W. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00319-0 · Cited by 311 · see citing works
Activity, modulation and role of basal forebrain cholinergic neurons innervating the cerebral cortex
Jones, B. E. (2004) · Progress in brain research · doi:10.1016/s0079-6123(03)45011-5 · Cited by 304 · see citing works
What Keeps Us Awake: the Neuropharmacology of Stimulants and Wakefulness Promoting Medications
Boutrel, B., & Koob, G. F. (2004) · SLEEP · doi:10.1093/sleep/27.6.1181 · Cited by 303 · see citing works
Concomitant loss of dynorphin, NARP, and orexin in narcolepsy
Crocker, A., España, R. A., Papadopoulou, M., Saper, C. B., Faraco, J., Sakurai, T., Honda, M., Mignot, E., & Scammell, T. E. (2005) · Neurology · doi:10.1212/01.wnl.0000168173.71940.ab · Cited by 301 · see citing works
Insular hypocretin transmission regulates nicotine reward
Hollander, J. A., Lu, Q., Cameron, M. D., Kamenecka, T. M., & Kenny, P. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808023105 · Cited by 296 · see citing works
Optogenetic activation of cholinergic neurons in the PPT or LDT induces REM sleep
Van Dort, C. J., Zachs, D. P., Kenny, J. D., Zheng, S., Goldblum, R. R., Gelwan, N. A., Ramos, D. M., Nolan, M. A., Wang, K., Weng, F.-J., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1423136112 · Cited by 296 · see citing works
Tandem-Pore K+ Channels Mediate Inhibition of Orexin Neurons by Glucose
Burdakov, D., Jensen, L. T., Alexopoulos, H., Williams, R. H., Fearon, I. M., O'Kelly, I., Gerasimenko, O. V., Fugger, L. H., & Verkhratsky, A. (2006) · Neuron · doi:10.1016/j.neuron.2006.04.032 · Cited by 294 · see citing works
Dahan, L., Astier, B., Vautrelle, N., Urbain, N., Kocsis, B., & Chouvet, G. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301251 · Cited by 289 · see citing works
Roles of orexin/hypocretin in regulation of sleep/wakefulness and energy homeostasis
Sakurai, T. (2005) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2004.07.007 · Cited by 286 · see citing works
Centrally administered orexin/hypocretin activates HPA axis in rats
Kuru, M., Ueta, Y., Serino, R., Nakazato, M., Yamamoto, Y., Shibuya, I., & Yamashita, H. (2000) · Neuroreport · doi:10.1097/00001756-200006260-00034 · Cited by 285 · see citing works
Mushroom bodies of the cockroach: Their participation in place memory
Mizunami, M., Weibrecht, J. M., & Strausfeld, N. J. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19981228)402:4 · Cited by 284 · see citing works
Burlet, S., Tyler, C. J., & Leonard, C. S. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-07-02862.2002 · Cited by 284 · see citing works
Dorsal Raphe Dopamine Neurons Modulate Arousal and Promote Wakefulness by Salient Stimuli
Cho, J. R., Treweek, J. B., Robinson, J. E., Xiao, C., Bremner, L. R., Greenbaum, A., & Gradinaru, V. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.020 · Cited by 276 · see citing works
Mechanism for Hypocretin-mediated sleep-to-wake transitions
Carter, M. E., Brill, J., Bonnavion, P., Huguenard, J. R., Huerta, R., & de Lecea, L. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1202526109 · Cited by 274 · see citing works
Basal forebrain control of wakefulness and cortical rhythms
Anaclet, C., Pedersen, N. P., Ferrari, L. L., Venner, A., Bass, C. E., Arrigoni, E., & Fuller, P. M. (2015) · Nature Communications · doi:10.1038/ncomms9744 · Cited by 273 · see citing works
Miller, J. D., Farber, J., Gatz, P., Roffwarg, H. P., & German, D. C. (1983) · Brain Research · doi:10.1016/0006-8993(83)91101-0 · Cited by 269 · see citing works
Possible Involvement of Orexin in the Stress Reaction in Rats
Ida, T., Nakahara, K., Murakami, T., Hanada, R., Nakazato, M., & Murakami, N. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2412 · Cited by 268 · see citing works
Differential Roles of Orexin Receptor-1 and -2 in the Regulation of Non-REM and REM Sleep
Mieda, M., Hasegawa, E., Kisanuki, Y. Y., Sinton, C. M., Yanagisawa, M., & Sakurai, T. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6506-10.2011 · Cited by 268 · see citing works
Behavioral correlates of dopaminergic unit activity in freely moving cats
Steinfels, G. F., Heym, J., Strecker, R. E., & Jacobs, B. L. (1983) · Brain Research · doi:10.1016/0006-8993(83)91145-9 · Cited by 261 · see citing works
Muschamp, J. W., Hollander, J. A., Thompson, J. L., Voren, G., Hassinger, L. C., Onvani, S., Kamenecka, T. M., Borgland, S. L., Kenny, P. J., & Carlezon, W. A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1315542111 · Cited by 250 · see citing works
Pharmacogenetic Modulation of Orexin Neurons Alters Sleep/Wakefulness States in Mice
Sasaki, K., Suzuki, M., Mieda, M., Tsujino, N., Roth, B. L., & Sakurai, T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020360 · Cited by 248 · see citing works
Inutsuka, A., & Yamanaka, A. (2013) · Frontiers in Endocrinology · doi:10.3389/fendo.2013.00018 · Cited by 244 · see citing works
Sleep Homeostasis Modulates Hypocretin-Mediated Sleep-to-Wake Transitions
Carter, M. E., Adamantidis, A., Ohtsu, H., Deisseroth, K. A., & de Lecea, L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1205-09.2009 · Cited by 242 · see citing works
Bäckberg, M., Hervieu, G. J., Wilson, S., & Meister, B. (2002) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01859.x · Cited by 235 · see citing works
Rodgers, R. J., Halford, J. C. G., de Souza, R. L. N., de Souza, A. L. C., Piper, D. C., Arch, J. R. S., Upton, N., Porter, R. A., Johns, A., & Blundell, J. E. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01518.x · Cited by 230 · see citing works
Wijnans, L., Lecomte, C., de Vries, C. S., Weibel, D. M., Sammon, C., Hviid, A. P., Svanström, H., Mølgaard‐Nielsen, D., Heijbel, H., Arnheim‐Dahlström, L., et al. (2012) · Vaccine · doi:10.1016/j.vaccine.2012.12.015 · Cited by 230 · see citing works
Choi, D. L., Davis, J. F., Fitzgerald, M. E., & Benoit, S. C. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.02.002 · Cited by 229 · see citing works
Dugovic, C., Shelton, J. E., Aluisio, L. E., Fraser, I. C., Jiang, X., Sutton, S. W., Bonaventure, P., Yun, S., Li, X., Lord, B., et al. (2009) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.109.152009 · Cited by 229 · see citing works
Regulation of orexin neurons by the monoaminergic and cholinergic systems
Yamanaka, A., Muraki, Y., Tsujino, N., Goto, K., & Sakurai, T. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)00299-7 · Cited by 226 · see citing works
Lateral hypothalamic neuropeptides in reward and drug addiction
Dileone, R., Georgescu, D., & Nestler, E. J. (2003) · Life Sciences · doi:10.1016/s0024-3205(03)00408-9 · Cited by 220 · see citing works
Håkansson, de Lecea, L., Sutcliffe, Yanagisawa, & Meister (1999) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1999.00378.x · Cited by 219 · see citing works
Adenosine and Sleep Homeostasis in the Basal Forebrain
Blanco‐Centurion, C., Xu, M., Murillo‐Rodríguez, E., Gerashchenko, D., Shiromani, A. M., Salín-Pascual, R. J., Hof, P. R., & Shiromani, P. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2181-06.2006 · Cited by 212 · see citing works
Theta activity in the waking EEG is a marker of sleep propensity in the rat
Vyazovskiy, V. V., & Tobler, I. (2005) · Brain Research · doi:10.1016/j.brainres.2005.05.022 · Cited by 210 · see citing works
Hansen, S., Ko¨hler, C., Goldstein, M., & Steinbusch, H. W. M. (1982) · Brain Research · doi:10.1016/0006-8993(82)90843-5 · Cited by 202 · see citing works
Szymusiak, R. S., Gvilia, I., & McGinty, D. (2007) · Sleep Medicine · doi:10.1016/j.sleep.2007.03.013 · Cited by 200 · see citing works
Stimulation of Gastric Acid Secretion by Centrally Administered Orexin-A in Conscious Rats
Takahashi, N., Okumura, T., Yamada, H., & Kohgo, Y. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.9994 · Cited by 199 · see citing works
Orexins (hypocretins) directly excite tuberomammillary neurons
Bayer, L., Eggermann, E., Serafin, M., Saint-Mleux, B., Machard, D., Jones, B. E., & Mühlethaler, M. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01777.x · Cited by 198 · see citing works
Liu, Z.-W., & Gao, X. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00873.2006 · Cited by 198 · see citing works
Modification of Motivated Behavior Elicited by Electrical Stimulation of the Hypothalamus
Valenstein, E. S., Cox, V. C., & Kakolewski, J. W. (1968) · Science · doi:10.1126/science.159.3819.1119 · Cited by 194 · see citing works
Awake dynamics and brain-wide direct inputs of hypothalamic MCH and orexin networks
González, J. A., Ιορδανίδου, Π., Strom, M., Adamantidis, A., & Burdakov, D. (2016) · Nature Communications · doi:10.1038/ncomms11395 · Cited by 193 · see citing works
A Role for Hypocretin (Orexin) in Male Sexual Behavior
Muschamp, J. W., Dominguez, J. M., Sato, S. M., Shen, R., & Hull, E. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4121-06.2007 · Cited by 192 · see citing works
Vittoz, N. M., & Berridge, C. W. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300807 · Cited by 189 · see citing works
Xi, M.-C., Morales, F. R., & Chase, M. H. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02317-4 · Cited by 188 · see citing works
Aphagia and Adipsia After Preferential Destruction of Nerve Cell Bodies in Hypothalamus
Grossman, S. P., Dacey, D. M., Halaris, A. E., Collier, T. J., & Routtenberg, A. (1978) · Science · doi:10.1126/science.705344 · Cited by 185 · see citing works
Orexin A in the nucleus accumbens stimulates feeding and locomotor activity
Thorpe, A. J., & Kotz, C. M. (2005) · Brain Research · doi:10.1016/j.brainres.2005.05.045 · Cited by 184 · see citing works
Griffond, B., Risold, P., Jacquemard, C., Colard, C., & FELLMANN, D. (1999) · Neuroscience Letters · doi:10.1016/s0304-3940(98)00976-8 · Cited by 182 · see citing works
Orexin/hypocretin role in reward: implications for opioid and other addictions
Baimel, C., Bartlett, S. E., Chiou, L., Lawrence, A. J., Muschamp, J. W., Patkar, O. L., Tung, L.-W., & Borgland, S. L. (2014) · British Journal of Pharmacology · doi:10.1111/bph.12639 · Cited by 180 · see citing works
Fujiki, N., Yoshida, Y., Ripley, B. A., Mignot, E. J.-M., & Nishino, S. (2003) · SLEEP · doi:10.1093/sleep/26.8.953 · Cited by 180 · see citing works
The autoimmune basis of narcolepsy
Mahlios, J., la Herrán-Arita, A. K. D., & Mignot, E. J.-M. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.04.013 · Cited by 179 · see citing works
Orexins in the paraventricular nucleus of the thalamus mediate anxiety-like responses in rats
Li, Y., Li, S., Wei, C., Wang, H., Sui, N., & Kirouac, G. J. (2010) · Psychopharmacology · doi:10.1007/s00213-010-1948-y · Cited by 178 · see citing works
Encephalitis Lethargica, Its Sequelae and Treatment.
(1932) · JAMA · doi:10.1001/jama.1932.02730290071039 · Cited by 178 · see citing works
Bonnavion, P., Jackson, A. C., Carter, M. E., & de Lecea, L. (2015) · Nature Communications · doi:10.1038/ncomms7266 · Cited by 175 · see citing works
Effects of Orexins on the Hypothalamic‐Pituitary‐Adrenal System
Jászberényi, M., Bujdosó, E., Pataki, I., & Telegdy, G. (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00572.x · Cited by 175 · see citing works
Circadian and Homeostatic Regulation of Structural Synaptic Plasticity in Hypocretin Neurons
Appelbaum, L., Wang, G. X., Yokogawa, T., Skariah, G. M., Smith, S. J., Mourrain, P., & Mignot, E. J.-M. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.006 · Cited by 172 · see citing works
España, R. A., Melchior, J. R., Roberts, D. C. S., & Jones, S. R. (2010) · Psychopharmacology · doi:10.1007/s00213-010-2048-8 · Cited by 170 · see citing works
Hypocretin/orexin depolarizes and decreases potassium conductance in locus coeruleus neurons
Ivanov, A., & Aston‐Jones, G. (2000) · Neuroreport · doi:10.1097/00001756-200006050-00031 · Cited by 169 · see citing works
Acute administration of leptin produces anxiolytic-like effects: a comparison with fluoxetine
Liu, J., Garza, J. C., Bronner, J., Kim, C. S., Zhang, W., & Lu, X. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1684-3 · Cited by 163 · see citing works
Trulson, M. E., & Preussler, D. W. (1984) · Experimental Neurology · doi:10.1016/s0014-4886(84)90105-5 · Cited by 162 · see citing works
Orexin-A (hypocretin-1) is possibly involved in generation of anxiety-like behavior
Suzuki, M., Beuckmann, C. T., Shikata, K., Ogura, H., & Sawai, T. (2005) · Brain Research · doi:10.1016/j.brainres.2005.03.002 · Cited by 161 · see citing works
Down regulation of the prepro-orexin gene expression in genetically obese mice
Yamamoto, Y., Ueta, Y., Date, Y., Nakazato, M., Hara, Y., Serino, R., Nomura, M. J., Shibuya, I., Matsukura, S., & Yamashita, H. (1999) · Molecular Brain Research · doi:10.1016/s0169-328x(98)00320-9 · Cited by 150 · see citing works
A role for cortical nNOS/NK1 neurons in coupling homeostatic sleep drive to EEG slow wave activity
Morairty, S. R., Dittrich, L., Pasumarthi, R. K., Valladao, D., Heiss, J. E., Gerashchenko, D., & Kilduff, T. S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1314762110 · Cited by 146 · see citing works
Cape, E. G., & Jones, B. E. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00099.x · Cited by 140 · see citing works
Selective activation of cholinergic basal forebrain neurons induces immediate sleep-wake transitions
Han, Y., Shi, Y.-F., Xi, W., Zhou, R., Tan, Z.-B., Wang, H., Li, X.-M., Chen, Z., Feng, G., Luo, M., et al. (2014) · Current Biology · doi:10.1016/j.cub.2014.02.011 · Cited by 137 · see citing works
Basal Forebrain Cholinergic Modulation of Sleep Transitions
Irmak, S. O., & de Lecea, L. (2014) · SLEEP · doi:10.5665/sleep.4246 · Cited by 134 · see citing works
Activity of substantia nigra units across the sleep-waking cycle in freely moving cats
Trulson, M. E., Preussler, D. W., & Howell, G. A. (1981) · Neuroscience Letters · doi:10.1016/0304-3940(81)90346-3 · Cited by 133 · see citing works
Nair, S. G., Golden, S. A., & Shaham, Y. (2008) · British Journal of Pharmacology · doi:10.1038/bjp.2008.3 · Cited by 132 · see citing works
Acute Suppressive and Long-Term Phase Modulation Actions of Orexin on the Mammalian Circadian Clock
Belle, M. D. C., Hughes, A. T. L., Bechtold, D. A., Cunningham, P. S., Pierucci, M., Burdakov, D., & Piggins, H. D. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3388-13.2014 · Cited by 131 · see citing works
Schöne, C., Cao, Z. F. H., Apergis‐Schoute, J., Adamantidis, A., Sakurai, T., & Burdakov, D. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0706-12.2012 · Cited by 131 · see citing works
Oishi, Y., Suzuki, Y., Takahashi, K., Yonezawa, T., Kanda, T., Takata, Y., Chérasse, Y., & Lazarus, M. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1365-7 · Cited by 130 · see citing works
Inflammation-Induced Lethargy Is Mediated by Suppression of Orexin Neuron Activity
Grossberg, A. J., Zhu, X., Leinninger, G. M., Levasseur, P. R., Braun, T. P., Myers, M. G., & Marks, D. L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2311-11.2011 · Cited by 130 · see citing works
Tsunematsu, T., Tabuchi, S., Tanaka, K. F., Boyden, E. S., Tominaga, M., & Yamanaka, A. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.021 · Cited by 125 · see citing works
Holst, M., Kelly, J. B., & Powley, T. L. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970428)381:1 · Cited by 124 · see citing works
Circadian and dark-pulse activation of orexin/hypocretin neurons
Marston, O. J., Williams, R. H., Canal, M. M., Samuels, R. E., Upton, N., & Piggins, H. D. (2008) · Molecular Brain · doi:10.1186/1756-6606-1-19 · Cited by 124 · see citing works
Orexin Neurons Are Directly and Indirectly Regulated by Catecholamines in a Complex Manner
Yamanaka, A., Muraki, Y., Ichiki, K., Tsujino, N., Kilduff, T. S., Goto, K., & Sakurai, T. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01361.2005 · Cited by 122 · see citing works
Sergeyev, V., Broberger, C., Gorbatyuk, O. S., & Hökfelt, T. (2000) · Neuroreport · doi:10.1097/00001756-200001170-00023 · Cited by 119 · see citing works
Mickelsen, L. E., Kolling, F. W., Chimileski, B. R., Fujita, A., Norris, C., Chen, K., Nelson, C. E., & Jackson, A. C. (2017) · eNeuro · doi:10.1523/eneuro.0013-17.2017 · Cited by 119 · see citing works
Adaptive sugar sensors in hypothalamic feeding circuits
Williams, R. H., Alexopoulos, H., Jensen, L. T., Fugger, L. H., & Burdakov, D. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802687105 · Cited by 119 · see citing works
Optogenetic Evidence for Inhibitory Signaling from Orexin to MCH Neurons via Local Microcircuits
Apergis‐Schoute, J., Ιορδανίδου, Π., Faure, C., Jego, S., Schöne, C., Aitta‐aho, T., Adamantidis, A., & Burdakov, D. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.5269-14.2015 · Cited by 118 · see citing works
Vassalli, A., & Franken, P. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1700983114 · Cited by 117 · see citing works
Regulation of Hypocretin (Orexin) Expression in Embryonic Zebrafish
Faraco, J. H., Appelbaum, L., Marin, W., Gaus, S. E., Mourrain, P., & Mignot, E. J.-M. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605811200 · Cited by 115 · see citing works
"Copulation-Reward Site" in the Posterior Hypothalamus
Caggiula, A. R., & Hoebel, B. G. (1966) · Science · doi:10.1126/science.153.3741.1284 · Cited by 114 · see citing works
Cape, E. G., Manns, I. D., Alonso, Á., Beaudet, A., & Jones, B. E. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08452.2000 · Cited by 111 · see citing works
Male Sexual Behavior Induced by Intracranial Electrical Stimulation
Vaughan, E. D., & Fisher, A. E. (1962) · Science · doi:10.1126/science.137.3532.758-a · Cited by 111 · see citing works
Genetic Ablation of Hypocretin Neurons Alters Behavioral State Transitions in Zebrafish
Elbaz, I., Yelin‐Bekerman, L., Nicenboim, J., Vatine, G. D., & Appelbaum, L. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1284-12.2012 · Cited by 111 · see citing works
Taylor, A. M. W., Castonguay, A., Ghogha, A., Vayssiere, P., Pradhan, A. A. A., Xue, L., Mehrabani, S., Wu, J., Levitt, P., Olmstead, M. C., et al. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.221 · Cited by 109 · see citing works
Intrahypothalamic injections of kainic acid produce feeding and drinking deficits in rats
Stricker, E. M., Swerdloff, A., & Zigmond, M. J. (1978) · Brain Research · doi:10.1016/0006-8993(78)90692-3 · Cited by 109 · see citing works
Lee, R., Steffensen, S. C., & Henriksen, S. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-05-01757.2001 · Cited by 109 · see citing works
Hypocretin underlies the evolution of sleep loss in the Mexican cavefish
Jaggard, J. B., Stahl, B. A., Lloyd, E., Prober, D. A., Duboué, E. R., & Keene, A. C. (2018) · eLife · doi:10.7554/elife.32637 · Cited by 108 · see citing works
Orexin (hypocretin)/dynorphin neurons control GABAergic inputs to tuberomammillary neurons
Eriksson, K. S., Sergeeva, O. A., Selbach, O., & Haas, H. L. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03243.x · Cited by 107 · see citing works
de Lecea, L., & Sutcliffe, J. G. (2005) · The FEBS Journal · doi:10.1111/j.1742-4658.2005.04981.x · Cited by 105 · see citing works
GABAB receptor‐mediated modulation of hypocretin/orexin neurones in mouse hypothalamus
Xie, X., Crowder, T. L., Yamanaka, A., Morairty, S. R., LeWinter, R. D., Sakurai, T., & Kilduff, T. S. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.108266 · Cited by 104 · see citing works
Gozzi, A., Turrini, G., Piccoli, L., Massagrande, M., Amantini, D., Antolini, M., Martinelli, P., Cesari, N., Montanari, D., Tessari, M., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016406 · Cited by 103 · see citing works
Centrally administered orexin A increases motivation for sweet pellets in rats
Thorpe, A. J., Cleary, J. P., Levine, A. S., & Kotz, C. M. (2005) · Psychopharmacology · doi:10.1007/s00213-005-0040-5 · Cited by 103 · see citing works
Zhang, W., Sakurai, T., Fukuda, Y., & Kuwaki, T. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00704.2005 · Cited by 103 · see citing works
Drinking induced by electrical stimulation of the lateral hypothalamus
Mogenson, G. J., & Stevenson, J. A. F. (1967) · Experimental Neurology · doi:10.1016/0014-4886(67)90139-2 · Cited by 102 · see citing works
Activation of the basal forebrain by the orexin/hypocretin neurones
Arrigoni, E., Mochizuki, T., & Scammell, T. E. (2009) · Acta Physiologica · doi:10.1111/j.1748-1716.2009.02036.x · Cited by 97 · see citing works
Kohlmeier, K. A., Inoue, T., & Leonard, C. S. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00076.2004 · Cited by 97 · see citing works
Tyree, S. M., & de Lecea, L. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00050 · Cited by 95 · see citing works
Self-citationIndividual differences in effects of hypothalamic stimulation: The role of stimulation locus
Wise, R. A. (1971) · Physiology & Behavior · doi:10.1016/0031-9384(71)90207-1 · Cited by 94 · see citing works
Rewarding effect of performance of gnawing aroused by hypothalamic stimulation in the rat.
Roberts, W. W., & Carey, R. J. (1965) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0022030 · Cited by 92 · see citing works
Tesoriero, C., Codita, A., Zhang, M., Cherninsky, A., Karlsson, H., Grassi-Zucconi, G., Bertini, G., Harkany, T., Ljungberg, K., Liljeström, P., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1521463112 · Cited by 91 · see citing works
Role of orexin input in the diurnal rhythm of locus coeruleus impulse activity
Gompf, H. S., & Aston‐Jones, G. (2008) · Brain Research · doi:10.1016/j.brainres.2008.05.060 · Cited by 89 · see citing works
Hara, J., Gerashchenko, D., Wisor, J. P., Sakurai, T., Xie, X., & Kilduff, T. S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0431-09.2009 · Cited by 89 · see citing works
Gulia, K. K., Mallick, H. N., & Kumar, V. M. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00877-1 · Cited by 85 · see citing works
Kohlmeier, K. A., Watanabe, S., Tyler, C. J., Burlet, S., & Leonard, C. S. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01388.2007 · Cited by 84 · see citing works
Fujita, A., Bonnavion, P., Wilson, M. H., Mickelsen, L. E., Bloit, J., de Lecea, L., & Jackson, A. C. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0580-17.2017 · Cited by 82 · see citing works
Hypothalamic Motivational Systems: Fixed or Plastic Neural Circuits?
Wise, R. A. (1968) · Science · doi:10.1126/science.162.3851.377 · Cited by 79 · see citing works
Narcolepsy and influenza A(H1N1) pandemic 2009 vaccination in the United States
Duffy, J., Weintraub, E., Vellozzi, C. J., & Destefano, F. R. (2014) · Neurology · doi:10.1212/wnl.0000000000000987 · Cited by 77 · see citing works
Dickman, M. S. (2001) · Archives of Neurology · doi:10.1001/archneur.58.10.1696 · Cited by 75 · see citing works
Swett, C. P., & Hobson, J. A. (1968) · PubMed · Cited by 74 · see citing works
Reduced Orexin System Function Contributes to Resilience to Repeated Social Stress
Grafe, L. A., Eacret, D., Dobkin, J., & Bhatnagar, S. (2018) · eNeuro · doi:10.1523/eneuro.0273-17.2018 · Cited by 73 · see citing works
Reliability-Weighted Integration of Audiovisual Signals Can Be Modulated by Top-down Attention
Rohe, T., & Noppeney, U. (2018) · eNeuro · doi:10.1523/eneuro.0315-17.2018 · Cited by 72 · see citing works
Chang, H., Saito, T., Ohiwa, N., Tateoka, M., Deocaris, C. C., Fujikawa, T., & Soya, H. (2006) · Neuroscience Research · doi:10.1016/j.neures.2006.11.009 · Cited by 71 · see citing works
Flagged first, then by citations
3 of the 236 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- [6]Elias CF Saper CB Maratos-Flier E Tritos NA Lee C Kelly J. Chemically defined projections linking the mediobasal hypothalamus and the lateral hypothalamic area. J Comp Neurol. (1998) 402: 442– 59. 10.1002/(SICI)1096-9861(19981228)402:4<442::AID-CNE2>3.0.CO;2-R 9862320 · DOI
Cited by
Sorted by citations
Ross, J. A., & Bockstaele, E. J. V. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.601519 · Cited by 223 · see citing works
To eat or to sleep: That is a lateral hypothalamic question
Arrigoni, E., Chee, M. J. S., & Fuller, P. M. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.11.017 · Cited by 124 · see citing works
Role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation
Karnani, M., Schöne, C., Bracey, E. F., González, J. A., Viskaitis, P., Li, H., Adamantidis, A., & Burdakov, D. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101771 · Cited by 89 · see citing works
Effects of orexin receptor antagonism on human sleep architecture: A systematic review
Clark, J. W., Brian, M. L., Drummond, S. P. A., Hoyer, D., & Jacobson, L. H. (2020) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2020.101332 · Cited by 86 · see citing works
Brunes, L. C., Baldi, F. S., Lopes, F. B., Lôbo, R. B., Espigolan, R., Costa, M. F. O. E., Stafuzza, N. B., & Magnabosco, C. D. U. (2020) · Journal of Animal Breeding and Genetics · doi:10.1111/jbg.12496 · Cited by 78 · see citing works
Sleep and alertness disturbance and substance use disorders: A bi-directional relation
Roehrs, T., Sibai, M., & Roth, T. G. (2021) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2021.173153 · Cited by 69 · see citing works
Ingested non-essential amino acids recruit brain orexin cells to suppress eating in mice
Viskaitis, P., Arnold, M., Garau, C., Jensen, L. T., Fugger, L. H., Peleg‐Raibstein, D., & Burdakov, D. (2022) · Current Biology · doi:10.1016/j.cub.2022.02.067 · Cited by 63 · 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
Kowalko, J. E. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.208835 · Cited by 63 · see citing works
Beuckmann, C. T., Ueno, T., Nakagawa, M., Suzuki, M., & Akasofu, S. (2019) · SLEEP · doi:10.1093/sleep/zsz076 · Cited by 53 · see citing works
Layer 6b controls brain state via apical dendrites and the higher-order thalamocortical system
Zolnik, T. A., Bronec, A., Ross, A., Staab, M., Sachdev, R. N. S., Molnár, Z., Eickholt, B. J., & Larkum, M. E. (2023) · Neuron · doi:10.1016/j.neuron.2023.11.021 · Cited by 51 · see citing works
Daily Fluctuation of Orexin Neuron Activity and Wiring: The Challenge of “Chronoconnectivity”
Azeez, I. A., Gallo, F. D., Cristino, L., & Bentivoglio, M. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.01061 · Cited by 44 · see citing works
Sleep Disruption and Cancer: Chicken or the Egg?
Berisha, A., Shutkind, K., & Borniger, J. C. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.856235 · Cited by 42 · see citing works
Self-citationNeuropsychiatric Correlates of Narcolepsy
BaHammam, A. S., Alnakshabandi, K., & Pandi-Perumal, S. R. (2020) · Current Psychiatry Reports · doi:10.1007/s11920-020-01159-y · Cited by 38 · see citing works
The Role of Hypothalamic Pathology for Non-Motor Features of Huntington’s Disease
Cheong, R. Y., Gabery, S., & Petersén, Å. (2019) · Journal of Huntington s Disease · doi:10.3233/jhd-190372 · Cited by 36 · see citing works
Stanton, L. M., Price, A. J., & Manning, E. E. (2023) · Journal of Neuroendocrinology · doi:10.1111/jne.13268 · Cited by 35 · see citing works
Yaeger, J. D. W., Krupp, K. T., Jacobs, B., Onserio, B. O., Meyerink, B. L., Cain, J. T., Ronan, P. J., Renner, K. J., Dileone, R., & Summers, C. H. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.12.019 · Cited by 34 · see citing works
D’Acci, L. S. (2021) · City Culture and Society · doi:10.1016/j.ccs.2021.100375 · Cited by 32 · see citing works
Bjorness, T. E., & Greene, R. W. (2021) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2021.173194 · Cited by 32 · see citing works
Dawson, M., Terstege, D. J., Jamani, N. F., Tsutsui, M., Pavlov, D., Bugescu, R., Epp, J. R., Leinninger, G. M., & Sargin, D. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112815 · Cited by 31 · see citing works
London, S., & Volkoff, H. (2019) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2019.06.011 · Cited by 30 · see citing works
The Orexin receptors: Structural and anti-tumoral properties
Couvineau, A., Nicole, P., Gratio, V., & Voisin, T. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.931970 · Cited by 30 · see citing works
Noritake, A., Ninomiya, T., & Isoda, M. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.02.018 · Cited by 29 · see citing works
At the intersection of sleep deficiency and opioid use: mechanisms and therapeutic opportunities
Greenwald, M. K., Moses, T. E. H., & Roehrs, T. (2021) · Translational research · doi:10.1016/j.trsl.2021.03.006 · Cited by 29 · see citing works
Hypothalamic deep brain stimulation as a strategy to manage anxiety disorders
Li, H., Donegan, D., Peleg‐Raibstein, D., & Burdakov, D. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2113518119 · Cited by 28 · see citing works
Cano, G., Hernan, S. L., & Sved, A. F. (2021) · Brain Sciences · doi:10.3390/brainsci11081005 · Cited by 27 · see citing works
Sánchez-Alavez, M., Benedict, J., Wills, D. N., & Ehlers, C. L. (2019) · SLEEP · doi:10.1093/sleep/zsz020 · Cited by 27 · see citing works
Neylan, T. C., Richards, A. L., Metzler, T. J., Yack, L. M., Varbel, J., O’Donovan, A., Sivasubramanian, M., Motraghi, T., Hlavin, J. A., Batki, S. L., et al. (2020) · SLEEP · doi:10.1093/sleep/zsaa080 · Cited by 27 · see citing works
He, X., Li, Y., Zhang, N., Huang, J., Ming, X., Guo, R., Hu, Y., Ji, P., & Guo, F. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.906057 · Cited by 25 · see citing works
Kaźmierczak, M., & Nicola, S. M. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.07.008 · Cited by 24 · see citing works
Sleep and orexin: A new paradigm for understanding behavioural-variant frontotemporal dementia?
Hwang, Y. T., Piguet, O., Hodges, J. R., Grunstein, R. R., & Burrell, J. R. (2020) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2020.101361 · Cited by 23 · see citing works
Bjorness, T. E., & Greene, R. W. (2020) · eNeuro · doi:10.1523/eneuro.0283-20.2020 · Cited by 21 · see citing works
Counterbalanced microcircuits for Orx1 and Orx2 regulation of stress reactivity
Yaeger, J. D. W., Krupp, K. T., Gale, J., & Summers, C. H. (2020) · Medicine in Drug Discovery · doi:10.1016/j.medidd.2020.100059 · Cited by 20 · see citing works
Cortical arousal frequency is increased in narcolepsy type 1
Brink-Kjær, A., Christensen, J. A. E., Cesari, M., Mignot, E. J.-M., Sørensen, H. B. D., & Jennum, P. (2020) · SLEEP · doi:10.1093/sleep/zsaa255 · Cited by 20 · see citing works
Central regulation of breast cancer growth and metastasis
Borniger, J. C. (2019) · Journal of Cancer Metastasis and Treatment · doi:10.20517/2394-4722.2018.107 · Cited by 20 · see citing works
Self-citationSleep and motivated behaviors, from physiology to pathology
Sotelo, M. I., Tyan, J., Dzera, J., & Eban-Rothschild, A. (2020) · Current Opinion in Physiology · doi:10.1016/j.cophys.2020.01.006 · Cited by 18 · see citing works
From Molecule to Behavior: Hypocretin/orexin Revisited From a Sex-dependent Perspective
Gao, X., & Horváth, T. L. (2021) · Endocrine Reviews · doi:10.1210/endrev/bnab042 · Cited by 17 · see citing works
Knez, R., Stevanović, D., Fernell, E., & Gillberg, C. (2022) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s358373 · Cited by 16 · see citing works
Melatonin: A Potential Antineoplastic Agent in Breast Cancer
Samanta, S. (2022) · Journal of Environmental Pathology Toxicology and Oncology · doi:10.1615/jenvironpatholtoxicoloncol.2022041294 · Cited by 14 · see citing works
Mild Traumatic Brain Injury Affects Orexin/Hypocretin Physiology Differently in Male and Female Mice
Somach, R. T., Jean, I. D., Farrugia, A. M., & Cohen, A. S. (2023) · Journal of Neurotrauma · doi:10.1089/neu.2023.0125 · Cited by 13 · see citing works
Macías-Triana, L., Romero-Cordero, K., Tatum-Kuri, A., Vera-Barrón, A., Millán‐Aldaco, D., Arankowsky‐Sandoval, G., Piomelli, D., & Murillo‐Rodríguez, E. (2020) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2020.172911 · Cited by 13 · see citing works
Neuroscience: Sleep Fragmentation Impairs Memory Formation
Joiner, W. J. (2019) · Current Biology · doi:10.1016/j.cub.2019.09.060 · Cited by 11 · see citing works
Characterization of mWake expression in the murine brain
Bell, B. J., Wang, A. A., Kim, D. W., Xiong, J., Blackshaw, S., & Wu, M. N. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.25066 · Cited by 11 · see citing works
Orexin-mediated motivated arousal and reward seeking
Bjorness, T. E., & Greene, R. W. (2024) · Peptides · doi:10.1016/j.peptides.2024.171280 · Cited by 10 · see citing works
Bergh, S., Cheong, R. Y., Petersén, Å., & Gabery, S. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.984317 · Cited by 9 · see citing works
Cancer as a tool for preclinical psychoneuroimmunology
Borniger, J. C. (2021) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2021.100351 · Cited by 9 · see citing works
Self-citationEmerging medications and pharmacological treatment approaches for substance use disorders
Raymond, J. S., Athanasopoulos, A. G., Badolato, C. J., Doolan, T. M., Scicluna, R. L., Everett, N. A., Bowen, M. T., & James, M. H. (2024) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2024.173952 · Cited by 8 · see citing works
Sleep deprivation engages the orexin/hypocretin system to regulate food reward seeking
Rojo, A. L. A., Barnhardt, T. R., Pham, T. Q., Heim, B., Cai, L., Tseng, G. C., & Huang, Y. H. (2025) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyaf047 · Cited by 8 · see citing works
Gratio, V., Dragan, P., Garcia, L., Saveanu, L., Nicole, P., Voisin, T., Latek, D., & Couvineau, A. (2024) · British Journal of Pharmacology · doi:10.1111/bph.17422 · Cited by 7 · see citing works
Luan, J., Zhang, Q., Zhou, X., Zhou, X., Gu, Q., Xia, J., & Song, N. (2023) · Andrology · doi:10.1111/andr.13444 · Cited by 7 · see citing works
Machine learning models to predict ligand binding affinity for the orexin 1 receptor
Zhang, V. Y., O’Connor, S. L., Welsh, W. J., & James, M. H. (2023) · Artificial Intelligence Chemistry · doi:10.1016/j.aichem.2023.100040 · Cited by 7 · see citing works
Pulver, A., Kiive, E., Kanarik, M., & Harro, J. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147013 · Cited by 7 · see citing works
Hopkins, K., Mukherjee, S., Ponce, D., Mangum, J. E., Jacobson, L. H., & Hoyer, D. (2021) · Medicine in Drug Discovery · doi:10.1016/j.medidd.2021.100102 · Cited by 6 · see citing works
Orexin neuron activity in mating mice - a pilot study
Burdakov, D., & Karnani, M. (2021) · Neuroanatomy and Behaviour · doi:10.35430/nab.2021.e17 · Cited by 6 · see citing works
Noritake, A., & Nakamura, K. (2023) · Scientific Reports · doi:10.1038/s41598-023-33026-0 · Cited by 5 · see citing works
Clark, P. J., Migovich, V. M., Das, S., Xu, W., Zhang, Y., Kortagere, S., & España, R. A. (2026) · Neuropsychopharmacology · doi:10.1038/s41386-025-02315-9 · Cited by 5 · see citing works
Sun, Y., Tisdale, R. K., Yamashita, A., & Kilduff, T. S. (2022) · Peptides · doi:10.1016/j.peptides.2023.171002 · Cited by 5 · see citing works
Costa, A., Monti, J. M., & Torterolo, P. (2020) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2020.101769 · Cited by 5 · see citing works
Murillo‐Rodríguez, E., Millán‐Aldaco, D., Arankowsky‐Sandoval, G., Yamamoto, T., Pertwee, R. G., Parker, L. A., & Mechoulam, R. (2021) · Journal of Cannabis Research · doi:10.1186/s42238-021-00081-1 · Cited by 4 · see citing works
Ionic Mechanisms Underlying the Excitatory Effect of Orexin on Rat Subthalamic Nucleus Neurons
Li, G., Zhuang, Q., Zhang, X., Wang, J.-J., & Zhu, J. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00153 · Cited by 4 · see citing works
Rapid sensory integration in orexin neurons governs probability of future movementsPreprint
Karnani, M., Schöne, C., Bracey, E. F., González, J. A., Viskaitis, P., Adamantidis, A., & Burdakov, D. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/620096 · Cited by 4 · see citing works
Wijdicks, E. F. M., & Boes, C. J. (2022) · Neurology · doi:10.1212/wnl.0000000000200800 · Cited by 3 · see citing works
Disentangling the Neural Circuits of Arousal and Anxiety-Like Behavior
Florido, A., Curtis, V. R., Pégard, N. C., & Rodríguez-Romaguera, J. (2024) · Current topics in behavioral neurosciences · doi:10.1007/7854_2024_539 · Cited by 3 · see citing works
Food restriction induces functional resilience to sleep restriction in rats
Loomis, S., McCarthy, A. P., Dijk, D., Gilmour, G., & Winsky‐Sommerer, R. (2020) · SLEEP · doi:10.1093/sleep/zsaa079 · Cited by 3 · see citing works
Effects of Traumatic Brain Injury on the Orexin/Hypocretin System
Somach, R. T., Lim, M. M., & Cohen, A. S. (2025) · Neurotrauma Reports · doi:10.1089/neur.2024.0111 · Cited by 2 · see citing works
Xiang, J., Shi, M., Kang, J., Zhang, X., Ling, J., Zhan, W., Li, D., Hu, R. K., & Xu, H. (2026) · Cell Discovery · doi:10.1038/s41421-025-00857-2 · Cited by 2 · see citing works
Mavanji, V., Teske, J. A., Kotz, C. M., & Pellizzer, G. (2023) · Journal of Neuroscience Research · doi:10.1002/jnr.25195 · Cited by 2 · see citing works
Neural bases of freedom and responsibility
Gruart, A., & Delgado-Garcia, J. M. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1191996 · Cited by 2 · see citing works
Dando, M. (2020) · Ethics Medicine and Public Health · doi:10.1016/j.jemep.2020.100513 · Cited by 2 · see citing works
Motivational Processes in the Regulation of Sleep/Wake States
Eban-Rothschild, A. (2019) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-813743-7.00035-9 · Cited by 2 · see citing works
Arousal-Mediated Sleep Disturbance Persists During Cocaine Abstinence in Male Mice
Bjorness, T. E., & Greene, R. W. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.868049 · Cited by 1 · see citing works
Stanton, L. M., Price, A. J., & Manning, E. E. (2022) · doi:10.31234/osf.io/2z9gw · Cited by 1 · see citing works
Lateral Hypothalamic Control of Sleep in the Context of Cancer
Borniger, J. C., & Nevárez, N. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-816658-1.00012-0
Self-citationDando, M. (2020) · Advanced sciences and technologies for security applications · doi:10.1007/978-3-030-53790-6_6
Ghrelin-dependent mechanisms of food reward. Part 1. Ghrelin and dopamine
Reikhardt, B. A., & Shabanov, P. D. (2022) · Reviews on Clinical Pharmacology and Drug Therapy · doi:10.17816/rcf20129-54
Genetics of Chronotype and Circadian Rhythm Disorders
Kunorozva, L., & Lane, J. M. (2024) · Springer eBooks · doi:10.1007/978-3-031-62723-1_11
Identifying Arousal Inputs to the Intergeniculate Leaflet in HamstersPreprint
Moshirpour, M., Horsley, K. G., Saud, S. P., McCance, C., Scotland, M., & Antle, M. C. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5139171
Moshirpour, M., Horsley, K. G., Saud, S. P., McCance, C., Scotland, M., & Antle, M. C. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.04.007
(2025) · Royal Society of Chemistry eBooks · doi:10.1039/9781837678174-00401
Hildebrandt, H., & Stuke, H. (2026) · Brain Disorders · doi:10.1016/j.dscb.2026.100318
Multisensory dysfunction across sleep disorders: A systematic review of 31 human modalities
Biabani, N., Ferri, R., Naismith, S. L., Mutti, C., Puligheddu, M., Parrino, L., Goadsby, P. J., & Rosenzweig, I. (2026) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2026.102363
Effort-based decision-making:A value-based dissection and arousal-focused synthesis
Clairis, N., & Tobler, P. N. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.107062
- Authors
- Tyree, S. M., Borniger, J. C., & de Lecea, L.
- Affiliations
- Stanford University (US)
- Venue
- Frontiers in Neurology
- Publisher
- Frontiers Media SA
- Published
- 2018-06-06
- Volume
- 9
- Pages
- 413-413
- ISSN
- 1664-2295 (ISSN-L)
- PMC
- PMC5997825
- OpenAlex
- W2806993167
- Cited by
- 83
- References
- 236
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 5 · 2023: 9 · 2022: 15 · 2021: 12 · 2020: 19 · 2019: 10 · 2018: 3
- FWCI
- 1.47
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Frontiers in Neurology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Neurological Foundation of New Zealand
- Foundation for the National Institutes of Health (F32MH11543, 5R01MH087592, R01MH1026380, 1R01AG047671)
- Boehringer Ingelheim
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroscience of respiration and sleep
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Keywords
- hypocretin/orexin neurons, lateral hypothalamus, arousal, motivation, sleep-wake regulation, hyperarousal, stress-induced anxiety, feeding behavior, drug-seeking behavior, sexual behavior, optogenetics, chemogenetics, fiber photometry
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