The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
CSF levels of prostaglandins, especially the level of prostaglandin D2, are correlated with increasing propensity towards sleep in rats
Abstract
The concentration of PGD2, PGE2, and of PGF2 alpha was measured in the cerebrospinal fluid (CSF) collected from the cisterna magna of conscious rats (n = 29), which, chronically implanted with a catheter for the CSF sampling, underwent deprivation of daytime sleep. Significant elevation of the CSF level of PGD2 was observed following 2.5-h sleep deprivation (SD), and the elevation became more marked following 5- and 10-h SD, apparently reaching the maximum at 5-h SD (703 +/- 140 pg/ml (mean +/- S.E.M.) for baseline vs. 1734 +/- 363 pg/ml for SD, n = 10). The levels of PGE2, and PGF2 alpha also significantly increased following 5- and 10-h SD, but not following 2.5-h SD. It is unlikely that these changes were simply caused by some responses of the animals to stress stimuli, because stress stimuli derived from restraint of the animal at the supine position to a board for 1 h did not produce any acute responses in the CSF levels of prostaglandins (n = 13). In a different group of animals (n = 11) implanted with electrodes for recording electroencephalogram (EEG) and electromyogram (EMG) in addition to the catheter, the levels of the prostaglandins in CSF were determined for slow-wave sleep (SWS) and wakefulness in the day and for SWS and wakefulness in the night. The highest PGD2 value was obtained at daytime SWS, whereas the lowest was at night wakefulness; furthermore, a significant difference was observed between SWS and wakefulness rather than between day and night. The CSF level of PGE2 also showed a similar tendency. In an additional group of animals (n = 6), not only PGD2 but also PGE2 and PGF2 alpha significantly increased the sleeping time of the animal when applied into the subarachnoid space underlying the ventral surface area of the rostral basal forebrain, the previously defined site of action for the sleep-promoting effect of PGD2. The promotion of sleep by PGE2 applied to the subarachnoid space was an effect completely opposite to the well-established awaking effect of the same prostaglandin demonstrated in the hypothalamic region in a series of previous studies. Based on these results, we conclude that increases in CSF levels of prostaglandins, especially that of PGD2, are correlated in rats with heightened propensity towards sleep and further with the depth of sleep under normal as well as SD conditions.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Additionally, COX-2 products, such as prostaglandin D2, are sleep-promoting in rat cerebrospinal fluid (CSF) (45), which may support the idea that sleep-promoting molecules are elevated during sleep loss.”
From Oxalic acid and diacylglycerol 36:3 are cross-species markers of sleep debt (2015) · cites this paper as [45]
In the citing paper
“moderate sleep deprivation caused an increase in CSF levels of PGD2, E2, and F2α in rats (455).”
From The Sleep-Immune Crosstalk in Health and Disease (2019) · cites this paper as [455]
Citations
Cites
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
Two-Process Model of Sleep Regulation
Binder, M. D., Hirokawa, N., & Windhorst, U. (2008) · Springer eBooks · doi:10.1007/978-3-540-29678-2_6166 · Cited by 3,900
Yamagata, K., Andreasson, K. I., Kaufmann, W. E., Barnes, C. A., & Worley, P. F. (1993) · Neuron · doi:10.1016/0896-6273(93)90192-t · Cited by 1,231
The interleukin‐1 family: 10 years of discovery 1
Dinarello, C. A. (1994) · The FASEB Journal · doi:10.1096/fasebj.8.15.8001745 · Cited by 783
Characterization of inducible cyclooxygenase in rat brain
Breder, C., Dewitt, D., & Kraig, R. (1995) · The Journal of comparative neurology · doi:10.1002/cne.903550208 · Cited by 550
Cloning Two Isoforms of Rat Cyclooxygenase: Differential Regulation of Their Expression
Feng, L., Sun, W. Q., Xia, Y. Y., Tang, W. W., Chanmugam, P., Soyoola, E., Wilson, C. B., & Hwang, D. (1993) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1993.1601 · Cited by 452
Cao, C., Matsumura, K., Yamagata, K., & Watanabe, Y. (1996) · Brain Research · doi:10.1016/0006-8993(96)00575-6 · Cited by 308
Endogenous sleep-promoting substances and sleep regulation
Borbely, A. A., & Tobler, I. (1989) · Physiological Reviews · doi:10.1152/physrev.1989.69.2.605 · Cited by 259
Cao, C., Matsumura, K., Yamagata, K., & Watanabe, Y. (1995) · Brain Research · doi:10.1016/0006-8993(95)00839-i · Cited by 252
Effects of sleep deprivation on human immune functions
Moldofsky, H., Lue, F. A., Davidson, J. R., & Gorczynski, R. (1989) · The FASEB Journal · doi:10.1096/fasebj.3.8.2785942 · Cited by 250
Cited by
Sorted by citations
The Sleep-Immune Crosstalk in Health and Disease
Besedovsky, L., Lange, T., & Haack, M. (2019) · Physiological Reviews · doi:10.1152/physrev.00010.2018 · Cited by 1,479
Control of sleep and wakefulness
Brown, R. E., Basheer, R., McKenna, J. T., Strecker, R. E., & McCarley, R. W. (2012) · Physiological Reviews · doi:10.1152/physrev.00032.2011 · Cited by 1,477
Sleep deficiency and chronic pain: potential underlying mechanisms and clinical implications
Haack, M., Simpson, N. S., Sethna, N. F., Kaur, S., & Mullington, J. M. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0439-z · Cited by 696
Haack, M., Sanchez, E., & Mullington, J. M. (2007) · Sleep · doi:10.1093/sleep/30.9.1145 · Cited by 615
Sustained sleep restriction reduces emotional and physical well-being
Haack, M., & Mullington, J. M. (2005) · Pain · doi:10.1016/j.pain.2005.09.011 · Cited by 422
Biochemical regulation of non-rapid-eye-movement sleep
Krueger, J. M. (2003) · Frontiers in Bioscience · doi:10.2741/1033 · Cited by 329
Datta, S., & MacLean, R. R. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.02.004 · Cited by 307
Prostaglandin D synthase: Structure and function
Urade, Y., & Hayaishi, O. (2000) · Vitamins and hormones · doi:10.1016/s0083-6729(00)58022-4 · Cited by 298
Self-citationSleep Neurobiology from a Clinical Perspective
España, R. A., & Scammell, T. E. (2011) · SLEEP · doi:10.5665/sleep.1112 · Cited by 294
The Role of Adenosine in the Regulation of Sleep
Huang, Z., Urade, Y., & Hayaishi, O. (2011) · Current Topics in Medicinal Chemistry · doi:10.2174/156802611795347654 · Cited by 230
Self-citationGallopin, T., Luppi, P.-H., Cauli, B., Urade, Y., Rossier, J., Hayaishi, O., Lambolez, B., & Fort, P. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.05.045 · Cited by 229
Self-citationThe Neurobiology of Sleep and Wakefulness
Schwartz, M. D., & Kilduff, T. S. (2015) · Psychiatric Clinics of North America · doi:10.1016/j.psc.2015.07.002 · Cited by 207
Regulation of the Blood–Brain Barrier by Circadian Rhythms and Sleep
Cuddapah, V. A., Zhang, S., & Sehgal, A. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.05.001 · Cited by 208
Prostaglandin D2 and sleep/wake regulation
Urade, Y., & Hayaishi, O. (2011) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2011.08.003 · Cited by 200
Self-citationMohri, I., Taniike, M., Taniguchi, H., Kanekiyo, T., Aritake, K., Inui, T., Fukumoto, N., Eguchi, N., Kushi, A., Sasai, H., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4531-05.2006 · Cited by 185
Oxalic acid and diacylglycerol 36:3 are cross-species markers of sleep debt
Weljie, A. M., Meerlo, P., Goel, N., Sengupta, A., Kayser, M. S., Abel, T., Birnbaum, M. J., Dinges, D. F., & Sehgal, A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1417432112 · Cited by 158
Haack, M., Lee, E., Cohen, D. A., & Mullington, J. M. (2009) · Pain · doi:10.1016/j.pain.2009.05.029 · Cited by 158
Prostaglandin D2 and sleep regulation
Urade, Y., & Hayaishi, O. (1999) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/s0005-2760(98)00163-5 · Cited by 159
Self-citationRoles of Adenosine and Its Receptors in Sleep–Wake Regulation
Huang, Z., Zhang, Z., & Qu, W. (2014) · International review of neurobiology · doi:10.1016/b978-0-12-801022-8.00014-3 · Cited by 156
Hirata, T., & Narumiya, S. (2011) · Chemical Reviews · doi:10.1021/cr200010h · Cited by 137
Gene Expression in the Brain across the Hibernation Cycle
O’Hara, B. F., Watson, F. L., Srere, H. K., Kumar, H., Wiler, S. W., Welch, S. K., Bitting, L., Heller, H. C., & Kilduff, T. S. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-10-03781.1999 · Cited by 108
Prostaglandin D2Protects Neonatal Mouse Brain from Hypoxic Ischemic Injury
Taniguchi, H., Mohri, I., Okabe-Arahori, H., Aritake, K., Wada, K., Kanekiyo, T., Narumiya, S., Nakayama, M., Ozono, K., Urade, Y., et al. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0321-07.2007 · Cited by 86
Brain oxidation is an initial process in sleep induction
Ikeda, M., Ikeda‐Sagara, M., Okada, T., Clément, P., Urade, Y., Nagai, T., Sugiyama, T., Yoshioka, T., Honda, K., & Inoue, S. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.09.057 · Cited by 80
Sleep and homeostatic control of plasticity
Lanza, G., DelRosso, L. M., & Ferri, R. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-12-819410-2.00004-7 · Cited by 78
Mechanisms of Sleep-Wake Cycle Modulation
Murillo‐Rodríguez, E., Arias-Carrión, Ó., Sanguino-Rodriguez, K., Gonzalez-Arias, M., & Haro, R. (2009) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/187152709788921654 · Cited by 74
Basic Sleep Mechanisms: An Integrative Review
Murillo‐Rodríguez, E., Arias-Carrión, Ó., Zavala-Garcia, A., Sarro-Ramírez, A., & Huitrón‐Reséndiz, S. (2012) · Central Nervous System Agents in Medicinal Chemistry · doi:10.2174/187152412800229107 · Cited by 71
Fatty-Acid Binding Proteins Modulate Sleep and Enhance Long-Term Memory Consolidation in Drosophila
Gerstner, J. R., Vanderheyden, W. M., Shaw, P. J., Landry, C. F., & Yin, J. C. P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0015890 · Cited by 71
Molecular mechanisms of sleep–wake regulation: a role of prostaglandin D 2
Hayaishi, O. (2000) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2000.0564 · Cited by 71
Self-citationTerao, A., Matsumura, H., & Saito, M. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-16-06599.1998 · Cited by 70
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 77
Singh, D. K. K., Ghosh, S., Bhola, A., Verma, P., Amist, A. D., Sharma, H., Sachdeva, P., & Sinha, J. K. (2024) · Annals of Neurosciences · doi:10.1177/09727531241275347 · Cited by 64
Night eating and obesity in the EP3R-deficient mouse
Sánchez-Alavez, M., Klein, I., Brownell, S. E., Tabarean, I. V., Davis, C. N., Conti, B., & Bartfai, T. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611209104 · Cited by 63
Brain Mechanisms of COVID-19-Sleep Disorders
Semyachkina-Glushkovskaya, O. V., Mamedova, A., Telnova, V., Klimova, M., Saranceva, E. I., Ageev, V., Yu, T., Zhu, D. Y., Penzel, T., & Kurths, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136917 · Cited by 63
Ribeiro, A. C. D. M., Pfaff, D. W., & Devidze, N. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06620.x · Cited by 59
Pinzar, E., Miyano, M., Kanaoka, Y., Urade, Y., & Hayaishi, O. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m000750200 · Cited by 59
Self-citationLight-Dependent Regulation of Sleep and Wake States by Prokineticin 2 in Zebrafish
Chen, S., Reichert, S., Singh, C., Oikonomou, G., Rihel, J., & Prober, D. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.001 · Cited by 62
Inhibitory G proteins and their receptors: emerging therapeutic targets for obesity and diabetes
Kimple, M. E., Neuman, J. C., Linnemann, A. K., & Casey, P. J. (2014) · Experimental & Molecular Medicine · doi:10.1038/emm.2014.40 · Cited by 54
Evidence for a role of the arachidonic acid cascade in affective disorders: a review
Sublette, M. E., Russ, M. J., & Smith, G. S. (2004) · Bipolar Disorders · doi:10.1046/j.1399-5618.2003.00094.x · Cited by 54
Central prostaglandin D2 stimulates food intake via the neuropeptide Y system in mice
Ohinata, K., Takagi, K., Biyajima, K., Fujiwara, Y., Fukumoto, S., Eguchi, N., Urade, Y., Asakawa, A., Fujimiya, M., Inui, A., et al. (2008) · FEBS Letters · doi:10.1016/j.febslet.2008.01.050 · Cited by 52
The Mutual Interaction Between Sleep and Epilepsy on the Neurobiological Basis and Therapy
Wang, Y., Zhang, M., Li, R., Qu, W., & Huang, Z. (2017) · Current Neuropharmacology · doi:10.2174/1570159x15666170509101237 · Cited by 52
Osborn, O., Gram, H., Zorrilla, E., Conti, B., & Bartfai, T. (2008) · Swiss Medical Weekly · doi:10.4414/smw.2008.12276 · Cited by 53
Fatty acids and sleep in depressed inpatients
Irmisch, G., Schläfke, D., Gierow, W., Herpertz, S. C., & Richter, J. (2006) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2006.09.001 · Cited by 46
Role of the L-PGDS-PGD2-DP1 receptor axis in sleep regulation and neurologic outcomes
Ahmad, A. S., Ottallah, H., Maciel, C. B., Strickland, M. R., & Doré, S. (2019) · SLEEP · doi:10.1093/sleep/zsz073 · Cited by 42
Nesbitt, A. D., Leschziner, G. D., & Peatfield, R. C. (2014) · Cephalalgia · doi:10.1177/0333102414542662 · Cited by 40
Luo, G., Yao, Y., Tao, J., Wang, T., & Yan, M. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1074605 · Cited by 38
The roles of prostaglandin E2 and D2 in lipopolysaccharide-mediated changes in sleep
Oishi, Y., Yoshida, K., Scammell, T. E., Urade, Y., Lazarus, M., & Saper, C. B. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.11.019 · Cited by 34
Kaneko, K., Yoshikawa, M., & Ohinata, K. (2012) · Neuropeptides · doi:10.1016/j.npep.2012.10.003 · Cited by 32
Gerashchenko, D., Okano, Y., Urade, Y., Inoué, S., & Hayaishi, O. (2000) · Journal of Sleep Research · doi:10.1046/j.1365-2869.2000.00175.x · Cited by 32
Self-citationBegemann, M., Sargin, D., Rossner, M. J., Bartels, C., Theis, F. J., Wickert, S. P., Stender, N., Fischer, B., Sperling, S., Stawicki, S., et al. (2008) · Molecular Medicine · doi:10.2119/2008-00053.begemann · Cited by 30
Sleep-Promoting Mechanisms in Mammals
McGinty, D., & Szymusiak, R. S. (2005) · Elsevier eBooks · doi:10.1016/b0-72-160797-7/50020-3 · Cited by 28
Yoshida, H., Kubota, T., & Krueger, J. M. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00609.2002 · Cited by 28
Microglial activation and neuroinflammation in acute and chronic cognitive deficits in sepsis
Denver, P., & Cunningham, C. M. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.110285 · Cited by 33
Central prostaglandin D2 exhibits anxiolytic-like activity via the DP1 receptor in mice
Zhao, H., Ohinata, K., & Yoshikawa, M. (2008) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2008.10.001 · Cited by 26
Biochemical modulation of the sleep–wake cycle: Endogenous sleep‐inducing factors
Arias-Carrión, Ó., Huitrón‐Reséndiz, S., Arankowsky‐Sandoval, G., & Murillo‐Rodríguez, E. (2011) · Journal of Neuroscience Research · doi:10.1002/jnr.22666 · Cited by 26
Cui, Y., Kataoka, Y., Inui, T., Mochizuki, T., Onoe, H., Matsumura, K., Urade, Y., Yamada, H., & Watanabe, Y. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21531 · Cited by 26
Wodarski, R., Schuh‐Hofer, S., Yurek, D. A., Wafford, K. A., Gilmour, G., Treede, R., & Kennedy, J. D. (2014) · European Journal of Pain · doi:10.1002/ejp.580 · Cited by 24
Genetic Mechanisms in Neural and Hormonal Controls over Female Reproductive Behaviors
Lee, A. W., Kow, L., Devidze, N., Ribeiro, A., Martín‐Alguacil, N., Schober, J. M., & Pfaff, D. W. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00034-6 · Cited by 23
Effects of COX-2 Inhibitor in Temporomandibular Joint Acute Inflammation
Schütz, T. C. B., Andersen, M. L., & Tufik, S. B. (2007) · Journal of Dental Research · doi:10.1177/154405910708600516 · Cited by 21
Central prostaglandins in food intake regulation
Ohinata, K., & Yoshikawa, M. (2008) · Nutrition · doi:10.1016/j.nut.2008.06.006 · Cited by 21
Porkka‐Heiskanen, T. (2010) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-13443-2_12 · Cited by 21
Rhythms in barriers and fluids: Circadian clock regulation in the aging neurovascular unit
Skapetze, L., Owino, S., Lo, E. H., Arai, K., Merrow, M. W., & Harrington, M. E. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106120 · Cited by 20
Lee, B., Hirst, J. J., & Walker, D. W. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05679.2002 · Cited by 20
Ferreira, M. T., Gomes, R. N., Panagopoulos, A., de Almeida, F. G., Veiga, J. C. E., & Colquhoun, A. (2017) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2017.10.002 · Cited by 19
Zhao, J., Bree, D., Harrington, M. G., Strassman, A. M., & Levy, D. (2016) · Cephalalgia · doi:10.1177/0333102416663466 · Cited by 18
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 19
The EP3 Receptor: Exploring a New Target for Type 2 Diabetes Therapeutics.
Neuman, J. C., & Kimple, M. E. (2013) · PubMed · Cited by 17
Santos, M. R. D. L., Rivalan, M., David, F. S., Stumpf, A., Pitsch, J., Tsortouktzidis, D., Velasquez, L. M., Voigt, A., Schilling, K., Mattei, D., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2014481118 · Cited by 16
Prostaglandins and sleep–wake regulation
Urade, Y., & Hayaishi, O. (2008) · CRC Press eBooks · doi:10.3109/9780203091715-28 · Cited by 15
Self-citationAlcohol, toxins, and medications as a cause of sleep dysfunction
Conroy, D. A., & Brower, K. J. (2010) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52006-7.00038-1 · Cited by 14
Suppression by resveratrol of prostaglandin D2-stimulated osteoprotegerin synthesis in osteoblasts
Kuroyanagi, G., Mizutani, J., Kondo, A., Yamamoto, N., Matsushima‐Nishiwaki, R., Otsuka, T., Kozawa, O., & Tokuda, H. (2014) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2014.04.003 · Cited by 14
Yang, J., Liu, C., Wu, G., & Zhao, S. (2024) · Experimental Gerontology · doi:10.1016/j.exger.2024.112602 · Cited by 13
Anatomy and Physiology of Normal Sleep
Schneider, L. D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804074-4.00001-7 · Cited by 17
An Interaction between L-prostaglandin D Synthase and Arrestin Increases PGD2 Production
Mathurin, K., Gallant, M. A., Germain, P., Allard‐Chamard, H., Brisson, J., Iorio‐Morin, C., de Brum-Fernandes, A. J., Caron, M. G., Laporte, S. A., & Parent, J. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.178277 · Cited by 13
Muraki, T., Fujimori, K., Ishizaka, M., Ohe, Y., Urade, Y., Okajima, F., & Ishikawa, K. (2004) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200404000-00006 · Cited by 13
Prostaglandin D2 sustains the pyrogenic effect of prostaglandin E2
Gao, W., Schmidtko, A., Lu, R., Brenneis, C., Angioni, C., Schmidt, R., & Geißlinger, G. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.01.051 · Cited by 12
Effect of rapid-eye-movement sleep deprivation on rat hypothalamic prostaglandins
Gelir, E., Arslan, S. O., Sayan, H., & Pınar, L. (2005) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2005.05.021 · Cited by 12
Werner, M. F. D. P., de Souza, G. E. P., & Zampronio, A. R. (2006) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2006.05.029 · Cited by 11
Gallopin, T., Fort, P., & Luppi, P. (2004) · CRC Press eBooks · doi:10.1201/9780203496732.ch3 · Cited by 11
Lipopolysaccharide-mediated effects of the microbiota on sleep and body temperature
Szentirmai, É., Buckley, K., Massie, A. R., & Kapás, L. (2024) · Scientific Reports · doi:10.1038/s41598-024-78431-1 · Cited by 10
Prostaglandin D2in the regulation of sleep
Urade, Y., & Lazarus, M. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139649469.010 · Cited by 10
Gene expression in the rat brain during prostaglandin D2 and adenosinergically‐induced sleep
Terao, A., Huang, Z., Wisor, J. P., Mochizuki, T., Gerashchenko, D., Urade, Y., & Kilduff, T. S. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05257.x · Cited by 7
Self-citationSzentirmai, É., Buckley, K., & Kapás, L. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.08.014 · Cited by 6
Palma, B. D., Nóbrega, J. N., Gomes, V. L., Esumi, L. A., Seabra, M. D. L. V., Tufik, S., & Hipólide, D. C. (2008) · Life Sciences · doi:10.1016/j.lfs.2008.12.009 · Cited by 6
CSF markers in sleep neurobiology
Rodríguez, J., & Santamaría, J. (2005) · Clinica Chimica Acta · doi:10.1016/j.cccn.2005.05.014 · Cited by 5
Why It Is Important to Consider the Effects of Analgesics on Sleep: A Critical Review
Iacovides, S., Kamerman, P. R., Baker, F. C., & Mitchell, D. (2021) · Comprehensive physiology · doi:10.1002/cphy.c210006 · Cited by 5
Fujitani, Y., Urade, Y., & Hayaishi, O. (1998) · Nippon Ronen Igakkai Zasshi Japanese Journal of Geriatrics · doi:10.3143/geriatrics.35.811 · Cited by 3
Self-citationKainuma, S., Tokuda, H., Kuroyanagi, G., Yamamoto, N., Ohguchi, R., Fujita, K., Matsushima‐Nishiwaki, R., Kozawa, O., & Otsuka, T. (2015) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2015.08.003 · Cited by 2
Neurochemistry of wakefulness and sleep
Strecker, R. E., & McKenna, J. T. (2012) · Cambridge University Press eBooks · doi:10.1017/cbo9780511783005.005 · Cited by 2
Regulation of Sleep and Wake Homeostasis
Goldstein, C. A., & Chervin, R. D. (2015) · Springer eBooks · doi:10.1007/978-3-7091-1631-9_1 · Cited by 1
Neuro-inflammatory Response and Immune–Brain Crosstalk in Sleep Regulation
Jha, P. K., & Bouâouda, H. (2024) · Progress in inflammation research · doi:10.1007/978-3-031-74744-1_5 · Cited by 1
Geneticsof sleep and circadian rhythms
Shaw, P. J., Tafti, M., & Thorpy, M. J. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139649469.006 · Cited by 1
Genetic and Epigenetic Mechanisms in Neural and Hormonal Controls over Female Reproductive Behaviors
Kow, L., Lee, A. W., Klinge, C. M., Warner, M. N., Gustafsson, J.-Α., & Pfaff, D. W. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803592-4.00045-6 · Cited by 1
Molecular Mechanisms of Sleep-Wake Regulation
Hayaishi, O. (2004) · CRC Press eBooks · doi:10.1201/9780203496732.ch4 · Cited by 1
Self-citationProstaglandin D2: An Endogenous Somnogen
Urade, Y., & Hayaishi, O. (2011) · Springer eBooks · doi:10.1007/978-1-4419-8390-9_9 · Cited by 1
Self-citationNew insights in the management of patients with obstructive sleep apnea
Chin, K. (2014) · Sleep and Biological Rhythms · doi:10.1111/sbr.12085
Sargin, D. (2009) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3247
Porkka‐Heiskanen, T., Alanko, L., & Stenberg, D. (2006) · Springer eBooks · doi:10.1007/978-0-387-30405-2_24
The Role of Endogenous Sleep-promoting Substances
Obál, F., García‐García, F., & Krueger, J. M. (2004) · Lung biology in health and disease · doi:10.3109/9780203998007-26
The Differential Role of Prostaglandin E2 Receptors in the CNS Response to Systemic Immune Challenge
Lazarus, M., & Saper, C. B. (2007) · Elsevier eBooks · doi:10.1016/b978-012088576-3/50020-4
Metadata
- Authors
- Ram, A., Pandey, H. P., Matsumura, H., Kasahara-Orita, K., Nakajima, T., Takahata, R., Satoh, S., Terao, A., & Hayaishi, O.
- Corresponding author
- Matsumura, Hitoshi
- ORCID
- Terao, Akira
- Venue
- Brain Research
- Publisher
- Elsevier BV
- Published
- 1997-03
- Volume
- 751
- Issue
- 1
- Pages
- 81-89
- ISSN
- 0006-8993 (ISSN-L)
- OpenAlex
- W2145858950
- Cited by
- 112
- References
- 47
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 6 · 2023: 2 · 2022: 4 · 2021: 6 · 2019: 5 · 2017: 4 · 2016: 3 · 2015: 5 · 2014: 8 · 2013: 3 · 2012: 5
- FWCI
- 1.81
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Takeda Science Foundation
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
- Keywords
- prostaglandin D2, prostaglandin E2, prostaglandin F2alpha, cerebrospinal fluid, sleep deprivation, slow-wave sleep, sleep-wake cycle, sleep promotion, basal forebrain, subarachnoid administration, rats, sleep propensity, hypothalamus, stress response, restraint stress, EEG, electromyography
- MeSH terms
- Animals, Antineoplastic Agents, Body Temperature, Consciousness, Male, Microelectrodes, Oxytocics, Prostaglandins, Synthetic, Sleep Deprivation, Stress, Physiological, Subarachnoid Space, Prostaglandin D2, Dinoprostone, Dinoprost, Prosencephalon, Rats, Sprague-Dawley, Rats
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