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.
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“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]
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Cites
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Characterization of inducible cyclooxygenase in rat brain
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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
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Effects of sleep deprivation on human immune functions
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Huang, Z., Zhang, Z., & Qu, W. (2022) · Translational medicine research · doi:10.1007/978-94-024-2168-2_3
Wang, C., Jiang, J., Liu, C., Wang, X., Wan, Q., Yuan, X., Liu, K., & Wu, W. (2023) · Research Square · doi:10.21203/rs.3.rs-3239691/v1
Jaggard, J. B., Ngo, K. J., & Mourrain, P. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780197602751.013.51
Integrative Real-Time NMR and X-ray Crystallography Reveal Prostaglandin D 2 Metabolism
Ohta, S., Shimamoto, S., Oda, H., Ohkubo, T., Oki, H., Shiraishi, Y., Kawahara, K., Yoshida, T., & Ueda, T. (2025) · Analytical Chemistry · doi:10.1021/acs.analchem.5c03604
Stewart, A. R., Bustillos, A., Beauregard, L. L., Link, C. D., Niemeyer, C. S., & Rowe, R. K. (2026) · Journal of Neuroinflammation · doi:10.1186/s12974-026-03944-7 · Cited by 1
Basic Mechanisms: Cognitive Performance and Sleep
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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
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