Cited by 480Sleep and Wakefulness ResearchNeural dynamics and brain functionNeuroscience and Neuropharmacology Research

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Microdialysis measurement of cortical and hippocampal acetylcholine release during sleep-wake cycle in freely moving cats

Marrosu, Francesco, Portas, Chiara, Mascia, Maria Stefania, Casu, Maria Antonietta, Fà, Mauro, Giagheddu, Marcello, Imperato, Assunta, Gessa, Gian Luigi·1995·Brain Research

DOI 10.1016/0006-8993(94)01399-3

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Abstract

The variations of Acetylcholine (ACh) release in the cerebral cortex and dorsal hippocampus were monitored by microdialysis during the electroencephalographically recorded sleep-waking cycle in freely moving cats. The results show a state-dependent variation in ACh output in both the cortex and the hippocampus. ACh release increased by approximately 100% during quiet waking (QW) and by 175% during active waking (AW) as referred to slow wave sleep (SWS) baseline. In contrast, a clear difference between the two areas was observed during REM sleep. During this stage ACh release in the cortex reached approximately the same values observed during QW, while in the hippocampus ACh release rose to about 4-fold the level obtained during SWS or twice that of QW. The results support the idea that the increase in ACh release in the cortex reflects the desynchronized EEG of wakefulness and REM sleep, while the marked increase of ACh during REM in the hippocampus may be related to the sustained theta activity in this area.

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Central cholinergic pathways in the rat: An overview based on an alternative nomenclature (Ch1–Ch6)
Mesulam, M. M., Mufson, E. J., Wainer, B. H., & Levey, A. I. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90108-2 · Cited by 2,329
The role of monoamines and acetylcholine-containing neurons in the regulation of the sleep-waking cycle
Jouvet, M. (1972) · Springer eBooks · doi:10.1007/3-540-05462-6_2 · Cited by 1,100
The physiology and pharmacology of hippocampal formation theta rhythms
Bland, B. H. (1986) · Progress in Neurobiology · doi:10.1016/0301-0082(86)90019-5 · Cited by 1,039
Effects of locus coeruleus activation on electroencephalographic activity in neocortex and hippocampus
Berridge, C. W., & Foote, S. L. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-10-03135.1991 · Cited by 434
Acetylcholine Liberation from Cerebral Cortex during Paradoxical (REM) Sleep
Jasper, H. H., & Tessier, J. (1971) · Science · doi:10.1126/science.172.3983.601 · Cited by 434
Microdialysis in the Neurosciences
(1991) · Techniques in the behavioral and neural sciences · doi:10.1016/c2013-0-04455-6 · Cited by 348
A small, removable microdialysis probe
Hernandez, L., Stanley, B. G., & Hoebel, B. G. (1986) · Life Sciences · doi:10.1016/0024-3205(86)90119-0 · Cited by 211
Enhancement of acetylcholine release during paradoxical sleep in the dorsal tegmental field of the cat brain stem
Kodama, T., Takahashi, Y., & Honda, Y. (1990) · Neuroscience Letters · doi:10.1016/0304-3940(90)90576-u · Cited by 179
The relation of hippocampal theta activity to arousal, attentive behaviour and somato-motor movements in unrestrained cats
Kemp, I. R., & Kaada, B. R. (1975) · Brain Research · doi:10.1016/0006-8993(75)90110-9 · Cited by 169
Brain stem generation of the hippocampal EEG
Vertes, R. P. (1982) · Progress in Neurobiology · doi:10.1016/0301-0082(82)90005-3 · Cited by 166

Show all 20 references

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Ripple-selective GABAergic projection cells in the hippocampus
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Volume transmission signalling via astrocytes
Hirase, H., Iwai, Y., Takata, N., Shinohara, Y., & Mishima, T. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0604 · Cited by 60
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Grabb, M. C., Sciotti, V. M., Gidday, J. M., Cohen, S. A., & Wylen, D. G. L. V. (1998) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(98)00025-9 · Cited by 54
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Hasselmo, M. E. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)63064-2 · Cited by 44
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Alreja, M., & Liu, W. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021485 · Cited by 43
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Authors: Marrosu, F., Portas, C., Mascia, M. S., Casu, M. A., Fà, M., Giagheddu, M., Imperato, A., & Gessa, G. L.
Affiliations: University of Cagliari (IT)
Corresponding author: Gessa, Gian Luigi
ORCID: Marrosu, Francesco
Casu, Maria Antonietta
Fà, Mauro
Gessa, Gian Luigi
Venue: Brain Research
Publisher: Elsevier BV
Published: 1995-02
Volume: 671
Issue: 2
Pages: 329-332
ISSN: 0006-8993 (ISSN-L)
DOI: 10.1016/0006-8993(94)01399-3
OpenAlex: W2092411461
Cited by: 480
References: 20
Citations by year: 2026: 6 · 2025: 16 · 2024: 10 · 2023: 12 · 2022: 16 · 2021: 20 · 2020: 13 · 2019: 18 · 2018: 20 · 2017: 31 · 2016: 18 · 2015: 22 · 2014: 23 · 2013: 11 · 2012: 24
FWCI: 3.18
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Brain Research (publishedVersion)
PubMed (publishedVersion)
UNICA IRIS Institutional Research Information System (University of Cagliari) (submittedVersion)
P-arch (Science and Technology Park of Sardinia) (submittedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: acetylcholine release, sleep-wake cycle, REM sleep, slow-wave sleep, cerebral cortex, dorsal hippocampus, cholinergic neurotransmission, theta activity, EEG desynchronization
MeSH terms: Acetylcholine, Animals, Cats, Cerebral Cortex, Electroencephalography, Hippocampus, Male, Sleep, Sleep, REM, Wakefulness, Microdialysis

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Microdialysis measurement of cortical and hippocampal acetylcholine release during sleep-wake cycle in freely moving cats

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