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26 - Adenosine and glycine in REM-sleep regulation

from Section IV - Neuroanatomy and neurochemistry

Published online by Cambridge University Press:  07 September 2011

Mahesh M. Thakkar
Affiliation:
University of Missouri
Rishi Sharma
Affiliation:
University of Missouri
Samuel C. Engemann
Affiliation:
University of Missouri
Pradeep Sahota
Affiliation:
University of Missouri
Birendra N. Mallick
Affiliation:
Jawaharlal Nehru University
S. R. Pandi-Perumal
Affiliation:
Somnogen Canada Inc, Toronto
Robert W. McCarley
Affiliation:
Harvard University, Massachusetts
Adrian R. Morrison
Affiliation:
University of Pennsylvania
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Summary

Summary

The discovery of rapid eye movement (REM) sleep revolutionized the field of sleep research. REM sleep is that state in which most of our dreams occur. During REM sleep, the brain is active, while the body is asleep. These characteristics make REM sleep a unique and a paradoxical state. While we are struggling to understand the function of REM sleep, major advances have been made in understanding the cellular mechanisms responsible for REM-sleep control. In this chapter, we have described two neurochemical substrates involved in REM-sleep regulation. One of them is adenosine and the other is glycine.

Adenosine is implicated to be the homeostatic regulator of sleep. It has been suggested that adenosine acts via A1 receptors to inhibit wake-promoting neurons and promote the transition from wakefulness to sleep. Adenosine acts on multiple wake-promoting systems including the basal forebrain cholinergic and the non-cholinergic systems, namely the orexinergic, and the histaminergic systems. There are reports suggesting that adenosine may act via A2A receptors and activate sleep-promoting neurons of the preoptic region. In addition, studies suggest a direct role of adenosine in the modulation of REM sleep.

During REM sleep, there is a tonic muscle atonia coupled with phasic muscle twitches. This phenomenon is regulated by the dorsolateral pons and ventromedial medulla along with local neurons within the spinal cord. Glycinergic mechanisms are responsible for the control of muscle tone during REM sleep. However, the exact role is under debate.

Type
Chapter
Information
Rapid Eye Movement Sleep
Regulation and Function
, pp. 256 - 265
Publisher: Cambridge University Press
Print publication year: 2011

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References

Alam, M. N., Szymusiak, R., Gong, H., King, J. & McGinty, D. (1999) Adenosinergic modulation of rat basal forebrain neurons during sleep and waking: neuronal recording with microdialysis. J Physiol 521(3): –90.CrossRefGoogle ScholarPubMed
Aserinsky, E. & Kleitman, N. (1953) Regularly occurring periods of eye motility and concomitant phenomenon during sleep. Science 118: –4.CrossRefGoogle Scholar
Basheer, R., Strecker, R. E., Thakkar, M. M. & McCarley, R. W. (2004) Adenosine and sleep-wake regulation. Progress in Neurobiology 73(6): 379–96.CrossRefGoogle ScholarPubMed
Brooks, P. L. & Peever, J. H. (2008) Glycinergic and GABA(A)-mediated inhibition of somatic motoneurons does not mediate rapid eye movement sleep motor atonia. J Neurosci 28( 3535–45.CrossRefGoogle Scholar
Chase, M. H., Chandler, S. H. & Nakamura, Y. (1980) Intracellular determination of membrane potential of trigeminal motoneurons during sleep and wakefulness. J Neurophysiol 44( 349–58.CrossRefGoogle ScholarPubMed
Chase, M. H. & Morales, F. R. (1990) The atonia and myoclonia of active (REM) sleep. Ann Rev Psychol 41: –84.CrossRefGoogle ScholarPubMed
Clarke, W. P., Yocca, F. D. & Maayani, S. (1996) Lack of 5-hydroxytryptamine1A-mediated inhibition of adenylyl cyclase in dorsal raphe of male and female rats. J Pharmacol Exp Ther 277(3): –66.Google ScholarPubMed
Coleman, C. G., Baghdoyan, H. A. & Lydic, R. (2006) Dialysis delivery of an adenosine A2A agonist into the pontine reticular formation of C57BL/6J mouse increases pontine acetylcholine release and sleep. J Neurochem 96(6): –9.CrossRefGoogle ScholarPubMed
Datta, S. & Maclean, R. R. (2007). Neurobiological mechanisms for the regulation of mammalian sleep-wake behavior: reinterpretation of historical evidence and inclusion of contemporary cellular and molecular evidence. Neurosci Biobehav Rev 31(5): –824.CrossRefGoogle ScholarPubMed
Datta, S., Mavanji, V., Patterson, E. H. & Ulloor, J. (2003) Regulation of rapid eye movement sleep in the freely moving rat: local microinjection of serotonin, norepinephrine, and adenosine into the brainstem. Sleep 26(5): –20.CrossRefGoogle ScholarPubMed
Dement, W. C. (2000) History of sleep physiology and medicine. InPrinciples and Practice of Sleep Medicine, 3rd edn, ed. M. Kryger, T. Roth & W. Dement. Philadelphia: W. B. Saunders Company, pp. 1–14.Google Scholar
Drury, A. N. & Szent-GyÖrgyi, A. (1929) The physiological activity of adenine compounds with especial reference to their actions upon the mammalian heart. J Physiol 68: –37.CrossRefGoogle Scholar
Fredholm, B. B., Jonzon, B. & Lindgren, E. (1983) Inhibition of noradrenaline release from hippocampal slices by a stable adenosine analogue. Acta Physiol Scand Suppl 515: 7–10.Google ScholarPubMed
Gallopin, T., Luppi, P. H., Cauli, B. . (2005) The endogenous somnogen adenosine excites a subset of sleep-promoting neurons via A2A receptors in the ventrolateral preoptic nucleus. Neuroscience 134(4): –90.CrossRefGoogle ScholarPubMed
Gundersen, R. Y., Vaagenes, P., Breivik, T., Fonnum, F. & Opstad, P. K. (2005). Glycine – an important neurotransmitter and cytoprotective agent. Acta Anaesthesiol Scand 49(8): –16.CrossRefGoogle ScholarPubMed
Hajnik, T., Lai, Y. Y. & Siegel, J. M. (2000) Atonia-related regions in the rodent pons and medulla. J Neurophysiol 84(4): –8.CrossRefGoogle ScholarPubMed
Hendricks, J. C., Morrison, A. R. & Mann, G. L. (1982) Different behaviors during paradoxical sleep without atonia depend on pontine lesion site. Brain Res 239(1): –105.CrossRefGoogle ScholarPubMed
Huston, J. P., Haas, H. L., Boix, F. . (1996) Extracellular adenosine levels in neostriatum and hippocampus during rest and activity periods of rats. Neuroscience 73(1): –107.CrossRefGoogle ScholarPubMed
Jouvet, M. (1979) What does a cat dream about?Trends Neurosci 2: –2.CrossRefGoogle Scholar
Kumar, S., Rai, S., Szymusiak, R., McGinty, D. & Alam, N. (2006) Effects of adenosine A1 receptor agonist into the perifornical lateral hypothalamic area on sleep. Society for Neuroscience Program No. 458.12. 2006.
Lai, Y. Y. & Siegel, J. M. (1988) Medullary regions mediating atonia. J Neurosci 8(12): –6.CrossRefGoogle ScholarPubMed
Lai, Y. Y. & Siegel, J. M. (1990) Muscle tone suppression and stepping produced by stimulation of midbrain and rostral pontine reticular formation. J Neurosci 10(8): –34.CrossRefGoogle ScholarPubMed
Liu, Z. W. & Gao, X. B. (2007) Adenosine inhibits activity of hypocretin/orexin neurons by the A1 receptor in the lateral hypothalamus: a possible sleep-promoting effect. J Neurophysiol 97(1): –48.CrossRefGoogle ScholarPubMed
Magoun, H. W. & Rhines, R. (1946) An inhibitory mechanism in the bulbar reticular formation. J Neurophysiol 9:–71.CrossRefGoogle ScholarPubMed
Marks, G. A., Shaffery, J. P., Speciale, S. G. & Birabil, C. G. (2003) Enhancement of rapid eye movement sleep in the rat by actions at A1 and A2a adenosine receptor subtypes with a differential sensitivity to atropine. Neuroscience 116(3): –20.CrossRefGoogle ScholarPubMed
McCarley, R., Strecker, R. E., Porkka-Heiskanen, T. . (1997) Modulation of cholinergic neurons by serotonin and adenosine in the control of REM and non-REM sleep. In Sleep and Sleep Disorders: From Molecule to Behavior, eds. Hayaishi, O. & Inoue, S.. Tokyo: Academic Press, pp. 63–79.Google Scholar
McCarley, R. W. (2007) Neurobiology of REM and NREM sleep. Sleep Med 8(4): –30.CrossRefGoogle ScholarPubMed
Methippara, M. M., Kumar, S., Alam, M. N., Szymusiak, R. & McGinty, D. (2005) Effects on sleep of microdialysis of adenosine A1 and A2a receptor analogs into the lateral preoptic area of rats. Am J Physiol Regul Integr Comp Physiol 289(6): –23.CrossRefGoogle ScholarPubMed
Morairty, S., Rainnie, D., McCarley, R. & Greene, R. (2004) Disinhibition of ventrolateral preoptic area sleep-active neurons by adenosine: a new mechanism for sleep promotion. Neuroscience 123(2): –7.CrossRefGoogle ScholarPubMed
Oishi, Y., Huang, Z. L., Fredholm, B. B., Urade, Y. & Hayaishi, O. (2008) Adenosine in the tuberomammillary nucleus inhibits the histaminergic system via A1 receptors and promotes non-rapid eye movement sleep. Proc Natl Acad Sci U S A 105(50): –7.CrossRefGoogle ScholarPubMed
Pompeiano, O. (1975) The control of posture and movements during REM sleep: neurophysiological and neurochemical mechanisms. Acta Astronaut 2(3/4): –39.CrossRefGoogle ScholarPubMed
Porkka-Heiskanen, T., Strecker, R. E. & McCarley, R. W. (2000) Brain site-specificity of extracellular adenosine concentration changes during sleep deprivation and spontaneous sleep: an in vivo microdialysis study. Neuroscience 99(3): –17.CrossRefGoogle Scholar
Porkka-Heiskanen, T., Strecker, R. E., Thakkar, M. . (1997) Adenosine: a mediator of the sleep-inducing effects of prolonged wakefulness. Science 276(5316) –8.CrossRefGoogle ScholarPubMed
Portas, C. M., Thakkar, M., Rainnie, D. G., Greene, R. W. & McCarley, R. W. (1997) Role of adenosine in behavioral state modulation: a microdialysis study in the freely moving cat. Neuroscience 79(1): –35.CrossRefGoogle ScholarPubMed
Radulovacki, M. (1985) Role of adenosine in sleep in rats. Rev Clin Basic Pharm 5(3/4): –39.Google ScholarPubMed
Sakurai, T. (2007) The neural circuit of orexin (hypocretin): maintaining sleep and wakefulness. Nat Rev Neurosci 8(3): –81.CrossRefGoogle ScholarPubMed
Schenck, C. H. & Mahowald, M. W. (1996) REM sleep parasomnias. Neurol Clin 14(4): –720.CrossRefGoogle ScholarPubMed
Soja, P. J., Finch, D. M. & Chase, M. H. (1987) Effect of inhibitory amino acid antagonists on masseteric reflex suppression during active sleep. Exp Neurol 96(1): –93.CrossRefGoogle ScholarPubMed
Steriade, M. & McCarley, R. W. (1990) Brainstem Control of Wakefulness and Sleep. New York: Plenum Press.CrossRefGoogle Scholar
Szymusiak, R. & McGinty, D. (2008) Hypothalamic regulation of sleep and arousal. Ann N Y Acad Sci 1129: –86.CrossRefGoogle Scholar
Takahashi, K., Lin, J. S. & Sakai, K. (2006) Neuronal activity of histaminergic tuberomammillary neurons during wake-sleep states in the mouse. J Neurosci 26(40): –8.CrossRefGoogle ScholarPubMed
Thakkar, M. & Mallick, B. N. (1996) Effect of rapid eye movement sleep deprivation on 5´- nucleotidase activity in the rat brain. Neurosci Lett 206(2/3): –80.CrossRefGoogle ScholarPubMed
Thakkar, M. M. & Datta, S. (2009) The evolution of REM sleep. In Evolution of Sleep: Phylogenetic and Functional Perspectives, ed. McNamara, P., Barton, R. & Nunn, C.. New York: Cambridge University Press 197–217.Google Scholar
Thakkar, M. M., Delgiacco, R. A., Strecker, R. E. & McCarley, R. W. (2003) Adenosinergic inhibition of basal forebrain wakefulness-active neurons: a simultaneous unit recording and microdialysis study in freely behaving cats. Neuroscience 122(4): –13.CrossRefGoogle ScholarPubMed
Thakkar, M. M., Engemann, S. C., Walsh, K. M. & Sahota, P. K. (2008) Adenosine and the homeostatic control of sleep: effects of A1 receptor blockade in the perifornical lateral hypothalamus on sleep-wakefulness. Neuroscience 153(4): –80.CrossRefGoogle ScholarPubMed
Thakkar, M. M. & McCarley, R. W. (2008) Histamine in the control of sleep-wakefulness. In Neurochemistry of Sleep and Wakefulness, ed. Monti, J. M., Pandi-Perumal, S. R. & Sinton, C. M.. New York: Cambridge University Press, pp. 144–78.Google Scholar
Thakkar, M. M., Ramesh, V., Cape, E. G. . (1999) REM sleep enhancement and behavioral cataplexy following orexin (hypocretin)-II receptor antisense perfusion in the pontine reticular formation. Sleep Res Online 2(4): –20.Google ScholarPubMed
Thakkar, M. M., Ramesh, V., Strecker, R. E. & McCarley, R. W. (2001) Microdialysis perfusion of orexin-A in the basal forebrain increases wakefulness in freely behaving rats. Arch Ital Biol 139(3): –28.Google Scholar
Thakkar, M. M., Strecker, R. E. & McCarley, R. W. (1998) Behavioral state control through differential serotonergic inhibition in the mesopontine cholinergic nuclei: a simultaneous unit recording and microdialysis study. J Neurosci 18(14): –7.CrossRefGoogle ScholarPubMed
Thakkar, M. M., Winston, S. & McCarley, R. W. (2002) Orexin neurons of the hypothalamus express adenosine A1 receptors. Brain Res 944(1/2) –4.CrossRefGoogle ScholarPubMed

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