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28 - Pontine areas inhibiting REM sleep

from Section IV - Neuroanatomy and neurochemistry

Published online by Cambridge University Press:  07 September 2011

Priyattam J. Shiromani
Affiliation:
Harvard Medical School
Carlos Blanco-Centurion
Affiliation:
Harvard Medical School
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

In the first half of the twentieth century, research by von Economo and Walle Nauta implicated the hypothalamus in sleep and waking. In the subsequent 50 years the hypothalamus was abandoned and instead the pons was considered to house the neurons regulating states of consciousness. In 1999, the linkage of a hypothalamic peptide, hypocretin, with narcolepsy shifted the emphasis back to the hypothalamus. However, since REM sleep originates from the pons, we sought to identify how the hypothalamus links with the pons, which would elucidate a network map of regions responsible for all three states. In this review we summarize our hypothesis that hypothalamic wake and non-REM sleep active neurons link with a group of i nhibitory pontine neurons to gate the transition to REM sleep. This hypothesis was first publically presented by us at the Society for Neuroscience meeting in 2004. We suggest that the pontine areas inhibiting REM sleep (PAIRS) represent GABA neurons; that these neurons are activated by glucosensing neurons, and neurons involved in emotion and arousal, and that their purpose is to keep the animal upright, mobile, and vigilant as it forages for food.

Type
Chapter
Information
Rapid Eye Movement Sleep
Regulation and Function
, pp. 280 - 284
Publisher: Cambridge University Press
Print publication year: 2011

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References

Arias-Carrion, O., Murillo-Rodriguez, E., Xu, M. . (2004) Transplantation of hypocretin neurons into the pontine reticular formation: preliminary results. Sleep 27: –70.CrossRefGoogle ScholarPubMed
Blanco-Centurion, C., Gerashchenko, D., Salin-Pascual, R. J. & Shiromani, P. J. (2004) Effects of hypocretin2-saporin and antidopamine-beta-hydroxylase-saporin neurotoxic lesions of the dorsolateral pons on sleep and muscle tone. Eur J Neurosci 19: –52.CrossRefGoogle ScholarPubMed
Boissard, R., Fort, P., Gervasoni, D., Barbagli, B. & Luppi, P. H. (2003) Localization of the GABAergic and non-GABAergic neurons projecting to the sublaterodorsal nucleus and potentially gating paradoxical sleep onset. Eur J Neurosci 18: –39.CrossRefGoogle ScholarPubMed
Chemelli, R. M., Willie, J. T., Sinton, C. M. . (1999) Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation. Cell 98: –51.CrossRefGoogle ScholarPubMed
Dahlstrom, A. & Fuxe, K. (1964) Evidence for the existence of monoamines in the cell bodies of brain stem neurons. Acta Physiol 62: –55.Google Scholar
Hendricks, J. C., Finn, S. M., Panckeri, K. A. . (1999) Rest in Drosophila is a sleep-like state. Neuron 25: –38.Google Scholar
Jones, B. E. (2004) Paradoxical REM sleep promoting and permitting neuronal networks. Arch Ital Biol 142: –96.Google ScholarPubMed
Kaur, S., Thankachan, S., Begum, S. . (2009) Hypocretin-2 saporin lesions of the ventrolateral periaquaductal gray (vlPAG) increase REM sleep in hypocretin knockout mice. PLoS ONE 4: .CrossRefGoogle ScholarPubMed
Lin, L., Faraco, J., Li, R. . (1999) The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene. Cell 98: –76.CrossRefGoogle ScholarPubMed
Liu, M., Thankachan, S., Kaur, S. . (2008) Orexin (hypocretin) gene transfer diminishes narcoleptic sleep behavior in mice. Eur J Neurosci 28: –93.CrossRefGoogle ScholarPubMed
Mitler, M. M., Carskadon, M. A., Czeisler, C.A. . (1988) Catastrophes, sleep, and public policy: consensus Report. Sleep 11: –9.CrossRefGoogle ScholarPubMed
Moldofsky, H. (1994) Central nervous system and peripheral immune functions and the sleep–wake system. J Psychiatry Neurosci 19: –74.Google ScholarPubMed
Moruzzi, G. & Magoun, H. W. (1949) Brain stem reticular formation and activation of the EEG. Electroencephalogr Clin Neurophysiol 1: –73.CrossRefGoogle ScholarPubMed
Oliva, A. A. Jr., Jiang, M., Lam, T., Smith, K. L. & Swann, J. W. (2000) Novel hippocampal interneuronal subtypes identified using transgenic mice that express green fluorescent protein in GABAergic interneurons. J Neurosci 20: –68.CrossRefGoogle ScholarPubMed
Peyron, C., Faraco, J., Rogers, W. . (2000) A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains. Nat Med 6: –7.CrossRefGoogle Scholar
Sakurai, T., Nagata, R., Yamanaka, A. . (2005) Input of orexin/hypocretin neurons revealed by a genetically encoded tracer in mice. Neuron 46: –308.CrossRefGoogle ScholarPubMed
Sherin, J. E., Shiromani, P. J., McCarley, R. W. & Saper, C. B. (1996) Activation of ventrolateral preoptic neurons during sleep. Science 271: –19.CrossRefGoogle ScholarPubMed
Shiromani, P. J., Kilduff, T. S., Bloom, F. E. & McCarley, R. W. (1992) Cholinergically induced REM sleep triggers Fos-like immunoreactivity in dorsolateral pontine regions associated with REM sleep. Brain Res 580: –7.CrossRefGoogle ScholarPubMed
Stefansson, H., Rye, D. B., Hicks, A. . (2007) A genetic risk factor for periodic limb movements in sleep. N Engl J Med 357: –47.CrossRefGoogle ScholarPubMed
Steriade, M. & McCarley, R. W. (1990) Brainstem Control of Wakefulness and Sleep. New York: Plenum Press.CrossRefGoogle Scholar
Thankachan, S., Kaur, S. & Shiromani, P. J. (2009) Activity of pontine neurons during sleep and cataplexy in hypocretin knock-out mice. J Neurosci 29: –5.CrossRefGoogle ScholarPubMed
Thannickal, T. C., Moore, R. Y., Nienhuis, R. . (2000) Reduced number of hypocretin neurons in human narcolepsy. Neuron 27: –74.CrossRefGoogle ScholarPubMed
Winkelmann, J., Schormair, B., Lichtner, P. . (2007) Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nat Genet 39: –6.CrossRefGoogle ScholarPubMed
Zimmerman, J. E., Naidoo, N., Raizen, D. M. & Pack, A. I. (2008) Conservation of sleep: insights from non-mammalian model systems. Trends Neurosci 31: –6.CrossRefGoogle ScholarPubMed

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