Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-jbqgn Total loading time: 0 Render date: 2024-07-01T12:22:56.603Z Has data issue: false hasContentIssue false

12 - Amygdalar regulation of REM sleep

from Section III - Neuronal regulation

Published online by Cambridge University Press:  07 September 2011

Larry D. Sanford
Affiliation:
Eastern Virginia Medical School, USA
Richard J. Ross
Affiliation:
University of Pennsylvania School of Medicine
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
Get access

Summary

Summary

The amygdala has a long-recognized role in emotion, and a growing body of work demonstrates that it plays an important part in the regulation of arousal state. Primary findings are that the amygdala, especially its central nucleus, is a strong regulator of rapid eye movement sleep (REMS) and related phenomena, though a smaller body of research indicates a role for the amygdala in regulating non-REM (NREM). Considering its vital place in the limbic circuitry that controls emotion, it is likely that the amygdala mediates fear- and stress-induced alterations in sleep, and investigations in animals have begun to provide confirmatory evidence. In particular, GABAergic regulation of the central nucleus of the amygdala appears to play a significant role in stress-induced reductions in REM. In humans, neuroimaging studies suggest that the pathophysiological mechanisms of narcolepsy and post-traumatic stress disorder (PTSD), two central nervous system disorders with a prominent emotional component and a demonstrated abnormality of REM, involve an amygdalar-mediated reorganization of fundamental REM systems.

Type
Chapter
Information
Rapid Eye Movement Sleep
Regulation and Function
, pp. 110 - 120
Publisher: Cambridge University Press
Print publication year: 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Adrien, J., Dugovic, C. & Martin, P. (1991) Sleep-wakefulness patterns in the helpless rat. Physiol Behav 49: –62.CrossRefGoogle ScholarPubMed
Amaral, D., Price, J., Pitkanen, A. & Carmichael, S. (1992) Anatomical organization of the primate amydaloid complex. In The Amygdala: Neurobiological Aspects of Emotion, Memory, and Mental Dysfunction, ed. J. Aggleton. New York: Wiley-Liss, Inc.Google Scholar
Bordi, F., Ledoux, J., Clugnet, M. C. & Pavlides, C. (1993) Single-unit activity in the lateral nucleus of the amygdala and overlying areas of the striatum in freely behaving rats: rates, discharge patterns, and responses to acoustic stimuli. Behav Neurosci 107: –69.CrossRefGoogle ScholarPubMed
Braun, A. R., Balkin, T. J., Wesensten, N. J. . (1998) Dissociated pattern of activity in visual cortices and their projections during human rapid eye movement sleep. Science 279: –5.CrossRefGoogle ScholarPubMed
Buysse, D. J., Germain, A., Hall, M. L. . (2008) EEG spectral analysis in primary insomnia: NREM period effects and sex differences. Sleep 31: –82.CrossRefGoogle ScholarPubMed
Buysse, D. J., Tu, X. M., Cherry, C. R. . (1999) Pretreatment REM sleep and subjective sleep quality distinguish depressed psychotherapy remitters and nonremitters. Biol Psychiatry 45: –13.CrossRefGoogle ScholarPubMed
Calvo, J., Simón-Arceo, K. & Fernández-Mas, R. (1996) Prolonged enhancement of REM sleep produced by carbachol microinjection into the amygdala. NeuroRep 7: –80.CrossRefGoogle ScholarPubMed
Calvo, J. M., Badillo, S., Morales-Ramirez, M. & Palacios-Salas, P. (1987) The role of the temporal lobe amygdala in ponto-geniculo-occipital activity and sleep organization in cats. Brain Res 403: –30.CrossRefGoogle ScholarPubMed
Calvo, J. M. & Fernandez-Guardiola, A. (1984) Phasic activity of the basolateral amygdala, cingulate gyrus, and hippocampus during REM sleep in the cat. Sleep 7: –10.CrossRefGoogle ScholarPubMed
Cape, E. G., Manns, I. D., Alonso, A., Beaudet, A. & Jones, B. E. (2000) Neurotensin-induced bursting of cholinergic basal forebrain neurons promotes gamma and theta cortical activity together with waking and paradoxical sleep. J Neurosci 20: –61.CrossRefGoogle ScholarPubMed
Davis, M. (1992) The role of the amygdala in fear and anxiety. Ann Rev Neurosci 15: –75.CrossRefGoogle ScholarPubMed
Davis, M. & Whalen, P. J. (2001) The amygdala: vigilance and emotion. Mol Psychiatry 6: –34.CrossRefGoogle ScholarPubMed
Fosse, R., Stickgold, R. & Hobson, J. A. (2002) Emotional experience during rapid-eye-movement sleep in narcolepsy. Sleep 25: –32.CrossRefGoogle ScholarPubMed
Frysinger, R., Zhang, J. & Harper, R. (1988) Cardiovascular and respiratory relationships with neuronal discharge in the central nucleus of the amygdala during sleep–waking states. Sleep 11: –32.Google ScholarPubMed
Gaudreau, H. & Pare, D. (1996) Projection neurons of the lateral amygdaloid nucleus are virtually silent throughout the sleep–waking cycle. J Neurophysiol 75: –5.CrossRefGoogle ScholarPubMed
Germain, A., Buysse, D. J., Wood, A. & Nofzinger, E. (2004) Functional neuroanatomical correlates of eye movements during rapid eye movement sleep in depressed patients. Psychiatry Res 130: –68.CrossRefGoogle ScholarPubMed
Jacobs, B. L. & McGinty, D. J. (1971) Amygdala unit activity during sleep and waking. Exp Neurol 33: –15.CrossRefGoogle ScholarPubMed
Jha, S. K., Ross, R. J. & Morrison, A. R. (2005) Sleep-related neurons in the central nucleus of the amygdala of rats and their modulation by the dorsal raphe nucleus. Physiol Behav 86: –26.CrossRefGoogle ScholarPubMed
Kreindler, A. & Steriade, M. (1964) EEG patterns of arousal and sleep induced by stimulating various amygdaloid levels in the cat. Arch Ital Biol 102: –86.Google ScholarPubMed
Lehmann, J., Nagy, J. I., Atmadia, S. & Fibiger, H. C. (1980) The nucleus basalis magnocellularis: the origin of a cholinergic projection to the neocortex of the rat. Neuroscience 5: –74.CrossRefGoogle ScholarPubMed
Liberzon, I. & Garfinkel, S. N. (2009) Functional neuroimaging in post-traumatic stress disorder. In Post-Traumatic Stress Disorder: Basic Science and Clinical Practice, eds. P. J. Shiromani, T. M. Keane & J. E. LeDoux. New York: Humana Press, pp. 297–318.Google Scholar
Liu, X., Lonart, G. & Sanford, L. D. (2007) Transient fear-induced alterations in evoked release of norepinephrine and GABA in amygdala slices. Brain Res 1142: –53.CrossRefGoogle ScholarPubMed
Liu, X., Tang, X. & Sanford, L. D. (2003) Fear-conditioned suppression of REM sleep: relationship to Fos expression patterns in limbic and brainstem regions in BALB/cJ mice. Brain Res 991: –17.CrossRefGoogle ScholarPubMed
Liu, X., Yang, L., Wellman, L. L., Tang, X. & Sanford, L. D. (2009) GABAergic antagonism of the central nucleus of the amygdala attenuates reductions in rapid eye movement sleep after inescapable footshock stress. Sleep 32: –96.CrossRefGoogle ScholarPubMed
Lydic, R., Baghdoyan, H. A., Hibbard, L. . (1991) Regional brain glucose metabolism is altered during rapid eye movement sleep in the cat: a preliminary study. J Comp Neurol 304: –29.CrossRefGoogle ScholarPubMed
Maquet, P., Peters, J., Aerts, J. . (1996) Functional neuroanatomy of human rapid-eye-movement sleep and dreaming. Nature 383: –6.CrossRefGoogle ScholarPubMed
Mellman, T. A. (2006) Sleep and anxiety disorders. Psychiatr Clin North Am 29: –58.CrossRefGoogle ScholarPubMed
Morrison, A. R., Sanford, L. D. & Ross, R. J. (2000) The amygdala: a critical modulator of sensory influence on sleep. Biol Signals Recept 9: –96.CrossRefGoogle Scholar
Nofzinger, E. A., Buysse, D. J., Germain, A. . (2004) Increased activation of anterior paralimbic and executive cortex from waking to rapid eye movement sleep in depression. Arch Gen Psychiatry 61: –702.CrossRefGoogle ScholarPubMed
Pawlyk, A. C., Morrison, A. R., Ross, R. J. & Brennan, F. X. (2008) Stress-induced changes in sleep in rodents: Models and mechanisms. Neurosci Biobehav Rev 32: –117.CrossRefGoogle ScholarPubMed
Perlis, M. L., Smith, M. T. & Pigeon, W. R. (2005) Etiology and pathophysiology of insomnia. In Principles and Practice of Sleep Medicine, 4th edn. eds. , M. H.Kryger, T. Roth, & Dement, W. C.. Philadelphia: Elsevier Saunders.Google Scholar
Reynolds, C. F., Gillin, J. C. & Kupfer, D. J. (1987) Sleep and affective disorders. In Psychopharmacology: The Third Generation of Progress. ed. Meltzer, H. Y.. New York: Raven Press.Google Scholar
Ross, R. J., Ball, W. A., Sullivan, K. A. & Caroff, S. N. (1989) Sleep disturbance as the hallmark of posttraumatic stress disorder. Am J Psychiatry 146: –707.CrossRefGoogle ScholarPubMed
Sanford, L. D., Yang, L., Liu, X. & Tang, X. (2006a) Effects of tetrodotoxin (TTX) inactivation of the central nucleus of the amygdala (CNA) on dark period sleep and activity. Brain Res 1084: –8.CrossRefGoogle ScholarPubMed
Sanford, L. D., Yang, L., Tang, X. . (2006b) Cholinergic regulation of the central nucleus of the amygdala in rats: effects of local microinjections of cholinomimetics and cholinergic antagonists on arousal and sleep. Neuroscience, 141, –76.CrossRefGoogle ScholarPubMed
Schwartz, S. & Maquet, P. (2002) Sleep imaging and the neuro-psychological assessment of dreams. Trends Cogn Sci 6: –30.CrossRefGoogle ScholarPubMed
Schwartz, S., Ponz, A., Poryazova, R. . (2008) Abnormal activity in hypothalamus and amygdala during humour processing in human narcolepsy with cataplexy. Brain 131: –22.CrossRefGoogle ScholarPubMed
Steriade, M. & McCarley, R. (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
Van der Zee, E., Roozendaal, B., Bohus, B., Koolhaas, J. & Luiten, P. (1997) Muscarinic acetylcholine receptor immunoreactivity in the amygdala – I Cellular distribution correlated with fear-induced behaviorNeurosci 76: –73.Google ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×