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'''Sleep spindles''' are bursts of [[neural oscillation|neural oscillatory activity]] that are generated by interplay of the [[thalamic reticular nucleus]] (TRN) and other thalamic nuclei during [[Neuroscience of sleep#NREM 2|stage 2 NREM sleep]] in a frequency range of ~11 to 16&nbsp;Hz (usually 12–14 Hz) with a duration of 0.5 seconds or greater (usually 0.5–1.5 seconds).<ref>{{cite book |last1=Berry |first1=Richard B. |last2=Wagner |first2=Mary H. | name-list-style = vanc |title=Sleep Medicine Pearls |date=2015 |publisher=Elsevier |isbn=978-1-4557-7051-9 |pages=10–14 |url=https://linkinghub.elsevier.com/retrieve/pii/B9781455770519000024 |access-date=5 June 2019}}</ref><ref>{{cite book | vauthors = Rechtschaffen A, Kales A | date = 1968 | title = A Manual of Standardized Terminology, Techniques and Scoring System For Sleep Stages of Human Subjects. | publisher = US Dept of Health, Education, and Welfare; National Institutes of Health | oclc = 2518321 }}</ref><ref>{{cite journal | vauthors = De Gennaro L, Ferrara M | title = Sleep spindles: an overview | journal = Sleep Medicine Reviews | volume = 7 | issue = 5 | pages = 423–40 | date = October 2003 | pmid = 14573378 | doi = 10.1053/smrv.2002.0252 }}</ref> After generation in the TRN, spindles are sustained and relayed to the cortex by thalamo-thalamic and thalamo-cortical feedback loops regulated by both [[GABAergic]] and [[NMDA]]-receptor mediated glutamatergic neurotransmission.<ref>{{cite journal | vauthors = Pinault D | title = The thalamic reticular nucleus: structure, function and concept | journal = Brain Research. Brain Research Reviews | volume = 46 | issue = 1 | pages = 1–31 | date = August 2004 | pmid = 15297152 | doi = 10.1016/j.brainresrev.2004.04.008 | s2cid = 26291991 }}</ref> Sleep spindles have been found in all tested mammalian species and in vitro cells.
'''Sleep spindles''' are bursts of [[neural oscillation|neural oscillatory activity]] that are generated by interplay of the [[thalamic reticular nucleus]] (TRN) and other thalamic nuclei during [[Neuroscience of sleep#NREM 2|stage 2 NREM sleep]] in a frequency range of ~11 to 16&nbsp;Hz (usually 12–14 Hz) with a duration of 0.5 seconds or greater (usually 0.5–1.5 seconds).<ref>{{cite book |last1=Berry |first1=Richard B. |last2=Wagner |first2=Mary H. | name-list-style = vanc |title=Sleep Medicine Pearls |date=2015 |publisher=Elsevier |isbn=978-1-4557-7051-9 |pages=10–14 |url=https://linkinghub.elsevier.com/retrieve/pii/B9781455770519000024 |access-date=5 June 2019}}</ref><ref>{{cite book | vauthors = Rechtschaffen A, Kales A | date = 1968 | title = A Manual of Standardized Terminology, Techniques and Scoring System For Sleep Stages of Human Subjects. | publisher = US Dept of Health, Education, and Welfare; National Institutes of Health | oclc = 2518321 }}</ref><ref>{{cite journal | vauthors = De Gennaro L, Ferrara M | title = Sleep spindles: an overview | journal = Sleep Medicine Reviews | volume = 7 | issue = 5 | pages = 423–40 | date = October 2003 | pmid = 14573378 | doi = 10.1053/smrv.2002.0252 }}</ref> After generation in the TRN, spindles are sustained and relayed to the cortex by thalamo-thalamic and thalamo-cortical feedback loops regulated by both [[GABAergic]] and [[NMDA]]-receptor mediated glutamatergic neurotransmission.<ref>{{cite journal | vauthors = Pinault D | title = The thalamic reticular nucleus: structure, function and concept | journal = Brain Research. Brain Research Reviews | volume = 46 | issue = 1 | pages = 1–31 | date = August 2004 | pmid = 15297152 | doi = 10.1016/j.brainresrev.2004.04.008 | s2cid = 26291991 }}</ref> Sleep spindles have been found in all tested mammalian species and in vitro cells.


Research supports that spindles (sometimes referred to as "sigma bands" or "sigma waves") play an essential role in both sensory processing and long term memory consolidation. Until recently, it was believed that each sleep spindle oscillation peaked at the same time throughout the neocortex. It was determined that oscillations sweep across the neocortex in circular patterns around the neocortex, peaking in one area, and then a few milliseconds later in an adjacent area. It has been suggested that this spindle organization allows for neurons to communicate across cortices. The time scale at which the waves travel at is the same speed it takes for neurons to communicate with each other.
Research supports that spindles (sometimes referred to as "sigma bands" or "sigma waves") play an essential role in both sensory processing and long term memory consolidation. Until recently, it was believed that each sleep spindle oscillation peaked at the same time throughout the neocortex. It was determined that oscillations sweep across the neocortex in circular patterns around the neocortex, peaking in one area, and then a few milliseconds later in an adjacent area. It has been suggested that this spindle organization allows for neurons to communicate across cortices. The time scale at which the waves travel at is the same speed it takes for neurons to communicate with each other.<ref>{{Cite journal|last=Muller|first=Lyle|last2=Piantoni|first2=Giovanni|last3=Koller|first3=Dominik|last4=Cash|first4=Sydney S|last5=Halgren|first5=Eric|last6=Sejnowski|first6=Terrence J|date=2016-11-15|editor-last=Skinner|editor-first=Frances K|title=Rotating waves during human sleep spindles organize global patterns of activity that repeat precisely through the night|url=https://doi.org/10.7554/eLife.17267|journal=eLife|volume=5|pages=e17267|doi=10.7554/eLife.17267|issn=2050-084X}}</ref>


Although the function of sleep spindles is unclear, it is believed that they actively participate in the consolidation of overnight declarative memory through the reconsolidation process. The density of spindles has been shown to increase after extensive learning of declarative memory tasks and the degree of increase in stage 2 spindle activity correlates with memory performance.
Although the function of sleep spindles is unclear, it is believed that they actively participate in the consolidation of overnight declarative memory through the reconsolidation process. The density of spindles has been shown to increase after extensive learning of declarative memory tasks and the degree of increase in stage 2 spindle activity correlates with memory performance.

Revision as of 04:27, 8 December 2021

For other uses, see Spindle (disambiguation).

Sleep spindles are bursts of neural oscillatory activity that are generated by interplay of the thalamic reticular nucleus (TRN) and other thalamic nuclei during stage 2 NREM sleep in a frequency range of ~11 to 16 Hz (usually 12–14 Hz) with a duration of 0.5 seconds or greater (usually 0.5–1.5 seconds).[1][2][3] After generation in the TRN, spindles are sustained and relayed to the cortex by thalamo-thalamic and thalamo-cortical feedback loops regulated by both GABAergic and NMDA-receptor mediated glutamatergic neurotransmission.[4] Sleep spindles have been found in all tested mammalian species and in vitro cells.

Research supports that spindles (sometimes referred to as "sigma bands" or "sigma waves") play an essential role in both sensory processing and long term memory consolidation. Until recently, it was believed that each sleep spindle oscillation peaked at the same time throughout the neocortex. It was determined that oscillations sweep across the neocortex in circular patterns around the neocortex, peaking in one area, and then a few milliseconds later in an adjacent area. It has been suggested that this spindle organization allows for neurons to communicate across cortices. The time scale at which the waves travel at is the same speed it takes for neurons to communicate with each other.[5]

Although the function of sleep spindles is unclear, it is believed that they actively participate in the consolidation of overnight declarative memory through the reconsolidation process. The density of spindles has been shown to increase after extensive learning of declarative memory tasks and the degree of increase in stage 2 spindle activity correlates with memory performance.

Among other functions, spindles facilitate somatosensory development, thalamocortical sensory gating, synaptic plasticity, and offline memory consolidation.[6] Sleep spindles closely modulate interactions between the brain and its external environment; they essentially moderate responsiveness to sensory stimuli during sleep.[7] Recent research has revealed that spindles distort the transmission of auditory information to the cortex; spindles isolate the brain from external disturbances during sleep.[8] Another study found that re-exposure to olfactory cues during sleep initiate reactivation, an essential part of long term memory consolidation that improves later recall performance.[9] Spindles generated in the thalamus have been shown to aid sleeping in the presence of disruptive external sounds. A correlation has been found between the amount of brainwave activity in the thalamus and a sleeper's ability to maintain tranquility.[10] Spindles play an essential role in both sensory processing and long term memory consolidation because they are generated in the TRN.

During sleep, these spindles are seen in the brain as a burst of activity immediately following muscle twitching. Researchers think the brain, particularly in the young, is learning about what nerves control what specific muscles when asleep.[11][12]

Sleep spindle activity has furthermore been found to be associated with the integration of new information into existing knowledge[13] as well as directed remembering and forgetting (fast sleep spindles).[14]

During NREM sleep, the brain waves produced by people with schizophrenia lack the normal pattern of slow and fast spindles.[15] Loss of sleep spindles are also a feature of familial fatal insomnia, a prion disease.[16] Changes in spindle density are observed in disorders. There are some studies that show an increase in sleep spindles in autistic children. Also some studies suggest a lack of sleep spindles in epilepsy.[17][18]/

Sex differences

Sleep spindles play a crucial role in declarative memory consolidation, however, most studies neglect to control for sex [citation needed], although both sex and menstruation affect sleep[19] and online learning periods.[20] Studies have shown that the influence of sleep spindles during the declarative memory process may be affected by modulatory menstrual cycle effects in females.[21]

Women tend to have 0.16 more sleep spindles per minute than men[22] ( ⁠i.e. roughly 9–⁠10 more over an hour's time). A female advantage has been found for episodic, emotional, and spatial memories as well as recognition of odours, faces, and pictures.[23] These differences are believed to be due to hormonal influence, especially that of estrogen. The female sex hormone estrogen primarily influences sexual maturation and reproduction, but has also been found to facilitate other brain functions, including cognition and memory. On verbal tasks where women scored higher than men, women scored higher during the mid-luteal phase, when women have higher estrogen levels, when compared to the menstrual phase.[19] A recent study found that local brain estrogen production within cognitive circuits may be important for the acquisition and consolidation of memories.[24] Recent experiments concerning the relationship between estrogen and the process of offline memory consolidation have also focused on sleep spindles. Genzel and colleagues determined that there was a menstrual effect on declarative and motor performance, meaning that women in the mid-luteal phase (high estrogen) performed higher than the other female participants.[21] Women in the luteal phase were also the only participants to experience an increase in spindles after learning, which led to the conclusion that the effect of the menstrual cycle may be mediated by spindles and female hormones.[21]

References

  1. ^ Berry RB, Wagner MH (2015). Sleep Medicine Pearls. Elsevier. pp. 10–14. ISBN 978-1-4557-7051-9. Retrieved 5 June 2019.
  2. ^ Rechtschaffen A, Kales A (1968). A Manual of Standardized Terminology, Techniques and Scoring System For Sleep Stages of Human Subjects. US Dept of Health, Education, and Welfare; National Institutes of Health. OCLC 2518321.
  3. ^ De Gennaro L, Ferrara M (October 2003). "Sleep spindles: an overview". Sleep Medicine Reviews. 7 (5): 423–40. doi:10.1053/smrv.2002.0252. PMID 14573378.
  4. ^ Pinault D (August 2004). "The thalamic reticular nucleus: structure, function and concept". Brain Research. Brain Research Reviews. 46 (1): 1–31. doi:10.1016/j.brainresrev.2004.04.008. PMID 15297152. S2CID 26291991.
  5. ^ Muller, Lyle; Piantoni, Giovanni; Koller, Dominik; Cash, Sydney S; Halgren, Eric; Sejnowski, Terrence J (2016-11-15). Skinner, Frances K (ed.). "Rotating waves during human sleep spindles organize global patterns of activity that repeat precisely through the night". eLife. 5: e17267. doi:10.7554/eLife.17267. ISSN 2050-084X.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  6. ^ Holz J, Piosczyk H, Feige B, Spiegelhalder K, Baglioni C, Riemann D, Nissen C (December 2012). "EEG Σ and slow-wave activity during NREM sleep correlate with overnight declarative and procedural memory consolidation". Journal of Sleep Research. 21 (6): 612–9. doi:10.1111/j.1365-2869.2012.01017.x. PMID 22591117.
  7. ^ Lüthi A (June 2014). "Sleep Spindles: Where They Come From, What They Do". The Neuroscientist. 20 (3): 243–56. doi:10.1177/1073858413500854. PMID 23981852. S2CID 206658010.
  8. ^ Dang-Vu TT, Bonjean M, Schabus M, Boly M, Darsaud A, Desseilles M, et al. (September 2011). "Interplay between spontaneous and induced brain activity during human non-rapid eye movement sleep". Proceedings of the National Academy of Sciences of the United States of America. 108 (37): 15438–43. Bibcode:2011PNAS..10815438D. doi:10.1073/pnas.1112503108. PMC 3174676. PMID 21896732.
  9. ^ Rihm JS, Diekelmann S, Born J, Rasch B (August 2014). "Reactivating memories during sleep by odors: odor specificity and associated changes in sleep oscillations" (PDF). Journal of Cognitive Neuroscience. 26 (8): 1806–18. doi:10.1162/jocn_a_00579. PMID 24456392. S2CID 22066368.
  10. ^ Dang-Vu TT, McKinney SM, Buxton OM, Solet JM, Ellenbogen JM (August 2010). "Spontaneous brain rhythms predict sleep stability in the face of noise". Current Biology. 20 (15): R626-7. doi:10.1016/j.cub.2010.06.032. PMID 20692606.
  11. ^ Dingfelder SF (January 2006). "To sleep, perchance to twitch". Monitor. 37 (1). American Psychological Association: 51.
  12. ^ Harney É (April 1, 2009). "Wiring your brain at college – a new perspective on sleep". Blog at WordPress.com. Archived from the original on 2010-06-19.
  13. ^ Tamminen J, Payne JD, Stickgold R, Wamsley EJ, Gaskell MG (October 2010). "Sleep spindle activity is associated with the integration of new memories and existing knowledge". The Journal of Neuroscience. 30 (43): 14356–60. doi:10.1523/JNEUROSCI.3028-10.2010. PMC 2989532. PMID 20980591.
  14. ^ Saletin JM, Goldstein AN, Walker MP (November 2011). "The role of sleep in directed forgetting and remembering of human memories". Cerebral Cortex. 21 (11): 2534–41. doi:10.1093/cercor/bhr034. PMC 3183424. PMID 21459838.
  15. ^ Ferrarelli F, Huber R, Peterson MJ, Massimini M, Murphy M, Riedner BA, et al. (March 2007). "Reduced sleep spindle activity in schizophrenia patients". The American Journal of Psychiatry. 164 (3): 483–92. doi:10.1176/ajp.2007.164.3.483. PMID 17329474.
  16. ^ Niedermeyer E, Ribeiro M (October 2000). "Considerations of nonconvulsive status epilepticus". Clinical EEG. 31 (4): 192–5. doi:10.1177/155005940003100407. PMID 11056841. S2CID 30679161.
  17. ^ Iranmanesh S, Rodriguez-Villegas E (August 2017). "An Ultralow-Power Sleep Spindle Detection System on Chip". IEEE Transactions on Biomedical Circuits and Systems. 11 (4): 858–866. doi:10.1109/TBCAS.2017.2690908. hdl:10044/1/46059. PMID 28541914. S2CID 206608057.
  18. ^ Warby SC, Wendt SL, Welinder P, Munk EG, Carrillo O, Sorensen HB, et al. (April 2014). "Sleep-spindle detection: crowdsourcing and evaluating performance of experts, non-experts and automated methods". Nature Methods. 11 (4): 385–92. doi:10.1038/nmeth.2855. PMC 3972193. PMID 24562424.
  19. ^ a b Manber R, Armitage R (August 1999). "Sex, steroids, and sleep: a review". Sleep. 22 (5): 540–55. doi:10.1093/sleep/22.5.540. PMID 10450590.
  20. ^ Maki PM, Rich JB, Rosenbaum RS (2002). "Implicit memory varies across the menstrual cycle: estrogen effects in young women". Neuropsychologia. 40 (5): 518–29. doi:10.1016/S0028-3932(01)00126-9. PMID 11749982. S2CID 15133827.
  21. ^ a b c Genzel L, Kiefer T, Renner L, Wehrle R, Kluge M, Grözinger M, et al. (July 2012). "Sex and modulatory menstrual cycle effects on sleep related memory consolidation". Psychoneuroendocrinology. 37 (7): 987–98. doi:10.1016/j.psyneuen.2011.11.006. PMID 22153362. S2CID 19797939.
  22. ^ Purcell SM, Manoach DS, Demanuele C, Cade BE, Mariani S, Cox R, et al. (June 2017). "Characterizing sleep spindles in 11,630 individuals from the National Sleep Research Resource". Nature Communications. 8 (1): 15930. Bibcode:2017NatCo...815930P. doi:10.1038/ncomms15930. PMC 5490197. PMID 28649997.
  23. ^ Dzaja A, Arber S, Hislop J, Kerkhofs M, Kopp C, Pollmächer T, et al. (January 2005). "Women's sleep in health and disease". Journal of Psychiatric Research. 39 (1): 55–76. doi:10.1016/j.jpsychires.2004.05.008. PMID 15504424.
  24. ^ Vahaba DM, Remage-Healey L (December 2015). "Brain estrogen production and the encoding of recent experience". Current Opinion in Behavioral Sciences. 6: 148–153. doi:10.1016/j.cobeha.2015.11.005. PMC 4955874. PMID 27453921.
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