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Sleep-slow oscillation-spindle coupling precedes spindle-ripple coupling during development
Abstract Study Objectives Sleep supports systems memory consolidation through the precise temporal coordination of specific oscillatory events during slow-wave sleep, i.e. the neocortical slow oscillations (SOs), thalamic spindles, and hippocampal ripples. Beneficial effects of sleep on memory are a...
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Published in: | Sleep (New York, N.Y.) N.Y.), 2024-05, Vol.47 (5), p.1 |
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creator | Fechner, Julia Contreras, María P Zorzo, Candela Shan, Xia Born, Jan Inostroza, Marion |
description | Abstract
Study Objectives
Sleep supports systems memory consolidation through the precise temporal coordination of specific oscillatory events during slow-wave sleep, i.e. the neocortical slow oscillations (SOs), thalamic spindles, and hippocampal ripples. Beneficial effects of sleep on memory are also observed in infants, although the contributing regions, especially hippocampus and frontal cortex, are immature. Here, we examined in rats the development of these oscillatory events and their coupling during early life.
Methods
EEG and hippocampal local field potentials were recorded during sleep in male rats at postnatal days (PD)26 and 32, roughly corresponding to early (1–2 years) and late (9–10 years) human childhood, and in a group of adult rats (14–18 weeks, corresponding to ~22–29 years in humans).
Results
SO and spindle amplitudes generally increased from PD26 to PD32. In parallel, frontocortical EEG spindles increased in density and frequency, while changes in hippocampal ripples remained nonsignificant. The proportion of SOs co-occurring with spindles also increased from PD26 to PD32. Whereas parietal cortical spindles were phase-locked to the depolarizing SO-upstate already at PD26, over frontal cortex SO-spindle phase-locking emerged not until PD32. Co-occurrence of hippocampal ripples with spindles was higher during childhood than in adult rats, but significant phase-locking of ripples to the excitable spindle troughs was observed only in adult rats.
Conclusions
Results indicate a protracted development of synchronized thalamocortical processing specifically in frontocortical networks (i.e. frontal SO-spindle coupling). However, synchronization within thalamocortical networks generally precedes synchronization of thalamocortical with hippocampal processing as reflected by the delayed occurrence of spindle-ripple phase-coupling.
Graphical Abstract
Graphical Abstract |
doi_str_mv | 10.1093/sleep/zsae061 |
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Study Objectives
Sleep supports systems memory consolidation through the precise temporal coordination of specific oscillatory events during slow-wave sleep, i.e. the neocortical slow oscillations (SOs), thalamic spindles, and hippocampal ripples. Beneficial effects of sleep on memory are also observed in infants, although the contributing regions, especially hippocampus and frontal cortex, are immature. Here, we examined in rats the development of these oscillatory events and their coupling during early life.
Methods
EEG and hippocampal local field potentials were recorded during sleep in male rats at postnatal days (PD)26 and 32, roughly corresponding to early (1–2 years) and late (9–10 years) human childhood, and in a group of adult rats (14–18 weeks, corresponding to ~22–29 years in humans).
Results
SO and spindle amplitudes generally increased from PD26 to PD32. In parallel, frontocortical EEG spindles increased in density and frequency, while changes in hippocampal ripples remained nonsignificant. The proportion of SOs co-occurring with spindles also increased from PD26 to PD32. Whereas parietal cortical spindles were phase-locked to the depolarizing SO-upstate already at PD26, over frontal cortex SO-spindle phase-locking emerged not until PD32. Co-occurrence of hippocampal ripples with spindles was higher during childhood than in adult rats, but significant phase-locking of ripples to the excitable spindle troughs was observed only in adult rats.
Conclusions
Results indicate a protracted development of synchronized thalamocortical processing specifically in frontocortical networks (i.e. frontal SO-spindle coupling). However, synchronization within thalamocortical networks generally precedes synchronization of thalamocortical with hippocampal processing as reflected by the delayed occurrence of spindle-ripple phase-coupling.
Graphical Abstract
Graphical Abstract</description><identifier>ISSN: 0161-8105</identifier><identifier>EISSN: 1550-9109</identifier><identifier>DOI: 10.1093/sleep/zsae061</identifier><identifier>PMID: 38452190</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Animals ; Brain ; Brain Waves - physiology ; Electroencephalography ; Hippocampus - physiology ; Male ; Neocortex - physiology ; Rats ; Sleep ; Sleep - physiology ; Sleep, Slow-Wave - physiology ; Thalamus - physiology</subject><ispartof>Sleep (New York, N.Y.), 2024-05, Vol.47 (5), p.1</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of Sleep Research Society. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com. 2024</rights><rights>The Author(s) 2024. Published by Oxford University Press on behalf of Sleep Research Society. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.</rights><rights>COPYRIGHT 2024 Oxford University Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c377t-fb089600d91d5b46c6b8a565c2c993c3b4d4a4a1fca598d1f84b0166861344f43</cites><orcidid>0000-0002-4424-5697 ; 0000-0002-2959-6632</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38452190$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fechner, Julia</creatorcontrib><creatorcontrib>Contreras, María P</creatorcontrib><creatorcontrib>Zorzo, Candela</creatorcontrib><creatorcontrib>Shan, Xia</creatorcontrib><creatorcontrib>Born, Jan</creatorcontrib><creatorcontrib>Inostroza, Marion</creatorcontrib><title>Sleep-slow oscillation-spindle coupling precedes spindle-ripple coupling during development</title><title>Sleep (New York, N.Y.)</title><addtitle>Sleep</addtitle><description>Abstract
Study Objectives
Sleep supports systems memory consolidation through the precise temporal coordination of specific oscillatory events during slow-wave sleep, i.e. the neocortical slow oscillations (SOs), thalamic spindles, and hippocampal ripples. Beneficial effects of sleep on memory are also observed in infants, although the contributing regions, especially hippocampus and frontal cortex, are immature. Here, we examined in rats the development of these oscillatory events and their coupling during early life.
Methods
EEG and hippocampal local field potentials were recorded during sleep in male rats at postnatal days (PD)26 and 32, roughly corresponding to early (1–2 years) and late (9–10 years) human childhood, and in a group of adult rats (14–18 weeks, corresponding to ~22–29 years in humans).
Results
SO and spindle amplitudes generally increased from PD26 to PD32. In parallel, frontocortical EEG spindles increased in density and frequency, while changes in hippocampal ripples remained nonsignificant. The proportion of SOs co-occurring with spindles also increased from PD26 to PD32. Whereas parietal cortical spindles were phase-locked to the depolarizing SO-upstate already at PD26, over frontal cortex SO-spindle phase-locking emerged not until PD32. Co-occurrence of hippocampal ripples with spindles was higher during childhood than in adult rats, but significant phase-locking of ripples to the excitable spindle troughs was observed only in adult rats.
Conclusions
Results indicate a protracted development of synchronized thalamocortical processing specifically in frontocortical networks (i.e. frontal SO-spindle coupling). However, synchronization within thalamocortical networks generally precedes synchronization of thalamocortical with hippocampal processing as reflected by the delayed occurrence of spindle-ripple phase-coupling.
Graphical Abstract
Graphical Abstract</description><subject>Animals</subject><subject>Brain</subject><subject>Brain Waves - physiology</subject><subject>Electroencephalography</subject><subject>Hippocampus - physiology</subject><subject>Male</subject><subject>Neocortex - physiology</subject><subject>Rats</subject><subject>Sleep</subject><subject>Sleep - physiology</subject><subject>Sleep, Slow-Wave - physiology</subject><subject>Thalamus - physiology</subject><issn>0161-8105</issn><issn>1550-9109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkc1rFTEUxYMo9lldupUHbtykTSYfkyxLqVoouNCuXIRMcqekZCYxmVHsX29e-9qqCJLFJbm_e3IPB6HXlBxRotlxjQD5-KZaIJI-QRsqBMG6tZ6iDaGSYkWJOEAvar0m7c41e44OmOKio5ps0NfPu3lcY_qxTdWFGO0S0oxrDrOPsHVpzTHMV9tcwIGHut13cAk5_w74tdwW-A4x5Qnm5SV6NtpY4dW-HqLL92dfTj_ii08fzk9PLrBjfb_gcSBKS0K8pl4MXDo5KCukcJ3Tmjk2cM8tt3R0Vmjl6aj40JxIJSnjfOTsEL27080lfVuhLmYK1UGzMkNaq-m04L3USpKGvv0LvU5rmdt2htFOEdoLwR6pKxvBhHlMS7FuJ2pOei3av6rbaR39g2rHwxRcmmEM7f2PAXw34EqqtcBocgmTLT8NJWYXprkN0-zDbPyb_bLrMIF_oO_TezTeMviP1i-54amU</recordid><startdate>20240510</startdate><enddate>20240510</enddate><creator>Fechner, Julia</creator><creator>Contreras, María P</creator><creator>Zorzo, Candela</creator><creator>Shan, Xia</creator><creator>Born, Jan</creator><creator>Inostroza, Marion</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4424-5697</orcidid><orcidid>https://orcid.org/0000-0002-2959-6632</orcidid></search><sort><creationdate>20240510</creationdate><title>Sleep-slow oscillation-spindle coupling precedes spindle-ripple coupling during development</title><author>Fechner, Julia ; Contreras, María P ; Zorzo, Candela ; Shan, Xia ; Born, Jan ; Inostroza, Marion</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-fb089600d91d5b46c6b8a565c2c993c3b4d4a4a1fca598d1f84b0166861344f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Brain</topic><topic>Brain Waves - physiology</topic><topic>Electroencephalography</topic><topic>Hippocampus - physiology</topic><topic>Male</topic><topic>Neocortex - physiology</topic><topic>Rats</topic><topic>Sleep</topic><topic>Sleep - physiology</topic><topic>Sleep, Slow-Wave - physiology</topic><topic>Thalamus - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fechner, Julia</creatorcontrib><creatorcontrib>Contreras, María P</creatorcontrib><creatorcontrib>Zorzo, Candela</creatorcontrib><creatorcontrib>Shan, Xia</creatorcontrib><creatorcontrib>Born, Jan</creatorcontrib><creatorcontrib>Inostroza, Marion</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Sleep (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fechner, Julia</au><au>Contreras, María P</au><au>Zorzo, Candela</au><au>Shan, Xia</au><au>Born, Jan</au><au>Inostroza, Marion</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sleep-slow oscillation-spindle coupling precedes spindle-ripple coupling during development</atitle><jtitle>Sleep (New York, N.Y.)</jtitle><addtitle>Sleep</addtitle><date>2024-05-10</date><risdate>2024</risdate><volume>47</volume><issue>5</issue><spage>1</spage><pages>1-</pages><issn>0161-8105</issn><eissn>1550-9109</eissn><abstract>Abstract
Study Objectives
Sleep supports systems memory consolidation through the precise temporal coordination of specific oscillatory events during slow-wave sleep, i.e. the neocortical slow oscillations (SOs), thalamic spindles, and hippocampal ripples. Beneficial effects of sleep on memory are also observed in infants, although the contributing regions, especially hippocampus and frontal cortex, are immature. Here, we examined in rats the development of these oscillatory events and their coupling during early life.
Methods
EEG and hippocampal local field potentials were recorded during sleep in male rats at postnatal days (PD)26 and 32, roughly corresponding to early (1–2 years) and late (9–10 years) human childhood, and in a group of adult rats (14–18 weeks, corresponding to ~22–29 years in humans).
Results
SO and spindle amplitudes generally increased from PD26 to PD32. In parallel, frontocortical EEG spindles increased in density and frequency, while changes in hippocampal ripples remained nonsignificant. The proportion of SOs co-occurring with spindles also increased from PD26 to PD32. Whereas parietal cortical spindles were phase-locked to the depolarizing SO-upstate already at PD26, over frontal cortex SO-spindle phase-locking emerged not until PD32. Co-occurrence of hippocampal ripples with spindles was higher during childhood than in adult rats, but significant phase-locking of ripples to the excitable spindle troughs was observed only in adult rats.
Conclusions
Results indicate a protracted development of synchronized thalamocortical processing specifically in frontocortical networks (i.e. frontal SO-spindle coupling). However, synchronization within thalamocortical networks generally precedes synchronization of thalamocortical with hippocampal processing as reflected by the delayed occurrence of spindle-ripple phase-coupling.
Graphical Abstract
Graphical Abstract</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>38452190</pmid><doi>10.1093/sleep/zsae061</doi><orcidid>https://orcid.org/0000-0002-4424-5697</orcidid><orcidid>https://orcid.org/0000-0002-2959-6632</orcidid></addata></record> |
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subjects | Animals Brain Brain Waves - physiology Electroencephalography Hippocampus - physiology Male Neocortex - physiology Rats Sleep Sleep - physiology Sleep, Slow-Wave - physiology Thalamus - physiology |
title | Sleep-slow oscillation-spindle coupling precedes spindle-ripple coupling during development |
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