通过磁共振量化大脑氧代谢随睡眠阶段而发生的变化。

IF 2.9 3区 医学 Q2 NEUROSCIENCES
Jing Xu, Andrew Wiemken, Michael C. Langham, Hengyi Rao, Marianne Nabbout, Alessandra S. Caporale, Richard J. Schwab, John A. Detre, Felix W. Wehrli
{"title":"通过磁共振量化大脑氧代谢随睡眠阶段而发生的变化。","authors":"Jing Xu,&nbsp;Andrew Wiemken,&nbsp;Michael C. Langham,&nbsp;Hengyi Rao,&nbsp;Marianne Nabbout,&nbsp;Alessandra S. Caporale,&nbsp;Richard J. Schwab,&nbsp;John A. Detre,&nbsp;Felix W. Wehrli","doi":"10.1002/jnr.25313","DOIUrl":null,"url":null,"abstract":"<p>A key function of sleep is to provide a regular period of reduced brain metabolism, which is critical for maintenance of healthy brain function. The purpose of this work was to quantify the sleep-stage-dependent changes in brain energetics in terms of cerebral metabolic rate of oxygen (CMRO<sub>2</sub>) as a function of sleep stage using quantitative magnetic resonance imaging (MRI) with concurrent electroencephalography (EEG) during sleep in the scanner. Twenty-two young and older subjects with regular sleep hygiene and Pittsburgh Sleep Quality Index (PSQI) in the normal range were recruited for the study. Cerebral blood flow (CBF) and venous oxygen saturation (SvO<sub>2</sub>) were obtained simultaneously at 3 Tesla field strength and 2.7-s temporal resolution during an 80-min time series using OxFlow, an in-house developed imaging sequence. The method yields whole-brain CMRO<sub>2</sub> in absolute physiologic units via Fick's Principle. Nineteen subjects yielded evaluable data free of subject motion artifacts. Among these subjects, 10 achieved slow-wave (N3) sleep, 16 achieved N2 sleep, and 19 achieved N1 sleep while undergoing the MRI protocol during scanning. Mean CMRO<sub>2</sub> was 98 ± 7(μmol min<sup>−1</sup>)/100 g awake, declining progressively toward deepest sleep stage: 94 ± 10.8 (N1), 91 ± 11.4 (N2), and 76 ± 9.0 μmol min<sup>−1</sup>/100 g (N3), with each level differing significantly from the wake state. The technology described is able to quantify cerebral oxygen metabolism in absolute physiologic units along with non-REM sleep stage, indicating brain oxygen consumption to be closely associated with depth of sleep, with deeper sleep stages exhibiting progressively lower CMRO<sub>2</sub> levels.</p>","PeriodicalId":16490,"journal":{"name":"Journal of Neuroscience Research","volume":"102 3","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2024-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sleep-stage-dependent alterations in cerebral oxygen metabolism quantified by magnetic resonance\",\"authors\":\"Jing Xu,&nbsp;Andrew Wiemken,&nbsp;Michael C. Langham,&nbsp;Hengyi Rao,&nbsp;Marianne Nabbout,&nbsp;Alessandra S. Caporale,&nbsp;Richard J. Schwab,&nbsp;John A. Detre,&nbsp;Felix W. Wehrli\",\"doi\":\"10.1002/jnr.25313\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A key function of sleep is to provide a regular period of reduced brain metabolism, which is critical for maintenance of healthy brain function. The purpose of this work was to quantify the sleep-stage-dependent changes in brain energetics in terms of cerebral metabolic rate of oxygen (CMRO<sub>2</sub>) as a function of sleep stage using quantitative magnetic resonance imaging (MRI) with concurrent electroencephalography (EEG) during sleep in the scanner. Twenty-two young and older subjects with regular sleep hygiene and Pittsburgh Sleep Quality Index (PSQI) in the normal range were recruited for the study. Cerebral blood flow (CBF) and venous oxygen saturation (SvO<sub>2</sub>) were obtained simultaneously at 3 Tesla field strength and 2.7-s temporal resolution during an 80-min time series using OxFlow, an in-house developed imaging sequence. The method yields whole-brain CMRO<sub>2</sub> in absolute physiologic units via Fick's Principle. Nineteen subjects yielded evaluable data free of subject motion artifacts. Among these subjects, 10 achieved slow-wave (N3) sleep, 16 achieved N2 sleep, and 19 achieved N1 sleep while undergoing the MRI protocol during scanning. Mean CMRO<sub>2</sub> was 98 ± 7(μmol min<sup>−1</sup>)/100 g awake, declining progressively toward deepest sleep stage: 94 ± 10.8 (N1), 91 ± 11.4 (N2), and 76 ± 9.0 μmol min<sup>−1</sup>/100 g (N3), with each level differing significantly from the wake state. The technology described is able to quantify cerebral oxygen metabolism in absolute physiologic units along with non-REM sleep stage, indicating brain oxygen consumption to be closely associated with depth of sleep, with deeper sleep stages exhibiting progressively lower CMRO<sub>2</sub> levels.</p>\",\"PeriodicalId\":16490,\"journal\":{\"name\":\"Journal of Neuroscience Research\",\"volume\":\"102 3\",\"pages\":\"\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2024-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Neuroscience Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jnr.25313\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neuroscience Research","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jnr.25313","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

睡眠的一个关键功能是提供一个规律的大脑新陈代谢降低期,这对维持健康的大脑功能至关重要。这项研究的目的是在扫描仪中使用定量磁共振成像(MRI)和同期脑电图(EEG),以脑氧代谢率(CMRO2)的形式量化大脑能量随睡眠阶段而发生的变化。研究招募了 22 名年轻和年长的受试者,他们有规律的睡眠卫生习惯,匹兹堡睡眠质量指数(PSQI)处于正常范围。在 3 特斯拉场强和 2.7 秒的时间分辨率下,使用自行开发的成像序列 OxFlow,在 80 分钟的时间序列中同时获得脑血流(CBF)和静脉血氧饱和度(SvO2)。该方法通过费克原理获得以绝对生理单位表示的全脑 CMRO2。19 名受试者获得了无受试者运动伪影的可评估数据。在这些受试者中,有 10 人在扫描期间进行了慢波(N3)睡眠,16 人进行了 N2 睡眠,19 人在扫描期间进行了 N1 睡眠。平均 CMRO2 为 98 ± 7 (μmol min-1 )/100 g 清醒状态,向最深睡眠阶段逐渐下降:94 ± 10.8 (N1)、91 ± 11.4 (N2) 和 76 ± 9.0 μmol min-1 /100 g (N3),每个水平都与清醒状态有显著差异。所述技术能够以绝对生理单位量化大脑缺氧代谢和非快速眼动睡眠阶段,表明大脑缺氧与睡眠深度密切相关,较深睡眠阶段的 CMRO2 水平逐渐降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sleep-stage-dependent alterations in cerebral oxygen metabolism quantified by magnetic resonance

Sleep-stage-dependent alterations in cerebral oxygen metabolism quantified by magnetic resonance

A key function of sleep is to provide a regular period of reduced brain metabolism, which is critical for maintenance of healthy brain function. The purpose of this work was to quantify the sleep-stage-dependent changes in brain energetics in terms of cerebral metabolic rate of oxygen (CMRO2) as a function of sleep stage using quantitative magnetic resonance imaging (MRI) with concurrent electroencephalography (EEG) during sleep in the scanner. Twenty-two young and older subjects with regular sleep hygiene and Pittsburgh Sleep Quality Index (PSQI) in the normal range were recruited for the study. Cerebral blood flow (CBF) and venous oxygen saturation (SvO2) were obtained simultaneously at 3 Tesla field strength and 2.7-s temporal resolution during an 80-min time series using OxFlow, an in-house developed imaging sequence. The method yields whole-brain CMRO2 in absolute physiologic units via Fick's Principle. Nineteen subjects yielded evaluable data free of subject motion artifacts. Among these subjects, 10 achieved slow-wave (N3) sleep, 16 achieved N2 sleep, and 19 achieved N1 sleep while undergoing the MRI protocol during scanning. Mean CMRO2 was 98 ± 7(μmol min−1)/100 g awake, declining progressively toward deepest sleep stage: 94 ± 10.8 (N1), 91 ± 11.4 (N2), and 76 ± 9.0 μmol min−1/100 g (N3), with each level differing significantly from the wake state. The technology described is able to quantify cerebral oxygen metabolism in absolute physiologic units along with non-REM sleep stage, indicating brain oxygen consumption to be closely associated with depth of sleep, with deeper sleep stages exhibiting progressively lower CMRO2 levels.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Neuroscience Research
Journal of Neuroscience Research 医学-神经科学
CiteScore
9.50
自引率
2.40%
发文量
145
审稿时长
1 months
期刊介绍: The Journal of Neuroscience Research (JNR) publishes novel research results that will advance our understanding of the development, function and pathophysiology of the nervous system, using molecular, cellular, systems, and translational approaches. JNR covers both basic research and clinical aspects of neurology, neuropathology, psychiatry or psychology. The journal focuses on uncovering the intricacies of brain structure and function. Research published in JNR covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of the nervous system, with emphasis on how disease modifies the function and organization.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信