The Impact of Emotional Salience and Aging on Selective Sleep-Based Memory Consolidation
情绪显着性和衰老对选择性睡眠记忆巩固的影响
基本信息
- 批准号:9186478
- 负责人:
- 金额:$ 4.95万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2015
- 资助国家:美国
- 起止时间:2015-01-01 至 2017-08-31
- 项目状态:已结题
- 来源:
- 关键词:AdultAgeAgingBiologicalBiological PreservationBrainClinicalComplexCuesDataDevelopmentElectroencephalographyEmotionalEmotionsEthicsEventFosteringFoundationsFrequenciesFunctional Magnetic Resonance ImagingGoalsIndividualInterventionKnowledgeLearningLiteratureLongevityMemoryMentorsMethodsModelingNappingNaturePerformancePeriodicityPhasePhysiologyPilot ProjectsPlayPopulationPositioning AttributePublic HealthReadingRecruitment ActivityResearchResearch TrainingRoleSleepSleep StagesSlow-Wave SleepStagingStimulusTechniquesTestingTimeTrainingTraining ProgramsWakefulnessWorkage effectage groupage relatedaging populationawakebaseclinical applicationcohortdensitydesignhealthy agingimprovedmemory consolidationmemory recognitionmiddle ageneural correlateneuromechanismnon rapid eye movementnovelprogramspublic health relevancerelating to nervous systemresearch and developmentsymposiumundergraduate studentwardyoung adult
项目摘要
DESCRIPTION (provided by applicant): Sleep preferentially preserves aspects of memory that are most salient and valuable to remember over less relevant details, but the majority of these provocative studies were conducted on young adults. Little is known about which aspects of sleep are crucially involved in selective consolidation and how these sleep phenomena vary with age. The objective of the proposed studies is to detect potential mechanisms, and the age- and salience-related influences, underlying sleep-based selectivity in memory. Based on preliminary data, the central hypothesis is that selective consolidation of salient parts of memory
will occur during sleep rich in slow waves and spindles, with emotional salience overriding other salience cues, and that these effects will decrease with age. The rationale for this project is tha an understanding of nuanced sleep-based consolidation and the role of emotion beyond the restricted cohort of young adults will foster the ability to determine the underlying age-related changes in the phenomenon. This research training program includes coursework, mentoring, and training designed to enable the candidate to examine mechanisms of, and age-effects on, selective memory consolidation in sleep. A novel dual nap paradigm will be used to control for time-of-day effects and to capitalize on the tendency of early and late naps to naturally differ with respect to sleep stage composition. Subjects 18-39 years (young) and 45-64 years (middle age) will be recruited to participate. Study 1 (n=90) will aim to identify sleep physiology correlates of selective consolidation of emotional components of memory. Subjects will be shown complex scenes of negative or neutral foreground objects on neutral backgrounds and then nap or remain awake. Memory for individual scene components (objects, backgrounds) will be assessed both before and after the sleep/wake retention period. Study 2 (n=90) will assess the relative importance of emotional salience in selective sleep-based consolidation by examining the interaction of emotional salience with another task-related salience cue (remember/forget). Negative and neutral stimuli will be presented, each followed by a cue to remember or forget the item, before a nap/wake retention period. Recognition memory for stimuli will be tested to directly assess how emotional salience influences the ability to remember important and forget irrelevant information. [An exploratory pilot study (n=15) using functional MRI will follow the general methods of Study 1 to investigate the feasibility of examining the neural mechanisms behind altered sleep-based selective consolidation of emotional memory with age.] EEG recordings will be analyzed to determine sleep staging, spectral frequency power, and sleep spindle density to correlate with age and memory performance data in all studies. The results will move the field forward by clarifying the interaction between aging, emotion, and sleep in nuanced memory consolidation in a healthy population, positioning the candidate to take a crucial step to- ward determining the underlying neural mechanisms, and modeling normal and abnormal processing for potential clinical applications.
描述(申请人提供):睡眠优先保留记忆中最重要和最有价值的部分,而不是相关的细节,但这些挑衅性的研究大多是在年轻人身上进行的。关于睡眠的哪些方面与选择性巩固有关,以及这些睡眠现象如何随着年龄的变化而变化,人们知之甚少。这项研究的目的是发现记忆中基于睡眠的选择性的潜在机制,以及与年龄和显着性相关的影响。根据初步数据,中心假设是选择性地巩固记忆的显著部分
在睡眠中会出现大量的慢波和纺锤波,情绪上的突出会压倒其他突出的暗示,这些影响会随着年龄的增长而减弱。这个项目的基本原理是,了解基于睡眠的细微差别巩固,以及超越有限的年轻人队列的情绪的作用,将培养确定这一现象潜在的与年龄相关的变化的能力。这项研究培训计划包括课程作业、指导和培训,旨在使应试者能够检查睡眠中选择性记忆巩固的机制和年龄效应。一种新的双午睡模式将被用来控制一天中的时间效应,并利用早睡和晚睡在睡眠阶段组成方面自然不同的趋势。将招募18-39岁(青年)和45-(中年)的受试者参加。研究1(n=90)的目的是确定选择性巩固记忆的情绪成分与睡眠生理学的相关性。受试者将被展示在中性背景上的负面或中性前景物体的复杂场景,然后打盹或保持清醒。将在睡眠/唤醒保持期之前和之后评估单个场景组件(对象、背景)的记忆。研究2(n=90)将通过考察情绪突显与另一个任务相关的突显线索(记住/忘记)的交互作用来评估情绪突显在选择性睡眠巩固中的相对重要性。将呈现消极和中性的刺激,每个刺激之后都会有一个提示,让你记住或忘记这一项,然后是午睡/清醒保持期。将测试对刺激的识别记忆,以直接评估情绪突显如何影响记住重要信息和忘记无关信息的能力。[一项使用功能磁共振成像的探索性初步研究(n=15)将遵循研究1的一般方法,以调查随着年龄增长而改变的基于睡眠的选择性巩固情绪记忆背后的神经机制的可行性。]将对脑电记录进行分析,以确定睡眠分期、频谱功率和睡眠纺锤密度,以与所有研究中的年龄和记忆表现数据相关联。这些结果将通过澄清健康人群中细微差别记忆巩固中衰老、情绪和睡眠之间的相互作用来推动这一领域的发展,为确定潜在的神经机制和为潜在的临床应用模拟正常和异常的处理过程定位候选者迈出关键的一步。
项目成果
期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Do different salience cues compete for dominance in memory over a daytime nap?
- DOI:10.1016/j.nlm.2018.06.005
- 发表时间:2019-04
- 期刊:
- 影响因子:2.7
- 作者:Alger SE;Chen S;Payne JD
- 通讯作者:Payne JD
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Sara Alger其他文献
Sara Alger的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Sara Alger', 18)}}的其他基金
The Impact of Emotional Salience and Aging on Selective Sleep-Based Memory Consolidation
情绪显着性和衰老对选择性睡眠记忆巩固的影响
- 批准号:
8984823 - 财政年份:2015
- 资助金额:
$ 4.95万 - 项目类别:
The Impact of Emotional Salience and Aging on Selective Sleep-Based Memory Consolidation
情绪显着性和衰老对选择性睡眠记忆巩固的影响
- 批准号:
8834408 - 财政年份:2015
- 资助金额:
$ 4.95万 - 项目类别:
相似国自然基金
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
- 批准号:JCZRQN202500010
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
- 批准号:2025JJ70209
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
- 批准号:
- 批准年份:2024
- 资助金额:0 万元
- 项目类别:面上项目
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
- 批准号:2023JJ50274
- 批准年份:2023
- 资助金额:0.0 万元
- 项目类别:省市级项目
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
- 批准号:
- 批准年份:2022
- 资助金额:33 万元
- 项目类别:地区科学基金项目
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
- 批准号:
- 批准年份:2022
- 资助金额:52 万元
- 项目类别:面上项目
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
- 批准号:n/a
- 批准年份:2022
- 资助金额:10.0 万元
- 项目类别:省市级项目
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
- 批准号:81973577
- 批准年份:2019
- 资助金额:55.0 万元
- 项目类别:面上项目
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
- 批准号:81602908
- 批准年份:2016
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
高血糖激活滑膜AGE-RAGE-PKC轴致骨关节炎易感的机制研究
- 批准号:81501928
- 批准年份:2015
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
相似海外基金
The Phenomenon of Stem Cell Aging according to Methylation Estimates of Age After Hematopoietic Stem Cell Transplantation
根据造血干细胞移植后甲基化年龄估算干细胞衰老现象
- 批准号:
23K07844 - 财政年份:2023
- 资助金额:
$ 4.95万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Analysis of Age-dependent Functional Changes in Skeletal Muscle CB1 Receptors by an in Vitro Model of Aging-related Muscle Atrophy
通过衰老相关性肌肉萎缩的体外模型分析骨骼肌 CB1 受体的年龄依赖性功能变化
- 批准号:
22KJ2960 - 财政年份:2023
- 资助金额:
$ 4.95万 - 项目类别:
Grant-in-Aid for JSPS Fellows
Joint U.S.-Japan Measures for Aging and Dementia Derived from the Prevention of Age-Related and Noise-induced Hearing Loss
美日针对预防与年龄相关和噪声引起的听力损失而导致的老龄化和痴呆症联合措施
- 批准号:
23KK0156 - 财政年份:2023
- 资助金额:
$ 4.95万 - 项目类别:
Fund for the Promotion of Joint International Research (International Collaborative Research)
The Effects of Muscle Fatigability on Gait Instability in Aging and Age-Related Falls Risk
肌肉疲劳对衰老步态不稳定性和年龄相关跌倒风险的影响
- 批准号:
10677409 - 财政年份:2023
- 资助金额:
$ 4.95万 - 项目类别:
Characterizing gut physiology by age, frailty, and sex: assessing the role of the aging gut in "inflamm-aging"
按年龄、虚弱和性别表征肠道生理学特征:评估衰老肠道在“炎症衰老”中的作用
- 批准号:
497927 - 财政年份:2023
- 资助金额:
$ 4.95万 - 项目类别:
Role of AGE/RAGEsignaling as a driver of pathological aging in the brain
AGE/RAGE信号传导作为大脑病理性衰老驱动因素的作用
- 批准号:
10836835 - 财政年份:2023
- 资助金额:
$ 4.95万 - 项目类别:
Deciphering the role of osteopontin in the aging eye and age-related macular degeneration
破译骨桥蛋白在眼睛老化和年龄相关性黄斑变性中的作用
- 批准号:
10679287 - 财政年份:2023
- 资助金额:
$ 4.95万 - 项目类别:
Elucidation of the protein kinase NLK-mediated aging mechanisms and treatment of age-related diseases
阐明蛋白激酶NLK介导的衰老机制及年龄相关疾病的治疗
- 批准号:
23K06378 - 财政年份:2023
- 资助金额:
$ 4.95万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Underlying mechanisms of age-related changes in ingestive behaviors: From the perspective of the aging brain and deterioration of the gustatory system.
与年龄相关的摄入行为变化的潜在机制:从大脑老化和味觉系统退化的角度来看。
- 批准号:
23K10845 - 财政年份:2023
- 资助金额:
$ 4.95万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Targeting Age-Activated Proinflammatory Chemokine Signaling by CCL2/11 to Enhance Skeletal Muscle Regeneration in Aging
通过 CCL2/11 靶向年龄激活的促炎趋化因子信号传导以增强衰老过程中的骨骼肌再生
- 批准号:
478877 - 财政年份:2023
- 资助金额:
$ 4.95万 - 项目类别:
Operating Grants