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中文摘要
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描述(由申请人提供):我们记住的东西很少。是什么决定了哪些记忆最终会被保留,以及依赖睡眠的记忆巩固在确保记忆保留中的作用,这些都是未知的。长期目标是了解清醒和睡眠时的离线记忆处理如何相互作用,以控制我们记住和忘记的内容。本研究的目的是确定编码后觉醒期间的记忆加工对睡眠依赖性记忆巩固的影响。核心假设是,最近形成的记忆的强度和显著性导致它们以某种方式进行修改,从而提高了它们随后依赖睡眠的巩固的可能性。(术语“清醒时的记忆修正”(MMW)指的是在训练后的清醒过程中,调节随后依赖睡眠的记忆巩固的过程。)进一步的假设是,毫米波通过在睡眠中触发记忆的再激活,并通过调节睡眠结构来增强修改后的记忆的巩固,从而促进睡眠依赖性巩固。这项研究的基本原理是,了解清醒时的离线记忆处理如何与睡眠依赖的记忆巩固相互作用,以确定我们最终记住的内容,将增加我们对记忆随时间的正常进化的理解,并为这些过程和相互作用的中断如何导致与一系列精神和神经疾病相关的记忆缺陷提供线索。三个具体目标测试了这一假设:(i)测量新形成的记忆的强度和显著性对其在清醒和睡眠中保持的影响,期望在睡眠中产生更大的影响;(ii)使用功能连接(fc) MRI和高密度(hd) EEG测量编码后休息时与记忆相关的大脑活动来量化毫米波,并将这些测量与随后的记忆保留相关联;(iii)确定特定睡眠阶段的记忆再激活在介导毫米波对记忆保持的影响中的作用。目标1和目标3将使用被证明可以操纵记忆强度和显著性,以及睡眠阶段和记忆再激活的方法。在目标1和目标3中,研究人员将使用hdEEG记录训练后安静休息期间与学习相关的大脑活动,在目标2中使用fcMRI记录学习相关的大脑活动,并用于识别训练后大脑活动模式,预测随后的睡眠依赖性记忆保留。这种方法是创新的,因为它首次尝试对清醒和睡眠期间依赖睡眠的记忆处理的调节进行综合描述。这项研究意义重大,因为它可以增加我们对编码后醒来和随后睡眠期间记忆处理的认识。获得这些知识是确定这些过程中的故障如何导致精神和神经疾病中出现的记忆功能障碍的第一步,也是开发逆转这些故障的治疗方法的第一步。
英文摘要
DESCRIPTION (provided by applicant): We remember little of what we commit to memory. What determine which memories will ultimately be retained, and the role of sleep-dependent memory consolidation in ensuring their retention, are unknown. The long-term goal is to understand how offline memory processing in wake and sleep interact to control what we remember and what we forget. The objective of the proposed research is to determine the impact of memory processing during post-encoding wake on sleep-dependent memory consolidation. The central hypothesis is that the strength and salience of recently formed memories lead to their modification in a manner that enhances the likelihood of their subsequent sleep-dependent consolidation. (The term "memory modification during wake" (MMW) is used to denote processes during post-training wake that modulate the subsequent sleep-dependent consolidation of those memories.) It is further hypothesized that MMW facilitates sleep-dependent consolidation by triggering the reactivation of memories during sleep and by modulating the structure of sleep to enhance consolidation of the modified memories. The rationale for this research is that understanding how offline memory processing during wake interacts with sleep-dependent memory consolidation to determine what we ultimately remember will increase our understanding of the normal evolution of memories over time, and provide clues into how breakdowns in these processes and interactions contribute to the memory deficits associated with a range of psychiatric and neurologic disorders. Three Specific Aims test this hypothesis: (i) Measure the impact of the strength and salience of newly formed memories on their retention across wake and sleep, expecting larger effects across sleep; (ii) Use functional connectivity (fc) MRI and high density (hd) EEG measures of memory related brain activity in post- encoding rest to quantify MMW, and correlate these measures with subsequent memory retention; and (iii) Determine the role of memory reactivation during specific sleep stages in mediating the effects of MMW on memory retention. Methods shown to manipulate memory strength and salience, as well as sleep stages and memory reactivation, will be used for Aims 1 and 3. Learning-related brain activity will be recorded during post-training quiet rest with hdEEG in Aims 1 and 3 and with fcMRI for Aim 2, and used to identify patterns of post-training brain activity that predict subsequent sleep-dependent memory retention. This approach is innovative because it represents the first attempt to produce an integrated description of the regulation of sleep-dependent memory processing across wake and sleep. This research is significant because it is can increase our knowledge of memory processing during both post-encoding wake and subsequent sleep. Gaining this knowledge is the first step toward identifying how breakdowns in these processes contribute to the memory dysfunction seen in psychiatric and neurologic disorders, and in developing treatments to reverse these breakdowns.
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会议论文
EEG Signatures of Offline Memory Reactivation and Consolidation
DREAMS, SLEEP MENTATION AND MEMORY
STATE DEPENDENT ASPECTS OF COGNITION
DREAMS, SLEEP MENTATION AND MEMORY
国内基金
海外基金
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
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
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
  • 依托单位:
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
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
    雷芬芳
  • 依托单位:
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:
    --
  • 项目类别:
    面上项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    万荣
  • 依托单位: