Improving multi-step planning in aging by overcoming deficits in memory encoding

通过克服记忆编码的缺陷来改善衰老的多步骤计划

基本信息

项目摘要

Project Summary/Abstract The objective of this R21 proposal is to investigate the behavioral and neural signatures of age-related decline in memory function in service of multi-step planning. We anticipate that the results obtained here will serve as preliminary findings in support of a research program using neuroimaging to evaluate how these circuits are altered in diseases of aging, such as Alzheimer's Disease and Mild Cognitive Impairment (MCI). Previous research into decision-making in aging has focused primarily on tasks that involve repeated reinforcement of specific actions or stimuli (e.g. sequential reinforcement learning tasks), or on comparisons between items whose values are directly instructed (e.g. gambles). A separate form of decisions, arguably more germane to everyday experience, are those in which choices depend on planning: searching through disparate events from our past experience, and reassembling them to achieve new goals introduced in the moment (e.g. seeking an ice cream store you may have passed by but never entered). These types of decisions, in addition to being relatively under-studied in older adults, are also distinct in that they depend on long-term, episodic memory. Episodic memory is known to decline in age. A specific aspect of episodic memory that is known to decline with age is the computation called pattern separation: the ability to create divergent neural patterns that reflect inputs with similar or overlapping sensory features (e.g. two flavors of ice cream). Pattern separation allows us to rapidly retrieve and re-use information even in the face of interference. We can measure pattern separation in behavior using the Mnemonic Similarity Task (MST), a short, widely used assay that predicts cognitive and neural deficits across the lifespan. While we know that pattern separation and planning both decline with age, and we know that both functions are supported by the same neural structures in healthy adults, we do not know if they co-exist in the same neural circuits, nor do we know if a decline in pattern separation yields a decline in planning ability. Here, we aim to fill this gap in knowledge, examining (Aim 1) the ability of older adults to construct multi-step plans, and how it corresponds to pattern separation; (Aim 2) to further ask whether taking account of an individual’s decline in pattern separation can allow us to structure their experiences in a way that improves their ability to later construct plans on the basis of those experiences; (Aim 3) whether neural circuits for pattern separation and planning overlap, and how they interact in normal cognitive aging. In sum, the proposed research will determine whether we can improve individual decision-making by taking account of individual differences in memory function; the findings will inform research into early detection and treatment of a wide range of diseases of aging.
项目总结/摘要 这项R21提案的目的是调查与年龄相关的衰退的行为和神经特征 在记忆功能服务的多步规划。我们预计,这里获得的结果将作为 支持一项研究计划的初步发现,该计划使用神经成像来评估这些回路是如何 在老年性疾病中,如阿尔茨海默病和轻度认知障碍(MCI)中,这些蛋白质会发生改变。 以前对老龄化决策的研究主要集中在涉及重复的任务上。 特定动作或刺激的强化(例如顺序强化学习任务),或比较 在直接指示其值的项目之间(例如赌博)。一种独立的决策形式, 与日常经验更密切相关的是那些选择取决于计划的选择: 从我们过去的经验不同的事件,并重新组装它们,以实现新的目标, 例如,寻找一家你可能经过但从未进入的冰淇淋店。 这些类型的决定,除了在老年人中相对研究不足之外,在老年人中也是不同的。 他们依赖于长期的情景记忆众所周知,情景记忆会随着年龄的增长而下降。特定 已知情景记忆的一个方面是随着年龄的增长而下降的称为模式分离的计算: 创造不同神经模式的能力,这些模式反映具有相似或重叠感觉特征的输入(例如, 两种口味的冰淇淋)。模式分离使我们能够快速检索和重用信息, 面对干扰。我们可以使用助记符相似性任务来衡量行为中的模式分离 (MST)这是一种短而广泛使用的检测方法,可以预测整个生命周期中的认知和神经缺陷。 虽然我们知道模式分离和计划都随着年龄的增长而下降,我们知道这两者都是 功能是由相同的神经结构在健康成人的支持,我们不知道他们是否共存于 同样的神经回路,我们也不知道模式分离的下降是否会导致规划能力的下降。 在这里,我们的目标是填补这一知识空白,检查(目标1)老年人的能力, 多步骤计划,以及它如何对应于模式分离;(目的2)进一步询问是否考虑到 一个人在模式分离方面的下降可以让我们以一种改进的方式来构建他们的经历, 他们在这些经验的基础上构建计划的能力;(目标3)是否神经回路 模式分离和规划重叠,以及它们在正常认知老化中如何相互作用。总而言之,拟议的 研究将确定我们是否可以通过考虑个人因素来改善个人决策 记忆功能的差异;研究结果将为早期发现和治疗广泛的 一系列的衰老疾病。

项目成果

期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ 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 }}

Aaron Michael Bornstein其他文献

Aaron Michael Bornstein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('Aaron Michael Bornstein', 18)}}的其他基金

Improving multi-step planning in aging by overcoming deficits in memory encoding
通过克服记忆编码的缺陷来改善衰老的多步骤计划
  • 批准号:
    10222051
  • 财政年份:
    2021
  • 资助金额:
    $ 37.77万
  • 项目类别:
Computational mechanisms of goal-directed control
目标导向控制的计算机制
  • 批准号:
    8324841
  • 财政年份:
    2011
  • 资助金额:
    $ 37.77万
  • 项目类别:
Computational mechanisms of goal-directed control
目标导向控制的计算机制
  • 批准号:
    8205292
  • 财政年份:
    2011
  • 资助金额:
    $ 37.77万
  • 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
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:
    $ 37.77万
  • 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:
    $ 37.77万
  • 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:
    $ 37.77万
  • 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:
    $ 37.77万
  • 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:
    $ 37.77万
  • 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:
    $ 37.77万
  • 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:
    $ 37.77万
  • 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:
    $ 37.77万
  • 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:
    $ 37.77万
  • 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:
    $ 37.77万
  • 项目类别:
    Operating Grants
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了