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DESCRIPTION (provided by applicant): There is substantial evidence that changes in memory function occur during healthy aging. Recent findings with aged rats suggest that aging is associated with impairment in pattern separation or the process of creating different representations from similar inputs. Additional evidence also suggests that this impairment may be linked to hyperactivity in CA3 hippocampal neurons. Functional MRI has been used extensively to study memory changes with aging, but due to the method's coarse resolution, studying activation at the level of hippocampal subfields in a manner similar to the animal studies has posed quite a challenge. However, recent technological advances have allowed us to overcome this limitation giving us the potential to assess subtle changes in function and corresponding changes in neural computations. The aim of the current proposal is to study these changes using high-resolution (1.5 mm) fMRI coupled with sophisticated alignment techniques that respect individuals' anatomy at the level of hippocampal subfields, and tasks designed to test computations specific to hippocampal subfields. We propose to test young healthy and aged healthy individuals using two tasks: a continuous paired-associate learning task and a incidental encoding task, both of which manipulate demand on pattern separation in different ways. We hypothesize that as pattern separation demands increase, behavioral and neural differences between groups will be more pronounced, and that the earliest neural changes will be detected in the CA3 region. If successful, this study will provide a clear picture of the exact locus and nature of the changes in memory computations with healthy aging. This will help us make the critical link between animal and human studies, enhance our understanding of aging as the primary risk factor for dementia, and pave the way to identifying pre-clinical markers and developing therapies to decelerate progression to dementia. PUBLIC HEALTH RELEVANCE: The proposed research examines detailed aspects about the neural bases of age-related memory decline (the most common cognitive complaint associated with aging). If successful, this study will provide a clear picture of the exact locus and nature of the changes in memory computations with healthy aging. This will help us make the critical link between animal and human studies, enhance our understanding of aging as the primary risk factor for dementia, and pave the way to identifying pre-clinical markers for disorders such as Mild Cognitive Impairment and Alzheimer's disease.
期刊论文(5)
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科研奖励(0)
会议论文
DOI: 10.1016/j.nlm.2012.03.010
发表时间: 2012-05
期刊: NEUROBIOLOGY OF LEARNING AND MEMORY
影响因子: 2.7
作者: [Segal, Sabrina K., Stark, Shauna M., Kattan, David, Stark, Craig E., Yassa, Michael A.]
通讯作者: Yassa, Michael A.
Age-Specific Seasonal Influenza Vaccine Effectiveness against Different Influenza Subtypes in the Hospitalized Population in Lithuania during the 2015-2019 Influenza Seasons.
2015 - 2019年流感季节,针对立陶宛住院人口中不同流感亚型的特定年龄季节性流感疫苗有效性。
DOI: 10.3390/vaccines9050455
发表时间: 2021-05-04
期刊: Vaccines
影响因子: 7.8
作者: [Kuliese M, Mickiene A, Jancoriene L, Zablockiene B, Gefenaite G, Study Group]
通讯作者: Study Group
Core G: Biomarker Core
  • 批准号:
    10188387
  • 项目类别:
  • 资助金额:
    $38.84万
  • 财政年份:
    2020
  • 负责人:
    Craig E Stark
  • 依托单位:
Core G: Biomarker Core
  • 批准号:
    9922106
  • 项目类别:
  • 资助金额:
    $23.54万
  • 财政年份:
    2020
  • 负责人:
    Craig E Stark
  • 依托单位:
Core G: Biomarker Core
  • 批准号:
    10582643
  • 项目类别:
  • 资助金额:
    $37.4万
  • 财政年份:
    2020
  • 负责人:
    Craig E Stark
  • 依托单位:
Development of the mnemonic similarity task as a tool to address age and dementia-related memory decline
  • 批准号:
    10571926
  • 项目类别:
  • 资助金额:
    $38.0万
  • 财政年份:
    2020
  • 负责人:
    Craig E Stark
  • 依托单位:
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: