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DESCRIPTION (provided by applicant): Our ability to encode the events that occur in our world, store that information, and then retrieve it at a later time is essential for survival. Our memory serves the essential capacity to integrate past events into current adaptive behavior. Thus, understanding brain processes involved in memory formation is of critical importance from a basic scientific perspective, as it can provide mechanistic insights into a fundamental aspect of cognitive behavior. The overarching goal of this research project is to elucidate brain mechanisms of memory by using a powerful model system, the marine mollusk Aplysia, to forge direct links between neuronal plasticity expressed at the cellular and molecular levels, and specific phases of enduring memory for sensitization expressed behaviorally. To accomplish this goal, there are three Specific Aims: A BEHAVIORAL ANALYSIS will be aimed at identifying the "rules" that govern memory formation for a range of temporally discrete forms of memory for sensitization. Of special importance will be the unique roles of different patterns of training in the formation of mechanistically distinct forms of memory. A SYNAPTIC ANALYSIS will be aimed at establishing synaptic analogs of the different forms of memory revealed in the Behavioral Analysis, and determining the synaptic mechanisms that are recruited into play in forming these diverse memories. A MOLECULAR ANALYSIS will be aimed at identifying "molecular profiles" for different forms of memory by examining the molecular cascades (the genes, messages and proteins) that are involved in altering synaptic strength during memory formation. Relevance to public health: The importance of understanding brain mechanisms underlying memory can be especially appreciated in cases where memory is impaired, such as in Alzheimer's Disease, Post-Traumatic Stress Disorders, and in victims of accidents or strokes. Thus a major challenge in mental health is to achieve a basic understanding of the brain mechanisms that are engaged in normal memory formation, and how those mechanisms are impaired when memory is compromised by disease or injury. Such an understanding is essential for developing effective therapies for cognitive problems involving memory impairment.
期刊论文(21)
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科研奖励(0)
会议论文
DOI: 10.1016/j.nlm.2013.05.003
发表时间: 2013-10
期刊: NEUROBIOLOGY OF LEARNING AND MEMORY
影响因子: 2.7
作者: [Philips, Gary T., Kopec, Ashley M., Carew, Thomas J.]
通讯作者: Carew, Thomas J.
DOI: 10.1016/j.neuron.2015.04.025
发表时间: 2015-06-03
期刊: Neuron
影响因子: 16.2
作者: [Kopec AM, Philips GT, Carew TJ]
通讯作者: Carew TJ
DOI: 10.1016/j.neuron.2010.09.013
发表时间: 2010-11-04
期刊: NEURON
影响因子: 16.2
作者: [Ye, Xiaojing, Carew, Thomas J.]
通讯作者: Carew, Thomas J.
DOI: 10.1016/j.neuron.2008.10.049
发表时间: 2009-01-15
期刊: Neuron
影响因子: 16.2
作者: [Shobe JL, Zhao Y, Stough S, Ye X, Hsuan V, Martin KC, Carew TJ]
通讯作者: Carew TJ
12
    Investigating the interface of epigenetics and metabolism underlying memory formation in the adult, aging, and AD brain
    • 批准号:
      10636957
    • 项目类别:
    • 资助金额:
      $73.67万
    • 财政年份:
      2022
    • 负责人:
      Marcelo Andres Wood
    • 依托单位:
    Training Program in Substance Use and Use Disorders
    • 批准号:
      10399427
    • 项目类别:
    • 资助金额:
      $18.97万
    • 财政年份:
      2020
    • 负责人:
      Marcelo Andres Wood
    • 依托单位:
    Training Program in Substance Use and Use Disorders
    • 批准号:
      10618200
    • 项目类别:
    • 资助金额:
      $19.38万
    • 财政年份:
      2020
    • 负责人:
      Marcelo Andres Wood
    • 依托单位:
    Role of HDAC3 in repressing memory formation in the aging brain
    • 批准号:
      9267406
    • 项目类别:
    • 资助金额:
      $19.31万
    • 财政年份:
      2016
    • 负责人:
      Marcelo Andres Wood
    • 依托单位:
    海外基金