Time-Dependent Effects of Stress on Learning: Physiological and Genetic Associations

Information

  • Research Project
  • 8851344
  • ApplicationId
    8851344
  • Core Project Number
    R15MH104836
  • Full Project Number
    1R15MH104836-01A1
  • Serial Number
    104836
  • FOA Number
    PA-13-313
  • Sub Project Id
  • Project Start Date
    5/1/2015 - 9 years ago
  • Project End Date
    4/30/2018 - 6 years ago
  • Program Officer Name
    TUMA, FARRIS K.
  • Budget Start Date
    5/1/2015 - 9 years ago
  • Budget End Date
    4/30/2018 - 6 years ago
  • Fiscal Year
    2015
  • Support Year
    01
  • Suffix
    A1
  • Award Notice Date
    2/27/2015 - 9 years ago
Organizations

Time-Dependent Effects of Stress on Learning: Physiological and Genetic Associations

? DESCRIPTION (provided by applicant): Stress-induced alterations of learning and memory have important implications for understanding the development of post-traumatic stress disorder (PTSD). Researchers have speculated that traumatic stress may promote the onset of PTSD as a result of pre-existing genetic factors and peri-traumatic physiological responses influencing learning and, thus, traumatic memory formation. Indeed, investigators have established a clear association between certain genetic polymorphisms, emotional memory and the onset of PTSD. However, systematic examination, in clinical samples, of susceptibility factors that could promote traumatic memory formation is problematic, making basic models of stress-memory interactions a necessity. It is still unclear as to what factors are most important for dictating te types of effects stress exerts on learning and memory and when the effects promote the formation of intrusive, debilitating memories. One leading theory regarding stress effects on learning is the temporal dynamics model of emotional memory processing. According to this theory, stress exerts biphasic effects on learning as a result of amygdala-induced modulation of hippocampal synaptic plasticity. Specifically, stress rapidly activates the amygdala, which enhances hippocampal plasticity and promotes the formation of powerful emotional memories; however, as stress continues, the hippocampus enters a refractory state during which hippocampal plasticity, and thus learning, is impaired. We have preliminary data supporting these predictions for declarative learning in humans; however, the mechanisms underlying these effects are still unclear, and an examination of how stressor timing influences other forms of learning that may relate better to traumatic memory formation, such as fear conditioning and extinction, has not yet been conducted. Moreover, sex differences are common in the stress-memory literature, yet little work has examined the role of sex in time-dependent effects of stress on learning. Thus, in Aim 1, we will examine how the timing of pre-learning stress interacts with individual characteristics (e.g., autonomic and endocrine stress responses, sex) to influence declarative learning and fear conditioning. Since there has been little work examining how genetic polymorphisms associated with emotional memory and stress increases one's risk for traumatic memory formation, this will be the focus of Aim 2. We will genotype participants from the studies in Aim 1 for single nucleotide polymorphisms (SNPs) that have been associated with the physiological stress response, emotional memory and/or risk for PTSD and examine whether such SNPs are associated with participants' physiological response to/recovery from stress exposure, as well as any observed stress-induced alterations of learning and memory. These studies will contribute important knowledge about when stress enhances versus impairs learning and memory and the physiological mechanisms underlying such effects. The findings may also lend insight into risk factors for traumatic memory formation and potentially facilitate the development of more targeted treatment options for PTSD in the future.

IC Name
NATIONAL INSTITUTE OF MENTAL HEALTH
  • Activity
    R15
  • Administering IC
    MH
  • Application Type
    1
  • Direct Cost Amount
    300000
  • Indirect Cost Amount
    123776
  • Total Cost
    423776
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    242
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIMH:423776\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    MESH
  • Study Section Name
    Biobehavioral Mechanisms of Emotion, Stress and Health Study Section
  • Organization Name
    OHIO NORTHERN UNIVERSITY
  • Organization Department
    PSYCHOLOGY
  • Organization DUNS
    051625564
  • Organization City
    ADA
  • Organization State
    OH
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    458106000
  • Organization District
    UNITED STATES