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Functional dissection of the Tac2-Nk3R pathway to prevent fear consolidation

Functional dissection of the Tac2-Nk3R pathway to prevent fear consolidation
Tac2-Nk3R 通路的功能解剖以防止恐惧巩固
批准号:
8689178
负责人:
KERRY J. RESSLER
金额:
$22.31万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-07-01 至 2015-05-31

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DESCRIPTION (provided by applicant): In our preclinical studies, we have found that the Tac2 pathway might be an attractive candidate to prevent the development of PTSD after exposure to a traumatic event. The Tac2 gene in rodents (Tac3 in humans) encodes the neurokinin B (NkB) neuropeptide which binds to the neurokinin 3 receptor (Nk3), a G-protein-coupled receptor. NkB and Nk3 are tachykinins, a family of neuropeptides widely distributed in the brain that act as neurotransmitters and neuromodulators having a variety of biological functions including modulation of emotion and learning. Previously, other tachykinin pathways, such as neurokinin 1 receptor (NK1) and substance P, have been described to be involved in fear processes. However, we provide the first evidence that Tac2, NkB and Nk3, all highly expressed in the central amygdala (CeA, a key substructure for the formation of fear memories) are involved in emotional learning processes. Specifically, using RNA microarray, qPCR and in situ hybridization approaches, we found that the Tac2 gene is dynamically regulated after cued-fear conditioning in the CeA. Moreover, a single systemic and intra-CeA dose of a Nk3 antagonist impaired cued-fear consolidation of memory. Thus, this Exploratory/Developmental R21 proposal is intended to gain a better understanding of the Tac2 pathway by overexpressing and silencing the Tac2 gene to further our understanding of its role in fear conditioning. Moreover, we aim to study the specific role of the Tac2 expressing cells within the CeA via optogenetic excitation and inhibition of Tac2-expressing cells during fear learning. Together these studies will provide a new understanding of the role of the Tac2/Nk3 pathway in the consolidation process underlying fear learning. These findings will energize and support a new research program aimed at translating the modulation of the Tac2/Nk3 pathway to provide novel approaches to intervention following fear and trauma exposure for the prevention of the PTSD.
期刊论文(1)
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会议论文
DOI: 10.1016/j.pnpbp.2015.02.007
发表时间: 2015-10-01
期刊: PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
影响因子: 5.6
作者: [Andero, Rauel]
通讯作者: Andero, Rauel
Neural circuit mechanisms of stress-induced alcohol seeking behavior
  • 批准号:
    9918818
  • 项目类别:
  • 资助金额:
    $19.48万
  • 财政年份:
    2019
  • 负责人:
    KERRY J. RESSLER
  • 依托单位:
Cell specific CRF-PACAP effects in mice (Ressler)
  • 批准号:
    10356103
  • 项目类别:
  • 资助金额:
    $48.86万
  • 财政年份:
    2019
  • 负责人:
    KERRY J. RESSLER
  • 依托单位:
Cell specific CRF-PACAP effects in mice (Ressler)
  • 批准号:
    10579995
  • 项目类别:
  • 资助金额:
    $48.86万
  • 财政年份:
    2019
  • 负责人:
    KERRY J. RESSLER
  • 依托单位:
Cell specific CRF-PACAP effects in mice (Ressler)
  • 批准号:
    10116477
  • 项目类别:
  • 资助金额:
    $48.86万
  • 财政年份:
    2019
  • 负责人:
    KERRY J. RESSLER
  • 依托单位:
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