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Mapping opioid-dependence state transitions across structural, functional, and transcriptomic topologies

Mapping opioid-dependence state transitions across structural, functional, and transcriptomic topologies
绘制结构、功能和转录组拓扑中阿片类药物依赖性状态转变的图谱
批准号:
10622531
负责人:
Julie A Blendy
金额:
$49.05万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-09-30 至 2026-05-31

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中文摘要
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英文摘要
PROJECT SUMMARY Opioid addiction is a chronic, progressive disorder that fuels the current US epidemic of opioid overdose deaths. Over the years, a tremendous amount of research effort has been devoted to understanding the biological roles of opioid receptors and developing newer generations of synthetic opioids to treat pain and combat opioid addiction. However, given the advancement of contemporary and novel neuroscience technologies, we have the tools to think beyond mu-opioid receptors (MORs) to develop improved OUD therapeutics. This proposal aims to investigate the architecture and function of endogenous MOR-expressing neural circuits in the brain and to determine how these circuits maintain cellular dependence and drive brain-wide maladaptive plasticity across different stages of the OUD cycle. In four complementary aims, we will first map the shifting structural and functional connectivity of opioidergic networks using viral-genetic and tissue clearing methods to identify monosynaptic inputs to withdrawal-active MOR-expressing cells and axonal output projections, as a function of opioid exposure and abstinence. We will then integrate these input/output maps with cell-type information and gene expression changes within dependence networks using hyper-multiplexed 3D in situ hybridizations to generate the anatomic localization of hundreds of dependence-related genes, targeted to cell types and retro- labeled connections. Finally, to reveal how MOR-expressing cells within core regions are modulated during opioid exposure in real-time, we will use miniature head-mounted microscopes to image the population activity— at cellular resolution—across weeks of opioid exposure and withdrawal. Our models will provide formal summaries of activity, connectivity, and gene expression as they evolve with repetitive opioid exposure and withdrawal, and our datasets will be made publicly available as they are generated. To bridge these experimental measurements and provide a common framework for our analyses, we will adopt Network Control Theory to identify brain nodes that drive the transition between opioid dependence states to identify potential candidates that disproportionately drive each state.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
DOI: 10.7554/elife.76886
发表时间: 2022-05-23
期刊: ELIFE
影响因子: 7.7
作者: [Beier, Kevin]
通讯作者: Beier, Kevin
A Brief Overview of the Neuropharmacology of Opioid Addiction.
阿片类药物成瘾的神经药理学简要概述。
DOI: 10.31480/2330-4871/165
发表时间: 2022
期刊: Translational perioperative and pain medicine
影响因子: --
作者: [Grothusen,JohnR, Blendy,JulieA, Barr,GordonA]
通讯作者: Barr,GordonA
Low-input profiling of brain-region and cell-type specific epigenomic dynamics to understand gene-environment interactions in opioid addiction
Mapping opioid-dependence state transitions across structural, functional, and transcriptomic topologies
  • 批准号:
    10293782
  • 项目类别:
  • 资助金额:
    $51.63万
  • 财政年份:
    2021
  • 负责人:
    Julie A Blendy
  • 依托单位:
Mapping opioid-dependence state transitions across structural, functional, and transcriptomic topologies
  • 批准号:
    10493185
  • 项目类别:
  • 资助金额:
    $48.25万
  • 财政年份:
    2021
  • 负责人:
    Julie A Blendy
  • 依托单位:
Neonatal Opioid Exposure and Withdrawal: Molecular and Behavioral Consequences
  • 批准号:
    10347354
  • 项目类别:
  • 资助金额:
    $69.65万
  • 财政年份:
    2020
  • 负责人:
    Julie A Blendy
  • 依托单位:
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