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In Vivo Discovery of Psychotropic Drugs by High-Throughput Behavioral Phenotyping

In Vivo Discovery of Psychotropic Drugs by High-Throughput Behavioral Phenotyping
通过高通量行为表型分析体内发现精神药物
批准号:
8259222
负责人:
RANDALL T PETERSON
金额:
$35.05万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-07-02 至 2013-04-30

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中文摘要
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英文摘要
In vivo discovery of psychotropic drugs by high-throughput behavioral phenotyping the challenge despite their ubiquity and impact, diseases of the central nervous system (CNS) remain among the most poorly treated medical conditions. New CNS drugs are needed, but the complexity of the nervous system has largely made CNS drug discovery refractory to reductionist and in vitro approaches. For this reason, most existing CNS drugs were discovered by serendipitous observation of behavioral effects in living animals, not by rational design or in vitro screening. Discovering new CNS drugs is limited by the difficulty of modeling complex brain function in vitro and the impracticality of screening for new drugs in vivo with existing mammalian behavioral assays. Our approach we propose to use high-throughput behavioral assays as a means of screening for novel neuroactive drugs. We are developing fully-automated systems capable of tracking and quantifying zebrafish behaviors in high- throughput, 96-well format. Using one of these assays, we have tested 700 psychotropic drugs from several functional classes and identified strong correlations between specific functional classes and the zebrafish behavioral profiles they induce. We now propose to expand the panel of automated behavioral assays and conduct screens of vast small molecule libraries to identify novel compounds with in vivo neurological activity. The potential impact the automated panel of zebrafish assays we are developing is the first high-throughput screen capable of assessing behavioral effects of small molecules in a vertebrate. Because the zebrafish behaviors integrate inputs from several major neurotransmitter systems, the assays can be used to identify compounds that act on the CNS through diverse mechanisms. Successful completion of this project will create a robust and flexible system for discovering neuroactive compounds. It will also lead directly to discovery of novel compounds that alter CNS function through diverse mechanisms of action. These compounds will be powerful tools for studying the nervous system and in some cases may be developed further for treating nervous system disorders. Nervous system disorders like schizophrenia and Alzheimer's disease are widespread and frequently devastating, but they remain poorly treated because conventional drug discovery methods are poorly equipped to deal with the complexity of the brain. This project proposes a bold new approach to nervous system drug discovery based on robotic testing of thousands of potential new drugs for their ability to alter brain function in microscopic zebrafish.
期刊论文(1)
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会议论文
DOI: 10.1016/b978-0-12-381320-6.00022-9
发表时间: 2011
期刊: METHODS IN CELL BIOLOGY
影响因子: --
作者: [Kokel, David, Peterson, Randall T.]
通讯作者: Peterson, Randall T.
Project 2: Advancing glyoxylate as a chemical countermeasure
  • 批准号:
    9981043
  • 项目类别:
  • 资助金额:
    $37.29万
  • 财政年份:
    2019
  • 负责人:
    RANDALL T PETERSON
  • 依托单位:
Training & Education Core
  • 批准号:
    9981038
  • 项目类别:
  • 资助金额:
    $13.91万
  • 财政年份:
    2019
  • 负责人:
    RANDALL T PETERSON
  • 依托单位:
Project 2: Advancing glyoxylate as a chemical countermeasure
  • 批准号:
    10426370
  • 项目类别:
  • 资助金额:
    $50.69万
  • 财政年份:
    2019
  • 负责人:
    RANDALL T PETERSON
  • 依托单位:
ADVANCING GENE-EDITING NUCLEASES FOR DIVERSE ZEBRAFISH APPLICATIONS
  • 批准号:
    10018919
  • 项目类别:
  • 资助金额:
    $47.04万
  • 财政年份:
    2019
  • 负责人:
    RANDALL T PETERSON
  • 依托单位:
国内基金
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新型F-18标记香豆素衍生物PET探针的研制及靶向Alzheimer's Disease 斑块显像研究
  • 批准号:
    81000622
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.0万元
  • 批准年份:
    2010
  • 负责人:
    梁胜
  • 依托单位:
阿尔茨海默病(Alzheimer's disease,AD)动物模型构建的分子机理研究
  • 批准号:
    31060293
  • 项目类别:
    地区科学基金项目
  • 资助金额:
    26.0万元
  • 批准年份:
    2010
  • 负责人:
    郭亚芬
  • 依托单位:
跨膜转运蛋白21(TMP21)对引起阿尔茨海默病(Alzheimer'S Disease)的γ分泌酶的作用研究