CONSTITUTIVELY ACTIVE DOPAMINE D1 AND D2 RECEPTORS

组成型活性多巴胺 D1 和 D2 受体

基本信息

  • 批准号:
    2891049
  • 负责人:
  • 金额:
    $ 10.04万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1998
  • 资助国家:
    美国
  • 起止时间:
    1998-07-01 至 2003-06-30
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (Adapted from applicant's abstract): The long-term objective of this project is to further our understanding of the physiological role of dopamine D1 and D2 receptors in normal CNS function and in the functional pathologies associated with schizophrenia and other mental health disorders. Evidence put forth by a number of investigators suggests that the overactivation of dopaminergic synaptic transmission may be important in the pathophysiology of schizophrenia. The precise relation of dopamine overactivation to schizophrenia, however, remaines vague. The present series of studies seeks to bridge this gap by investigating the consequences of overactivated dopamine systems on brain development and function by genetic manipulation of dopamine receptors, and by identifying the consequences of expression of mutant dopamine receptors in transgenic animals. In brief, these studies seek (a) to create constitutively active mutants of dopamine D1 and D2 receptors and to identify their pharmacological and biochemical characteristics, (b) to introduce selected constitutively active D1 and D2 receptor mutants into transgenic mice, (c) to characterize developmental abnormalities in animals with overactivated dopamine systems, and (d) to identify behavioral abnormalities in mice with constitutively active dopamine receptors. The studies will enhance our understanding of D1 and D2 receptors at the molecular level, lead to a better understanding of the action mechanisms for dopamine receptors, and may lead to the development of improved pharmacotherapies for dopamine system malfunctions. These studies will also lead to a better understanding of the developmental and functional consequences of dopamine overactivation and should provide us with some fundamental information pertaining to the relation of dopamine neurotransmission malfunctions with the development of the behavioral malfunctions underlying complex mental health disorders.
描述(改编自申请人摘要):的长期目标

项目成果

期刊论文数量(0)
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科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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QUN-YONG ZHOU其他文献

QUN-YONG ZHOU的其他文献

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{{ truncateString('QUN-YONG ZHOU', 18)}}的其他基金

Regulation of glucose homeostasis by prokineticin 2 signaling
通过前动力蛋白 2 信号传导调节葡萄糖稳态
  • 批准号:
    8095574
  • 财政年份:
    2011
  • 资助金额:
    $ 10.04万
  • 项目类别:
Regulation of glucose homeostasis by prokineticin 2 signaling
通过前动力蛋白 2 信号传导调节葡萄糖稳态
  • 批准号:
    8313920
  • 财政年份:
    2011
  • 资助金额:
    $ 10.04万
  • 项目类别:
Prokineticin 2 and Suprachiasmatic Circadian Output
前动力蛋白 2 和视交叉上昼夜节律输出
  • 批准号:
    7093485
  • 财政年份:
    2004
  • 资助金额:
    $ 10.04万
  • 项目类别:
Prokineticin 2 and Suprachiasmatic Circadian Output
前动力蛋白 2 和视交叉上昼夜节律输出
  • 批准号:
    6952007
  • 财政年份:
    2004
  • 资助金额:
    $ 10.04万
  • 项目类别:
Prokineticin 2 and Suprachiasmatic Circadian Output
前动力蛋白 2 和视交叉上昼夜节律输出
  • 批准号:
    7491461
  • 财政年份:
    2004
  • 资助金额:
    $ 10.04万
  • 项目类别:
Prokineticin 2 and Suprachiasmatic Circadian Output
前动力蛋白 2 和视交叉上昼夜节律输出
  • 批准号:
    6823853
  • 财政年份:
    2004
  • 资助金额:
    $ 10.04万
  • 项目类别:
Prokineticin 2 and Suprachiasmatic Circadian Output
前动力蛋白 2 和视交叉上昼夜节律输出
  • 批准号:
    7267757
  • 财政年份:
    2004
  • 资助金额:
    $ 10.04万
  • 项目类别:
PILOT STUDY--TRANSGENIC APPROACH TO PREDILECTION OF NICOTINE ABUSE
试点研究——通过转基因方法降低尼古丁滥用倾向
  • 批准号:
    6660950
  • 财政年份:
    2002
  • 资助金额:
    $ 10.04万
  • 项目类别:
PILOT STUDY--TRANSGENIC APPROACH TO PREDILECTION OF NICOTINE ABUSE
试点研究——通过转基因方法降低尼古丁滥用倾向
  • 批准号:
    6495110
  • 财政年份:
    2001
  • 资助金额:
    $ 10.04万
  • 项目类别:
PILOT STUDY--TRANSGENIC APPROACH TO PREDILECTION OF NICOTINE ABUSE
试点研究——通过转基因方法降低尼古丁滥用倾向
  • 批准号:
    6349046
  • 财政年份:
    2000
  • 资助金额:
    $ 10.04万
  • 项目类别:

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