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DESCRIPTION (provided by applicant): The behavioral effects of alcohol have long been considered to depend on gamma-amino-butyric acid (GABA) neurotransmission. Recently, the GABAA receptor isoform, 1424, has been proposed to mediate effects of alcohol at low-to-moderate concentrations. The current proposal will examine this possibility by testing the hypothesis that the 1424 GABAA receptor mediates aspects of the reinforcing properties of ethanol, thereby critically contributing to voluntary intake of ethanol. We will use viral-mediated RNA interference to knock down expression of the 14 and 4 GABAA receptor subunits in the nucleus accumbens, a brain region involved in processes of reward and reinforcement, to probe the contribution of the 1424 GABAA receptor to ethanol drinking behaviors by rats. Within our experimental aims we will test the contribution of this receptor to oral ethanol consumption, as well as to instrumental responding for ethanol. We will also initiate studies of the mechanism whereby ethanol in the NAc interacts with the 1424 GABAA receptor, using in vitro electrophysiogical techniques. Together, these studies will serve to define a role for two unique subunits of the GABAAR in a primary region of the brain reward circuitry, the NAc, in the reinforcing effects of ethanol. Understanding the neural mechanisms that mediate ethanol's reinforcing effects is critical for the development of treatments to assist in pharmacological therapies for alcohol abuse and alcoholism. PUBLIC HEALTH RELEVANCE The elucidation of the neurotransmitter and receptor systems that support alcohol drinking is critical for understanding how the pharmacological actions of alcohol lead to voluntary intake of alcohol, including under conditions of abuse. If the GABAA receptor studied in the experiments in this proposal is found to contribute to alcohol drinking, then future research on possible pharmaceutical approaches to reduce drinking by interacting with this receptor would be indicated.
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DOI: 10.1111/j.1369-1600.2011.00333.x
发表时间: 2012-03
期刊: Addiction biology
影响因子: 3.4
作者: [Rewal M, Donahue R, Gill TM, Nie H, Ron D, Janak PH]
通讯作者: Janak PH
Alpha4-containing GABAA receptors in the nucleus accumbens mediate moderate intake of alcohol.
伏隔核中含有 Alpha4 的 GABAA 受体介导适度的酒精摄入。
DOI: 10.1523/jneurosci.3199-08.2009
发表时间: 2009-01-14
期刊: The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子: --
作者: [Rewal M, Jurd R, Gill TM, He DY, Ron D, Janak PH]
通讯作者: Janak PH
Amygdala neural circuits in alcohol intake
  • 批准号:
    10518250
  • 项目类别:
  • 资助金额:
    $6.44万
  • 财政年份:
    2019
  • 负责人:
    Patricia H. Janak
  • 依托单位:
Amygdala neural circuits in alcohol intake
  • 批准号:
    10362742
  • 项目类别:
  • 资助金额:
    $39.49万
  • 财政年份:
    2019
  • 负责人:
    Patricia H. Janak
  • 依托单位:
Amygdala neural circuits in alcohol intake
  • 批准号:
    10795152
  • 项目类别:
  • 资助金额:
    $6.44万
  • 财政年份:
    2019
  • 负责人:
    Patricia H. Janak
  • 依托单位:
Amygdala neural circuits in alcohol intake
  • 批准号:
    10581530
  • 项目类别:
  • 资助金额:
    $39.49万
  • 财政年份:
    2019
  • 负责人:
    Patricia H. Janak
  • 依托单位:
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