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Molecular and cellular mechanisms of novel targets in alcohol reward

Molecular and cellular mechanisms of novel targets in alcohol reward
酒精奖励新靶点的分子和细胞机制
批准号:
8201635
负责人:
Igor Ponomarev
金额:
$14.51万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-05-04 至 2017-04-30

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英文摘要
OVERVIEW Persistent changes in gene expression may mediate many effects of alcohol including reward learning, tolerance and dependence, suggesting that agents effective in changing alcohol-induced gene expression could be considered as therapeutic agents. Drugs targeting gene expression through inhibition of enzymes that regulate chromatin structure (epigenetic drugs) have been widely used in cancer research and recently emerged as potential therapeutics for neurodegenerative disorders and drug addiction. The main goals of this project are: 1) to identify epigenetic drugs that affect alcohol reward through testing their effects on alcohol consumption and conditioned place preference (CPP) and 2) to investigate the effects of selected epigenetic drugs on gene expression and cellular physiology in the reward pathway including the ventral tegmental area (VTA) and the nucleus accumbens (NA). The overall hypothesis is that some epigenetic drugs will reduce the rewarding properties of alcohol through changes in gene expression and cellular physiology in the reward pathway. Integration of electrophysiological and gene expression data will elucidate the drug's mechanisms of action and identify novel targets for drug development. This research will provide initial mechanistic evidence for the therapeutic potential of epigenetic drugs in treating alcohol addiction.
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The neuroimmune model of excessive alcohol consumption: Transition to Alcohol Use Disorder.
The neuroimmune model of excessive alcohol consumption: Transition to Alcohol Use Disorder.
The neuroimmune model of excessive alcohol consumption: Transition to Alcohol Use Disorder.
The neuroimmune model of excessive alcohol consumption: Transition to Alcohol Use Disorder.
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