NEUROBIOLOGY OF REINFORCEMENT, CRAVING AND RELAPSE
NEUROBIOLOGY OF REINFORCEMENT, CRAVING AND RELAPSE
批准号:
6332502
负责人:
David W Self
金额:
$58.59万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-07-15 至 2000-12-31
关键词:
behavior test cAMP response element binding protein dopamine receptor drug abuse drug addiction gene expression gene targeting genetic regulation glutamate receptor laboratory mouse laboratory rat limbic system motivation neural plasticity neurobiology neurotransmitter metabolism neurotrophic factors nucleus accumbens psychological reinforcement relapse /recurrence stress transcription factor transfection transfection /expression vector
中文摘要
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英文摘要
Repeated exposure to drugs of abuse produces specific neuroadaptations in
the mesolimbic dopamine system that could alter both the primary and
secondary reinforcing properties of the drugs, and contribute to relapse
of drug-seeking behavior. In the nucleus accumbens (NAc), some of these
neuroadaptations could result from altered gene expression mediated by
drug-induced changes in the transcription factors, CREB (cAMP-Response
Element Binding protein) and deltaFosB, a Fos-related Antigen (FRA)
induced by chronic, but not acute, drug exposure. Similarly, repeated drug
exposure produce an up-regulation of GluR1, an AMPA glutamate receptor
subunit, in the ventral tegmental area (VTA), and a down-regulation of the
GluR2 subunit in the NAc. Our hypothesis is that these neuroadaptations
contribute to specific motivational changes associated with drug
addiction, for example with sensitization or tolerance to the reinforcing
properties of the drugs, or to enhance the ability of drugs, stress, and
drug-associated (conditioned) stimuli to trigger relapse of drug-seeking
behavior. The proposed studies will test the hypothesis by using animals
with genetically altered levels of these target proteins in the VTA and
NAc 1) by direct transfection with a viral vector containing the gene for
the target protein in rats; and 2) by using mutant mice that lack or over
express the gene for the target protein. Preliminary studies demonstrate
that these genetically modified animals exhibit altered responses to drugs
of abuse in other drug-related behaviors (see Behavioral Core). The
studies in Project 4 will extend these studies by testing the effects of
genetically modulating the target protein on direct behavioral measures of
the primary and secondary reinforcing properties of drugs, and relapse of
drug-seeking behavior triggered by drugs, conditioned stimuli, and stress.
Some neuroadaptations to chronic drug exposure resemble a
neurodegenerative process, and can be prevented or reversed by infusion or
neurotrophic factors into the VTA or NAc. Moreover, some of the
neuroadaptations mentioned above can be modified by these factors.
Preliminary studies have found highly potent actions of neurotrophic
factors on drug-related behaviors. Since these various neuroadaptations
are hypothesized to contribute to motivations changes associated with drug
addiction, the proposed studies will test whether treatment with
neurotrophic factors can alter direct behavioral measures of primary and
secondary drug reinforcement, and relapse of drug-seeking behavior
triggered by drugs, conditioned stimuli, and stress.
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会议论文
Role of Extinction in Circuit-Specific Modulation of Motivation and Mood in Cocaine Addiction
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批准号:10198877
-
项目类别:
-
资助金额:$36.45万
-
财政年份:2017
-
负责人:David W Self
-
依托单位:
Role of Extinction in Circuit-Specific Modulation of Motivation and Mood in Cocaine Addiction
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批准号:9551580
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项目类别:
-
资助金额:$36.45万
-
财政年份:2017
-
负责人:David W Self
-
依托单位:
Role of Extinction in Circuit-Specific Modulation of Motivation and Mood in Cocaine Addiction
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批准号:9238093
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项目类别:
-
资助金额:$36.45万
-
财政年份:2017
-
负责人:David W Self
-
依托单位:
Role of Extinction in Circuit-Specific Modulation of Motivation and Mood in Cocaine Addiction
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批准号:9974501
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项目类别:
-
资助金额:$36.45万
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财政年份:2017
-
负责人:David W Self
-
依托单位:
Role of Endogenous Opiate Systems in Cocaine Relapse after Long-Term Abstinence
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批准号:8044146
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项目类别:
-
资助金额:$34.27万
-
财政年份:2010
-
负责人:David W Self
-
依托单位:
Role of Endogenous Opiate Systems in Cocaine Relapse after Long-Term Abstinence
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批准号:8423318
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项目类别:
-
资助金额:$32.89万
-
财政年份:2010
-
负责人:David W Self
-
依托单位:
Role of Endogenous Opiate Systems in Cocaine Relapse after Long-Term Abstinence
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批准号:8605866
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项目类别:
-
资助金额:$34.27万
-
财政年份:2010
-
负责人:David W Self
-
依托单位:
Role of Endogenous Opiate Systems in Cocaine Relapse after Long-Term Abstinence
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批准号:8215776
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项目类别:
-
资助金额:$34.27万
-
财政年份:2010
-
负责人:David W Self
-
依托单位:
Behavioral Core
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批准号:7513615
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项目类别:
-
资助金额:$33.59万
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财政年份:2007
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负责人:David W Self
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依托单位:
Neuroadaptions in Drug Self-Administration and Relapse
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批准号:7513609
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项目类别:
-
资助金额:$22.34万
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财政年份:2007
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负责人:David W Self
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依托单位:
VTA Ionotropic Glutamate Receptors in Cocaine Addiction
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批准号:7169921
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项目类别:
-
资助金额:$29.58万
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财政年份:2005
-
负责人:David W Self
-
依托单位:
VTA Ionotropic Glutamate Receptors in Cocaine Addiction
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批准号:7356420
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项目类别:
-
资助金额:$28.99万
-
财政年份:2005
-
负责人:David W Self
-
依托单位:
VTA Ionotropic Glutamate Receptors in Cocaine Addiction
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批准号:7565663
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项目类别:
-
资助金额:$7.22万
-
财政年份:2005
-
负责人:David W Self
-
依托单位:
VTA Ionotropic Glutamate Receptors in Cocaine Addiction
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批准号:7022941
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项目类别:
-
资助金额:$30.47万
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财政年份:2005
-
负责人:David W Self
-
依托单位:
VTA Ionotropic Glutamate Receptors in Cocaine Addiction
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批准号:6851428
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项目类别:
-
资助金额:$31.2万
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财政年份:2005
-
负责人:David W Self
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依托单位:
VTA Ionotropic Glutamate Receptors in Cocaine Addiction
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批准号:7563955
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项目类别:
-
资助金额:$36.21万
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财政年份:2005
-
负责人:David W Self
-
依托单位:
GENE EXPRESSION AND COCAINE IN PROLONGED ABSTINENCE
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批准号:6620140
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项目类别:
-
资助金额:$14.11万
-
财政年份:2000
-
负责人:David W Self
-
依托单位:
GENE EXPRESSION AND COCAINE IN PROLONGED ABSTINENCE
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批准号:6379123
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项目类别:
-
资助金额:$14.11万
-
财政年份:2000
-
负责人:David W Self
-
依托单位:
GENE EXPRESSION AND COCAINE IN PROLONGED ABSTINENCE
-
批准号:6406283
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项目类别:
-
资助金额:$13.8万
-
财政年份:2000
-
负责人:David W Self
-
依托单位:
CORE--BEHAVIORAL
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批准号:6332504
-
项目类别:
-
资助金额:$58.59万
-
财政年份:2000
-
负责人:David W Self
-
依托单位:
海外基金