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ASSESSMENT OF POTENTIAL COCAINE TREATMENT MEDICATIONS

ASSESSMENT OF POTENTIAL COCAINE TREATMENT MEDICATIONS
潜在可卡因治疗药物的评估
批准号:
6078704
负责人:
MICHAEL J. FORSTER
金额:
$12.0万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-09-30 至 2001-09-29

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中文摘要
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英文摘要
This represents a competitive renewal of NIDA contract N01DA29305, entitled "Assessment of Potential Cocaine Treatment Medications in Rodents". The objectives of this research and development contract is to determine the effects of compounds in the rodent locomotor activity and drug discrimination procedures as a means of evaluating their potential efficacy as cocaine treatment medications. These tests have been selected by NIDA Medication Development Division's (MDD) Cocaine Treatment Discovery Program (CTDP) because they are believed to represent model systems that may be predictive of clinical efficacy of pharmacotherapies for cocaine dependence. The data generated by this contract will be utilized by the NIDA/MDD/CTDP in the selection of compounds for additional preclinical evaluation and subsequent development as pharmacotherapies for cocaine dependence. Briefly, the Contractor will be screening compounds in the mouse locomotor activity and rat drug discrimination test. We respect to the locomotor activity procedure, the effect of the compound, administered alone and in combination with cocaine, on locomotor activity in mice will be assessed. Depending on results obtained from the locomotor activity test, the compound will either be evaluated for the ability to antagonize the discriminative (subjective) effects of cocaine or to substitute for the discriminative (subjective) effects of cocaine. The anticipated end results of this contract will be written reports detailing study findings.
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Dietary targeting of dihydrolipoamide dehydrogenase for stroke tolerance
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Dietary targeting of dihydrolipoamide dehydrogenase for stroke tolerance
国内基金
海外基金
抗可卡因(Cocaine)抗体酶的研制及实验研究
  • 批准号:
    39570633
  • 项目类别:
    面上项目
  • 资助金额:
    8.5万元
  • 批准年份:
    1995
  • 负责人:
    段燕文
  • 依托单位: