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ORAL DRUG ABUSE--DETERMINANTS AND CONSEQUENCES

ORAL DRUG ABUSE--DETERMINANTS AND CONSEQUENCES
口服药物滥用——决定因素和后果
批准号:
2872038
负责人:
JOHN L FALK
金额:
$9.45万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-02-01 至 2000-01-31

项目摘要

项目成果

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中文摘要
翻译
申请ADAMHA研究科学家奖。(1)口头、日程安排 (S-I)药物过度放纵,与慢性药物偏好相比 车辆,将被研究,特别是由 环境刺激控制(S/D)的偏好,和当前 药理因素。被考虑的药物将从可卡因扩展到 咖啡因、咪达唑仑和尼古丁。重点将放在追踪 在有条件的情况下启动和维持药物滥用的情景来源 其中药理影响最小,但在功能上意义重大 (口服路线),而环境测定(S-I和S/D控制) 最大化的行为。这是为了澄清药物滥用。 通过对网关的分析来发起,包括情景和 从药理上讲,这使得它有可能被收购。(2)药物过量 摄入可能会损害随后的行为功能。都是无条件的 行为(例如,运动活动)和精神运动表现(例如, 精细运动控制和计时行为)将在急性和 慢性口服药物自我给药及由此产生的相关情况 一种药物测量的血药浓度-时间曲线。(3)结果: 口服自我给药将与静脉给药进行比较。 强制执行。其目的是预测血清药代动力学 母体化合物及其活性的浓度-时间分布 代谢物预测并发行为-时间分布。(4)研究 特别关注药物相互作用的行为和动力学, 由于合法和非法物质的同时使用和滥用, 通常会发生。
英文摘要
Request for ADAMHA Research Scientist Award. (1) Oral, schedule-induced (S-I) drug overindulgence, and chronic drug preference compared to vehicle, will be studied, especially as determined by the history of the environmental stimulus control (S/D) of preference, and current pharmacological factors. Drugs considered will be extended from cocaine to caffeine, midazolam and nicotine. Emphasis will be on tracing the situational sources initiating and maintaining drug abuse under conditions wherein pharmacologic impact is minimized, but functionally significant (oral route), while the environmental determination (S-I and S/D control) of the behavior maximized. This endeavors to clarify drug abuse initiation by an analysis of the gateways, both situational and pharmacologic, that make its acquisition probable. (2) Excessive drug intake can compromise ensuing behavioral functions. Both unconditioned behavior (e.g., locomotor activity) and psychomotor performance (e.g., fine-motor control and timing behaviors) will be measured after acute and chronic oral drug self-administration, and the resulting profiles related to a drug's measured serum concentration-time profile. (3) Results from oral self-administration will be compared to those of parenteral drug imposition. The aim is to predict whether serum pharmacokinetic concentration-time profiles of parent compounds and their active metabolites predict the concurrent behavior-time profiles. (4) Studies pay special attention to the behavior and kinetics of drug interactions, as concurrent use and abuse of substances, both licit and illicit, commonly occurs.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
Schedule-induced polydipsic consumption of hypertonic NaCl solutions: effects of chlordiazepoxide.
时间表引起的高渗氯化钠溶液的烦渴消耗:利眠宁的影响。
DOI: 10.1016/s0031-9384(97)00461-7
发表时间: 1998
期刊: Physiology & behavior
影响因子: 2.9
作者: [Lobarinas,E, Falk,JL]
通讯作者: Falk,JL
Comparison of benzodiazepines and the non-benzodiazepine agents zolpidem and zaleplon with respect to anxiolytic action as measured by increases in hypertonic NaCl-solution drinking in rats.
通过增加大鼠高渗氯化钠溶液饮用量来测量苯二氮卓类药物与非苯二氮卓类药物唑吡坦和扎来普隆的抗焦虑作用的比较。
DOI: 10.1007/s002139900354
发表时间: 2000
期刊: Psychopharmacology
影响因子: 3.4
作者: [Lobarinas,E, Falk,JL]
通讯作者: Falk,JL
Independent interaction of alprazolam and caffeine under chronic dose regimens on differential reinforcement of low-rate (DRL 45-s) performance.
慢性剂量方案下阿普唑仑和咖啡因对低速(DRL 45-s)表现差异强化的独立相互作用。
DOI: 10.1007/s002130050450
发表时间: 1997
期刊: Psychopharmacology
影响因子: 3.4
作者: [Lau,CE, Wang,Y, Falk,JL]
通讯作者: Falk,JL
Behavioral tolerance to flurazepam.
对氟西泮的行为耐受性。
DOI: 10.1016/0091-3057(91)90249-2
发表时间: 1991
期刊: Pharmacology, biochemistry, and behavior
影响因子: --
作者: [Lau,CE, Dolan,S, Tang,M, Falk,JL]
通讯作者: Falk,JL
共 6 条
    ORAL DRUG ABUSE--DETERMINANTS AND CONSEQUENCES
    • 批准号:
      2654336
    • 项目类别:
    • 资助金额:
      $9.27万
    • 财政年份:
      1995
    • 负责人:
      JOHN L FALK
    • 依托单位:
    ORAL DRUG ABUSE--DETERMINANTS AND CONSEQUENCES
    • 批准号:
      2115982
    • 项目类别:
    • 资助金额:
      $9.5万
    • 财政年份:
      1995
    • 负责人:
      JOHN L FALK
    • 依托单位:
    ORAL DRUG ABUSE--DETERMINANTS AND CONSEQUENCES
    • 批准号:
      2115981
    • 项目类别:
    • 资助金额:
      $10.03万
    • 财政年份:
      1995
    • 负责人:
      JOHN L FALK
    • 依托单位:
    ORAL DRUG ABUSE--DETERMINANTS AND CONSEQUENCES
    • 批准号:
      2331127
    • 项目类别:
    • 资助金额:
      $9.39万
    • 财政年份:
      1995
    • 负责人:
      JOHN L FALK
    • 依托单位:
    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: