Toward a General Theory of Drug Behavior Dynamics
药物行为动力学的一般理论
基本信息
- 批准号:6515322
- 负责人:
- 金额:$ 8.29万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-05-01 至 2004-04-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION: (provided by applicant)
In the proposed research, the PI will: 1) come to thoroughly understand
existing models of drug-behavior interactions in behavioral pharmacology. This
will be done by (a) deriving them from more basic principles, where that is
possible; (b) cataloging their applications, boundaries, strengths and
weaknesses; (c) gauging the psychometricproperties of their parameters; their
dimensions, sensitivities and intercorrelations. (2) Interrelate the existing
models with Killeen's (1994) Mathematical Principles of Reinforcement (MPR)
theory. (3) Develop appropriate tests of these interpretations and execute
them. A series of experiments will determine if models developed from Killeen's
theory can differentiate drugs based on these factors. Behavioral pharmacology
is replete with hopeful attempts to quantify drug-behavior interactions.
Examples 'include Hermstem's matching law/hyperbola, behavioral economics,
behavioral momentum, delay discounting and signal detection theory. These and
other techniques, procedures, theories and models are useful in describing
phenomena at a local level. When they are viewed globally, however, it is
unclear whether and how they are related to one another, or to the data just
outside their domain. There is a need for a general theory of behavior that
both incorporates the established correspondences between empirical
observations and current theories, and provides a framework for the development
of new models, of both local and global utility. Whereas existing models
potentially could embody these characteristics, success is not guaranteed;
meanwhile there exists one theory that has yet to be exploited to these ends.
Killeen (1994) developed a quantitative model of behavior that was based upon
three mechanisms; response constraint (ability), arousal (motivation) and
coupling (short-term memory). Responses are energized by incentives, directed
by coupling (more recent responses receive more of the weight of reinforcement
than earlier responses), and bounded by temporal and physical constraints.
These three mechanisms can be used to generate predictions about behavior under
the influence of drugs. I propose to 1) derive several existing models from the
theory; 2) generate new models based upon the theory; 3) test these
interpretations and extrapolations with appropriate experiments. This process
should help me perfect my education as a behavioral pharmacologist, deploy
those skills to further research on problems of substance abuse and participate
in the development of a comprehensive framework for the scientific modeling of
the control of behavior by drugs.
描述:(由申请人提供)
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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MARK P REILLY其他文献
MARK P REILLY的其他文献
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{{ truncateString('MARK P REILLY', 18)}}的其他基金
Toward a General Theory of Drug Behavior Dynamics
药物行为动力学的一般理论
- 批准号:
6634136 - 财政年份:2001
- 资助金额:
$ 8.29万 - 项目类别:
Toward a General Theory of Drug Behavior Dynamics
药物行为动力学的一般理论
- 批准号:
6333243 - 财政年份:2001
- 资助金额:
$ 8.29万 - 项目类别:
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