A PHARMACOLOGICAL ANALYSIS OF THC IN HUMANS (01)

THC 在人体中的药理学分析 (01)

• 批准号: 7607330
• 负责人: Joshua Anthony Lile
• 金额: $ 12.09万
• 依托单位: UNIVERSITY OF KENTUCKY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-04-01 至 2008-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7607330
• 关键词: Agonist; Behavior; Cannabis; Cognition; Computer Retrieval of Information on Scientific Projects Database; Funding; GABA Modulators; Grant; Human; Hydromorphone; Institution; Measures; Methylphenidate; Opioid; Oral; Research; Research Personnel; Resources; Source; Stimulus; System; Triazolam; United States National Institutes of Health; gamma-Aminobutyric Acid

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. To establish oral THC as a discriminative stimulus and characterize its effects on behavior and cognition. It is hypothesized that THC will function as a discriminative stimulus and produce other effects typically seen following cannabis administration. To determine if the effects of oral THC in humans can also be attributed to indirect involvement of the opioid, GABA and DA systems. It is hypothesized that the opioid agonist hydromorphone and GABA modulator triazolam will partially substitue for THC and will have similar effects to THC on most expermental measures. In contrast it is hypothesized that the indirect DA agonist methylphenidate will not share discriminative-stimulus effects with THC and will have opposite effects on most experimental measures.

这个子项目是许多研究子项目中利用 资源由NIH/NCRR资助的中心拨款提供。子项目和 调查员(PI)可能从NIH的另一个来源获得了主要资金， 并因此可以在其他清晰的条目中表示。列出的机构是 该中心不一定是调查人员的机构。 建立口服液THC作为辨别性刺激，并表征其对行为和认知的影响。假设THC将作为一种歧视性刺激发挥作用，并产生通常在服用大麻后出现的其他效果。为了确定口服THC对人类的影响是否也可以归因于阿片类药物、GABA和DA系统的间接参与。假设阿片激动剂氢吗啡酮和GABA调节剂三唑仑将部分替代THC，并在大多数实验指标上具有与THC相似的作用。相反，假设间接DA激动剂哌醋甲酯不会与THC分享辨别刺激效应，并将对大多数实验措施产生相反的影响。