Laboratory Models of Cocaine Self-Administration

可卡因自我给药的实验室模型

• 批准号: 7124685
• 负责人: Thomas Frederick Newton
• 金额: $ 37.72万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-09-20 至 2009-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7124685
• 关键词: behavior test; behavioral /social science research tag; behavioral genetics; blood chemistry; breath tests; clinical trials; cocaine; disulfiram; drug abuse chemotherapy; drug abuse prevention; drug screening /evaluation; genotype; human genetic material tag; human subject; human therapy evaluation; interview; outcomes research; questionnaires; self medication; statistics /biometry; substance abuse related behavior; urinalysis

DESCRIPTION (provided by applicant): The problem of cocaine dependence remains a major medical, social, and legal concern, with 2.3 million Americans estimated to be current users of cocaine. The outcome from medications development efforts has generally been discouraging, excepting for results recently obtained for disulfiram. A series of clinical trials have shown that disulfiram treatment was associated with reduced cocaine use, independent of co-morbid drug or alcohol use. The validation of a human laboratory model against outcomes observed in clinical trials would be a major step forward in developing even more effective treatments for cocaine dependence. This is a crucial undertaking, since there has not been good accord between animal or human laboratory model findings and results from clinical trials. Disulfiram has a variety of actions, one of which is to inhibit dopamine beta hydroxylase, the enzyme responsible for metabolizing dopamine into norepinephrine. Recently obtained data indicate that disulfiram is particularly effective in patients with a "T" allele of dopamine beta hydroxylase (DBH); the C/T genotype is associated with reduced enzyme activity compared to the C/C genotype. We therefore propose to evaluate effects of disulfiram treatment on cocaine self-administration in genetically characterized non-treatment seeking volunteers. Participants will be screened and only those with the DBH C/T genotype will be included. Effects of cocaine self-administration will be assessed using two established human laboratory models, one developed at Columbia University and the other developed at Johns Hopkins. Based on the observed effects of disulfiram treatment in clinical trials, especially effects of disulfiram in participants with the C/T genotype, we anticipate that disulfiram treatment will decrease cocaine self-administration in the laboratory.

描述（由申请人提供）：可卡因依赖问题仍然是主要的医疗，社会和法律关注，估计有230万美国人是可卡因的当前使用者。药物开发工作的结果通常令人沮丧，除了最近获得的二硫酸酯的结果。一系列临床试验表明，二硫仑治疗与可卡因的使用降低有关，而与合并药物或酒精使用无关。在临床试验中观察到的人类实验室模型的验证将是开发更有效的可卡因依赖治疗方法的重要一步。这是一项至关重要的事业，因为动物或人类实验室模型的发现与临床试验的结果之间没有良好的一致性。二硫仑具有多种作用，其中之一是抑制多巴胺β羟化酶，该酶是负责将多巴胺代谢为去甲肾上腺素的酶。最近获得的数据表明，多巴胺β羟化酶（DBH）的“ T”等位基因的患者特别有效。与C/C基因型相比，C/T基因型与酶活性降低有关。因此，我们建议评估二硫兰氏治疗对可卡因自我给药的影响在遗传表征的非治疗寻求志愿者中。将筛选参与者，并且只有具有DBH C/T基因型的参与者。可卡因自我管理的影响将使用两种已建立的人类实验室模型进行评估，一种模型是在哥伦比亚大学开发的，另一种是在约翰·霍普金斯（Johns Hopkins）开发的。基于二硫仑治疗在临床试验中观察到的影响，尤其是二硫仑在C/T基因型参与者中的影响，我们预计二硫仑治疗将降低实验室中可卡因的自我管理。