Rat Models of Alcohol Dependence for Evaluating Combined Medication Effects

用于评估综合药物效应的酒精依赖大鼠模型

• 批准号: 8101962
• 负责人: Wendy Jean Lynch
• 金额: $ 29.73万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-07-15 至 2013-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8101962
• 关键词: Abstinence; Alcohol dependence; Alcoholism; Alcohols; Animal Model; Animals; Basic Science; Behavioral; Biological; Brain region; Breeding; Clinical; Clinical Research; Development; Disease; Dopamine; Ethanol; Fingers; Future; Genetic; Genetic Load; Glutamates; Goals; Health; Heavy Drinking; Human; Individual; Ion Channel; Measurement; Measures; Medial; Mediating; Microdialysis; Modeling; Neurons; Nucleus Accumbens; Ondansetron; Pattern; Pharmaceutical Preparations; Population; Prefrontal Cortex; Printing; Procedures; Process; Property; Rattus; Self Administration; Serotonin; Signal Transduction; Site; Synapses; Testing; Ventral Tegmental Area; Western Blotting; Wistar Rats; Work; alcohol effect; alcohol reinforcement; alcohol seeking behavior; base; dopaminergic neuron; effective therapy; gamma-Aminobutyric Acid; neuroadaptation; neurochemistry; neuroregulation; preference; receptor; response; topiramate

DESCRIPTION (provided by applicant): Neuromodulation of cortico-mesolimbic dopamine (CMDA) function may be more effective for the treatment of alcohol dependence than DA receptor blockade, and consistent with this hypothesis, we have shown that ondansetron a serotonin-3 antagonist that modulates CMDA primarily in the ventral tegmental area and nucleus accumbens (NAc), is efficacious treatment for a subtype of alcohol dependent humans with high biological loading for the disease. We have also demonstrated that topiramate, a GABA/glutamate (GLU) modulator that is believe to produce widespread suppression of CMDA, is an efficacious treatment for a heterogeneous group of alcohol dependent individuals. Because ondansetron and topiramate manifest their effects through different neuronal processes, both resulting in modulation of CMDA function, it is reasonable to hypothesize that their combination shall be more efficacious than either alone in the treatment of alcohol dependence. Therefore, we propose to characterize the mechanistic process by which ondansetron and topiramate, both alone and in combination, exert their behavioral and neurochemical effects using different rat self-administration models and strains. In Aim 1 and 2 we will examine the prediction that both ondansetron and topiramate alone and in combination will reduce ethanol reinforcement, and in Aim 2 and 3 we will examine the prediction that both ondansetron and topiramate alone and in combination will reduce ethanol reinstatement. The combination is expected to be associated with added or synergistic decreases in ethanol reinforcement and reinstatement as well as associated modulation in CMDA and GLU concentrations. This pharmaco-behavioral response pattern or "finger-print" will enable us to identify future promising putative medications with similar effects as well as enable us to understand which of their properties can be harnessed to develop even more potent medications. PUBLIC HEALTH RELEVANCE Our study is significant because it focuses on determining the biological basis for the effects of two potential medications, ondansetron and topiramate, for treating alcohol dependence. The overall goals of this basic science work is to helping to identify populations that may be ideally suited for treating alcohol dependence with these two medications, and to provide information that may guide the development of even more effective medications.

描述（由申请人提供）：皮质-中边缘多巴胺（CMDA）功能的神经调节可能比DA受体阻断对酒精依赖的治疗更有效，并且与这一假设相一致，我们已经证明，昂丹西酮是一种主要调节腹侧被盖区和伏隔核（NAc）的CMDA的5 -羟色胺-3拮抗剂，对具有高生物负荷的酒精依赖人群亚型有效。我们还证明了托吡酯，一种GABA/谷氨酸（GLU）调节剂，被认为可以产生广泛的CMDA抑制，是一种有效的治疗酒精依赖个体的异质组。由于昂丹司琼和托吡酯通过不同的神经元过程发挥作用，都导致CMDA功能的调节，因此我们有理由假设它们联合使用在治疗酒精依赖方面比单独使用更有效。因此，我们建议通过不同的大鼠自我给药模型和菌株来表征昂丹司琼和托吡酯单独或联合发挥其行为和神经化学作用的机制过程。在目标1和2中，我们将研究预测，昂丹司琼和托吡酯单独和联合将减少乙醇强化，在目标2和3中，我们将研究预测，昂丹司琼和托吡酯单独和联合将减少乙醇恢复。该组合预计与乙醇强化和恢复的添加或协同减少以及CMDA和GLU浓度的相关调节有关。这种药物-行为反应模式或“指纹”将使我们能够识别具有类似效果的未来有希望的假定药物，并使我们能够了解它们的哪些特性可以被利用来开发更有效的药物。我们的研究意义重大，因为它着重于确定两种治疗酒精依赖的潜在药物——昂丹司琼和托吡酯的生物学基础。这项基础科学工作的总体目标是帮助确定最适合用这两种药物治疗酒精依赖的人群，并提供可能指导开发更有效药物的信息。