Behavioral and Epigenetic Mechanisms in Extinction of Cocaine-Induced Memories

可卡因诱发记忆消退的行为和表观遗传机制

• 批准号: 7840553
• 负责人: K Matthew Lattal
• 金额: $ 48.02万
• 依托单位: OREGON HEALTH & SCIENCE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-09-15 至 2013-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7840553
• 关键词: Abbreviations; Affect; Animal Model; Applications Grants; Behavior; Behavior Therapy; Behavioral; Binding; Brain; Brain region; CREB-binding protein; CREB1 gene; Chromatin; Chromatin Structure; Chronic; Cocaine; Cocaine Dependence; Conditioned Stimulus; Cues; Cyclic AMP-Responsive DNA-Binding Protein; DNA Packaging; Data; Dependovirus; Development; Drug Addiction; Drug Exposure; Drug abuse; Drug usage; Effectiveness; Enzymes; Epigenetic Process; Essential Drugs; Ethanol; Exposure to; Extinction (Psychology); FDA approved; Fright; Gene Expression; Gene Expression Regulation; Gene Mutation; Genetic; Genetic Transcription; Goals; Hippocampus (Brain); Histone Acetylation; Histone Deacetylase; Histone Deacetylase Inhibitor; Histones; Intervention; Learning; Memory; Methods; Modification; Molecular; Molecular Target; Mus; Mutant Strains Mice; Neurobiology; Pathway interactions; Pattern; Pharmaceutical Preparations; Pharmacological Treatment; Point Mutation; Procedures; Process; Public Health; Regulation; Relapse; Research; Role; Sodium Butyrate; Synaptic plasticity; System; Therapeutic Agents; Time; Transcriptional Regulation; Trichostatin A; United States; addiction; base; chromatin modification; chromatin remodeling; cocaine use; cofactor; conditioned fear; design; drug craving; drug seeking behavior; histone acetyltransferase; histone modification; human CREBBP protein; long term memory; memory process; mouse model; novel strategies; preference; protein complex; public health relevance; receptor function; recombinase; research study; therapy design; transcription factor

DESCRIPTION (provided by applicant): A common finding from studies of drug abuse is that exposure to the context in which drug use occurs can trigger relapse, resulting in an increase in drug-seeking behavior and subsequent drug use. A major goal of interventions designed to eliminate drug seeking therefore must be to eliminate the ability of contextual cues to elicit memories that result in relapse. Behavioral and neurobiological approaches to memory have identified extinction, in which the relation between the context and the drug is severed, as a way to eliminate conditioned behavior. A major challenge for extinction-based therapies, however, is that extinguished behavior often returns with time or after re-exposure to the drug. Thus, extinction-based behavioral interventions must focus on ways to enhance the development of extinction, as well as methods to make the extinction memory long- lasting, causing persistent suppression of the original context-drug association. At a molecular level, studies of memory and extinction have demonstrated the necessity of gene transcription for long-term memory storage. Our research has found that regulation of gene transcription necessary for long-term memory formation involves the concerted action of multiple transcription factors and cofactors that interact with chromatin, a protein complex that packages DNA. Chromatin modification is a main mechanism of epigenetic gene regulation, which is emerging as a major molecular pathway involved in the transcriptional regulation of gene expression required for synaptic plasticity and memory storage. Epigenetic gene regulation has been shown to underlie persistent long-term changes at the cellular level as well as the behavioral level. Importantly, in animal models of addiction, chronic drug exposure induces stable chromatin modification resulting in maintained gene expression, which is thought to drive persistent changes in behavior. Considering the substantial overlap in the circuitry involved in drug addiction and learning and memory pathways, the focus of this grant application is to modulate learning and memory pathways in order to extinguish context-drug associated memories. We will use a combined behavioral, pharmacological, and genetic strategy to examine ways to enhance the development of extinction of cocaine-induced conditioned place preferences to cause persistent suppression of the original context-drug association. In Specific Aim 1, we will determine the best temporal pattern of context presentations to extinguish context-cocaine associations using the conditioned place preference (CPP) procedure. In Specific Aim 2, we will examine the behavioral and molecular consequences of administration of systemic or intra-hippocampal drugs that relax chromatin structure, thereby enhancing gene transcription during extinction of cocaine-induced CPP. In Specific Aim 3, we will examine the effects of inhibiting a chromatin modifying enzyme called CREB-binding protein (CBP), which relaxes chromatin structure, through genetic mutations and focal deletions of CBP, thereby inhibiting transcription during extinction of cocaine-induced CPP. This novel approach promises to elucidate behavioral and epigenetic mechanisms of extinction and will allow us to identify further molecular targets and brain systems for pharmacological interventions. PUBLIC HEALTH RELEVANCE: Cocaine addiction is a major public health problem in the United States. In this project, we examine behavioral and pharmacological interventions in a mouse model of cocaine seeking that may help reverse cocaine seeking and reduce relapse.

描述(申请人提供)：药物滥用研究的一个常见发现是，暴露在药物使用发生的环境中会引发复发，导致寻求药物行为和随后的药物使用增加。因此，旨在消除毒品寻觅的干预措施的一个主要目标必须是消除背景线索引发导致复发的记忆的能力。行为和神经生物学的记忆方法已经确定了消亡，即背景和药物之间的关系被切断，作为消除条件性行为的一种方式。然而，基于灭绝的疗法的一个主要挑战是，消失的行为往往会随着时间的推移或在再次接触药物后恢复。因此，基于灭绝的行为干预必须着眼于如何促进灭绝的发展，以及如何使灭绝记忆持久，导致对原有语境-药物联系的持续抑制。在分子水平上，对记忆和灭绝的研究已经证明了基因转录对于长期记忆存储的必要性。我们的研究发现，长期记忆形成所需的基因转录调控涉及多个转录因子和辅助因子的协同作用，这些转录因子和辅因子与染色质相互作用，染色质是包装DNA的蛋白质复合体。染色质修饰是表观遗传基因调控的主要机制，是突触可塑性和记忆存储所需基因表达转录调控的主要分子途径。表观遗传基因调控已被证明是细胞水平和行为水平持久长期变化的基础。重要的是，在成瘾的动物模型中，慢性药物暴露诱导了稳定的染色质修饰，从而维持了基因表达，这被认为是推动行为持续变化的原因。考虑到参与药物成瘾和学习记忆通路的电路有很大的重叠，这项拨款申请的重点是调节学习和记忆通路，以消除与药物相关的背景记忆。我们将使用行为学、药理学和遗传学相结合的策略来研究如何促进可卡因诱导的条件性位置偏爱的消亡发展，以导致对原始上下文-药物联系的持续抑制。在具体目标1中，我们将使用条件化位置偏好(CPP)程序来确定消除语境-可卡因关联的语境呈现的最佳时间模式。在特定的目标2中，我们将研究全身或海马内给药的行为和分子后果，这些药物松弛染色质结构，从而在可卡因诱导的CPP消退期间增强基因转录。在具体目标3中，我们将研究抑制染色质修饰酶CREB结合蛋白(CBP)的效果，该酶通过CBP的遗传突变和局部缺失来松弛染色质结构，从而在可卡因诱导的CPP消退期间抑制转录。这一新的方法有望阐明灭绝的行为和表观遗传机制，并将使我们能够识别更多的分子靶点和大脑系统进行药物干预。 与公共健康相关：可卡因成瘾是美国的一个主要公共健康问题。在这个项目中，我们检查了可卡因寻找的小鼠模型中的行为和药物干预，这可能有助于逆转可卡因寻找和减少复发。