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: 7578155
• 负责人: K Matthew Lattal
• 金额: $ 40.05万
• 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/7578155
• 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; Complex; Condition; 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); Fright; Gene Expression; Gene Expression Regulation; Gene Mutation; Genetic; Genetic Transcription; Goals; Hippocampus (Brain); Histone Acetylation; Histone Deacetylase; 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; Proteins; Public Health; Regulation; Relapse; Research; Role; Sodium Butyrate; Synaptic plasticity; System; Therapeutic Agents; Thinking; Time; Transcriptional Regulation; Trichostatin A; United States; United States Food and Drug Administration; addiction; base; chromatin remodeling; cofactor; conditioned fear; design; drug craving; drug seeking behavior; histone acetyltransferase; human CREBBP protein; inhibitor/antagonist; long term memory; memory process; mouse model; novel strategies; preference; 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（由申请人提供）：药物滥用研究的一个常见发现是，暴露于药物使用发生的环境可能引发复发，导致寻求药物的行为和随后的药物使用增加。因此，旨在消除药物寻求的干预措施的一个主要目标必须是消除上下文线索引发导致复吸的记忆的能力。行为学和神经生物学研究记忆的方法已经确定了消退，其中背景和药物之间的关系被切断，作为消除条件行为的一种方式。然而，基于预防的治疗的一个主要挑战是，消失的行为通常会随着时间的推移或重新暴露于药物后而恢复。因此，基于预防的行为干预必须关注促进消退发展的方法，以及使消退记忆持久的方法，从而导致对原始背景-药物关联的持续抑制。在分子水平上，记忆和灭绝的研究已经证明了基因转录对长期记忆存储的必要性。我们的研究发现，长期记忆形成所必需的基因转录调控涉及多个转录因子和辅因子的协同作用，这些转录因子和辅因子与染色质（一种包装DNA的蛋白质复合物）相互作用。染色质修饰是表观遗传基因调控的主要机制之一，是参与突触可塑性和记忆储存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续长期变化的基础。重要的是，在成瘾的动物模型中，慢性药物暴露诱导稳定的染色质修饰，从而维持基因表达，这被认为是驱动行为持续变化的原因。考虑到药物成瘾与学习和记忆途径所涉及的电路的大量重叠，这项拨款申请的重点是调节学习和记忆途径，以消除与背景药物相关的记忆。我们将使用一个结合的行为，药理学和遗传策略，以研究如何提高发展的灭绝可卡因诱导的条件性位置偏好，造成持续抑制的原始上下文药物协会。在具体目标1中，我们将确定最佳的时间模式的背景介绍，以消除上下文可卡因协会使用条件位置偏好（CPP）程序。在具体目标2中，我们将研究给予全身或海马内放松染色质结构的药物的行为和分子后果，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，我们将研究抑制称为CREB结合蛋白（CBP）的染色质修饰酶的影响，该蛋白通过CBP的基因突变和局灶性缺失来松弛染色质结构，从而抑制可卡因诱导的CPP消退期间的转录。这种新的方法有望阐明灭绝的行为和表观遗传机制，并将使我们能够确定进一步的分子靶点和药物干预的大脑系统。 公共卫生相关性：可卡因成瘾是美国的一个主要公共卫生问题。在这个项目中，我们研究了行为和药物干预在可卡因寻求的小鼠模型，可能有助于扭转可卡因寻求和减少复发。