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Role of Novel VTA Neurons in Addiction

新型 VTA 神经元在成瘾中的作用

基本信息

批准号：
8990709
负责人：
Thomas Hnasko
金额：
$ 3.99万
依托单位：
UNIVERSITY OF CALIFORNIA, SAN DIEGO
依托单位国家：
美国
项目类别：
财政年份：
2014
资助国家：
美国
起止时间：
2014-04-01 至 2019-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8990709
关键词：
Adaptive Behaviors Addictive Behavior Amino Acid Neurotransmitters Behavior Behavior Control Behavior Disorders Behavioral Biological Assay Brain Cell Nucleus Cocaine Corpus striatum structure Data Development Discipline Disease Dopamine Drug Addiction Electrophysiology (science)Genetic Globus Pallidus Glutamates Goals Habenula Health Heterogeneity Intervention Knowledge Lateral Learning Mediating Mental disorders Methods Molecular Motivation Mus Neurobiology Neuronal Plasticity Neurons Neurosciences Nucleus Accumbens Physiological Population Process Property Psychological reinforcement Rewards Ribosomal Proteins Role Signal Transduction Slice Specific qualifier value Synapses System Testing Ventral Tegmental Area Viral Viral Vector addiction avoidance behavior behavioral response classical conditioning defined contribution dopaminergic neuron drug abuse prevention drug of abuse excitatory neuron gamma-Aminobutyric Acid in vivo motivated behavior mouse model neural circuit neuroadaptation neurotransmission novel optogenetics postsynaptic prevent receptor research study targeted treatment tool

项目摘要

DESCRIPTION (provided by applicant): The ventral tegmental area (VTA) is a core component of the neural circuitry that drives goal-directed behavior and a primary target upon which drugs of abuse manipulate behavior. Although generally regarded as a dopaminergic nucleus, about half of VTA neurons signal through release of the amino acid neurotransmitters GABA or glutamate. Unlike dopamine, these transmitters activate fast ionotropic postsynaptic receptors indicating VTA neurons signal across multiple modes and timescales. Recent evidence suggests important roles for VTA GABA neurons in encoding negative reward value, but little is known regarding the behavioral relevance of the recently identified glutamate neurons in the VTA. However, developmental, anatomical, and electrophysiological evidence suggests overlapping but distinct roles for VTA glutamate and dopamine signaling in the neural circuit processes underlying behavioral reinforcement. The goal of this proposal is to identify how excitatory VTA signaling contributes to the processes underlying behavioral reinforcement and how VTA glutamate neurons functionally integrate into the mesolimbic neural circuits that regulate motivated behavior. We will use mouse genetics, optogenetics, and viral vectors to selectively manipulate discrete excitatory VTA circuits. Behavioral, anatomical, electrophysiological, and molecular assays will then be used to assess VTA glutamate neurons, determine their physiological and behavioral functions, and define the anatomical and molecular factors distinguishing them from neighboring dopamine and GABA-releasing neurons. Together these studies comprise a comprehensive plan to define the form and function of a novel class of VTA neurons while enhancing our understanding of intrinsic VTA heterogeneity. These studies will identify new opportunities and specify new targets for the treatment and prevention of drug addiction and other compulsive behavioral disorders.

描述（由申请人提供）：腹侧被盖区（VTA）是驱动目标导向行为的神经回路的核心组成部分，也是滥用药物操纵行为的主要靶点。虽然通常被认为是多巴胺能核，但大约一半的VTA神经元通过释放氨基酸神经递质GABA或谷氨酸来发出信号。与多巴胺不同，这些递质激活快速嗜离子性突触后受体，表明VTA神经元在多种模式和时间尺度上发出信号。最近的证据表明VTA GABA神经元在编码负奖励值中起重要作用，但关于最近发现的VTA谷氨酸神经元的行为相关性知之甚少。然而，发育、解剖和电生理证据表明，VTA谷氨酸和多巴胺信号在行为强化的神经回路过程中具有重叠但不同的作用。本研究的目的是确定兴奋性VTA信号如何促进行为强化的过程，以及VTA谷氨酸神经元如何在功能上整合到调节动机行为的中边缘神经回路中。我们将使用小鼠遗传学、光遗传学和病毒载体来选择性地操纵离散的兴奋性VTA电路。行为、解剖、电生理和分子分析将用于评估VTA谷氨酸神经元，确定其生理和行为功能，并确定将其与邻近的多巴胺和gaba释放神经元区分开来的解剖和分子因素。这些研究共同构成了一个全面的计划，以定义一类新的VTA神经元的形式和功能，同时增强我们对内在VTA异质性的理解。这些研究将为药物成瘾和其他强迫性行为障碍的治疗和预防确定新的机会和指定新的目标。