Effects of exercise on dopaminergic mechanisms of cocaine relapse

运动对可卡因复吸的多巴胺能机制的影响

基本信息

批准号：
10553437
负责人：
Natalie Zlebnik
金额：
$ 24.9万
依托单位：
UNIVERSITY OF CALIFORNIA RIVERSIDE
依托单位国家：
美国
项目类别：
财政年份：
2019
资助国家：
美国
起止时间：
2019-08-01 至 2025-02-28
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10553437
关键词：
Abstinence Aerobic Exercise Animals Attenuated Behavior Behavior Therapy Brain Chronic Cocaine Corpus striatum structure Cues Data Development Dopamine Dopamine D1 Receptor Dopamine D2 Receptor Dopamine Receptor Dorsal Drug Addiction Drug abuse Drug usage Effectiveness Electrophysiology (science)Environment Event Exercise Exposure to Extinction (Psychology)Goals Human Intake Intervention Kinetics Maintenance Mediating Methods Molecular Mus Neurobiology Neurons Optics Periodicity Pharmaceutical Preparations Pharmacotherapy Phase Process Public Health Recording of previous events Relapse Reporting Rewards Rodent Role Running Scanning Signal Transduction Slice Technology Therapeutic Therapeutic Effect Treatment Efficacy Ventral Striatum Withdrawal addiction cell type cocaine relapse cocaine self-administration craving drug craving drug of abuse drug relapse effective therapy experimental study extracellular in vivo insight motivated behavior mouse model neurochemistry neurophysiology novel optogenetics paired stimuli prevent receptor expression recruit relating to nervous system response restoration reward circuitry sedentary spatiotemporal uptake

项目摘要

PROJECT SUMMARY Relapse to drug abuse is the single greatest challenge in addiction treatment. Relapse can occur even after prolonged abstinence and is often preceded by robust drug craving precipitated by exposure to drug-paired stimuli and environments. Aerobic exercise is a novel and promising behavioral treatment for drug addiction and relapse. However, the precise mechanism of its therapeutic effects is unknown. The long-term goal of this project is to characterize the striatal network dynamics that mediate the effects of exercise on addiction and relapse. The current aims of this proposal are to examine the impact of chronic wheel running on rapid subsecond dopamine release dynamics and dopamine terminal function as well as on the longitudinal development of phasic dopamine signals that promote cocaine-seeking behavior and on the recruitment of cell- type specific neural processing of cocaine seeking and cocaine-paired cues. It is hypothesized that chronic wheel running will (1) attenuate cocaine-evoked subsecond dopamine release in the striatum, (2) decrease striatal phasic dopaminergic signals accompanying cocaine-paired cues and cocaine seeking, and (3) attenuate D1-MSN and potentiate D2-MSN encoding of cocaine-paired cues and cocaine seeking. These experiments will employ a sophisticated mouse model of cocaine relapse, state-of-the-art in vivo fast-scan cyclic voltammetry recordings, in vivo multiple single-unit electrophysiological recordings, and chemogenetic and optogenetic technologies to examine these questions in behaving animals. The proposed experiments aim to increase our understanding of the neurobiological substrates that mediate drug craving and relapse and identify the neurochemical and neurophysiological mechanisms of the beneficial effects of exercise.

项目概要药物滥用复发是成瘾治疗中最大的挑战。即使术后也可能复发长期禁欲，并且通常在暴露于配对药物后引发强烈的药物渴望刺激和环境。有氧运动是一种新颖且有前途的药物成瘾行为治疗方法并复发。然而，其治疗作用的确切机制尚不清楚。本次活动的长远目标该项目的目的是描述纹状体网络动力学的特征，该网络动力学介导运动对成瘾和成瘾的影响复发。该提案当前的目的是研究长期车轮运行对快速行驶的影响亚秒多巴胺释放动力学和多巴胺末端功能以及纵向阶段性多巴胺信号的发展促进可卡因寻求行为以及细胞招募可卡因寻求和可卡因配对线索的类型特定神经处理。据推测，慢性车轮转动会 (1) 减弱可卡因引起的纹状体亚秒多巴胺释放，(2) 减少纹状体阶段性多巴胺能信号伴随可卡因配对线索和可卡因寻找，以及（3）减弱可卡因配对线索和可卡因寻找的 D1-MSN 编码并增强 D2-MSN 编码。这些实验将采用复杂的可卡因复发小鼠模型，最先进的体内快速扫描循环伏安法记录、体内多个单单元电生理记录和化学遗传学和光遗传学技术来研究动物行为中的这些问题。拟议的实验目标增加我们对介导药物渴望和复发的神经生物学底物的理解确定运动有益影响的神经化学和神经生理学机制。