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Modulation of Methamphetamine Actions in the CNS

Modulation of Methamphetamine Actions in the CNS
甲基苯丙胺在中枢神经系统中的作用的调节
批准号:
7587365
负责人:
Margarita L Dubocovich
金额:
$31.07万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-07-01 至 2012-03-31

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中文摘要
翻译
描述(由申请人提供):甲基苯丙胺的广泛使用,导致滥用和依赖,是一个重大的医学,精神病学和公共卫生问题。确定有效的药物疗法来管理甲基苯丙胺滥用和依赖是一个研究重点。甲基苯丙胺的使用与行为敏感化、睡眠和昼夜节律的改变、焦虑、情绪变化和易怒有关,无论是在滥用期间还是在戒断时。本申请的目的是研究选择性褪黑激素受体配体减弱与慢性甲基苯丙胺滥用相关的行为敏化、增加奖励行为和昼夜节律去兴奋化的潜力。褪黑激素受体(MT 1、MT 2)正在成为多巴胺介导的信号的调节、扰乱的行为昼夜节律的夹带和睡眠促进的靶标。将使用神经药理学方法来研究内源性和外源性褪黑激素在前脑区域中激活褪黑激素受体(MT 1,MT 2)以调节甲基苯丙胺诱导的运动敏化、奖赏行为和通过CREB通路的多巴胺能信号传导的作用。还将研究CLOCK和NPAS-2基因和褪黑激素受体对慢性甲基苯丙胺诱导昼夜节律紊乱和产生自由活动节律的机制的参与。最后,我们将开发小鼠模型,以评估褪黑激素和多巴胺配体的效力,夹带甲基苯丙胺诱导的视交叉上核独立的自由运行的节奏。这些研究的结果应该为发现和开发新型褪黑激素配体提供基础,以减轻与甲基苯丙胺类药物的医疗使用和滥用相关的失眠、昼夜睡眠障碍和抑郁症状(内源性抑郁)。
英文摘要
DESCRIPTION (provided by applicant): The wide spread use of methamphetamine, causing abuse and dependence, is a significant medical, psychiatric, and public health concern. Identifying effective pharmacotherapies for the management of methamphetamine abuse and dependence is a research priority. Methamphetamine use is associated with behavioral sensitization, alterations in sleep and circadian rhythmicity, anxiety, mood changes and irritability either during abuse or upon withdrawal. The goal of this application is to investigate the potential of selective melatonin receptor ligands to attenuate the behavioral sensitization, increase reward behavior and circadian rhythm desynchronization associated with chronic methamphetamine abuse. Melatonin receptors (MTi, MT2) are emerging as targets for the modulation of dopamine-mediated signals, entrainment of disrupted behavioral circadian rhythms and sleep promotion. Neuropharmacological approaches will be used to investigate the role of melatonin receptor (MTi, MT2) activation by endogenous and exogenous melatonin in forebrain areas to modulate methamphetamine-induced locomotor sensitization, reward behavior and dopaminergic signaling through the CREB pathway. The involvement of CLOCK and NPAS-2 genes and melatonin receptors on the mechanism(s) by which chronic methamphetamine induce circadian rhythms disorganization and generates free running activity rhythms will also be investigated. Finally, we will develop mouse models to assess the potency of melatonin and dopamine ligands to entrain methamphetamine-induced suprachiasmatic nucleus independent free running rhythms. Results from these studies should provide the basis for the discovery and development of novel melatonin ligands to alleviate insomnia, circadian sleep disorders and depressive symptoms (endogenous depression) associated with the medical use and abuse of methamphetamine-like drugs.
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