Orbitofrontal-Accumbens Interactions, Dopamine Modulation and Impulsive Choice
Orbitofrontal-Accumbens Interactions, Dopamine Modulation and Impulsive Choice
批准号:
7995475
负责人:
MATTHEW R ROESCH
金额:
$17.91万
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 2012-05-31
关键词:
AffectAgonistAnimal ModelAnimalsAreaAttenuatedBehaviorBehavioralChemicalsCocaineComorbidityDataDisciplineDiseaseDopamineDopamine D2 ReceptorDrug AddictionDrug ExposureDrug abuseDrug usageEducational process of instructingElectrophysiology (science)FacultyFecesFire - disastersFunctional disorderFutureGoalsHumanImpulsive BehaviorImpulsivityIncidenceJournalsLearningLengthLesionMarylandMeasuresMentored Research Scientist Development AwardMentorsModelingNeurobiologyNeuronsNeuropharmacologyNucleus AccumbensPatientsPatternPharmaceutical PreparationsPopulationProcessRattusResearchResearch PersonnelRewardsRoleSchizophreniaSignal TransductionTechniquesTestingTimeTrainingUniversitiesWorkaddictionawakecareercocaine exposuredesigndiscountdiscountingmemberneural circuitneurochemistryneurophysiologyrelating to nervous systemresearch studyresponseskillstheories
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The experiments in this proposal are designed to investigate the neurophysiology and neurochemistry underlying impulsivity in normal animals and in animal models of schizophrenia and drug abuse. Like humans, animals impulsively choose a small immediate reward over a larger delayed reward (i.e. time discounting). We will test whether impulsive choice is governed by dopaminergic modulation of time discounted reward signals to nucleus accumbens (NA) from the orbitofrontal cortex (OFC) and whether disrupted function in this circuit due to changes in encoding in OFC and dopaminergic tone in NA gives rise to abnormal levels of impulsivity in schizophrenia and drug abuse. Such complementary changes would explain the high incidence of drug abuse in schizophrenic patients. Through the Mentored Research Scientist Development Award I can acquire the necessary techniques and didactic training in new disciplines in order to achieve my immediate goal of testing these hypotheses and my long-term career goal of becoming a successful independent faculty member, competent in a variety of disciplines including neurophysiology, neuropharmacology and the study of schizophrenia and drug abuse. My training and specific research aims can be broken down into three main components: (1) To characterize neural correlates of impulsive choice in behaving animals. For this, I will continue my training under Dr. Schoenbaum, who is an expert in behavioral electrophysiology and learning theory. (2) To characterize the role of dopamine on interactions between OFC and NA. For this, I will learn how to record intracellularly in anesthetized rats during pharmacological manipulations under the mentoring of Dr. O'Donnell. (3) To characterize the impact of schizophrenia and cocaine on this circuit. For this, I will acquire new skills from both Dr. Schoenbaum and Dr. O'Donnell. In addition to technical and intellectual support from my mentors I will receive didactic training through courses, journal clubs and seminars offered at the University of Maryland and the MPRC. This research will increase our understanding of the neurobiology of impulsivity common to many psychiatric illnesses. Furthermore, it will serve as a platform to investigate impulsive choice in animal models of schizophrenia and drug abuse, which has relevance to understanding the high incidence of drug abuse comorbidity observed in the schizophrenic population.
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会议论文
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Restoration and Further Assessment of the Actor-Critic Circuit and Connected Areas After Cocaine Self-Administration
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Restoration and Further Assessment of the Actor-Critic Circuit and Connected Areas After Cocaine Self-Administration
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依托单位:
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依托单位:
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