Opioid Modulation of Cue-Triggered 'Wanting' in Amygdala
Opioid Modulation of Cue-Triggered 'Wanting' in Amygdala
批准号:
7298601
负责人:
Stephen Vincent Mahler
金额:
$3.26万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-30 至 2009-09-29
关键词:
AffectAgonistAmygdaloid structureAnxietyAreaBehaviorBehavioralCuesDataDependencyDiffusionDiseaseDorsalDoseDrug AddictionEnkephalin, Ala(2)-MePhe(4)-Gly(5)-EnvironmentExploratory BehaviorFOS geneFeeding behaviorsFellowshipFemaleFoodHumanIncentivesIndividualIndividual DifferencesInfusion proceduresInjection of therapeutic agentLearningLightMeasuresMediationMicroinjectionsMotivationNamesNatureNeuronsObesityOpioidOpioid ReceptorPharmaceutical PreparationsPredispositionProcessRattusRewardsRiskRoleSiteSpecificityStandards of Weights and MeasuresSucroseTestingThinkingTrainingVariantaddictionapproach behaviorbehavior testdaydrug relapseimmunoreactivitymu opioid receptorsnovelpreferencerelating to nervous systemresearch studyresponsereward processingtrait
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The aim of this proposal is to explore the involvement of mu opioid receptors (MORs) in the amygdala on the attribution of incentive motivation to natural reward-associated cues. Preliminary results indicate that infusion of the specific MOR agonist DAMGO (0.1 mu g) into the amygdala increases feeding behavior in female rats. Additionally, we found that DAMGO administered prior to each of the first six days of autoshaping training increases approaches to one of two reward associated cues, depending on individual differences between rats in 'preferred' cue. In the proposed experiments, we first seek to determine the dose dependency and MOR mediation of these enhancements in CS+ approach behavior. Second, we seek to determine whether observed appetitive effects of CeA DAMGO are specific to the amygdala. Third, we seek to determine whether individual differences in pre-autoshaping anxiety, exploratory, and reward sensitivity are related to individual differences observed in autoshaping. This project is relevant to understanding the neural substrates of, and role of individual differences in human appetitive disorders such as addiction and obesity.
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依托单位:
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依托单位: