Neurobiology of compulsive eating.
Neurobiology of compulsive eating.
批准号:
8815287
负责人:
Pietro Cottone
金额:
$32.25万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-03-01 至 2017-02-28
关键词:
AbstinenceAcuteAffectAffectiveAmygdaloid structureAnhedoniaAnimal ModelAnimalsAnxietyAnxiety DisordersAreaBehaviorBehavioralBinge EatingBrainCRF receptor type 1Cell NucleusChronicCorticotropin-Releasing HormoneDSM-VDependenceDevelopmentDietDrug AddictionDrug usageEatingEating DisordersEmotionalEpidemicEtiologyFoodHealthHyperphagiaInterventionLinkMeasuresMediatingMental disordersMolecularMood DisordersNegative ReinforcementsNeurobiologyNeurosecretory SystemsObesityOutcomePeptidesPeripheralPharmacological TreatmentRadioimmunoassayRattusRecording of previous eventsReinforcement ScheduleRelapseReverse Transcriptase Polymerase Chain ReactionRewardsRodent ModelRoleSelf MedicationSelf StimulationSiteStressSwimmingSystemTestingWithdrawalacute stressanxiety-like behaviorbasebehavioral outcomebiological adaptation to stressdepressive symptomsdrug of abusefeedingfood consumptionlensnegative emotional stateneuroadaptationnovelpreventresearch studyresponsesocialstressor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): In the last decades, the epidemic spreading of eating disorders and obesity has raised the question whether certain highly palatable foods may be responsible for the development of a "food dependence". In fact, epidemic eating disorders and obesity, like drug addiction, can be conceptualized as chronic relapsing conditions with alternating periods of abstinence (e.g., dieting to avoid "forbidden" foods) and relapse (uncontrollable eating of palatable foods) that continue despite negative consequences. Eating disorders and obesity very frequently occur comorbidly with anxiety and mood disorders; however the neurobiological link between the two pathological conditions is poorly understood. We have recently proposed a new reliable animal model of palatable food dependence which contributes to the understanding of the etiology of compulsive eating and comorbid anxiety and affective disorders. Compulsive eating may be generated by the recruitment of the extrahypothalamic corticotropin-releasing factor (CRF) brain stress systems and by the emergence of a negative emotional state during abstinence, analogous to withdrawal from abused drugs. Therefore, relying on the general hypothesis that withdrawal generates palatable food overeating as a form of "self-medication," the proposed application will investigate the relationship between compulsive eating and comorbid anxiety and mood disorders. Specifically, the experiments of the proposed Specific Aims use a combined behavioral, pharmacological and molecular approach to elucidate: i) the brain sites important for the pharmacological effects of CRF1 receptor antagonists on the consummatory, emotional and motivational components of compulsive eating; ii) the effects of acute mild stress on food consumption, affectivity, and HPA and CRF responses, in animals with a history of palatable diet-cycling during protracted abstinence; iii) the role of the CRF/CRF1 system in the adaptations of the brain reward system and in the depressive-like behavior induced by the palatable diet alternation. This proposal will elucidate the neurobiological relationship between compulsive eating and comorbid anxiety and mood disorders through the lens of negative reinforcement. A better understanding of the etiology of compulsive eating would help prevent the onset of eating disorders and obesity, and would increase the potential for pharmacological intervention for tens of millions of people.
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海外基金