Drug Abuse, Social Decision-Making, and Sex-Related Functional Brain Asymmetry
药物滥用、社会决策和与性别相关的大脑功能不对称
基本信息
- 批准号:7292654
- 负责人:
- 金额:$ 32.42万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2006
- 资助国家:美国
- 起止时间:2006-09-30 至 2011-03-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAdultAffectiveAlcohol abuseAlcoholsAmygdaloid structureAnxietyArchitectureBrainBrain PartBrain regionCharacteristicsChildChildhoodClinicalComorbidityDataDecision MakingDefectDevelopmentDiseaseDrug AddictionDrug abuseDrug usageEmotionalEmotionsEmployee StrikesExhibitsFeelingFemaleFunctional disorderFutureGamblingGenderGoalsHeartImpairmentIndividualInsula of ReilInvestigationIowaLeadLeftLesionLifeLightLinkMeasuresMood DisordersMyopiaNeurobiologyNeurologicNeurological ModelsNumbersOutcomePatientsPatternPersonal SatisfactionPersonality DisordersPersonsPharmaceutical PreparationsPlayPrefrontal CortexPreventionProcessPublic HealthRequest for ApplicationsResearchRoleSamplingSex CharacteristicsSideSocial EnvironmentSocial supportSourceStructureSubstance abuse problemSystemTestingTrustWomanWomen&aposs RightsWorkaddictionbrain behaviordesignearly onsetfocal brain damageinterestmalemenneuroeconomicsneuropsychologicalpatient registrypre-clinicalrelating to nervous systemresearch studyresponsesexsocialsocial modeltherapy development
项目摘要
DESCRIPTION (provided by applicant): This research application is in response to #RFA-DA-06-004. At the heart of drug and alcohol abuse is bad decision-making, especially in response to social influences. This decision-making defect is highly reminiscent of the social decision-making impairments that characterize neurological patients with damage to ventromedial prefrontal cortex (VMPC). The VMPC patients provide a neurological model of social decision- making gone awry. There is evidence at both preclinical and clinical levels that the VMPC is a key brain region in drug abuse, and we propose that VMPC dysfunction and defective social decision-making may characterize individuals who abuse and become addicted to drugs and alcohol. In this research application, we plan to conduct studies in neurological patients in order to flesh out the neurobiological underpinnings of social decision-making, taking advantage of the unique Iowa Patient Registry that contains neuropsychological and neuroanatomical data for thousands of patients. A particular focus is on gender differences. We have intriguing preliminary findings suggesting that there might be an important sex-related difference in the relationship between the VMPC and social decision-making: in men, the right VMPC might be critical, whereas in women, the left VMPC might be critical. The experiments will test three specific aims: (1) To determine whether there is sex-related functional asymmetry of the VMPC in regard to social decision- making, using tasks such as the Ultimatum Game, Trust Game, Iowa Gambling Task, and Ellsberg Tasks; (2) To extend the investigation of sex-related functional asymmetry to other brain structures known to be critical for social and affective processes related to decision-making, namely, the amygdala and the insular cortex; (3) To investigate developmental influences on the relationship between the VMPC and social- decision making and emotional processing, by studying patients who incurred VMPC damage early in life. The experiments will furnish important new information about the neurobiological underpinnings of social decision-making and emotional processing. The link with substance abuse is direct: the decision-making deficits in VMPC patients have striking similarities with those evident in drug and alcohol abusers and addicts ("myopia for the future"). Thus, our research could help pinpoint sources of neural dysfunction that contribute to bad decision-making of the type that characterizes drug and alcohol abuse. Public health relevance: This research will help us understand how various parts of the brain are important for social decision-making and emotional processing, whether there are gender differences in these brain- behavior relationships, and how these relationships develop. The research could help inform treatment and prevention of drug and alcohol abuse disorders, as well as social conduct disorders, personality disorders, and anxiety and mood disorders, all of which have high comorbidity with drug and alcohol abuse.
描述(由申请人提供):本研究申请是对#RFA-DA-06-004的回应。药物和酒精滥用的核心是错误的决策,特别是在应对社会影响时。这种决策缺陷与腹内侧前额叶皮质(VMPC)受损的神经系统患者的社会决策障碍非常相似。VMPC患者提供了一个社会决策错误的神经模型。有证据表明,在临床前和临床水平的VMPC是一个关键的大脑区域在药物滥用,我们建议,VMPC功能障碍和有缺陷的社会决策可能表征个人滥用和成瘾的药物和酒精。在这项研究应用中,我们计划在神经系统患者中进行研究,以充实社会决策的神经生物学基础,利用独特的爱荷华州患者登记处,其中包含数千名患者的神经心理学和神经解剖学数据。一个特别的重点是性别差异。我们有有趣的初步研究结果表明,VMPC和社会决策之间的关系可能存在重要的性别差异:在男性中,右VMPC可能是关键的,而在女性中,左VMPC可能是关键的。本实验将测试三个具体的目标:(1)使用最后通牒游戏、信任游戏、爱荷华州赌博任务和埃尔斯伯格任务等任务来确定VMPC在社会决策方面是否存在性别相关的功能不对称;(2)将与性别相关的功能不对称性的研究扩展到其他已知对与决策相关的社会和情感过程至关重要的大脑结构,(3)通过对早期VMPC受损患者的研究,探讨VMPC与社会决策和情绪加工之间的关系。这些实验将为社会决策和情绪处理的神经生物学基础提供重要的新信息。与药物滥用的联系是直接的:VMPC患者的决策缺陷与药物和酒精滥用者和成瘾者的决策缺陷有惊人的相似之处(“未来近视”)。因此,我们的研究可以帮助确定神经功能障碍的来源,这些神经功能障碍导致了以药物和酒精滥用为特征的错误决策。公共卫生相关性:这项研究将帮助我们了解大脑的各个部分对社会决策和情绪处理的重要性,这些大脑-行为关系中是否存在性别差异,以及这些关系如何发展。这项研究可以帮助治疗和预防药物和酒精滥用障碍,以及社会行为障碍,人格障碍,焦虑和情绪障碍,所有这些都与药物和酒精滥用有很高的共病率。
项目成果
期刊论文数量(0)
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Daniel T. Tranel其他文献
Daniel T. Tranel的其他文献
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{{ truncateString('Daniel T. Tranel', 18)}}的其他基金
Drug Abuse, Social Decision-Making, and Sex-Related Functional Brain Asymmetry
药物滥用、社会决策和与性别相关的大脑功能不对称
- 批准号:
7192900 - 财政年份:2006
- 资助金额:
$ 32.42万 - 项目类别:
Drug Abuse, Social Decision-Making, and Sex-Related Functional Brain Asymmetry
药物滥用、社会决策和与性别相关的大脑功能不对称
- 批准号:
7379984 - 财政年份:2006
- 资助金额:
$ 32.42万 - 项目类别:
Drug Abuse, Social Decision-Making, and Sex-Related Functional Brain Asymmetry
药物滥用、社会决策和与性别相关的大脑功能不对称
- 批准号:
7845392 - 财政年份:2006
- 资助金额:
$ 32.42万 - 项目类别:
Drug Abuse, Social Decision-Making, and Sex-Related Functional Brain Asymmetry
药物滥用、社会决策和与性别相关的大脑功能不对称
- 批准号:
7797636 - 财政年份:2006
- 资助金额:
$ 32.42万 - 项目类别:
Drug Abuse, Social Decision-Making, and Sex-Related Functional Brain Asymmetry
药物滥用、社会决策和与性别相关的大脑功能不对称
- 批准号:
7586092 - 财政年份:2006
- 资助金额:
$ 32.42万 - 项目类别:
Course Development in Neurobiology of Disease at the University of Iowa
爱荷华大学疾病神经生物学课程开发
- 批准号:
7125072 - 财政年份:2005
- 资助金额:
$ 32.42万 - 项目类别:
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