Adolescent brains, nicotine and endogenous prototoxins
青少年大脑、尼古丁和内源性原毒素
基本信息
- 批准号:7814634
- 负责人:
- 金额:$ 50万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-09-30 至 2011-08-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAdolescenceAdolescentAdolescent BehaviorAdultAffectAgonistAlcoholsAllelesAnimal BehaviorAnimalsAnxietyAreaBehaviorBehavioralBehavioral inhibitionBindingBlood specimenBrainCandidate Disease GeneCellular biologyCessation of lifeChildhoodChromosomes, Human, Pair 8CognitionCognitiveConsumptionDNADendritesDevelopmentDiseaseDrug abuseEpidemicEsthesiaExhibitsExposure toGenesGenetic PolymorphismGenotypeGrantHaplotypesHealthHippocampus (Brain)HumanImpulsivityIndividualLabelLeadMeasuresMethamphetamineModelingMolecularMusNeuronsNicotineNicotine DependenceNicotinic ReceptorsNucleus AccumbensOpiatesOutcomeOutcome MeasurePathway interactionsPatternPerformancePhysiologicalPlasticsPreventiveReportingResearch PersonnelRewardsSmokeSmokerSmokingStructureSystemTestingTobacco DependenceTransgenic OrganismsTranslational ResearchVertebral columnadolescent smokingbasal forebrainbasecholinergicdensitydrug of abusegenetic epidemiologyhigh risk behaviorinterdisciplinary approachnerve supplyneurochemistrynovel strategiespreferencepreventpublic health relevanceresponse
项目摘要
DESCRIPTION (provided by applicant): This application addresses broad Challenge Area (15) Translational Science and specific Challenge Topic, 15- DA-110: Determining if and how Adolescent Behaviors Affect Connections in the Developing Brain. The adverse impact of smoking on health is a world-wide epidemic that contributes to four million deaths a year, with an expected increase to 10 million per year world-wide by 2030. Tobacco dependence is viewed as a "pediatric disease" because most people begin smoking during adolescence. Adolescents display a greater sensitivity to the addictive effects of nicotine, becoming dependent upon smoking more rapidly than adults. Studies also show that smokers who began as adolescents smoke more frequently with a lower rate of quitting. Despite the many reports establishing a greater sensitivity of adolescent brains to nicotine, the fundamental basis of this greater sensitivity together with the long-term consequences of nicotine exposure on the wiring and neurochemistry of the brain is unknown. Most animal studies on adolescents have limited outcome measures of nicotine exposure to a single aspect such as behavior, agonist binding, or electrophysiological outcomes. Furthermore, none of the studies have examined plastic changes at the level of individual neurons with respect to the normal endogenous cholinergic system of the basal forebrain, and we know of no studies that integrate information from animal systems with human behavior. Thus, this Challenge Grant is a multidisciplinary approach that involves investigators from the fields of animal behavior, human cognition, genetic epidemiology, and molecular cell biology to test the validity of the following model: that the enhanced sensitivity of adolescents to nicotine is due to an imbalance between the endogenous cholinergic system and the function of nicotinic acetylcholine receptors (nAChRs). We predict that the cholinergic pathway from the basal forebrain to the cortex and hippocampus is not yet functionally mature in adolescents, yet an overabundance of terminals with nAChRs combined with a reduced level of prototoxin modulators of nAChRs allows exogenously administered nicotine to lead to long term changes that enhance reward pathways, while preventing full cholinergic maturation, leading to a beneficial effect of nicotine in cognitive performance that reinforces the use of nicotine. The specific aims of this application are: 1) to use adolescent and adult transgenic Thy-1-eYFP mice that demonstrate nicotine-induced conditioned place to determine whether changes in arborization of eYFP- labeled dendrites in layer 5 as well as changes in eYFP-terminals in nucleus accumbens occur; to determine if correlative changes in cholinergic innervation or dopaminergic interaction with eYFP-containing structures occur; 2) to determine whether mice that lack or carry only one copy of the prototoxin gene psca exhibit a greater physiological and behavioral response to nicotine and to determine whether this correlates with parameters examined in Aim 1; 3) to genotype human adolescent subjects that have been screened and tested for impulsivity, nicotine exposure, and drug abuse to determine whether specific alleles of prototoxin genes are correlated with increased impulsivity or nicotine dependence.
PUBLIC HEALTH RELEVANCE: The adverse impact of smoking on health is a world-wide epidemic that contributes to four million deaths a year. Studies show that smokers who began as adolescents smoke more frequently with a lower rate of quitting. Despite the many reports establishing a greater sensitivity of adolescent brains to nicotine, the fundamental basis of this greater sensitivity together with the long-term consequences of nicotine exposure on the wiring and neurochemistry of the brain is unknown. A greater understanding of these will lead to possible preventive measures and therapies, having a significant long-term impact on human health.
描述(由申请人提供):本申请涉及广泛的挑战领域(15)翻译科学和具体的挑战主题,15-DA-110:确定青少年的行为是否以及如何影响发育中的大脑的连接。吸烟对健康的不利影响是一种世界性的流行病,每年导致400万人死亡,预计到2030年全球每年将增加到1000万人。烟草依赖被视为一种“儿科疾病”,因为大多数人在青春期就开始吸烟。青少年对尼古丁的成瘾作用表现出更高的敏感性,比成年人更快地对吸烟产生依赖。研究还表明,从青少年时期开始吸烟的人吸烟频率更高,戒烟率更低。尽管许多报告证实青少年大脑对尼古丁更敏感,但这种更敏感的基本基础以及尼古丁暴露对大脑的神经化学和线路的长期后果尚不清楚。大多数关于青少年的动物研究对尼古丁暴露在单一方面的结果测量有限,如行为、激动剂结合或电生理结果。此外,没有一项研究检查单个神经元水平上相对于基底前脑正常内源性胆碱能系统的可塑性变化,我们也不知道有任何研究将动物系统的信息与人类行为相结合。因此,这项挑战赠款是一个多学科的方法,涉及动物行为、人类认知、遗传流行病学和分子细胞生物学领域的研究人员,以测试以下模型的有效性:青少年对尼古丁的敏感性增强是由于内源性胆碱能系统和尼古丁乙酰胆碱受体(NAChRs)功能之间的失衡。我们预测,在青少年中,从基底前脑到皮质和海马区的胆碱能通路在功能上尚未成熟,但过多的nAChRs终末与nAChRs原毒素调节剂水平的降低相结合,允许外源性给予尼古丁导致长期变化,从而增强奖励途径,同时阻止完全的胆碱能成熟,导致尼古丁在认知表现中的有益作用,从而加强尼古丁的使用。本应用的具体目的是:1)使用青少年和成年转基因Thy-1-EYFP小鼠,展示尼古丁诱导的条件性位置,以确定第5层EYFP标记树突的树枝是否发生变化以及伏隔核中EYFP终末的变化;确定胆碱能神经或多巴胺能与含EYFP结构的相互作用是否发生相关变化;2)确定是否缺乏或仅携带一个拷贝的原毒素基因PSCA的小鼠对尼古丁表现出更大的生理和行为反应,并确定这是否与目标1中检查的参数有关;3)对经过冲动、尼古丁暴露和药物滥用筛查和测试的青少年受试者进行基因分型,以确定原毒素基因的特定等位基因是否与冲动增加或尼古丁依赖有关。
公共卫生相关性:吸烟对健康的不利影响是一种世界性的流行病,每年导致400万人死亡。研究表明,从青少年时期开始吸烟的人吸烟频率更高,戒烟率更低。尽管许多报告证实青少年大脑对尼古丁更敏感,但这种更敏感的基本基础以及尼古丁暴露对大脑的神经化学和线路的长期后果尚不清楚。更好地了解这些将导致可能的预防措施和治疗,对人类健康产生重大的长期影响。
项目成果
期刊论文数量(0)
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科研奖励数量(0)
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{{ truncateString('Rae Nishi', 18)}}的其他基金
Nicotinic acetylcholine receptors and neuroblastoma
烟碱乙酰胆碱受体与神经母细胞瘤
- 批准号:
8231045 - 财政年份:2011
- 资助金额:
$ 50万 - 项目类别:
Nicotinic acetylcholine receptors and neuroblastoma
烟碱乙酰胆碱受体与神经母细胞瘤
- 批准号:
8326061 - 财政年份:2011
- 资助金额:
$ 50万 - 项目类别:
Adolescent brains, nicotine and endogenous prototoxins
青少年大脑、尼古丁和内源性原毒素
- 批准号:
7933994 - 财政年份:2009
- 资助金额:
$ 50万 - 项目类别:
Nicotinic Acetylcholine Receptors in Neural Development
神经发育中的烟碱乙酰胆碱受体
- 批准号:
7093071 - 财政年份:2005
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$ 50万 - 项目类别:
Nicotinic Acetylcholine Receptors in Neural Development
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- 批准号:
7228939 - 财政年份:2005
- 资助金额:
$ 50万 - 项目类别:
Nicotinic Acetylcholine Receptors in Neural Development
神经发育中的烟碱乙酰胆碱受体
- 批准号:
7429773 - 财政年份:2005
- 资助金额:
$ 50万 - 项目类别:
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