The role of medial striatum in spatial sequence learning
The role of medial striatum in spatial sequence learning
批准号:
10727401
负责人:
Janina Diana Ferbinteanu
金额:
$43.18万
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-09-01 至 2025-08-31
关键词:
Alzheimer&aposs DiseaseAnimal ModelAnimalsAreaBehaviorBehavioralBrainCellsCognitiveCollectionCompensationComplementComplexCorpus striatum structureCouplingDimensionsDorsalEnvironmentEpisodic memoryEventFire - disastersFutureGoalsHippocampusHuntington DiseaseImpairmentLearningLinkLiteratureLocationMedialMemoryMemory DisordersMental DepressionMental disordersModelingMonitorMotorNeurologicNeuronsOrganismOutcomeOutputPatternPost-Traumatic Stress DisordersPrefrontal CortexPublic HealthRecordsResearchRewardsRoleSchizophreniaStructureTemporal LobeTestingTimeWorkYinautism spectrum disorderenvironmental changeexperienceexperimental studyflexibilityhuman modelinsightmillisecondneuralneural circuitneural networkplace fieldsprefrontal loberesponsesequence learningtheoriestherapy developmentway finding
中文摘要
海马体(HPC)编码伴随当前,过去和未来的位置;并区分
发生在同一地点的事件,作为不同经历的一部分。HPC活动的这些方面可能会
支持情景记忆,编码个人经历的过去事件。然而,神经基质
支持使用这些情景记忆来实现灵活行为的证据仍然不足
因此,排除了记忆障碍治疗的发展。其中一种记忆-
基于灵活的行为可以通过HPC和其他本地设备之间的活动的瞬时协调来生成。
记忆网络,如背内侧纹状体(DSM),其涉及行为灵活性,
神经元以动作调制的方式(动作选择,AC)放电。这项研究的长期目标是
理解环境记忆需求如何导致不同局部的瞬时功能耦合
记忆电路,以指导行为(记忆的动态模型)。当前的目标
建议是评估DSM的贡献,消除歧义的重复遍历相同的物理
空间位置,而在不同的旅程(顺序上下文),一个任务相关的HPC功能和情节
记忆当前提议的中心假设是,行为任务的结构调节
在HPC-DSM中,如何将发生在同一空间的相似事件区分为不同事件的一部分
网络这项工作的基本原理是,
在类似但不同的情况下采取适当行动的信息将提供强有力的科学框架
由此可以开发记忆研究的新策略。我们提出以下两个具体目标:
目标1.确定HPC和DSM活动在顺序上下文消歧中的作用。
这一目标的工作假设是,HPC和DSM中的神经放电的组合是必要的,
成功区分共享轨迹段的扩展空间序列。目标2.识别
HPC/DSM神经活动模式与成功消除
我们的工作假设是,虽然HPC不区分顺序上下文,
在第二个尺度上,在毫秒尺度上区分位置细胞的活动组合
与编码AC的DSM神经元的活动有关。我们希望拟议研究的结果,
证明了顺序上下文的消歧涉及到一个神经网络,
HPC和DSM(目标1);分析神经活动的深层结构将揭示HPC如何
当适当的行动涉及记忆时,
在同一环境中发生的不同的过去事件(目标2)。拟议研究的结果将
有助于充分理解情景记忆的神经基础,这对几个方面都有影响。
神经和精神疾病,并将导致提交R 01等效提案。
英文摘要
The hippocampus (HPC) encodes concomitantly current, past and future locations; and distinguishes between
events that occur in the same place as part of distinct experiences. These aspects of HPC activity are likely to
support episodic memory, which encodes personally experienced past events. However, the neural substrate
that supports the use of these episodic memories to achieve flexible behavior remains insufficiently
understood, precluding thus the development of treatments in memory disorders. One way in which memory-
based flexible behavior may be generated is by transient coordination of activity between HPC and other local
memory networks such as dorso-medial striatum (DSM) which is involved in behavioral flexibility and whose
neurons fire in action-modulated manner (action choice, AC). The long-term goal of this line of research is to
understand how circumstantial mnemonic demand may lead to transient functional coupling of distinct local
memory circuits in order to guide behavior (the dynamic model of memory). The objective of the current
proposal is to evaluate the contribution of DSM to disambiguation of repeated traversals of the same physical
spatial locations while on distinct journeys (sequential context), a task relevant for HPC function and episodic
memory. The central hypothesis of the current proposal is that the structure of the behavioral task modulates
how similar events that occur in the same space are distinguished as part of different episodes in the HPC-DSM
network. The rationale of the proposed work is that a determination of how neural circuits use stored
information to act adequately in similar but yet distinct circumstances will offer a strong scientific framework
whereby new strategies in memory research can be developed.. We propose the following two specific aims:
Aim 1. Identify the roles of HPC and DSM activities in disambiguation of sequential contexts.
The working hypothesis of this aim is that a combination of neural firing in both HPC and DSM is necessary to
successfully distinguish the extended spatial sequences that share segments of trajectory. Aim 2. Identify
the HPC/DSM neural activity patterns that are correlated with successful disambiguation of
sequential contexts Our working hypothesis is that although HPC does not differentiate between sequential
contexts at the second scale, distinction is made at the millisecond scale in place cells' activity in combination
with the activity of DSM neurons which encode AC. We expect the results of the proposed research to
demonstrate that that disambiguation of sequential contexts involves a neural network encompassing both
HPC and DSM (Aim 1); and that analyzing the deep structure of neural activity will uncover how the HPC
representation combines with DSM activity to guide behavior when appropriate action involves memory of
distinct past events that occurred in the same environment (Aim 2). The results of the proposed research will
contribute to fully understanding the neural basis of episodic memory, which has implications for several
neurological and mental illnesses, and will lead to submission of an R01-equivalent proposal.
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会议论文
Hippocampal-Striatal Co-operative Synergistic Interaction
-
批准号:9435600
-
项目类别:
-
资助金额:$24.23万
-
财政年份:2017
-
负责人:Janina Diana Ferbinteanu
-
依托单位:
Physiological Mechanisms of Hippocampal-Striatal Interactions
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批准号:8970021
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项目类别:
-
资助金额:$24.23万
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财政年份:2015
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负责人:Janina Diana Ferbinteanu
-
依托单位:
Physiological Mechanisms of Hippocampal-Striatal Interactions
-
批准号:9116294
-
项目类别:
-
资助金额:$20.19万
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财政年份:2015
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负责人:Janina Diana Ferbinteanu
-
依托单位:
Cognitive and Physiological Mechanisms of Hippocampal Journey Dependent Coding
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批准号:8535306
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项目类别:
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资助金额:$3.81万
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财政年份:2012
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负责人:Janina Diana Ferbinteanu
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依托单位:
Cognitive and Physiological Mechanisms of Hippocampal Journey Dependent Coding
-
批准号:8447425
-
项目类别:
-
资助金额:$23.2万
-
财政年份:2012
-
负责人:Janina Diana Ferbinteanu
-
依托单位:
Cognitive and Physiological Mechanisms of Hippocampal Journey Dependent Coding
-
批准号:8300646
-
项目类别:
-
资助金额:$21.66万
-
财政年份:2012
-
负责人:Janina Diana Ferbinteanu
-
依托单位:
国内基金
海外基金
新型F-18标记香豆素衍生物PET探针的研制及靶向Alzheimer's Disease 斑块显像研究
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批准号:81000622
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项目类别:青年科学基金项目
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资助金额:20.0万元
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批准年份:2010
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负责人:梁胜
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依托单位:
阿尔茨海默病(Alzheimer's disease,AD)动物模型构建的分子机理研究
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批准号:31060293
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资助金额:26.0万元
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批准年份:2010
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负责人:郭亚芬
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依托单位:
跨膜转运蛋白21(TMP21)对引起阿尔茨海默病(Alzheimer'S Disease)的γ分泌酶的作用研究
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批准号:30960334
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项目类别:地区科学基金项目
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资助金额:22.0万元
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批准年份:2009
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负责人:董贵成
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依托单位: