The Role of Neuronal Ensembles Supporting Auditory Fear Conditioning (Engrams) in the Amygdala in Memory Formation, Generalization and Extinction
The Role of Neuronal Ensembles Supporting Auditory Fear Conditioning (Engrams) in the Amygdala in Memory Formation, Generalization and Extinction
批准号:
10553228
负责人:
Sheena A Josselyn
金额:
$33.78万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-04-01 至 2024-01-31
关键词:
AddressAmygdaloid structureAnxietyAnxiety DisordersArchitectureAuditoryBehaviorBrainCalciumCell NucleusCellsCodeDangerousnessDataDevelopmentDiseaseEligibility DeterminationEndoscopesEventExtinctionFluorescent in Situ HybridizationFreezingFrightFutureHalorhodopsinsHippocampusImageImmediate-Early GenesLateralLightMapsMediatingMemoryMental disordersMessenger RNAMicroscopyMusNeuronsNuclearOpsinPersonsPopulationPost-Traumatic Stress DisordersPrevention strategyProcessRecurrenceResearch PersonnelRetrievalRoleStimulusSystemTechniquesTestingTimeTissuesTrainingTraining ActivityVirusVisualizationbehavioral extinctionconditioned feardata analysis pipelineeffective therapyexperiencefear memorygraph theoryin vivo calcium imaginginnovationmachine learning algorithmmemory consolidationneuronal excitabilityoptogeneticspromoterrecruittherapy developmenttreatment strategy
中文摘要
项目总结/摘要
记忆可以被定义为随着时间的推移,通过以下方式获得的内部表征的保留
经验,以及在以后重建这些表征的能力(Dudai 2007)。
这些内部表征被认为是由持久的物理大脑编码的
变化(记忆痕迹或“痕迹”)(Josselyn,科勒& Frankland 2015,2017; Tonegawa等人
al. 2015; Schacter 2001)。记住引起恐惧的事件是适应性的;它有助于一个人
未来的选择基于过去的经验。它甚至可能是有益的概括一些可怕的
回忆然而,过度的恐惧泛化或将不再具有威胁性的刺激视为
危险可能是适应不良。事实上,反复出现或不恰当地表达恐惧,
记忆是几种精神疾病的主要组成部分,包括创伤后
应激障碍(PTSD)和焦虑。因此,了解记忆如何追踪恐惧
事件的形成,随时间的推移而变化,在什么条件下它们保持特殊性或普遍性,
以及它们是如何受到行为灭绝的影响是关键问题,
了解大脑如何使用信息,同时也为新事物的发展提供信息。
治疗/预防以不适当的恐惧记忆为特征的疾病的策略。
在这里,两位PI(Josselyn博士和Frankland博士),都是新的研究者,将联合收割机结合他们的
专业知识来解决这些重要问题。因为所有的技术都与
注意事项和限制,我们将使用各种技术,包括光遗传学操作,
全脑神经元活动绘图和使用图形理论产生“印迹图”
以及结合行为的真实的实时体内钙成像。团结起来,
操纵和观察记忆痕迹,因为它的形成,随着时间的推移和行为的变化,
灭绝是一种创新,可能会导致记忆痕迹定义的转变,
提高我们对开发旨在解决不适当恐惧的治疗方法的理解
回忆
英文摘要
Project Summary/Abstract
Memory may be defined as the retention over time of internal representations gained through
experience, and the capacity to reconstruct these representations at later times (Dudai 2007).
These internal representations are thought to be encoded by long-lasting physical brain
changes (memory traces or `engrams') (Josselyn, Kohler & Frankland 2015, 2017; Tonegawa et
al. 2015; Schacter 2001). Remembering fear-evoking events is adaptive; it helps one make
future choices based on past experience. It may even be beneficial to generalize some fearful
memories. However, excessive fear generalization or treating no-longer threatening stimuli as
dangerous may be maladaptive. Indeed, recurrent or inappropriately expressed fearful
memories are a major component of several psychiatric diseases, including post-traumatic
stress disorder (PTSD) and anxiety. Therefore, understanding how memory traces for fearful
events are formed, change over time, under what conditions they remain specific or generalize,
and how they are impacted by behavioral extinction are critical questions to not only
understanding how the brain uses information but also for informing the development of new
treatment/prevention strategies for disorders characterized by inappropriate fear memories.
Here two PIs (Drs. Josselyn and Frankland), both New Investigators, will combine their
expertise to address these important questions. Because all techniques are associated with
caveats and limitations, we will use a variety of techniques including optogenetic manipulation,
brain-wide neuronal activity mapping and the use of graph-theory to produce “engram maps”
and real time in vivo calcium imaging combined with behavior. Together, the ability to
manipulate and observe an engram as it forms, changes over time and with behavioral
extinction is innovative and may lead to a shift in the very definition of an engram, as well as
increase our understanding for developing treatments aimed at resolving inappropriate fear
memories.
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Neuronal competition: microcircuit mechanisms define the sparsity of the engram.
神经元竞争:微电路机制定义了印迹的稀疏性。
DOI:
10.1016/j.conb.2018.10.013
发表时间:
2019
期刊:
Current opinion in neurobiology
影响因子:
5.7
作者:
[Rao-Ruiz,Priyanka, Yu,Julia, Kushner,StevenA, Josselyn,SheenaA]
通讯作者:
Josselyn,SheenaA
Exercise accelerates place cell representational drift.
运动会加速位置细胞表征漂移。
DOI:
10.1016/j.cub.2022.12.033
发表时间:
2023
期刊:
Current biology : CB
影响因子:
--
作者:
[deSnoo,MitchellL, Miller,AdamMP, Ramsaran,AdamI, Josselyn,SheenaA, Frankland,PaulW]
通讯作者:
Frankland,PaulW
Examining memory linking and generalization using scFLARE2, a temporally precise neuronal activity tagging system.
使用 scFLARE2(一种时间精确的神经元活动标记系统)检查记忆链接和泛化。
DOI:
10.1016/j.celrep.2023.113592
发表时间:
2023
期刊:
Cell reports
影响因子:
8.8
作者:
[Jung,JungHoon, Wang,Ying, Rashid,AsimJ, Zhang,Tao, Frankland,PaulW, Josselyn,SheenaA]
通讯作者:
Josselyn,SheenaA
DOI:
10.1016/j.bbr.2019.112180
发表时间:
2019-12-30
期刊:
Behavioural brain research
影响因子:
2.7
作者:
[Tran LM, Josselyn SA, Richards BA, Frankland PW]
通讯作者:
Frankland PW
Neurogenesis-dependent transformation of hippocampal engrams.
海马印迹的神经发生依赖性转化。
DOI:
10.1016/j.neulet.2021.136176
发表时间:
2021
期刊:
Neuroscience letters
影响因子:
2.5
作者:
[Ko,SangyoonY, Frankland,PaulW]
通讯作者:
Frankland,PaulW
共 17 条
The Role of Neuronal Ensembles Supporting Auditory Fear Conditioning (Engrams) in the Amygdala in Memory Formation, Generalization and Extinction
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批准号:9891099
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项目类别:
-
资助金额:$35.56万
-
财政年份:2019
-
负责人:Sheena A Josselyn
-
依托单位:
The Role of Neuronal Ensembles Supporting Auditory Fear Conditioning (Engrams) in the Amygdala in Memory Formation, Generalization and Extinction
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批准号:10087966
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项目类别:
-
资助金额:$33.78万
-
财政年份:2019
-
负责人:Sheena A Josselyn
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依托单位: