Anterograde Amnesia for Contextual Fear

对情境恐惧的顺行性遗忘

• 批准号: 7590494
• 负责人: Michael S Fanselow
• 金额: $ 33.38万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2001
• 资助国家: 美国
• 起止时间: 2001-09-16 至 2011-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7590494
• 关键词: Abbreviations; Adaptive Behaviors; Amygdaloid structure; Anterior; Anterograde Amnesia; Anxiety; Anxiety Disorders; Attenuated; Behavior; Behavioral; Brain; Cell Nucleus; Complex; Data; Dorsal; Environment; Equilibrium; Failure; Financial compensation; Freezing; Fright; Gene Expression; Generations; Goals; Hippocampus (Brain); Homeostasis; Immediate-Early Genes; Knowledge; Learning; Lesion; Medial; Mediating; Memory; Modeling; Nature; Neural Pathways; Organism; Output; Pathway interactions; Prefrontal Cortex; Process; Psychological reinforcement; Rattus; Recruitment Activity; Regulation; Relative (related person); Research Personnel; Role; Route; Staging; Stimulus; System; Techniques; Testing; Training; behavior test; cingulate cortex; conditioned fear; conditioning; innovation; insight; midbrain central gray substance; motivated behavior; novel; prevent; programs; relating to nervous system; research study; response; theories

DESCRIPTION (provided by applicant): This proposal investigates how multiple alternate neural pathways mediate learned fear memories. Our approach identifies 4 key hypotheses: 1) There are primary & alternate pathways capable of mediating fear memory. 2) The alternate pathways are less efficient than the primary pathway. 3) The more efficient primary pathway dominates the learning, precluding significant learning in the alternate pathways. 4) The alternate pathways compensate when the dominant pathway is compromised. The specific aims are to use behavioral and anatomical techniques directed at 3 functional-anatomical stages of contextual fear conditioning, to determine what are these different pathways and how learning is being regulated between these pathways. These stages are: 1) Context Processing, 2) CS-US Association and 3) Response Generation, which are normally mediated by the hippocampus, basolateral amygdala and central amygdala, respectively. A key finding is that while posttraining lesions to a primary component of the network severely compromises contextual fear conditioning, pretraining lesions have lesser effects because alternate routes compensate for the disruption. This compensation is driven by regulatory mechanisms that control memory formation. This model is tested by determining if inactivating one region results in increased activity and behavioral importance in the alternate pathway using behavioral testing, immediate early gene expression and tract tracing. Regulatory mechanisms often preclude a role for the alternate pathways in Pavlovian fear conditioning. Identifying alternate fear pathways, understanding their function and how they are recruited, is essential for understanding the regulation of fear conditioning. From this perspective, anxiety disorders emerge when there is a lack of a balance between the threat in the environment and an organism's adaptive response. In other words, anxiety disorders are a failure of the normal regulatory mechanisms of fear and anxiety. A key goal is to develop an understanding of how the brain maintains a "homeostasis of fear," At the model's core is the regulation of fear between various pathways that generate adaptive behavior.

描述（由申请人提供）：该提案研究了多个备用神经通路如何介导学习的恐惧记忆。我们的方法确定了4个关键假设：1）存在能够介导恐惧记忆的主要和备用通路。2)替代途径的效率低于主要途径。3)更有效的主要途径主导学习，排除了替代途径中的重要学习。4)当主导通路受损时，备用通路进行补偿。具体的目标是使用行为和解剖学技术，针对3个功能解剖学阶段的背景恐惧条件反射，以确定这些不同的途径是什么，以及如何在这些途径之间调节学习。这些阶段是：1）上下文处理，2）CS-US关联和3）反应产生，其通常分别由海马、基底外侧杏仁核和中央杏仁核介导。一个关键的发现是，虽然训练后损伤网络的主要组成部分严重损害了情境恐惧条件反射，但训练前损伤的影响较小，因为替代路线补偿了中断。这种补偿由控制记忆形成的调节机制驱动。该模型通过使用行为测试、立即早期基因表达和束追踪确定一个区域的失活是否导致替代途径中的活性和行为重要性增加来测试。调节机制往往排除了巴甫洛夫恐惧条件反射的替代途径的作用。识别替代的恐惧途径，了解它们的功能以及它们是如何被招募的，对于理解恐惧条件反射的调节至关重要。从这个角度来看，当环境中的威胁和生物体的适应性反应之间缺乏平衡时，焦虑症就会出现。换句话说，焦虑症是恐惧和焦虑的正常调节机制的失败。一个关键目标是了解大脑如何维持“恐惧的稳态”，该模型的核心是产生适应性行为的各种途径之间的恐惧调节。