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Understanding whole-brain circuits mediating fear memory attenuation

Project description

Understanding the underlying mechanisms of chronic fear disorders

Individuals respond differently to unpleasant events, which can lead to chronic fear disorders such as phobias and post-traumatic stress disorder (PTSD). However, technical challenges in analysing neuronal activity across the entire brain hinder our understanding of the underlying mechanisms. In this context, the MSCA-funded TaggingMemory project aims to investigate the circuitry involved in fear memory extinction by generating detailed brain connectivity maps at a single-cell level. By pinpointing this circuitry, researchers aim to enhance our understanding of PTSD at an individual level. The project will develop a new quadruple transgenic mouse model to examine multiple memories within the same brain, identify brain regions crucial for successful memory extinction, and explore anatomical circuits.

Objective

The experience of aversive events is a component of everyone’s lives. People perceive aversive events and traumas differently but the explanation of this different perception is poorly understood. At times, this different perception leads to chronic fear disorders like phobias and post-traumatic stress disorder (PTSD). Despite the high prevalence of such disorders, effective treatments for traumatic memories remain scarce. Therefore, a good understanding of the time-evolution of fear memory is necessary to clarify how different neuronal circuits are disrupted in disease states but also to set the basis for the development of unified therapeutic strategy to attenuate PTSD. Currently, the limited knowledge of the mechanisms underlying fear memory at brain-wide level is mainly due to the technical limitations in large-scale analysis of neuronal activity.
TaggingMemory seeks to study the anatomical and functional circuitry underlying fear memory extinction reconstructing single-cell-resolution maps of whole-brain connectivity. The identification of this circuitry could pave the way for a better comprehension of PTSD circuitry at single-individual level. To reach this goal, I will develop a new quadruple transgenic mouse model able to capture multiple memories in the same brain. Using this transgenic line such as preclinical model of PTSD, I will reconstruct the evolutionary maps of fear memory. Then, I will test psychedelics as new promising drugs for PTSD treatment in order to analyze how fear attenuation changes with or without drug treatment, highlighting the connectivity differences that drive fear suppression. Finally, by identifying brain regions pivotal for a successful memory extinction, I will then unravel the anatomical circuits with sub-cellular resolution by a cutting-edge intelligent light-sheet microscope.
The present action will pioneer the anatomical and functional characterization of the well-known but poorly understood phenomenon of fear memory.

Coordinator

LABORATORIO EUROPEO DI SPETTROSCOPIE NON LINEARI
Net EU contribution
€ 265 099,20
Address
Via Nello Carrara 1
50019 Sesto-Fiorentino (Fi)
Italy

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Region
Centro (IT) Toscana Firenze
Activity type
Research Organisations
Links
Total cost
No data

Partners (1)