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Fear memory, a profound emotional memory formed in response to threatening events, is vital to the survival and adaptation of individuals. The amygdala, a central hub in the formation, storage, and expression of fear memory, extensively connects with other brain regions, particularly the hippocampus and hypothalamus, allowing it to rapidly integrate sensory information and generate emotional responses. Past research on the regulatory circuits of fear memory has focused on the amygdala, prefrontal cortex, and hippocampus, emphasizing their interactive roles in the formation, consolidation, and extinction of fear memory. However, new circuits and signaling pathways have been identified, leaving many unresolved mysteries about the specific mechanisms of signaling pathways and circuits that depend on the amygdala in fear memories. Therefore, this review focuses on the roles of the different signaling pathways and circuits of the amygdala in fear memories, including their interactions with the hippocampus, cortex, and other brain regions. Further, synaptic plasticity and the regulation of inhibitory interneurons in the amygdala by the ventral prefrontal cortex are discussed. The aims of this review are to advance our understanding of the amygdala's mechanism in fear memory, provide new insights for the prevention and treatment of related disorders such as post-traumatic stress disorder (PTSD), and offer guidance for future research.
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http://dx.doi.org/10.1002/syn.70026 | DOI Listing |
Dev Psychobiol
September 2025
Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio, USA.
Social buffering may reduce the persistent impacts of acute early life stress (aELS) and, thus, has important implications for anxiety- and trauma-related disorders. First, we assessed whether aELS would induce maladaptive fear incubation in adult mice, a PTSD-like phenotype. Overall, animals showed incubation of fear memory in adulthood, independent of aELS condition.
View Article and Find Full Text PDFLearn Mem
September 2025
Department of Psychological and Brain Sciences, Indiana University, Bloomington, Indiana 47405, USA
While cognitive function remains stable for majority of the lifespan, many functions sharply decline in later life. Women have higher rates of neurodegenerative diseases that involve memory loss, including Alzheimer's disease. This sex disparity may be due to longer life expectancies when compared to men; women outlive men by roughly 5 years globally.
View Article and Find Full Text PDFBackgroundNurses suffered an unprecedented number of potentially morally injurious events (PMIEs) during the COVID-19 pandemic. Their long-term associations with organizational well-being remain unknown.Research aimWe aimed to assess whether psychological basic need thwarting characteristic of nurses' episodic memories of PMIEs from the pandemic, either enacted (self-PMIEs) or passively witnessed (other-PMIEs), explained unique burnout and turnover intentions variance 2 years after the events.
View Article and Find Full Text PDFStudy Objectives: Brief sleep loss alters cognition and the activity and synaptic structures of both principal neurons and interneurons in hippocampus. However, although sleep-dependent coordination of activity between hippocampus and neocortex is essential for memory consolidation, much less is known about how sleep loss affects neocortical input to hippocampus, or excitatory-inhibitory balance within neocortical structures. We aimed to test how the synaptic structures of SST+ interneurons in lateral and medial entorhinal cortex (LEC and MEC), which are the major neocortical input to hippocampus, are affected by brief sleep disruption in the hours following learning.
View Article and Find Full Text PDFFront Aging Neurosci
August 2025
Laboratory of Molecular Neurodegeneration, Graduate School of Biomedical Systems and Technologies, Institute of Biomedical Systems and Biotechnology, Peter the Great St. Petersburg Polytechnic University, Saint Petersburg, Russia.
Alzheimer's disease (AD) is a neurodegenerative disorder that leads to progressive cognitive decline and significant disruptions in hippocampal neural networks, critically impacting memory and learning. Understanding the neural mechanisms underlying these impairments is essential for developing effective therapies. The 5xFAD mouse model, known for progressive neurodegeneration and cognitive deficits, provides a valuable platform for investigating associative learning and memory impairments related to AD.
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