Abstract
Witnessing pain and distress in others can cause psychological trauma and increase odds of developing PTSD in the future, on exposure to another stressful event. However, the underlying synaptic process remains unknown. Here we report that mice exposed to a conspecific receiving electrical footshocks exhibited enhanced passive avoidance (PA) learning when trained 24 h after the exposure. The exposure activated neurons in the dorsomedial prefrontal cortex (dmPFC) and basolateral amygdala (BLA) and altered synaptic transmission from dmPFC to BLA. It increased amplitude, slowed decay of NMDA receptor-mediated currents, and generated silent synapses. Administration of sub-anesthetic ketamine immediately after the exposure prevented the enhancement of PA learning and silent synapse formation. These findings suggest that ketamine can prevent pathophysiological consequences of psychological trauma.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Avoidance Learning / drug effects
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Avoidance Learning / physiology*
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Basolateral Nuclear Complex / drug effects
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Basolateral Nuclear Complex / physiopathology*
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Disease Models, Animal
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Electroshock
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Fear / drug effects
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Fear / physiology
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Glutamic Acid / metabolism
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Ketamine / pharmacology*
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Male
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Mice, 129 Strain
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Mice, Inbred C57BL
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Neural Pathways / drug effects
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Neural Pathways / physiopathology
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Prefrontal Cortex / drug effects
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Prefrontal Cortex / physiopathology*
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Psychotropic Drugs / pharmacology*
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Receptors, AMPA / metabolism
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Receptors, N-Methyl-D-Aspartate / metabolism
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Stress, Psychological / drug therapy
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Stress, Psychological / physiopathology*
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Synapses / drug effects
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Synapses / physiology
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Synaptic Transmission / drug effects
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Synaptic Transmission / physiology
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Tissue Culture Techniques
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Visual Perception
Substances
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Psychotropic Drugs
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Receptors, AMPA
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Receptors, N-Methyl-D-Aspartate
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Glutamic Acid
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Ketamine