AI Article Synopsis

  • Fear learning is crucial for survival, but traumatic experiences can lead to excessive fear responses, as seen in PTSD, through abnormal fear consolidation and overgeneralization.* -
  • Research examined the role of adenosine A receptors (AR) in fear memory; blocking these receptors after fear conditioning increased fear generalization, while activating them reduced it.* -
  • Findings indicate that ARs influence long-term potentiation in key brain areas during fear consolidation, suggesting they could be a target for treatments addressing fear-related disorders like PTSD.*

Article Abstract

Fear learning is essential to survival, but traumatic events may lead to abnormal fear consolidation and overgeneralization, triggering fear responses in safe environments, as occurs in post-traumatic stress disorder (PTSD). Adenosine A receptors (AR) control emotional memory and fear conditioning, but it is not known if they affect the consolidation and generalization of fear, which was now investigated. We now report that AR blockade through systemic administration of the AR antagonist SCH58261 immediately after contextual fear conditioning (within the consolidation window), accelerated fear generalization. Conversely, AR activation with CGS21680 decreased fear generalization. Ex vivo electrophysiological recordings of field excitatory post-synaptic potentials (fEPSPs) in CA3-CA1 synapses and of population spikes in the lateral amygdala (LA), showed that the effect of SCH58261 is associated with a reversion of fear conditioning-induced decrease of long-term potentiation (LTP) in the dorsal hippocampus (DH) and with increased amplitude of LA LTP in conditioned animals. These data suggest that AR are engaged during contextual fear consolidation, controlling long-term potentiation mechanisms in both DH and LA during fear consolidation, impacting on fear generalization; this supports targeting AR during fear consolidation to control aberrant fear processing in PTSD and other fear-related disorders.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570294PMC
http://dx.doi.org/10.1038/s41398-023-02613-0DOI Listing

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