<p>Aversive signals such as pain serve an instructive role in aversive learning to promote animal survival. While negative valence of aversive signals is considered to be innately assigned, the valence can be scaled by internal state and previous experiences. However, the neuronal mechanisms underlying state and experience-dependent valence modulation remain unexplored. Previous studies demonstrated synaptic potentiation in instructive signal pathways following robust aversive learning. Here, we hypothesized that long-term potentiation (LTP) in the parabrachial-to-central amygdala (PB-CeC/L) pathway, an important nociceptive circuit for producing pain and emotional learning, enhances the negative valence and thereby alter future learning rules. To test this hypothesis, we developed pathway-specific in vivo LTP induction methods and mathematical models. Our results suggest that LTP in the PB-CeC/L pathway alters aversive valence and future learning rules by enhancing subsequent learning and memory generalization. These results may help to identify a therapeutic target for post-traumatic stress disorder.</p>

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Aversive experiences induce valence plasticity of instructive signals to change future learning rules in mice

  • Suguru Tohyama,
  • Takashi Nagashima,
  • Iori Higashino,
  • Fumiko Arima-Yoshida,
  • Kanae Hiyoshi,
  • Masashi Nagase,
  • Yuichiro Yada,
  • Naoki Honda,
  • Ayako M. Watabe

摘要

Aversive signals such as pain serve an instructive role in aversive learning to promote animal survival. While negative valence of aversive signals is considered to be innately assigned, the valence can be scaled by internal state and previous experiences. However, the neuronal mechanisms underlying state and experience-dependent valence modulation remain unexplored. Previous studies demonstrated synaptic potentiation in instructive signal pathways following robust aversive learning. Here, we hypothesized that long-term potentiation (LTP) in the parabrachial-to-central amygdala (PB-CeC/L) pathway, an important nociceptive circuit for producing pain and emotional learning, enhances the negative valence and thereby alter future learning rules. To test this hypothesis, we developed pathway-specific in vivo LTP induction methods and mathematical models. Our results suggest that LTP in the PB-CeC/L pathway alters aversive valence and future learning rules by enhancing subsequent learning and memory generalization. These results may help to identify a therapeutic target for post-traumatic stress disorder.