<p>Understanding how the brain evaluates aversion and appetition to guide behavior is an important question. Here, we investigated the role of dopamine signaling in the tail of the striatum (TS) in regulating competing valence-based behaviors and learning. TS dopamine dynamics were monitored as mice performed a classical conditioning task in which an odor cue predicted either an aversive air puff or a water reward. Initially, mice exhibited anticipatory blinking, which diminished over time, while anticipatory licking emerged later, coinciding with adaptation to the air puff. Dopamine responses in the TS to the air puff and its associated odor were initially elevated but declined with repeated exposure. Ablation of TS dopamine inhibited avoidance learning and accelerated appetitive learning. Optogenetic disruption of dopaminergic decline suppressed adaptation and hindered appetitive learning. These findings demonstrate that TS dopamine dynamics are essential for avoidance and adaptation to aversive stimuli, which indirectly modulates appetitive learning, underscoring a regulatory mechanism for shifting between defensive and reward-seeking behaviors.</p><p></p>

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Dopamine dynamics as a regulatory mechanism for shifting between defensive and reward-seeking behaviors

  • Ryota Tsuruga,
  • Yu Tajika,
  • Masabumi Minami,
  • Iku Tsutsui-Kimura

摘要

Understanding how the brain evaluates aversion and appetition to guide behavior is an important question. Here, we investigated the role of dopamine signaling in the tail of the striatum (TS) in regulating competing valence-based behaviors and learning. TS dopamine dynamics were monitored as mice performed a classical conditioning task in which an odor cue predicted either an aversive air puff or a water reward. Initially, mice exhibited anticipatory blinking, which diminished over time, while anticipatory licking emerged later, coinciding with adaptation to the air puff. Dopamine responses in the TS to the air puff and its associated odor were initially elevated but declined with repeated exposure. Ablation of TS dopamine inhibited avoidance learning and accelerated appetitive learning. Optogenetic disruption of dopaminergic decline suppressed adaptation and hindered appetitive learning. These findings demonstrate that TS dopamine dynamics are essential for avoidance and adaptation to aversive stimuli, which indirectly modulates appetitive learning, underscoring a regulatory mechanism for shifting between defensive and reward-seeking behaviors.