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Functional diversity of dopamine axons in prefrontal cortex during classical conditioning.
Abe, Kenta; Kambe, Yuki; Majima, Kei; Hu, Zijing; Ohtake, Makoto; Momennezhad, Ali; Izumi, Hideki; Tanaka, Takuma; Matunis, Ashley; Stacy, Emma; Itokazu, Takahide; Sato, Takashi R; Sato, Tatsuo.
Afiliação
  • Abe K; Department of Neuroscience, Medical University of South Carolina, Charleston, United States.
  • Kambe Y; Department of Pharmacology, Kagoshima University, Kagoshima, Japan.
  • Majima K; Institute for Quantum Life Science, National Institutes for Quantum Science and Technology, Chiba, Japan.
  • Hu Z; Japan Science and Technology PRESTO, Saitama, Japan.
  • Ohtake M; Department of Physiology, Monash University, Clayton, Australia.
  • Momennezhad A; Neuroscience Program, Biomedicine Discovery Institute, Monash University, Clayton, Australia.
  • Izumi H; Department of Neuroscience, Medical University of South Carolina, Charleston, United States.
  • Tanaka T; Department of Pharmacology, Kagoshima University, Kagoshima, Japan.
  • Matunis A; Faculty of Data Science, Shiga University, Shiga, Japan.
  • Stacy E; Faculty of Data Science, Shiga University, Shiga, Japan.
  • Itokazu T; Department of Neuroscience, Medical University of South Carolina, Charleston, United States.
  • Sato TR; Department of Biology, College of Charleston, Charleston, United States.
  • Sato T; Department of Neuro-Medical Science, Osaka University, Osaka, Japan.
Elife ; 122024 May 15.
Article em En | MEDLINE | ID: mdl-38747563
ABSTRACT
Midbrain dopamine neurons impact neural processing in the prefrontal cortex (PFC) through mesocortical projections. However, the signals conveyed by dopamine projections to the PFC remain unclear, particularly at the single-axon level. Here, we investigated dopaminergic axonal activity in the medial PFC (mPFC) during reward and aversive processing. By optimizing microprism-mediated two-photon calcium imaging of dopamine axon terminals, we found diverse activity in dopamine axons responsive to both reward and aversive stimuli. Some axons exhibited a preference for reward, while others favored aversive stimuli, and there was a strong bias for the latter at the population level. Long-term longitudinal imaging revealed that the preference was maintained in reward- and aversive-preferring axons throughout classical conditioning in which rewarding and aversive stimuli were paired with preceding auditory cues. However, as mice learned to discriminate reward or aversive cues, a cue activity preference gradually developed only in aversive-preferring axons. We inferred the trial-by-trial cue discrimination based on machine learning using anticipatory licking or facial expressions, and found that successful discrimination was accompanied by sharper selectivity for the aversive cue in aversive-preferring axons. Our findings indicate that a group of mesocortical dopamine axons encodes aversive-related signals, which are modulated by both classical conditioning across days and trial-by-trial discrimination within a day.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Axônios / Córtex Pré-Frontal / Condicionamento Clássico / Neurônios Dopaminérgicos Limite: Animals Idioma: En Revista: Elife Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Axônios / Córtex Pré-Frontal / Condicionamento Clássico / Neurônios Dopaminérgicos Limite: Animals Idioma: En Revista: Elife Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos