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Sato, T. R.

Publications and source records attributed to Sato, T. R..

2 recordsLinked to original sources

A design principle of slow-wave sleep firing pattern with Na+ dynamics

Non-rapid eye movement (NREM) sleep is characterized by electroencephalography (EEG) signals with high amplitude and low frequency. This signal is thought to originate from the synchronized activity of cortical neurons, showing the alternating bursting state (up state) and resting state (down state). This activity is termed as slow-wave sleep (SWS) firing pattern. We previously proposed the importance of Ca2+-dependent hyperpolarization pathway in generating this firing pattern by introducing the averaged-neuron (AN) model, which describes neuronal activity based on the Hodgkin-Huxley type model. In the AN model, Ca2+-dependent K+ channels are involved in the transition from the up to the down state. Here we focus on the intracellular Na+ dynamics which are not explicitly described in the AN model. A revised AN model, termed as Na+-centered AN (NAN) model, proposes that the activation of voltage-gated Na+ channels leads to intracellular Na+ accumulation, which in turn triggers the activation of Na+-dependent K+ (KNa) channels or Na+/K+ ATPases, resulting in the down state. Changes in the activation kinetics of voltage-gated Na+ channels are important in shaping SWS firing pattern as well as explaining the inter-spike interval changes between SWS and AWAKE firing pattern. Mathematically, transition from the up state to the down state occurs in accordance with the change in the number of the fixed point in the dynamical system with the changes in the intracellular Na+ concentration. The importance of Na+-dependent pathway is elucidated even with the coexistence of Ca2+-dependent pathway. Subsequent analysis with network model suggests that the result of averaged neuron model with Na+ pathway can be extended to the population of neurons. Therefore, our model proposes that voltage-gated Na+ channels and Na+-dependent K+ channels or Na+/K+ ATPases are also the candidate pathways for the generation of SWS firing pattern.

systems biology↗

Enhanced Aversive Signals During Classical Conditioning in Dopamine Axons in Medial Prefrontal Cortex

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. Impact statementTwo-photon calcium imaging revealed that many mesocortical dopamine axons show enhanced selectivity for aversive cue processing during classical conditioning.

neuroscience↗