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Sitzia, G.

Publications and source records attributed to Sitzia, G..

3 recordsLinked to original sources

Motor cortex somatostatin interneurons adaptively shape the structure of motor sequences

The brain can flexibly reorganize the structure of action sequence, or motor programs, to efficiently reach positive outcomes. These behavioral adaptations are primarily driven by reinforcement learning, leading to structural and kinematic modifications of consolidated motor programs. While the motor cortex is recognized as a crucial neural substrate for adaptive motor control and skill learning, the mechanisms by which cortical microcircuits actively fine-tune the timing and structure of action sequences, enabling organisms to adaptively maintain motor efficiency across varying task demands, remain unclear. Here, we found that the calcium activity of somatostatin (SST) interneurons (INs) in the primary motor cortex (M1) exhibits highly action-locked and synchronized calcium responses during the acquisition of a single lever-press task in freely moving mice. This neural representation contrasts with the sequential activation of pyramidal (PYR) neurons during the same task. After extended training with a consistent schedule and subsequent motor consolidation, M1 SST IN activity was no longer related to action execution. However, when the training schedule was progressively updated, leading mice to adapt their motor programs for more time-constrained, rapid action sequences, the action-related SST IN activity redistributed and did not decrease. Notably, this redistributed calcium activity of M1 SST INs correlated with structural modulation of ongoing action sequences. We identified two distinct neural activity patterns among non-overlapping SST IN populations: one encoding the initiation of action sequences and the other encoding trial-by-trial structural changes during the execution of complex action sequences. Moreover, inhibition of SST INs disrupted temporal structure of action sequences and decreased the efficiency of motor program execution. These findings highlight the unexpected role of M1 SST interneurons in actively refining motor programs into more efficient and task-specific structures. HIGHLIGHTSO_LIActivation of somatostatin (SST) interneurons in the primary motor cortex (M1) correlates with learning new motor actions and execution of complex motor programs. C_LIO_LIDistinct activity patterns of M1 SST interneurons actively encode the initiation and temporal structure of complex action sequences on a trial-by-trial basis C_LIO_LIInhibition of SST interneuron activity leads to inefficient execution of complex motor programs, with effects dependent on task specificity. C_LI

neuroscience↗

Chronic alcohol induces subcircuit-specific striatonigral plasticity shifting action control to the sensorimotor striatum

While cortico-striatal circuit deficits contribute to Alcohol Use Disorder, the impact of alcohol on synaptic function in the basal ganglia output, the substantia nigra pars reticulata (SNr), remains unclear. Here, we found that the inputs from the dorsomedial (DMS) and dorsolateral striatum (DLS) differ in their presynaptic properties and target molecularly distinct subpopulations of SNr neurons. We also discovered that indirect pathway subthalamic (STN) inputs to the medial and lateral SNr have different presynaptic properties and that STN inputs are stronger in the lateral SNr. Chronic alcohol exposure (CIE) potentiated DLS inputs but did not affect the strength and presynaptic release properties of DMS and subthalamic inputs to SNr neurons. Chemogenetic inhibition of DLS direct pathway projection neurons impaired action performance in an operant conditioning task in CIE mice but not control mice. Overall, our work identifies a synaptic mechanism whereby chronic alcohol induces a gain of function for action control in direct pathway neurons in the dorsolateral striatum. TeaserChronic alcohol selectively potentiates DLS synaptic inputs to the SNr, enhancing their role in action control.

neuroscience↗

Distinct mechanisms of CB1 and GABAB receptor presynaptic modulation of striatal indirect pathway projections to mouse Globus Pallidus

Presynaptic modulation is a fundamental process regulating synaptic transmission. Striatal indirect pathway projections originate from A2A- expressing spiny projection neurons (iSPNs), targeting the globus pallidus external segment (GPe) and control the firing of the tonically active GPe neurons via GABA release. It is unclear if and how the presynaptic GPCRs, GABAB and CB1 receptors, modulate iSPN-GPe projections. Here we used an optogenetic platform to study presynaptic Ca2+ and GABAergic transmission at iSPN projections, using a genetic strategy to express the calcium sensor GCaMP6f or the excitatory channelrhodopsin (hChR2) on iSPNs. We found that P/Q-type calcium channels are the primary VGCC-subtype controlling presynaptic calcium and GABA release at iSPN-GPe projections. N-type and L-type VGCCs contribute to GABA release at iSPN-GPe synapses. GABAB receptor activation resulted in a reversible inhibition of presynaptic Ca2+ transients (PreCaTs) and an inhibition of GABAergic transmission at iSPN-GPe synapses. CB1 receptor activation did not inhibit PreCaTs while inhibiting GABAergic transmission at iSPN-GPe projections. CB1 effects on GABAergic transmission persisted in experiments where NaV and KV1 were blocked, indicating a VGCC- and KV1 independent presynaptic mechanism of action of CB1 receptors. Taken together, presynaptic modulation of iSPN-GPe projections by CB1 and GABAB receptors is mediated by distinct mechanisms. Key PointsP/Q-type are the predominant VGCC controlling presynaptic Ca2+ and GABA release on the striatal indirect pathway projections GABAB receptor modulate of iSPN-GPe projections via a VGCC- dependent mechanism CB1 receptors modulate iSPN-GPe projections via a VGCC- independent mechanism

neuroscience↗