Short term depression shapes information transmission in a constitutively active GABAergic synapse
Abstract
Short-term depression is a low pass filter of synaptic information that reduces and flattens synaptic information transfer at high presynaptic firing frequencies. This view questions the relevance of spontaneous high firing rates in some networks. In the indirect pathway of the basal ganglia, spontaneously active neurons in the globus pallidus (GP) form depressing inhibitory synapses in the basal ganglia output nuclei. Using numerical modeling and whole-cell recordings from single entopeduncular nucleus (EP) neurons in rat brain slices we investigated the contribution of the different firing rates of GP neurons to information transmission in the indirect pathway. Wholecell recordings showed significant variability in steady-state depression which decreased as stimulation frequency increased. Modeling predicted that this variability would translate into different postsynaptic noise levels during constitutive presynaptic activity. Our simulations further predicted that individual GP-EP synapses mediate gain control. However, when we consider integration of multiple inputs, the large range of GP firing rates would enable different modes of information transmission in which the magnitude and temporal features of postsynaptic modulation would change as a function of present and past firing rates of GP neurons. Finally, we predict that changes in dopamine levels can shift the action of GP neurons from rate coding to gain modulation. Our results thus demonstrate how short-term synaptic depression shapes information transmission in the basal ganglia in particular and via GABAergic synapses in general.\n\nSignificant statementSynapses displaying short-term depression are low-pass filters of synaptic input. Consequently, when presynaptic firing is high, little information passes to the postsynaptic neuron. However, many neurons fire at relatively high frequencies all the time. Are their synapses constantly silenced by depression? We tested this apparent contradiction in the indirect pathway of the basal ganglia, where neurons from the globus pallidus (GP) form constitutively active depressing synapses on basal ganglia output. We hypothesized that the different rates of ongoing activity underlie different modes of action for GP neurons. We show that the synaptic and structural properties of the indirect pathway map GP baseline frequencies to different postsynaptic signals, thus demonstrating how short-term synaptic depression shapes information transmission in the basal ganglia.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 13
- FWCI
- 0.60
- Field percentile
- top 39%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Short-term plasticity at Purkinje to deep cerebellar nuclear neuron synapses supports a slow gain-control mechanism enabling scaled linear encoding over second-long time windows
Christine M. Pedroarena·bioRxiv·Aug 29, 2019
- Opposing regulation of short-term memory by basal ganglia direct and indirect pathways that are coactive during behavior
Yingjun Tang, Hongjiang Yang, … Zengcai V. Guo·bioRxiv·Dec 15, 2021
- Transient response of basal ganglia network in healthy and low-dopamine state
Kingshuk Chakravarty, Sangheeta Roy, … Arvind Kumar·eNeuroPeer-reviewed·Feb 9, 2022
- Gamma oscillations in basal ganglia stem from the interplay between local inhibition and beta synchronization
Federico Fattorini, Mahboubeh Ahmadipour, … Nicolò Meneghetti·bioRxiv·Mar 19, 2025
- Tonic GABAA conductance favors temporal over rate coding in the rat hippocampus
Yulia Dembitskaya, Yu‐Wei Wu, Alexey V. Semyanov·bioRxiv·Aug 19, 2019
- Differential Synaptic Input to External Globus Pallidus Neuronal Subpopulations In Vivo.
Maya Ketzef, Gilad Silberberg·NeuronPeer-reviewed·Nov 27, 2020