ArticleJournal of neurophysiology2015
A model of order-selectivity based on dynamic changes in the balance of excitation and inhibition produced by short-term synaptic plasticity.
Article in Journal of neurophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Induction and propagation of transient synchronous activity in neural networks endowed with short-term plasticity.Cognitive neurodynamics · 2021Article
- The Adaptation Model Offers a Challenge for the Predictive Coding Account of Mismatch Negativity.Frontiers in human neuroscience · 2021Article
- Differential Short-Term Plasticity of PV and SST Neurons Accounts for Adaptation and Facilitation of Cortical Neurons to Auditory Tones.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020Article
- Attractor-state itinerancy in neural circuits with synaptic depression.Journal of mathematical neuroscience · 2020Article
- Sensory Stream Adaptation in Chaotic Networks.Scientific reports · 2017Article
- Diverse effects of stimulus history in waking mouse auditory cortex.Journal of neurophysiology · 2017Article
- Article
- Dynamic balance of excitation and inhibition rapidly modulates spike probability and precision in feed-forward hippocampal circuits.Journal of neurophysiology · 2016Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Determining the order of sensory events separated by a few hundred milliseconds is critical to many forms of sensory processing, including vocalization and speech discrimination. Although many experimental studies have recorded from auditory order-sensitive and order-selective neurons, the underlying mechanisms are poorly understood. Here we demonstrate that universal properties of cortical synapses-short-term synaptic plasticity of excitatory and inhibitory synapses-are well suited for the generation of order-selective neural responses. Using computational models of canonical disynaptic circuits, we show that the dynamic changes in the balance of excitation and inhibition imposed by short-term plasticity lead to the generation of order-selective responses. Parametric analyses predict that among the forms of short-term plasticity expressed at excitatory-to-excitatory, excitatory-to-inhibitory, and inhibitory-to-excitatory synapses, the single most important contributor to order-selectivity is the paired-pulse depression of inhibitory postsynaptic potentials (IPSPs). A topographic model of the auditory cortex that incorporates short-term plasticity accounts for both context-dependent suppression and enhancement in response to paired tones. Together these results provide a framework to account for an important computational problem based on ubiquitous synaptic properties that did not yet have a clearly established computational function. Additionally, these studies suggest that disynaptic circuits represent a fundamental computational unit that is capable of processing both spatial and temporal information.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.