Computational Advances in Taste Perception: From Ion Channels to Neural Coding

Recent advances in computational neuroscience demand models that balance biophysical realism with scalability. We present a hybrid neuron model combining the biophysical fidelity of Hodgkin-Huxley (HH) dynamics for taste receptor cells with the computational efficiency of Izhikevich spiking neurons for large-network simulations. Our framework incorporates biomorphic taste cell models, featuring modality-specific receptor dynamics (T1R/T2R, ENaC, PKD) and Goldman-Hodgkin-Katz (GHK)-driven ion currents to accurately simulate gustatory transduction. Synaptic interactions are modeled via glutamate release kinetics with alpha-function profiles, AMPA receptor trafficking regulated by phosphorylation, and spike-timing-dependent plasticity (STDP) to enforce temporal coding. At the network level, we optimize multiscale learning, leveraging both temporal spike synchrony (van Rossum metrics) and combinatorial population coding (rank-order patterns). This approach bridges single-cell biophysics with ensemble-level computation, enabling efficient simulation of gustatory pathways while retaining biological fidelity.

Publication Details

Journal
ArXiv.org
Published
2025-09-16
Primary Topic
EFL/ESL Teaching and Learning
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article
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article

Computational Advances in Taste Perception: From Ion Channels to Neural Coding

ArXiv.org
EFL/ESL Teaching and Learning
article

Computational Advances in Taste Perception: From Ion Channels to Neural Coding

article en

Abstract

Recent advances in computational neuroscience demand models that balance biophysical realism with scalability. We present a hybrid neuron model combining the biophysical fidelity of Hodgkin-Huxley (HH) dynamics for taste receptor cells with the computational efficiency of Izhikevich spiking neurons for large-network simulations. Our framework incorporates biomorphic taste cell models, featuring modality-specific receptor dynamics (T1R/T2R, ENaC, PKD) and Goldman-Hodgkin-Katz (GHK)-driven ion currents to accurately simulate gustatory transduction. Synaptic interactions are modeled via glutamate release kinetics with alpha-function profiles, AMPA receptor trafficking regulated by phosphorylation, and spike-timing-dependent plasticity (STDP) to enforce temporal coding. At the network level, we optimize multiscale learning, leveraging both temporal spike synchrony (van Rossum metrics) and combinatorial population coding (rank-order patterns). This approach bridges single-cell biophysics with ensemble-level computation, enabling efficient simulation of gustatory pathways while retaining biological fidelity.

ArXiv.org
Openalex Percentile: Top 36%
EFL/ESL Teaching and Learning
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