Information Content in Neuronal Calcium Spike Trains: Entropy Rate Estimation based on Empirical Probabilities

TL;DR

This paper introduces a new empirical probability-based entropy rate estimator for neuronal calcium spike trains, addressing nonstationarity and short interval encoding to better understand neural information processing and disease signatures.

Contribution

The paper presents a novel entropy rate estimation method tailored for short, nonstationary neuronal spike trains, improving accuracy and convergence over existing algorithms.

Findings

Proposed method outperforms Lempel-Ziv algorithms in accuracy and speed.

Detected structural heterogeneity in neuronal responses.

Facilitates large-scale analysis of neural information content.

Abstract

Quantification of information content and its temporal variation in intracellular calcium spike trains in neurons helps one understand functions such as memory, learning, and cognition. Such quantification could also reveal pathological signaling perturbation that potentially leads to devastating neurodegenerative conditions including Parkinson's, Alzheimer's, and Huntington's diseases. Accordingly, estimation of entropy rate, an information-theoretic measure of information content, assumes primary significance. However, such estimation in the present context is challenging because, while entropy rate is traditionally defined asymptotically for long blocks under the assumption of stationarity, neurons are known to encode information in short intervals and the associated spike trains often exhibit nonstationarity. Against this backdrop, we propose an entropy rate estimator based on empirical probabilities that operates within windows, short enough to ensure approximate stationarity. Specifically, our estimator, parameterized by the length of encoding contexts, attempts to model the underlying memory structures in neuronal spike trains. In an example Markov process, we compared the performance of the proposed method with that of versions of the Lempel-Ziv algorithm as well as with that of a certain stationary distribution method and found the former to exhibit higher accuracy levels and faster convergence. Also, in experimentally recorded calcium responses of four hippocampal neurons, the proposed method showed faster convergence. Significantly, our technique detected structural heterogeneity in the underlying process memory in the responses of the aforementioned neurons. We believe that the proposed method facilitates large-scale studies of such heterogeneity, which could in turn identify signatures of various diseases in terms of entropy rate estimates.