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Richard Bertram

Publications and source records attributed to Richard Bertram.

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A Persistent Homology Pipeline for the Analysis of Neural Spike Train Data

In this article, we introduce a Topological Data Analysis (TDA) pipeline for neural spike train data. Understanding how the brain transforms sensory information into perception and behavior requires analyzing coordinated neural population activity. Modern electrophysiology enables simultaneous recording of spike train ensembles, but extracting meaningful information from these datasets remains a central challenge in neuroscience. A fundamental question is how ensembles of neurons discriminate between different stimuli or behavioral states, particularly when individual neurons exhibit weak or no stimulus selectivity, yet their coordinated activity may still contribute to network-level encoding. We describe a TDA framework that identifies stimulus-discriminative structure in spike train ensembles recorded from the mouse insular cortex during presentation of deionized water stimuli at distinct non-nociceptive temperatures. We show that population-level topological signatures effectively differentiate oral thermal stimuli even when individual neurons provide little or no discrimination. These findings demonstrate that ensemble organization can carry perceptually relevant information that standard single-unit analysis may miss. The framework builds on a mathematical representation of spike train ensembles that enables persistent homology to be applied to collections of point processes. At its core is the widely-used Victor-Purpura (VP) distance. Using this metric, we construct persistence-based descriptors that capture multiscale topological features of ensemble geometry. Two key theoretical results support the method: a stability theorem establishing robustness of persistent homology to perturbations in the VP metric parameter, and a probabilistic stability theorem ensuring robustness of topological signatures.

stat.ME

Dynamic homeostasis in relaxation and bursting oscillations

Homeostasis, broadly speaking, refers to the maintenance of a stable internal state when faced with external stimuli. Failure to manage these regulatory processes can lead to different diseases or death. Most physiologists and cell biologists around the world agree that homeostasis is a fundamental tenet of their disciplines. Nevertheless, a precise definition of homeostasis is hard to come by. Often times, homeostasis is simply defined as ``you know it when you see it''. Mathematical treatments of homeostasis involve studying equilibria of dynamical systems that are relatively invariant with respect to parameters. However, physiological processes are rarely static and often involve dynamic processes such as oscillations. In such dynamic environments, quantities such as average values may be relatively invariant with respect to parameters. This has been referred to as ``homeodynamics''. We present a general framework for homeodynamics involving systems with two or more time scales that elicits homeostasis in the temporal average of a species. The key point is that homeostasis manifests when measuring the slow variable responsible for driving oscillations and is not apparent in the fast variables. We demonstrate this in the Fitzhugh-Nagumo model for relaxation oscillations and then in two models for electrical bursting activity and calcium oscillations in pancreatic $\beta$-cells. One of these models has multiple slow variables, each driving the bursting oscillations in different parameter regimes, but homeodynamics is only present in the variable currently engaged in this role.

math.DS

Why Pacing Frequency Affects the Production of Early Afterdepolarizations in Cardiomyocytes: An Explanation Revealed by Slow/Fast Analysis of a Minimal Model

Early afterdepolarizations (EADs) are pathological voltage oscillations in cardiomyocytes that have been observed in response to a number of pharmacological agents and disease conditions. EADs are small voltage fluctuations that occur during the plateau of an action potential. Although a single-cell behavior, EADs can lead to tissue-level arrhythmias, including ventricular tachycardia. Much is currently known about the biophysical mechanisms (i.e., the roles of ion channels and intracellular calcium stores) for EADs, due partially to the development and analysis of mathematical models. This includes the application of slow/fast analysis, which takes advantage of timescale separation inherent in the system to simplify its analysis. We take this further, using a minimal 3D model to demonstrate that the phase-2 EADs are canards that are formed in the neighborhood of a folded node singularity. This knowledge allows us to determine the number of EADs that can be produced for a given parameter set without performing computer simulations, and provides guidance on parameter changes that can facilitate or inhibit EAD production. With this approach, we demonstrate why periodic stimulation, as would occur in an intact heart, preferentially facilitates EAD production when applied at low frequencies,. We also explain the origin of complex alternan dynamics that can occur with intermediate-frequency stimulation, in which varying numbers of EADs are produced with each stimulation. These revelations fall out naturally from an understanding of folded node singularities, but are hard or impossible to glean from a knowledge of the biophysical mechanism for EADs alone. Therefore, an understanding of the canard mechanism is a useful complement to an understanding of the biophysical mechanism that has been developed over years of experimental and computational investigations.

q-bio.TO