Burst-to-burst information resetting in sequential rhythmic neural activity

In multiple neural systems, networks of bursting neurons generate and coordinate robust sequential rhythms, such as those observed in central pattern generators (CPGs) that control motor activity. In this paper, we combine electrophysiological experiments and biophysical models of the pyloric CPG to investigate cycle-by-cycle coordination resetting in sequential rhythms. In particular, we focus our analysis on the variability constraints of sequence intervals defined by the burst onset and offset time references, which structure the timing of the rhythmic CPG sequence cycle-by-cycle. We identified the conditions under which sequential dynamical invariants emerge as robust relationships between specific intervals within the same cycle, and when such relations reset at each cycle or extend between intervals of consecutive cycles. Our results help understand the mechanisms underlying the autonomous cycle-by-cycle sequential coordination and the relationships between intervals from consecutive cycles when a slow modulatory action establishes a common trend across the rhythm.

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Journal
PLoS Computational Biology
Published
2026-11-11
DOI
https://doi.org/10.1371/journal.pcbi.1014953
Primary Topic
Neural dynamics and brain function
Type
article
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article

Burst-to-burst information resetting in sequential rhythmic neural activity

Francisco B. Rodrı́guez, Rafael Levi, P. Terradillos Sánchez, Alicia Garrido-Peña et al.
PLoS Computational Biology
Neural dynamics and brain function
article

Burst-to-burst information resetting in sequential rhythmic neural activity

Francisco B. Rodrı́guez, Rafael Levi, P. Terradillos Sánchez, Alicia Garrido-Peña, Carlos García-Saura, Irene Elices, Pablo Varona
article en

Abstract

In multiple neural systems, networks of bursting neurons generate and coordinate robust sequential rhythms, such as those observed in central pattern generators (CPGs) that control motor activity. In this paper, we combine electrophysiological experiments and biophysical models of the pyloric CPG to investigate cycle-by-cycle coordination resetting in sequential rhythms. In particular, we focus our analysis on the variability constraints of sequence intervals defined by the burst onset and offset time references, which structure the timing of the rhythmic CPG sequence cycle-by-cycle. We identified the conditions under which sequential dynamical invariants emerge as robust relationships between specific intervals within the same cycle, and when such relations reset at each cycle or extend between intervals of consecutive cycles. Our results help understand the mechanisms underlying the autonomous cycle-by-cycle sequential coordination and the relationships between intervals from consecutive cycles when a slow modulatory action establishes a common trend across the rhythm.

PLoS Computational BiologyVol. 22(11)
Universidad Autónoma de Madrid (ES)
Neural dynamics and brain function
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