Evidence map›Paper›PMID 27549764›Full record

ArticleJournal of mathematical biology2017

Homeostatic dynamics, hysteresis and synchronization in a low-dimensional model of burst suppression.

Sensen Liu, ShiNung Ching

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Article in Journal of mathematical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Quiescence during burst suppression and postictal generalized EEG suppression are distinct patterns of activity.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Network dynamics in the healthy and epileptic developing brain.Network neuroscience (Cambridge, Mass.) · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Sensen LiuDepartment of Electrical and Systems Engineering, Washington University in St. Louis, St. Louis, MO, 63130, USA.
ShiNung ChingDepartment of Electrical and Systems Engineering, Division of Biology and Biomedical Sciences, Washington University in St. Louis, St. Louis, MO, 63130, USA. shinung@ese.wustl.edu.
Washington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Burst suppression, a pattern of the electroencephalogram characterized by quasi-periodic alternation of high-voltage activity (burst) and isoelectric silence (suppression), is typically associated with states of unconsciousness, such as in deep general anesthesia and certain etiologies of coma. Recent computational models for burst suppression have attributed the slow (up to tens of seconds) time-scale of burst termination and re-initiation to cycling in supportive physiological process, such as cerebral metabolism. That is, activity-dependent substrate ('energy') depletion during bursts, followed by substrate recovery during suppression. Such a model falls into the category of a fast-slow dynamical system, commonly used to describe neuronal bursting more generally. Here, following this basic paradigm, we develop a low dimensional mean field model for burst suppression that adds several new features and capabilities to previous models. Most notably, this new model includes explicit homeostatic interactions wherein the rates of substrate recovery are tied to neuronal activity in a supply demand loop, creating a physiologically consistent, reciprocal interaction between the neural and substrate processes. We develop formal analysis of the model dynamics, showing, in particular, the capability of the model to produce burst-like activity as a consequence of neuronal downregulation only, without any direct perturbation to the substrate dynamics. Further, we use a synchronization analysis to contrast different mechanisms for spatially local versus global bursting. The analysis performed generates characterizations that are consistent with experimental observations of spatiotemporal features such as burst onset, duration, and spatial organization and, moreover, generates predictions regarding the presence of bistability and hysteresis in the underlying system. Thus, the model provides new dynamical insight into the mechanisms of burst suppression and, moreover, a tractable platform for more detailed future characterizations.

Indexed as

Models, NeurologicalCortical SynchronizationElectroencephalographyHomeostasisHumansNeuronsBurst suppressionBurst synchronizationHomeostasisHysteresisMean field modelMetabolism

Identifiers

PMID27549764
OpenAlexW2509940611

What OpenQuestion holds

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Registered trials

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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.