Evidence map›Paper›PMID 22658080›Full record

ArticleJournal of mathematical neuroscience2012

Explicit maps to predict activation order in multiphase rhythms of a coupled cell network.

Jonathan E Rubin, David Terman

Abstract read
In one paragraph

Article in Journal of mathematical neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Jonathan E RubinDepartment of Mathematics, University of Pittsburgh, Pittsburgh, PA, 15260, USA. jonrubin@pitt.edu.
David Terman

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a novel extension of fast-slow analysis of clustered solutions to coupled networks of three cells, allowing for heterogeneity in the cells' intrinsic dynamics. In the model on which we focus, each cell is described by a pair of first-order differential equations, which are based on recent reduced neuronal network models for respiratory rhythmogenesis. Within each pair of equations, one dependent variable evolves on a fast time scale and one on a slow scale. The cells are coupled with inhibitory synapses that turn on and off on the fast time scale. In this context, we analyze solutions in which cells take turns activating, allowing any activation order, including multiple activations of two of the cells between successive activations of the third. Our analysis proceeds via the derivation of a set of explicit maps between the pairs of slow variables corresponding to the non-active cells on each cycle. We show how these maps can be used to determine the order in which cells will activate for a given initial condition and how evaluation of these maps on a few key curves in their domains can be used to constrain the possible activation orders that will be observed in network solutions. Moreover, under a small set of additional simplifying assumptions, we collapse the collection of maps into a single 2D map that can be computed explicitly. From this unified map, we analytically obtain boundary curves between all regions of initial conditions producing different activation patterns.

Identifiers

PMID22658080
PMCPMC3489566

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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.