Evidence map›Paper›PMID 21708954›Full record

ArticleThe Journal of general physiology2011

Time-dependent changes in membrane excitability during glucose-induced bursting activity in pancreatic β cells.

Chae Young Cha, Enrique Santos, Akira Amano, Takao Shimayoshi, Akinori Noma

Abstract read
In one paragraph

Article in The Journal of general physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

18 citing papers in PubMed.

  1. Review
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  18. Dynamical systems theory in physiology.The Journal of general physiology · 2011
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Chae Young ChaBiosimulation Project, Ritsumeikan University, Kusatsu, Shiga, Japan.
Enrique Santos
Akira Amano
Takao Shimayoshi
Akinori Noma

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In our companion paper, the physiological functions of pancreatic β cells were analyzed with a new β-cell model by time-based integration of a set of differential equations that describe individual reaction steps or functional components based on experimental studies. In this study, we calculate steady-state solutions of these differential equations to obtain the limit cycles (LCs) as well as the equilibrium points (EPs) to make all of the time derivatives equal to zero. The sequential transitions from quiescence to burst-interburst oscillations and then to continuous firing with an increasing glucose concentration were defined objectively by the EPs or LCs for the whole set of equations. We also demonstrated that membrane excitability changed between the extremes of a single action potential mode and a stable firing mode during one cycle of bursting rhythm. Membrane excitability was determined by the EPs or LCs of the membrane subsystem, with the slow variables fixed at each time point. Details of the mode changes were expressed as functions of slowly changing variables, such as intracellular [ATP], [Ca(2+)], and [Na(+)]. In conclusion, using our model, we could suggest quantitatively the mutual interactions among multiple membrane and cytosolic factors occurring in pancreatic β cells.

Indexed as

Action PotentialsAdenosine TriphosphateCell MembraneCytosolGlucoseInsulin-Secreting CellsMembrane PotentialsTime FactorsAdenosine TriphosphateGlucose

Identifiers

PMID21708954
PMCPMC3137027

What Socratic holds

Textmetadata
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Registered trials

None linked

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 Socratic graph.