Evidence map›Paper›PMID 25322829›Full record

ReviewIslets2014

Mathematical models of electrical activity of the pancreatic β-cell: a physiological review.

Gerardo J Félix-Martínez, J Rafael Godínez-Fernández

Abstract readReview
In one paragraph

Review in Islets, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Mechanisms and Functions of Sweet Reception in Oral and Extraoral Organs.International journal of molecular sciences · 2024
    Review
  3. Review
  4. CaAmerican journal of physiology. Endocrinology and metabolism · 2023
    Review
  5. TRPC3 Regulates Islet Beta-Cell Insulin Secretion.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  6. A Review ofMolecules (Basel, Switzerland) · 2023
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Bayesian metamodeling of complex biological systems across varying representations.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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.

Gerardo J Félix-MartínezDepartment of Electrical Engineering; Universidad Autónoma Metropolitana-Iztapalapa ; México , DF , México.
J Rafael Godínez-FernándezDepartment of Electrical Engineering; Universidad Autónoma Metropolitana-Iztapalapa ; México , DF , México.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mathematical modeling of the electrical activity of the pancreatic β-cell has been extremely important for understanding the cellular mechanisms involved in glucose-stimulated insulin secretion. Several models have been proposed over the last 30 y, growing in complexity as experimental evidence of the cellular mechanisms involved has become available. Almost all the models have been developed based on experimental data from rodents. However, given the many important differences between species, models of human β-cells have recently been developed. This review summarizes how modeling of β-cells has evolved, highlighting the proposed physiological mechanisms underlying β-cell electrical activity.

Indexed as

Models, BiologicalAnimalsCalciumComputer SimulationGlucoseHumansInsulinInsulin-Secreting CellsInsulin SecretionPotassium ChannelsCalciumGlucoseInsulinPotassium Channelsaction potentialsADP, adenosine diphosphateATP, adenosine triphosphate[ATP]i, cytosolic ATPburstingCa2+, calcium ions[Ca2+]i, intracellular calcium concentration[Ca2+]m, mitochondrial calciumcalciumcAMP, cyclic AMPCK, Chay-KeizerCRAC, calcium release-activated currentDOM, dual oscillator modelelectrical activityER, endoplasmic reticulumF6P, fructose-6-phosphateFBP, fructose-1,6-bisphosphateGLUT, glucose transporterGSIS, glucose-stimulated insulin secretionHERG, human eter à-go-go related geneion channelsIP3R, inositol-1,4,5-trisphosphate receptorsKATP, ATP-sensitive K+ channelsKCa, Ca2+-dependent K+ channelsKv, voltage-dependent K+ channelsmathematical modelMCU, mitochondrial Ca2+ uniportermNCX, mitochondrial Na+/Ca2+ exchanger[Na+], Na+ concentrationNCX, Na+/Ca2+ exchangerPFK, phosphofructokinasePMCA, plasma membrane Ca2+-ATPaseROS, reactive oxygen speciesRyR, ryanodine receptorsSERCA, sarco-endoplasmic reticulum Ca2+-ATPaseT2D, Type 2 DiabetesTCA, trycarboxylic acid cycleTRP, transient receptor potentialVDCC, voltage-dependent Ca2+ channelsVm, membrane potentialβ-cell

Identifiers

PMID25322829
PMCPMC4292577

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.