Evidence map›Paper›PMID 30726280›Full record

ArticlePloS one2019

Synchronization of pancreatic islets by periodic or non-periodic muscarinic agonist pulse trains.

Joel E Adablah, Ryan Vinson, Michael G Roper, Richard Bertram

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Coordination of pancreatic islet rhythmic activity by delayed negative feedback.American journal of physiology. Endocrinology and metabolism · 2022
    Article
  6. Article
  7. Review
  8. Article
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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

4 authors at 1 institution in 1 country.

Joel E AdablahDepartment of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida, United States of America.
Ryan VinsonDepartment of Mathematics, Florida State University, Tallahassee, Florida, United States of America.
Michael G RoperDepartment of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida, United States of America.
Richard BertramDepartment of Mathematics and Programs in Molecular Biophysics and Neuroscience, Florida State University, Tallahassee, Florida, United States of America.ORCID 0000-0001-8577-2592
Florida State University · US

Funding

Microfluidic Devices to Determine Roles of Islet-Secreted LeptinR01DK080714 · NIDDK · FLORIDA STATE UNIVERSITY · PI ROPER, MICHAEL GABRIEL · 2008 to 2025
$5.5M
NIDDK NIH HHS R01 DK080714
6 · The paper itself

Abstract

Pulsatile insulin secretion into the portal vein from the many pancreatic islets of Langerhans is critical for efficient glucose homeostasis. The islets are themselves endogenous oscillators, but since they are not physically coupled it is not obvious how their oscillations are synchronized across the pancreas. It has been proposed that synchronization of islets is achieved through periodic activity of intrapancreatic ganglia, and indeed there are data supporting this proposal. Postganglionic nerves are cholinergic, and their product, acetylcholine, can influence islet β-cells through actions on M3 muscarinic receptors which are coupled to Gq type G-proteins. In addition, the neurons secrete several peptide hormones that act on β-cell receptors. The data supporting synchronization via intrapancreatic ganglia are, however, limited. In particular, it has not been shown that trains of muscarinic pulses are effective at synchronizing islets in vitro. Also, if as has been suggested, there is a ganglionic pacemaker driving islets to a preferred frequency, no neural circuitry for this pacemaker has been identified. In this study, both points are addressed using a microfluidic system that allows for the pulsed application of the muscarinic agonist carbachol. We find that murine islets are entrained and synchronized over a wide range of frequencies when the carbachol pulsing is periodic, adding support to the hypothesis that ganglia can synchronize islets in vivo. We also find that islet synchronization is very effective even if the carbachol pulses are applied at random times. This suggests that a neural pacemaker is not needed; all that is required is that islets receive occasional coordinated input from postganglionic neurons. The endogenous rhythmic activity of the islets then sets the frequency of the islet population rhythm, while the input from ganglia acts only to keep the islet oscillators in phase.

Indexed as

Lab-On-A-Chip DevicesMicrofluidic Analytical TechniquesAnimalsCarbacholCell Culture TechniquesCells, CulturedInsulinInsulin-Secreting CellsMaleMiceMuscarinic AgonistsCarbacholInsulinMuscarinic Agonists

Identifiers

PMID30726280
PMCPMC6364940
OpenAlexW2912284839

What Socratic holds

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LicenceCC BY
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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.