Evidence map›Paper›PMID 24841202›Full record

ArticleThe Journal of biological chemistry2014

Control of insulin secretion by cytochrome C and calcium signaling in islets with impaired metabolism.

Austin M Rountree, Adam S Neal, Mark Lisowski, Norma Rizzo, Jared Radtke, Sarah White, Dan S Luciani, Francis Kim, Christiane S Hampe, Ian R Sweet

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. The neuronal KScientific reports · 2017
    Article
  16. Article
  17. 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

10 authors at 2 institutions in 2 countries.

Austin M RountreeFrom the Diabetes and Obesity Center, Department of Medicine, University of Washington, Seattle, Washington 98195 and.
Adam S NealFrom the Diabetes and Obesity Center, Department of Medicine, University of Washington, Seattle, Washington 98195 and.
Mark LisowskiFrom the Diabetes and Obesity Center, Department of Medicine, University of Washington, Seattle, Washington 98195 and.
Norma RizzoFrom the Diabetes and Obesity Center, Department of Medicine, University of Washington, Seattle, Washington 98195 and.
Jared RadtkeFrom the Diabetes and Obesity Center, Department of Medicine, University of Washington, Seattle, Washington 98195 and.
Sarah Whitethe Department of Surgery, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.
Dan S Lucianithe Department of Surgery, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.
Francis KimFrom the Diabetes and Obesity Center, Department of Medicine, University of Washington, Seattle, Washington 98195 and.
Christiane S HampeFrom the Diabetes and Obesity Center, Department of Medicine, University of Washington, Seattle, Washington 98195 and.
Ian R SweetFrom the Diabetes and Obesity Center, Department of Medicine, University of Washington, Seattle, Washington 98195 and isweet@u.washington.edu.
University of Washington · USUniversity of British Columbia · CA

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Sakeneh Zraika · 1986 to 2026
$41.4M
ISLET CELL MEMBRANE ANTIBODIES IN DIABTESR01DK026190 · NIDDK · UNIVERSITY OF WASHINGTON · PI HAMPE, CHRISTIANE S · 1986 to 2016
$4.9M
NIDDK NIH HHS DK17047NIDDK NIH HHS P30 DK017047NIDDK NIH HHS R01 DK026190
6 · The paper itself

Abstract

The aim of the study was to assess the relative control of insulin secretion rate (ISR) by calcium influx and signaling from cytochrome c in islets where, as in diabetes, the metabolic pathways are impaired. This was achieved either by culturing isolated islets at low (3 mm) glucose or by fasting rats prior to the isolation of the islets. Culture in low glucose greatly reduced the glucose response of cytochrome c reduction and translocation and ISR, but did not affect the response to the mitochondrial fuel α-ketoisocaproate. Unexpectedly, glucose-stimulated calcium influx was only slightly reduced in low glucose-cultured islets and was not responsible for the impairment in glucose-stimulated ISR. A glucokinase activator acutely restored cytochrome c reduction and translocation and ISR, independent of effects on calcium influx. Islets from fasted rats had reduced ISR and cytochrome c reduction in response to both glucose and α-ketoisocaproate despite normal responses of calcium. Our data are consistent with the scenario where cytochrome c reduction and translocation are essential signals in the stimulation of ISR, the loss of which can result in impaired ISR even when calcium response is normal.

Indexed as

Calcium SignalingAnimalsCytochromes cDose-Response Relationship, DrugEnergy MetabolismFastingGlucoseGlycolysisInsulinInsulin SecretionIn Vitro TechniquesIslets of LangerhansKeto AcidsMetabolic DiseasesMitochondriaOxidation-Reductionalpha-ketoisocaproic acidCytochromes cGlucoseInsulinKeto AcidsOxygenCalciumCalcium SignalingCytochrome cCytochrome c TranslocationInsulin SecretionMitochondrial MetabolismOxygen ConsumptionPancreatic Islet

Identifiers

PMID24841202
PMCPMC4081948
OpenAlexW2102782562

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.