Evidence map›Paper›PMID 37294632›Full record

ArticleCell reports2023

Pancreatic islet protection at the expense of secretory function involves serine-linked mitochondrial one-carbon metabolism.

Angela Pelligra, Jessica Mrugala, Kerstin Griess, Philip Kirschner, Oliver Nortmann, Barbara Bartosinska, Andrea Köster, Natalia I Krupenko, Dominik Gebel, Philipp Westhoff and 8 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Genetics and diet shape the relationship between islet function and whole body metabolism.American journal of physiology. Endocrinology and metabolism · 2024
    Article
  8. The N-Methyl-D-Aspartate Receptor Antagonist Dextromethorphan Improves Glucose Homeostasis and Preserves Pancreatic Islets in NOD Mice.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 2 countries.

Angela PelligraInstitute of Metabolic Physiology, Heinrich Heine University, 40225 Düsseldorf, Germany.
Jessica MrugalaInstitute of Metabolic Physiology, Heinrich Heine University, 40225 Düsseldorf, Germany; Institute for Vascular and Islet Cell Biology, German Diabetes Center (DDZ), Leibniz Center for Diabetes Research at Heinrich Heine University, 40225 Düsseldorf, Germany; German Center for Diabetes Research (DZD e.V.), Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Kerstin GriessInstitute of Metabolic Physiology, Heinrich Heine University, 40225 Düsseldorf, Germany.
Philip KirschnerInstitute of Metabolic Physiology, Heinrich Heine University, 40225 Düsseldorf, Germany.
Oliver NortmannInstitute of Metabolic Physiology, Heinrich Heine University, 40225 Düsseldorf, Germany.
Barbara BartosinskaInstitute of Metabolic Physiology, Heinrich Heine University, 40225 Düsseldorf, Germany.
Andrea KösterInstitute of Metabolic Physiology, Heinrich Heine University, 40225 Düsseldorf, Germany.
Natalia I KrupenkoUniversity of North Carolina (UNC) Nutrition Research Institute, UNC Chapel Hill, Chapel Hill, NC, USA.
Dominik GebelInstitute of Metabolic Physiology, Heinrich Heine University, 40225 Düsseldorf, Germany.
Philipp WesthoffInstitute of Plant Biochemistry, Cluster of Excellence on Plant Science (CEPLAS), Heinrich Heine University, 40225 Düsseldorf, Germany; Cluster of Excellence on Plant Science (CEPLAS), Heinrich Heine University, 40225 Düsseldorf, Germany.
Bodo SteckelDepartment of Molecular Cardiology, Heinrich Heine University, 40225 Düsseldorf, Germany.
Daniel EberhardInstitute of Metabolic Physiology, Heinrich Heine University, 40225 Düsseldorf, Germany; Institute for Vascular and Islet Cell Biology, German Diabetes Center (DDZ), Leibniz Center for Diabetes Research at Heinrich Heine University, 40225 Düsseldorf, Germany.
Diran HerebianDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University, 40225 Düsseldorf, Germany.
Bengt-Frederik BelgardtInstitute for Vascular and Islet Cell Biology, German Diabetes Center (DDZ), Leibniz Center for Diabetes Research at Heinrich Heine University, 40225 Düsseldorf, Germany; German Center for Diabetes Research (DZD e.V.), Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Jürgen SchraderDepartment of Molecular Cardiology, Heinrich Heine University, 40225 Düsseldorf, Germany.
Andreas P M WeberInstitute of Plant Biochemistry, Cluster of Excellence on Plant Science (CEPLAS), Heinrich Heine University, 40225 Düsseldorf, Germany; Cluster of Excellence on Plant Science (CEPLAS), Heinrich Heine University, 40225 Düsseldorf, Germany.
Sergey A KrupenkoUniversity of North Carolina (UNC) Nutrition Research Institute, UNC Chapel Hill, Chapel Hill, NC, USA.
Eckhard LammertInstitute of Metabolic Physiology, Heinrich Heine University, 40225 Düsseldorf, Germany; Institute for Vascular and Islet Cell Biology, German Diabetes Center (DDZ), Leibniz Center for Diabetes Research at Heinrich Heine University, 40225 Düsseldorf, Germany; German Center for Diabetes Research (DZD e.V.), Helmholtz Zentrum München, 85764 Neuherberg, Germany. Electronic address: lammert@hhu.de.
Heinrich Heine University Düsseldorf · DEDeutsches Diabetes-Zentrum e.V. · DEUniversity of North Carolina at Chapel Hill · USGerman Center for Diabetes Research · DE

Funding

Regulation of mitochondrial function by folate enzyme ALDH1L2 in health and diseaseR01DK117854 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KRUPENKO, SERGEY A · 2019 to 2023
$2.4M
NIDDK NIH HHS R01 DK117854
6 · The paper itself

Abstract

Type 2 diabetes is characterized by insulin hypersecretion followed by reduced glucose-stimulated insulin secretion (GSIS). Here we show that acute stimulation of pancreatic islets with the insulin secretagogue dextrorphan (DXO) or glibenclamide enhances GSIS, whereas chronic treatment with high concentrations of these drugs reduce GSIS but protect islets from cell death. Bulk RNA sequencing of islets shows increased expression of genes for serine-linked mitochondrial one-carbon metabolism (OCM) after chronic, but not acute, stimulation. In chronically stimulated islets, more glucose is metabolized to serine than to citrate, and the mitochondrial ATP/ADP ratio decreases, whereas the NADPH/NADP

Indexed as

Diabetes Mellitus, Type 2Insulin-Secreting CellsIslets of LangerhansCarbonGlucoseHumansInsulinCarbonGlucoseInsulinActivating transcription factor-4 (Atf4)beta cell exhaustionbeta cell survivalCP: Metabolismde novo serine synthesisdiabetesK(ATP) channelmitochondriaone-carbon metabolismpancreatic beta cellpancreatic islets

Identifiers

PMID37294632
PMCPMC10592470
OpenAlexW4380046759

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.