Evidence map›Paper›PMID 37523232›Full record

ArticleThe Journal of endocrinology2023

Metabolic regulation of glucagon secretion.

Sarah L Armour, Jade E Stanley, James Cantley, E Danielle Dean, Jakob G Knudsen

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

16 citing papers in PubMed, 18 citations in OpenAlex.

  1. mNature metabolism · 2026
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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

5 authors at 3 institutions in 3 countries.

Sarah L ArmourSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Denmark.
Jade E StanleyDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
James CantleyDivision of Cellular and Systems Medicine, School of Medicine, University of Dundee, UK.ORCID 0000-0003-2509-1271
E Danielle DeanDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Jakob G KnudsenSection for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Denmark.ORCID 0000-0001-7237-8457
University of Copenhagen · DKVanderbilt University · USUniversity of Dundee · GB

Funding

Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Marcela Brissova · 2012 to 2026
$29.3M
Molecular Mechanisms of Postnatal Islet alpha-cell ProliferationR01DK117147 · NIDDK · VANDERBILT UNIVERSITY · PI CHEN, WENBIAO, POWERS, ALVIN C · 2019 to 2023
$3.1M
Arginine regulation of alpha cell proliferation and functionR01DK132669 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Erika Danielle Dean · 2022 to 2026
$2.2M
The Role of Ceramides in the Pancreatic Beta CellR01DK130296 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI HOLLAND, WILLIAM L, SUMMERS, SCOTT A · 2022 to 2025
$2.2M
The Role of Arginine Transport on Pancreatic Alpha Cell Proliferation and FunctionF31DK134158 · NIDDK · VANDERBILT UNIVERSITY · PI STANLEY, JADE ELISE · 2023 to 2024
$67k
Medical Research Council MR/W019590/1NIDDK NIH HHS F31 DK134158NIDDK NIH HHS P30 DK020593NIDDK NIH HHS R01 DK117147NIDDK NIH HHS R01 DK130296NIDDK NIH HHS R01 DK132669
6 · The paper itself

Abstract

Since the discovery of glucagon 100 years ago, the hormone and the pancreatic islet alpha cells that produce it have remained enigmatic relative to insulin-producing beta cells. Canonically, alpha cells have been described in the context of glucagon's role in glucose metabolism in liver, with glucose as the primary nutrient signal regulating alpha cell function. However, current data reveal a more holistic model of metabolic signalling, involving glucagon-regulated metabolism of multiple nutrients by the liver and other tissues, including amino acids and lipids, providing reciprocal feedback to regulate glucagon secretion and even alpha cell mass. Here we describe how various nutrients are sensed, transported and metabolised in alpha cells, providing an integrative model for the metabolic regulation of glucagon secretion and action. Importantly, we discuss where these nutrient-sensing pathways intersect to regulate alpha cell function and highlight key areas for future research.

Indexed as

GlucagonGlucagon-Secreting CellsGlucoseInsulinLiverSignal TransductionGlucagonGlucoseInsulinamino acidsendocrine pancreasfatty acidsglucose metabolismTCA cycle

Identifiers

PMID37523232
PMCPMC10681275
OpenAlexW4385406300

What OpenQuestion holds

Textmetadata
LicenceTDM
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.