Evidence map›Paper›PMID 24735892›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2014

Neuronostatin inhibits glucose-stimulated insulin secretion via direct action on the pancreatic α-cell.

Alison S Salvatori, Mollisa M Elrick, Willis K Samson, John A Corbett, Gina L C Yosten

Abstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 20 citations in OpenAlex.

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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 2 institutions in 1 country.

Alison S SalvatoriDepartment of Pharmacological and Physiological Science, Saint Louis University School of Medicine, St. Louis, Missouri; and.
Mollisa M ElrickDepartment of Pharmacological and Physiological Science, Saint Louis University School of Medicine, St. Louis, Missouri; and.
Willis K SamsonDepartment of Pharmacological and Physiological Science, Saint Louis University School of Medicine, St. Louis, Missouri; and.
John A CorbettDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin.
Gina L C YostenDepartment of Pharmacological and Physiological Science, Saint Louis University School of Medicine, St. Louis, Missouri; and gyosten@slu.edu.
Saint Louis University · USMedical College of Wisconsin · US

Funding

BIOCHEMICAL MECHANISM OF BETA-CELL DESTRUCTIONR01DK052194 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CORBETT, JOHN A · 1998 to 2025
$8.8M
MECHANISMS OF VIRAL INDUCED BETA CELL DAMAGER01AI044458 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CORBETT, JOHN A · 1998 to 2024
$7.5M
NHLBI NIH HHS HL-06623NIAID NIH HHS R01 AI044458NIDDK NIH HHS DK-052194NIDDK NIH HHS R01 DK052194
6 · The paper itself

Abstract

Neuronostatin is a recently described peptide hormone encoded by the somatostatin gene. We previously showed that intraperitoneal injection of neuronostatin into mice resulted in c-Jun accumulation in pancreatic islets in a pattern consistent with the activation of glucagon-producing α-cells. We therefore hypothesized that neuronostatin could influence glucose homeostasis via a direct effect on the α-cell. Neuronostatin enhanced low-glucose-induced glucagon release in isolated rat islets and in the immortalized α-cell line αTC1-9. Furthermore, incubation with neuronostatin led to an increase in transcription of glucagon mRNA, as determined by RT-PCR. Neuronostatin also inhibited glucose-stimulated insulin secretion from isolated islets. However, neuronostatin did not alter insulin release from the β-cell line INS 832/13, indicating that the effect of neuronostatin on insulin secretion may be secondary to a direct action on the α-cell. In agreement with our in vitro data, intra-arterial infusion of neuronostatin in male rats delayed glucose disposal and inhibited insulin release during a glucose challenge. These studies suggest that neuronostatin participates in maintaining glucose homeostasis through cell-cell interactions between α-cells and β-cells in the endocrine pancreas, leading to attenuation in insulin secretion.

Indexed as

AnimalsArea Under CurveBlood GlucoseBlotting, WesternBradykininCell LineCyclic AMPCyclic AMP-Dependent Protein KinasesElectrophoresis, Polyacrylamide GelGlucagon-Secreting CellsGlucoseInjections, IntraperitonealInositol 1,4,5-TrisphosphateInsulinIslets of LangerhansMaleBlood GlucoseBradykininCyclic AMPCyclic AMP-Dependent Protein KinasesGlucoseInositol 1,4,5-TrisphosphateInsulinneuronostatin protein, ratPeptide FragmentsSomatostatinglucagonglucose homeostasisislet functionneuronostatin

Identifiers

PMID24735892
PMCPMC4042099
OpenAlexW1972202396

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.