Evidence map›Paper›PMID 28536182›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2017

Glucagon's effect on liver protein metabolism in vivo.

Guillaume Kraft, Katie C Coate, Jason J Winnick, Dominique Dardevet, E Patrick Donahue, Alan D Cherrington, Phillip E Williams, Mary Courtney Moore

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 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

8 authors at 2 institutions in 2 countries.

Guillaume KraftDepartment of Molecular Physiology and Biophysics,Vanderbilt University School of Medicine, Nashville, Tennessee; and guillaume.kraft@vanderbilt.edu.
Katie C CoateDepartment of Molecular Physiology and Biophysics,Vanderbilt University School of Medicine, Nashville, Tennessee; and.
Jason J WinnickDepartment of Molecular Physiology and Biophysics,Vanderbilt University School of Medicine, Nashville, Tennessee; and.
Dominique DardevetUniversité Clermont Auvergne, Institut National de la Recherche Agronomique, Unité de Nutrition Humaine, Clermont-Ferrand, France.
E Patrick DonahueDepartment of Molecular Physiology and Biophysics,Vanderbilt University School of Medicine, Nashville, Tennessee; and.
Alan D CherringtonDepartment of Molecular Physiology and Biophysics,Vanderbilt University School of Medicine, Nashville, Tennessee; and.
Phillip E WilliamsDepartment of Molecular Physiology and Biophysics,Vanderbilt University School of Medicine, Nashville, Tennessee; and.
Mary Courtney MooreDepartment of Molecular Physiology and Biophysics,Vanderbilt University School of Medicine, Nashville, Tennessee; and.
Vanderbilt University · USUniversité Clermont Auvergne · FR

Funding

GLUCONEOGENESIS &GLYCOGENOLYSIS:ROLE &REGULATIONR01DK018243 · NIDDK · VANDERBILT UNIVERSITY · PI Alan D Cherrington, Dale S Edgerton · 1986 to 2026
$12.2M
REGULATION OF NET HEPATIC GLUCOSE UPTAKE IN VIVOR01DK043706 · NIDDK · VANDERBILT UNIVERSITY · PI CHERRINGTON, ALAN D · 1991 to 2009
$4.6M
The effect of exercise on hepatic glucose metabolism in type 2 diabetes mellitusK01DK093799 · NIDDK · VANDERBILT UNIVERSITY · PI WINNICK, JASON · 2012 to 2014
$338k
NIDDK NIH HHS K01 DK093799NIDDK NIH HHS R01 DK018243NIDDK NIH HHS R01 DK043706
6 · The paper itself

Abstract

The postprandial state is characterized by a storage of nutrients in the liver, muscle, and adipose tissue for later utilization. In the case of a protein-rich meal, amino acids (AA) stimulate glucagon secretion by the α-cell. The aim of the present study was to determine the impact of the rise in glucagon on AA metabolism, particularly in the liver. We used a conscious catheterized dog model to recreate a postprandial condition using a pancreatic clamp. Portal infusions of glucose, AA, and insulin were used to achieve postprandial levels, while portal glucagon infusion was either maintained at the basal level or increased by three-fold. The high glucagon infusion reduced the increase in arterial AA concentrations compared with the basal glucagon level (-23%,

Indexed as

Amino AcidsAMP-Activated Protein KinasesAnimalsBlood GlucoseDogsGlucagonGluconeogenesisGlucoseHormonesHypoglycemic AgentsInfusions, IntravenousInsulinLiverPhosphorylationPortal VeinPostprandial PeriodAmino AcidsAMP-Activated Protein KinasesBlood GlucoseGlucagonGlucoseHormonesHypoglycemic AgentsInsulinProteinsUreaamino acid metabolismglucagonliver

Identifiers

PMID28536182
PMCPMC5625084
OpenAlexW2620519156

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.