Evidence map›Paper›PMID 25269484›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2014

Differential impact of selective GH deficiency and endogenous GH excess on insulin-mediated actions in muscle and liver of male mice.

Jose Cordoba-Chacon, Manuel D Gahete, Owen P McGuinness, Rhonda D Kineman

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 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

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  18. Insulin signaling in the whole spectrum of GH deficiency.Archives of endocrinology and metabolism
    Review
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

4 authors at 3 institutions in 2 countries.

Jose Cordoba-ChaconResearch and Development Division, Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois; Section of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois;
Manuel D GaheteResearch and Development Division, Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois; Section of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois; Department of Cell Biology, Physiology, and Immunology, University of Córdoba, Instituto Maimónides de Investigación Biomédica de Córdoba/Hospital Universitario Reina Sofia, and CIBER de la Fisiopatología de la Obesidad y Nutrición, Córdoba, Spain; and.
Owen P McGuinnessDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Rhonda D KinemanResearch and Development Division, Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois; Section of Endocrinology, Diabetes, and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois; kineman@uic.edu.
University of Illinois Chicago · USJesse Brown VA Medical Center · USVanderbilt University · US

Funding

Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALVIN C POWERS · 2012 to 2026
$29.3M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Vanderbilt Mouse Metabolic Phenotyping CenterU2CDK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2016 to 2021
$6.3M
Growth hormone and adult physiologyR01DK088133 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KINEMAN, RHONDA D · 2010 to 2013
$1.0M
Interrelationship between the GH-axis and metabolismI01BX001114 · VA · JESSE BROWN VA MEDICAL CENTER · PI KINEMAN, RHONDA D · 2013 to 2016
–
INTERACTION OF NUCLEOTIDES AND STEROID RECEPTORSR01DK020893 · NIDDK · OAKLAND UNIVERSITY · PI MOUDGIL, VIRINDER K · 1986 to 1996
–
BLRD VA I01 BX001114NIDDK NIH HHS DK-020893NIDDK NIH HHS DK-059637NIDDK NIH HHS P30 DK020593NIDDK NIH HHS R01-DK-088133NIDDK NIH HHS U24 DK059637
6 · The paper itself

Abstract

A reciprocal relationship between insulin sensitivity and glucose tolerance has been reported in some mouse models and humans with isolated changes in growth hormone (GH) production and signaling. To determine if this could be explained in part by tissue-specific changes in insulin sensitivity, hyperinsulinemic-euglycemic clamps were performed in mice with adult-onset, isolated GH deficiency and in mice with elevated endogenous GH levels due to somatotrope-specific loss of IGF-I and insulin receptors. Our results demonstrate that circulating GH levels are negatively correlated with insulin-mediated glucose uptake in muscle but positively correlated with insulin-mediated suppression of hepatic glucose production. A positive relationship was also observed between GH levels and endpoints of hepatic lipid metabolism known to be regulated by insulin. These results suggest hepatic insulin resistance could represent an early metabolic defect in GH deficiency.

Indexed as

Insulin ResistanceAcromegalyAnimalsGlucoseGlucose Clamp TechniqueGrowth HormoneInsulinLiverMaleMiceMice, TransgenicMuscle, SkeletalGlucoseGrowth HormoneInsulinglucose disposalgrowth hormonehepatic glucose productionhyperinsulinemic-euglycemic clampstriglycerides

Identifiers

PMID25269484
PMCPMC4233257
OpenAlexW2327737248

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.