Evidence map›Paper›PMID 18334611›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2008

Effect of acute physiological hyperinsulinemia on gene expression in human skeletal muscle in vivo.

Dawn K Coletta, Bogdan Balas, Alberto O Chavez, Muhammad Baig, Muhammad Abdul-Ghani, Sangeeta R Kashyap, Franco Folli, Devjit Tripathy, Lawrence J Mandarino, John E Cornell and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

49 citing papers in PubMed, 96 citations in OpenAlex.

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  7. Insulin Resistance, Obesity, and Lipotoxicity.Advances in experimental medicine and biology · 2024
    Review
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  9. A stepwise activation model for the insulin receptor.Experimental & molecular medicine · 2023
    Review
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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

12 authors at 3 institutions in 1 country.

Dawn K ColettaDivision of Diabetes, Department of Medicine, University of Texas Health Science Centre, San Antonio, TX, USA. richardsond2@uthscsa.edu
Bogdan Balas
Alberto O Chavez
Muhammad Baig
Muhammad Abdul-Ghani
Sangeeta R Kashyap
Franco Folli
Devjit Tripathy
Lawrence J Mandarino
John E Cornell
Ralph A Defronzo
Christopher P Jenkinson
The University of Texas Health Science Center at San Antonio · USArizona State University · USCleveland Clinic · US

Funding

MOLECULAR REGULATION OF MUSCLE GLUCOSE METABOLISM IN MANR01DK047936 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI MANDARINO, LAWRENCE J · 1994 to 2022
$10.7M
PGC-1 & Muscle Mitochondrial Dysfunction in DiabetesR01DK066483 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI MANDARINO, LAWRENCE J · 2004 to 2018
$6.7M
Identification of Prediabetes Genes by Expression Linkage AnalysisR01DK079195 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JENKINSON, CHRISTOPHER P · 2008 to 2013
$2.5M
NIDDK NIH HHS R01 DK047936NIDDK NIH HHS R01 DK066483NIDDK NIH HHS R01 DK079195
6 · The paper itself

Abstract

This study was undertaken to test the hypothesis that short-term exposure (4 h) to physiological hyperinsulinemia in normal, healthy subjects without a family history of diabetes would induce a low grade inflammatory response independently of glycemic status. Twelve normal glucose tolerant subjects received a 4-h euglycemic hyperinsulinemic clamp with biopsies of the vastus lateralis muscle. Microarray analysis identified 121 probe sets that were significantly altered in response to physiological hyperinsulinemia while maintaining euglycemia. In normal, healthy human subjects insulin increased the mRNAs of a number of inflammatory genes (CCL2, CXCL2 and THBD) and transcription factors (ATF3, BHLHB2, HES1, KLF10, JUNB, FOS, and FOSB). A number of other genes were upregulated in response to insulin, including RRAD, MT, and SGK. CITED2, a known coactivator of PPARalpha, was significantly downregulated. SGK and CITED2 are located at chromosome 6q23, where we previously detected strong linkage to fasting plasma insulin concentrations. We independently validated the mRNA expression changes in an additional five subjects and closely paralleled the results observed in the original 12 subjects. A saline infusion in healthy, normal glucose-tolerant subjects without family history of diabetes demonstrated that the genes altered during the euglycemic hyperinsulinemic clamp were due to hyperinsulinemia and were unrelated to the biopsy procedure per se. The results of the present study demonstrate that insulin acutely regulates the levels of mRNAs involved in inflammation and transcription and identifies several candidate genes, including HES1 and BHLHB2, for further investigation.

Indexed as

AdultColoring AgentsDatabases, GeneticDietFemaleGene ExpressionGlucoseGlucose Clamp TechniqueHumansHyperinsulinismImage Processing, Computer-AssistedImmunohistochemistryInflammationIn Situ HybridizationMaleMuscle, SkeletalColoring AgentsGlucoseRNA, Messenger

Identifiers

PMID18334611
PMCPMC3581328
OpenAlexW2102088252

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.