Evidence map›Paper›PMID 23680665›Full record

ArticleBiochemical and biophysical research communications2013

Neuronal nitric oxide synthase is phosphorylated in response to insulin stimulation in skeletal muscle.

Kathryn Hinchee-Rodriguez, Neha Garg, Priya Venkatakrishnan, Madeline G Roman, Martin L Adamo, Bettie Sue Masters, Linda J Roman

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.9field-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

26 citing papers in PubMed, 44 citations in OpenAlex.

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  8. How Postural Muscle Senses Disuse? Early Signs and Signals.International journal of molecular sciences · 2020
    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

7 authors at 1 institution in 1 country.

Kathryn Hinchee-RodriguezDepartment of Biochemistry, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr., San Antonio, TX 78229-7760, USA.
Neha Garg
Priya Venkatakrishnan
Madeline G Roman
Martin L Adamo
Bettie Sue Masters
Linda J Roman
The University of Texas Health Science Center at San Antonio · US

Funding

Structure/Function Modularity in Nitric Oxide SynthaseR01GM052419 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI MASTERS, BETTIE SUE SILER, ROMAN, LINDA J · 1996 to 2012
$3.5M
NIGMS NIH HHS GM052419NIGMS NIH HHS R01 GM052419
6 · The paper itself

Abstract

Type 2 Diabetes (T2DM) is the seventh leading cause of death in the United States, and is quickly becoming a global pandemic. T2DM results from reduced insulin sensitivity coupled with a relative failure of insulin secretion. Reduced insulin sensitivity has been associated with reduced nitric oxide synthase (NOS) activity and impaired glucose uptake in T2DM skeletal muscle. Upon insulin stimulation, NO synthesis increases in normal adult skeletal muscle, whereas no such increase is observed in T2DM adults. Endothelial NOS is activated by phosphorylation in the C-terminal tail in response to insulin. Neuronal NOS (nNOS), the primary NOS isoform in skeletal muscle, contains a homologous phosphorylation site, raising the possibility that nNOS, too, may undergo an activating phosphorylation event upon insulin treatment. Yet it remains unknown if or how nNOS is regulated by insulin in skeletal muscle. Data shown herein indicate that nNOS is phosphorylated in response to insulin in skeletal muscle and that this phosphorylation event occurs rapidly in C2C12 myotubes, resulting in increased NO production. In vivo phosphorylation of nNOS was also observed in response to insulin in mouse skeletal muscle. These results indicate, for the first time, that nNOS is phosphorylated in skeletal muscle in response to insulin and in association with increased NO production.

Indexed as

AnimalsCell LineDiabetes Mellitus, Type 2InsulinInsulin ResistanceMaleMiceMice, Inbred C57BLMuscle Fibers, SkeletalMuscle, SkeletalNitric OxideNitric Oxide Synthase Type IPhosphorylationInsulinNitric OxideNitric Oxide Synthase Type INos1 protein, mouse

Identifiers

PMID23680665
PMCPMC3703775
OpenAlexW2089274031

What Socratic 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 Socratic graph.