Evidence map›Paper›PMID 23995100›Full record

ArticleExperimental physiology2014

Differential vasomotor effects of insulin on gastrocnemius and soleus feed arteries in the OLETF rat model: role of endothelin-1.

Nathan T Jenkins, Jaume Padilla, Jeffrey S Martin, Jacqueline M Crissey, John P Thyfault, R Scott Rector, M Harold Laughlin

Open access · bronzeAbstract read
In one paragraph

Article in Experimental physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-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

12 citing papers in PubMed, 19 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

7 authors at 2 institutions in 2 countries.

Nathan T JenkinsN. T. Jenkins: 115M Ramsey Center, Department of Kinesiology, University of Georgia, 330 River Road, Athens, GA 30602-6554, USA. jenkinsn@uga.edu.
Jaume Padilla
Jeffrey S Martin
Jacqueline M Crissey
John P Thyfault
R Scott Rector
M Harold Laughlin
University of Missouri · USCanadian Society for Exercise Physiology · CA

Funding

TRAINING: MUSCLE BLOOD FLOW &CAPILLARY DYNAMICSR01HL036088 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI LAUGHLIN, M HAROLD · 1985 to 2013
$4.0M
Exercise &Health: Integration from Molecule to PatientT32AR048523 · NIAMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI TERJUNG, RONALD L · 2003 to 2013
$2.5M
Hepatic Mitochondria and Insulin Resistance in Fatty Liver and Type 2 DiabetesIK2BX001299 · VA · HARRY S. TRUMAN MEMORIAL VA HOSPITAL · PI RECTOR, RANDY SCOTT · 2011 to 2015
–
BLRD VA IK2 BX001299NHLBI NIH HHS R01 HL036088NHLBI NIH HHS R01-HL036088NIAMS NIH HHS T32 AR048523NIAMS NIH HHS T32-AR48523
6 · The paper itself

Abstract

The vascular actions of insulin are complex, because it can stimulate both nitric oxide-mediated dilatation and endothelin (ET)-1-mediated constriction. We examined vasoreactivity to insulin in isolated feed arteries of the gastrocnemius (GFA) and soleus muscles (SFA) of 32-week-old Long-Evans Tokushima Otsuka (LETO) and Otsuka Long-Evans Tokushima fatty (OLETF) rats, a hyperphagic rodent model of obesity and insulin resistance. The insulin-induced vasoreactivity of SFA and GFA was similar in LETO (healthy) and OLETF (obese/insulin-resistant) rats. However, examination of between-vessel effects revealed a number of novel insights into the heterogeneous vascular effects of insulin. Soleus feed arteries dilated more than GFA in LETO at 100 and 1000 μIU ml(-1) insulin (23 versus 6 and 28 versus 0%, respectively; P < 0.05 for between-vessel differences). Likewise, in OLETF rats there was significantly greater dilatation in SFA than GFA at 10, 100 and 1000 μIU ml(-1) insulin (28 versus 3, 30 versus 0 and 34 versus 0%, respectively; all P < 0.05). In the presence of 3 μm tezosentan, a non-specific endothelin-1 receptor blocker, insulin-induced dilatation of the GFA was enhanced such that differences between vessels were largely abolished in both groups. Furthermore, acetylecholine-induced dilatation was significantly greater in SFA than GFA within each group, whereas sodium nitroprusside-induced dilatory responses were greater in the GFA compared with the SFA. Overall, our findings indicate that the insulin/endothelin-1 vasoconstrictor pathway is more active in GFA than in SFA, independent of obesity in the OLETF rat model.

Indexed as

AnimalsArteriesEndothelin-1Endothelin A Receptor AntagonistsInsulinInsulin ResistanceMaleMuscle, SkeletalObesityRatsRats, Inbred OLETFReceptor, Endothelin AVasoconstrictionVasodilationVasodilator AgentsVasomotor SystemEndothelin-1Endothelin A Receptor AntagonistsInsulinReceptor, Endothelin AVasodilator Agents

Identifiers

PMID23995100
PMCPMC4427248
OpenAlexW1918192531

What OpenQuestion holds

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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 OpenQuestion graph.