Evidence map›Paper›PMID 20634354›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2010

Daily physical activity enhances reactivity to insulin in skeletal muscle arterioles of hyperphagic Otsuka Long-Evans Tokushima Fatty rats.

Catherine R Mikus, R Scott Rector, Arturo A Arce-Esquivel, Jessica L Libla, Frank W Booth, Jamal A Ibdah, M Harold Laughlin, John P Thyfault

Open access · greenAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
14.2field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 56 citations in OpenAlex.

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  7. Microvascular insulin resistance in skeletal muscle and brain occurs early in the development of juvenile obesity in pigs.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
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  17. Retention of sedentary obese visceral white adipose tissue phenotype with intermittent physical activity despite reduced adiposity.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
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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 3 institutions in 2 countries.

Catherine R MikusDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, USA.
R Scott Rector
Arturo A Arce-Esquivel
Jessica L Libla
Frank W Booth
Jamal A Ibdah
M Harold Laughlin
John P Thyfault
University of Missouri · USHarry S. Truman Memorial Veterans' Hospital · USInstitute of Biomedical Science · GB

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
Exercise, mitochondrial function, and fatty acid oxidation in fatty liver diseaseF32DK083182 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI RECTOR, RANDY SCOTT · 2008 to 2009
$88k
NHLBI NIH HHS HL-36088NHLBI NIH HHS R01 HL036088NIAMS NIH HHS T32 AR048523NIAMS NIH HHS T32-AR-048523NIDDK NIH HHS F32 DK083182NIDDK NIH HHS F32-DK-83182
6 · The paper itself

Abstract

Insulin-mediated glucose disposal is dependent on the vasodilator effects of insulin. In type 2 diabetes, insulin-stimulated vasodilation is impaired as a result of an imbalance in NO and ET-1 production. We tested the hypothesis that chronic voluntary wheel running (RUN) prevents impairments in insulin-stimulated vasodilation associated with obesity and type 2 diabetes independent of the effects of RUN on adiposity by randomizing Otsuka Long Evans Tokushima Fatty (OLETF) rats, a model of hyperphagia-induced obesity and type 2 diabetes, to 1) RUN, 2) caloric restriction (CR; diet adjusted to match body weights of RUN group), or 3) sedentary control (SED) groups (n = 8/group) at 4 wk. At 40 wk, NO- and ET-1-mediated vasoreactivity to insulin (1-1,000 μIU/ml) was assessed in the presence of a nonselective ET-1 receptor blocker (tezosentan) or a NO synthase (NOS) inhibitor [N(G)-nitro-L-arginine methyl ester (L-NAME)], respectively, in second-order arterioles isolated from the white portion of the gastrocnemius muscle. Body weight, fasting plasma glucose, and hemoglobin A1c were lower in RUN and CR than SED (P < 0.05); however, the glucose area under the curve (AUC) following the intraperitoneal glucose tolerance test was lower only in the RUN group (P < 0.05). Vasodilator responses to all doses of insulin were greater in RUN than SED or CR in the presence of a tezosentan (P < 0.05), but group differences in vasoreactivity to insulin with coadministration of L-NAME were not observed. We conclude daily wheel running prevents obesity and type 2 diabetes-associated declines in insulin-stimulated vasodilation in skeletal muscle arterioles through mechanisms that appear to be NO mediated and independent of attenuating excess adiposity in hyperphagic rats.

Indexed as

Insulin ResistanceMotor ActivityVasodilationAdiposityAnimalsArteriolesBlood GlucoseBody CompositionBody WeightCaloric RestrictionDiabetes Mellitus, Type 2Disease Models, AnimalEatingEndothelin-1Enzyme InhibitorsGlycated HemoglobinBlood GlucoseEndothelin-1Enzyme InhibitorsGlycated HemoglobinInsulinNitric OxideNitric Oxide Synthase Type IIINos3 protein, rat

Identifiers

PMID20634354
PMCPMC2963325
OpenAlexW2041156347

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.