Evidence map›Paper›PMID 25830228›Full record

ArticlePloS one2015

Positive effects of voluntary running on metabolic syndrome-related disorders in non-obese hereditary hypertriacylglycerolemic rats.

Vojt ch Škop, Hana Malínská, Jaroslava Trnovská, Martina Hüttl, Monika Cahová, Agnieszka Blachnio-Zabielska, Marcin Baranowski, Martin Burian, Olena Oliyarnyk, Ludmila Kazdová

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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  6. Non-alcoholic fatty liver disease: Insights from sphingolipidomics.Biochemical and biophysical research communications · 2018
    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

10 authors at 2 institutions in 2 countries.

Vojt ch ŠkopCenter for experimental medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic; Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Czech Republic.
Hana MalínskáCenter for experimental medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Jaroslava TrnovskáCenter for experimental medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Martina HüttlCenter for experimental medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Monika CahováCenter for experimental medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Agnieszka Blachnio-ZabielskaDepartment of Physiology, Medical University of Bialystok, Bialystok, Poland.
Marcin BaranowskiDepartment of Physiology, Medical University of Bialystok, Bialystok, Poland.
Martin BurianCenter for experimental medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Olena OliyarnykCenter for experimental medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Ludmila KazdováCenter for experimental medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Institute of Clinical and Experimental Medicine · CZMedical University of Białystok · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While metabolic syndrome is often associated with obesity, 25% of humans suffering from it are not obese and the effect of physical activity remains unclear in such cases. Therefore, we used hereditary hypertriaclyglycerolemic (HHTg) rats as a unique model for studying the effect of spontaneous physical activity [voluntary running (VR)] on metabolic syndrome-related disorders, such as dyslipidemia, in non-obese subjects. Adult HHTg males were fed standard (CD) or high-sucrose (HSD) diets ad libitum for four weeks. Within both dietary groups, some of the rats had free access to a running wheel (CD+VR, HSD+VR), whereas the controls (CD, HSD) had no possibility of extra physical activity. At the end of the four weeks, we measured the effects of VR on various metabolic syndrome-associated parameters: (i) biochemical parameters, (ii) the content and composition of triacylglycerols (TAG), diacylglycerols (DAG), ceramides and membrane phospholipids, and (iii) substrate utilization in brown adipose tissue. In both dietary groups, VR led to various positive effects: reduced epididymal and perirenal fat depots; increased epididymal adipose tissue lipolysis; decreased amounts of serum TAG, non-esterified fatty acids and insulin; a higher insulin sensitivity index. While tissue ceramide content was not affected, decreased TAG accumulation resulted in reduced and modified liver, heart and skeletal muscle DAG. VR also had a beneficial effect on muscle membrane phospholipid composition. In addition, compared with the CD group, the CD+VR rats exhibited increased fatty acid oxidation and protein content in brown adipose tissue. Our results confirm that physical activity in a non-obese model of severe dyslipidemia has many beneficial effects and can even counteract the negative effects of sucrose consumption. Furthermore, they suggest that the mechanism by which these effects are modulated involves a combination of several positive changes in lipid metabolism.

Indexed as

Lipid MetabolismAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsCell MembraneCeramidesHypertriglyceridemiaMaleMetabolic SyndromeMuscle CellsMuscle, SkeletalOxidative StressPhospholipidsRatsRunningTriglyceridesCeramidesPhospholipidsTriglycerides

Identifiers

PMID25830228
PMCPMC4382201
OpenAlexW2156618386

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.