Evidence map›Paper›PMID 22709650›Full record

ArticleExperimental physiology2013

Differential changes in vascular mRNA levels between rat iliac and renal arteries produced by cessation of voluntary running.

Jaume Padilla, Nathan T Jenkins, Michael D Roberts, Arturo A Arce-Esquivel, Jeffrey S Martin, M Harold Laughlin, Frank W Booth

Open access · bronzeAbstract read
In one paragraph

Article in Experimental physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  6. Prolonged sitting leg vasculopathy: contributing factors and clinical implications.American journal of physiology. Heart and circulatory physiology · 2017
    Review
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  8. Review
  9. Loss of UCP1 exacerbates Western diet-induced glycemic dysregulation independent of changes in body weight in female mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2017
    Article
  10. Article
  11. 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
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Divergent phenotype of rat thoracic and abdominal perivascular adipose tissues.American journal of physiology. Regulatory, integrative and comparative physiology · 2013
    Article
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.

Jaume PadillaDepartment of Biomedical Sciences, E102 Veterinary Medicine, 1600 East Rollins Road, University of Missouri, Columbia, MO 65211, USA. padillaja@missouri.edu
Nathan T Jenkins
Michael D Roberts
Arturo A Arce-Esquivel
Jeffrey S Martin
M Harold Laughlin
Frank W Booth
Cardiovascular Research Center · BRUniversity of Missouri · US

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
NHLBI NIH HHS R01 HL036088NHLBI NIH HHS R01HL036088NIAMS NIH HHS T32 AR048523NIAMS NIH HHS T32-AR048523
6 · The paper itself

Abstract

Early vascular changes at the molecular level caused by adoption of a sedentary lifestyle are incompletely characterized. Herein, we employed the rodent wheel-lock model to identify mRNAs in the arterial wall that are responsive to the acute transition from higher to lower levels of daily physical activity. Specifically, we evaluated whether short-term cessation of voluntary wheel running alters vascular mRNA levels in rat conduit arteries previously reported to have marked increases (i.e. iliac artery) versus marked decreases (i.e. renal artery) in blood flow during running. We used young female Wistar rats with free access to voluntary running wheels. Following 23 days of voluntary running (average distance of ∼15 km per night; ∼4.4 h per night), rats in one group were rapidly transitioned to a sedentary state by locking the wheels for 7 days (n = 9; wheel-lock 7 day rats) or remained active in a second group for an additional 7 days (n = 9; wheel-lock 0 day rats). Real-time PCR was conducted on total RNA isolated from iliac and renal arteries to evaluate expression of 25 pro-atherogenic and anti-atherogenic genes. Compared with the iliac arteries of wheel-lock 0 day rats, iliac arteries of wheel-lock 7 day rats exhibited increased expression of TNFR1 (+19%), ET1 (+59%) and LOX-1 (+31%; all P < 0.05). Moreover, compared with renal arteries of wheel-lock 0 day rats, renal arteries of wheel-lock 7 day rats exhibited decreased expression of ETb (-23%), p47phox (-32%) and p67phox (-19%; all P < 0.05). These data demonstrate that cessation of voluntary wheel running for 7 days produces modest, but differential changes in mRNA levels between the iliac and renal arteries of healthy rats. This heterogeneous influence of short-term physical inactivity could be attributed to the distinct alteration in haemodynamic forces between arteries.

Indexed as

AnimalsArteriesEndothelin-1FemaleIliumMotor ActivityNADPH OxidasesPhosphoproteinsRatsRats, WistarReceptor, Endothelin BReceptors, Tumor Necrosis Factor, Type IRenal ArteryRNA, MessengerRunningScavenger Receptors, Class EEndothelin-1NADPH Oxidasesneutrophil cytosol factor 67Kneutrophil cytosolic factor 1OLR1 protein, ratPhosphoproteinsReceptor, Endothelin BReceptors, Tumor Necrosis Factor, Type IRNA, MessengerScavenger Receptors, Class ETnfrsf1a protein, rat

Identifiers

PMID22709650
PMCPMC3474882
OpenAlexW1621653565

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Registered trials

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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.