Evidence map›Paper›PMID 29025901›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2018

Effects of age and exercise training on coronary microvascular smooth muscle phenotype and function.

Judy M Muller-Delp, Kazuki Hotta, Bei Chen, Bradley J Behnke, Joshua J Maraj, Michael D Delp, Tiffani R Lucero, Jeremy A Bramy, David B Alarcon, Hannah E Morgan and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Coronary microvascular adaptations distal to epicardial artery stenosis.American journal of physiology. Heart and circulatory physiology · 2021
    Review
  9. As time flies by: Investigating cardiac aging in the short-lived Drosophila model.Biochimica et biophysica acta. Molecular basis of disease · 2019
    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

12 authors at 3 institutions in 1 country.

Judy M Muller-DelpDepartment of Biomedical Sciences, Florida State University , Tallahassee, Florida.ORCID 0000-0001-5322-0611
Kazuki HottaDepartment of Biomedical Sciences, Florida State University , Tallahassee, Florida.
Bei ChenDepartment of Physiology and Functional Genomics, University of Florida , Gainesville, Florida.
Bradley J BehnkeDepartment of Kinesiology and Johnson Cancer Research Center, Kansas State University , Manhattan, Kansas.
Joshua J MarajDepartment of Physiology and Functional Genomics, University of Florida , Gainesville, Florida.
Michael D DelpDepartment of Nutrition, Food & Exercise Sciences, Florida State University , Tallahassee, Florida.
Tiffani R LuceroDepartment of Biomedical Sciences, Florida State University , Tallahassee, Florida.
Jeremy A BramyDepartment of Biomedical Sciences, Florida State University , Tallahassee, Florida.
David B AlarconDepartment of Biomedical Sciences, Florida State University , Tallahassee, Florida.
Hannah E MorganDepartment of Biomedical Sciences, Florida State University , Tallahassee, Florida.
Morgan R CowanDepartment of Biomedical Sciences, Florida State University , Tallahassee, Florida.
Anthony D HaynesDepartment of Biomedical Sciences, Florida State University , Tallahassee, Florida.
Florida State University · USUniversity of Florida · USKansas State University · US

Funding

Aging, Estrogen, and Coronary Endothelial FunctionR01HL077224 · NHLBI · WEST VIRGINIA UNIVERSITY · PI DELP, JUDY M · 2005 to 2008
$1.4M
Microvascular Aging and eNOS UncouplingR01HL090937 · NHLBI · UNIVERSITY OF FLORIDA · PI DELP, JUDY M, WYSOLMERSKI, ROBERT B. · 2009 to 2010
$825k
Ankle dorsiflexion splinting enhances endothelial function of aged leg musclesR21AG044858 · NIA · UNIVERSITY OF FLORIDA · PI CHRISTOU, DEMETRA, DELP, JUDY M · 2013 to 2014
$401k
NHLBI NIH HHS R01 HL077224NHLBI NIH HHS R01 HL090937
6 · The paper itself

Abstract

Coronary microvascular function and blood flow responses during acute exercise are impaired in the aged heart but can be restored by exercise training. Coronary microvascular resistance is directly dependent on vascular smooth muscle function in coronary resistance arterioles; therefore, we hypothesized that age impairs contractile function and alters the phenotype of vascular smooth muscle in coronary arterioles. We further hypothesized that exercise training restores contractile function and reverses age-induced phenotypic alterations of arteriolar smooth muscle. Young and old Fischer 344 rats underwent 10 wk of treadmill exercise training or remained sedentary. At the end of training or cage confinement, contractile responses, vascular smooth muscle proliferation, and expression of contractile proteins were assessed in isolated coronary arterioles. Both receptor- and non-receptor-mediated contractile function were impaired in coronary arterioles from aged rats. Vascular smooth muscle shifted from a differentiated, contractile phenotype to a secretory phenotype with associated proliferation of smooth muscle in the arteriolar wall. Expression of smooth muscle myosin heavy chain 1 (SM1) was decreased in arterioles from aged rats, whereas expression of phospho-histone H3 and of the synthetic protein ribosomal protein S6 (rpS6) were increased. Exercise training improved contractile responses, reduced smooth muscle proliferation and expression of rpS6, and increased expression of SM1 in arterioles from old rats. Thus age-induced contractile dysfunction of coronary arterioles and emergence of a secretory smooth muscle phenotype may contribute to impaired coronary blood flow responses, but arteriolar contractile responsiveness and a younger smooth muscle phenotype can be restored with late-life exercise training. NEW & NOTEWORTHY Aging impairs contractile function of coronary arterioles and induces a shift of the vascular smooth muscle toward a proliferative, noncontractile phenotype. Late-life exercise training reverses contractile dysfunction of coronary arterioles and restores a young phenotype to the vascular smooth muscle.

Indexed as

15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidAgingAnimalsCoronary VesselsMaleMicrovesselsMuscle, Smooth, VascularPhysical Conditioning, AnimalRats, Inbred F344Vasoconstriction15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acidadiponectincontractile phenotypesecretory phenotypevascular smooth musclevasoconstriction

Identifiers

PMID29025901
PMCPMC5866446
OpenAlexW2760951855

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.