Evidence mapPaperPMID 23262133Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2013

Blunted temporal activity of microvascular perfusion heterogeneity in metabolic syndrome: a new attractor for peripheral vascular disease?

Joshua T Butcher, Adam G Goodwill, Shyla C Stanley, Jefferson C Frisbee

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Cardiovascular consequences of metabolic syndrome.Translational research : the journal of laboratory and clinical medicine · 2017
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. β(2)-Adrenoreceptor blockade improves early posttrauma hyperglycemia and pulmonary injury in obese rats.American journal of physiology. Heart and circulatory physiology · 2014
    Article
  17. Inhibition of NADPH oxidase prevents acute lung injury in obese rats following severe trauma.American journal of physiology. Heart and circulatory physiology · 2014
    Article
  18. 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

4 authors at 1 institution in 1 country.

Joshua T ButcherDepartment of Physiology and Pharmacology and Center for Cardiovascular and Respiratory Sciences, West Virginia University Health Sciences Center, Morgantown, WV 26506, USA.
Adam G Goodwill
Shyla C Stanley
Jefferson C Frisbee
West Virginia University · US

Funding

Skeletal Muscle Microcirculation in Obese Zucker RatsR01DK064668 · WEST VIRGINIA UNIVERSITY · 2004 to 2005
$516k
NHLBI NIH HHS T32 HL090610NHLBI NIH HHS T32-HL-90610NIAMS NIH HHS RR-2865ARNIDDK NIH HHS DK-R01-64668
6 · The paper itself

Abstract

A key clinical outcome for peripheral vascular disease (PVD) in patients is a progressive decay in skeletal muscle performance and its ability to resist fatigue with elevated metabolic demand. We have demonstrated that PVD in obese Zucker rats (OZR) is partially due to increased perfusion distribution heterogeneity at successive microvascular bifurcations within skeletal muscle. As this increased heterogeneity (γ) is longitudinally present in the network, its cumulative impact is a more heterogeneous distribution of perfusion between terminal arterioles than normal, causing greater regional tissue ischemia. To minimize this negative outcome, a likely compensatory mechanism against an increased γ should be an increased temporal switching at arteriolar bifurcations to minimize downstream perfusion deficits. Using in situ cremaster muscle, we determined that temporal activity (the cumulative sum of absolute differences between successive values of γ, taken every 20 s) was lower in OZR than in control animals, and this difference was present in both proximal (1A-2A) and distal (3A-4A) arteriolar bifurcations. Although adrenoreceptor blockade (phentolamine) improved temporal activity in 1A-2A arteriolar bifurcations in OZR, this was without impact in the distal microcirculation, where only interventions against oxidant stress (Tempol) and thromboxane A(2) activity (SQ-29548) were effective. Analysis of the attractor for γ indicated that it was not only elevated in OZR but also exhibited severe reductions in range, suggesting that the ability of the microcirculation to respond to any challenge is highly restricted and may represent the major contributor to the manifestation of poor muscle performance at this age in OZR.

Indexed as

Adrenergic alpha-AntagonistsAnimalsAntioxidantsArteriolesBridged Bicyclo Compounds, HeterocyclicCyclic N-OxidesDisease Models, AnimalFatty Acids, UnsaturatedHumansHydrazinesMaleMetabolic SyndromeMicrovesselsMuscle, SkeletalObesityOxidative StressAdrenergic alpha-AntagonistsAntioxidantsBridged Bicyclo Compounds, HeterocyclicCyclic N-OxidesFatty Acids, UnsaturatedHydrazinesPhentolamineSpin LabelsSQ 29548tempol

Identifiers

PMID23262133
PMCPMC3566484
OpenAlexW2152297749

What Socratic 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 Socratic graph.