Evidence map›Paper›PMID 23645465›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2013

Mechanisms of rapid vasodilation after a brief contraction in human skeletal muscle.

Anne R Crecelius, Brett S Kirby, Gary J Luckasen, Dennis G Larson, Frank A Dinenno

Open access · greenAbstract 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 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 75 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Prolonged adenosine triphosphate infusion and exercise hyperemia in humans.Journal of applied physiology (Bethesda, Md. : 1985) · 2016
    Trial
  5. Trial
  6. Article
  7. Article
  8. Review
  9. Article
  10. Swimming motions evoke Piezo1-dependent CaCurrent biology : CB · 2025
    Article
  11. Article
  12. Review
  13. The role of the endothelium in the hyperemic response to passive leg movement: looking beyond nitric oxide.American journal of physiology. Heart and circulatory physiology · 2021
    Article
  14. Sex-related differences in rapid-onset vasodilation: impact of aging.Journal of applied physiology (Bethesda, Md. : 1985) · 2021
    Article
  15. KThe Journal of physiology · 2020
    Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

5 authors at 4 institutions in 1 country.

Anne R CreceliusHuman Cardiovascular Physiology Laboratory, Department of Health and Exercise Science, Colorado State University, Fort Collins, CO 80523, USA.
Brett S Kirby
Gary J Luckasen
Dennis G Larson
Frank A Dinenno
Colorado State University · USColorado Health Foundation · USDuke Medical Center · USUniversity of Colorado Health · US

Funding

Role of circulating ATP and smooth muscle cell hyperpolarization in vascular contR21HL102720 · NHLBI · COLORADO STATE UNIVERSITY · PI DINENNO, FRANK A · 2010 to 2011
$393k
NHLBI NIH HHS HL-102720
6 · The paper itself

Abstract

A monophasic increase in skeletal muscle blood flow is observed after a brief single forearm contraction in humans, yet the underlying vascular signaling pathways remain largely undetermined. Evidence from experimental animals indicates an obligatory role of vasodilation via K⁺-mediated smooth muscle hyperpolarization, and human data suggest little to no independent role for nitric oxide (NO) or vasodilating prostaglandins (PGs). We tested the hypothesis that K⁺-mediated vascular hyperpolarization underlies the rapid vasodilation in humans and that combined inhibition of NO and PGs would have a minimal effect on this response. We measured forearm blood flow (Doppler ultrasound) and calculated vascular conductance 10 s before and for 30 s after a single 1-s dynamic forearm contraction at 10%, 20%, and 40% maximum voluntary contraction in 16 young adults. To inhibit K⁺-mediated vasodilation, BaCl₂ and ouabain were infused intra-arterially to inhibit inwardly rectifying K⁺ channels and Na⁺-K⁺-ATPase, respectively. Combined enzymatic inhibition of NO and PG synthesis occurred via NG-monomethyl-L-arginine (L-NMMA; NO synthase) and ketorolac (cyclooxygenase), respectively. In protocol 1 (n = 8), BaCl₂ + ouabain reduced peak vasodilation (range: 30-45%, P < 0.05) and total postcontraction vasodilation (area under the curve, ~55-75% from control) at all intensities. Contrary to our hypothesis, L-NMMA + ketorolac had a further impact (peak: ~60% and area under the curve: ~80% from control). In protocol 2 (n = 8), the order of inhibitors was reversed, and the findings were remarkably similar. We conclude that K⁺-mediated hyperpolarization and NO and PGs, in combination, significantly contribute to contraction-induced rapid vasodilation and that inhibition of these signaling pathways nearly abolishes this phenomenon in humans.

Indexed as

Muscle ContractionVasodilationAdultArteriesCyclooxygenase InhibitorsFemaleForearmHumansMaleMembrane PotentialsMuscle, SkeletalNitric OxideNitric Oxide SynthasePotassiumPotassium Channel BlockersPotassium Channels, Inwardly RectifyingCyclooxygenase InhibitorsNitric OxideNitric Oxide SynthasePotassiumPotassium Channel BlockersPotassium Channels, Inwardly RectifyingProstaglandinsSodium-Potassium-Exchanging ATPaseexercisehyperemiapotassium

Identifiers

PMID23645465
PMCPMC3727098
OpenAlexW1990376116

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.