Evidence map›Paper›PMID 27561916›Full record

ArticleThe Journal of physiology2016

Endothelium-dependent vasodilatory signalling modulates α

Christopher M Hearon, Brett S Kirby, Gary J Luckasen, Dennis G Larson, Frank A Dinenno

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 48 citations in OpenAlex.

  1. Short-term water deprivation does not increase blood pressure variability or impair neurovascular function in healthy young adults.American journal of physiology. Regulatory, integrative and comparative physiology · 2020
    Trial
  2. Trial
  3. Review
  4. Endogenous muscarinic acetylcholine receptor signaling blunts αAmerican journal of physiology. Regulatory, integrative and comparative physiology · 2025
    Article
  5. Article
  6. Article
  7. Adrenergic control of skeletal muscle blood flow during chronic hypoxia in healthy males.American journal of physiology. Regulatory, integrative and comparative physiology · 2023
    Article
  8. Article
  9. Article
  10. ATP and acetylcholine interact to modulate vascular tone and αJournal of applied physiology (Bethesda, Md. : 1985) · 2021
    Article
  11. Functional sympatholysis is preserved in healthy young Black men during rhythmic handgrip exercise.American journal of physiology. Regulatory, integrative and comparative physiology · 2020
    Article
  12. Article
  13. Healthy active older adults have enhanced KAmerican journal of physiology. Regulatory, integrative and comparative physiology · 2020
    Article
  14. KThe Journal of physiology · 2020
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  15. Article
  16. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Christopher M HearonHuman Cardiovascular Physiology Laboratory, Department of Health and Exercise Science, Colorado State University, Fort Collins, CO, 80523, USA.
Brett S KirbyHuman Cardiovascular Physiology Laboratory, Department of Health and Exercise Science, Colorado State University, Fort Collins, CO, 80523, USA.
Gary J LuckasenMedical Center of the Rockies Foundation, University of Colorado Health System, Loveland, CO, 80538, USA.
Dennis G LarsonMedical Center of the Rockies Foundation, University of Colorado Health System, Loveland, CO, 80538, USA.
Frank A DinennoHuman Cardiovascular Physiology Laboratory, Department of Health and Exercise Science, Colorado State University, Fort Collins, CO, 80523, USA.
Colorado State University · USColorado Health Foundation · USUniversity of Colorado Health · US

Funding

Exercise Hyperemia in HumansR01HL119337 · NHLBI · MAYO CLINIC ROCHESTER · PI DINENNO, FRANK A, JOYNER, MICHAEL J · 2014 to 2017
$3.0M
Aging, Sleep Apnea, & Vascular Control During Systemic HypoxiaR01HL095573 · NHLBI · COLORADO STATE UNIVERSITY · PI DINENNO, FRANK A · 2010 to 2014
$1.8M
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 R01 HL095573NHLBI NIH HHS R01 HL119337NHLBI NIH HHS R21 HL102720
6 · The paper itself

Abstract

key points'Functional sympatholysis' describes the ability of contracting skeletal muscle to attenuate sympathetic vasoconstriction, and is critical to ensure proper blood flow and oxygen delivery to metabolically active skeletal muscle. The signalling mechanism responsible for sympatholysis in healthy humans is unknown. Evidence from animal models has identified endothelium-derived hyperpolarization (EDH) as a potential mechanism capable of attenuating sympathetic vasoconstriction. In this study, increasing endothelium-dependent signalling during exercise significantly enhanced the ability of contracting skeletal muscle to attenuate sympathetic vasoconstriction in humans. This is the first study in humans to identify endothelium-dependent regulation of sympathetic vasoconstriction in contracting skeletal muscle, and specifically supports a role for EDH-like vasodilatory signalling. Impaired functional sympatholysis is a common feature of cardiovascular ageing, hypertension and heart failure, and thus identifying fundamental mechanisms responsible for sympatholysis is clinically relevant. ABSTRACT: Stimulation of α-adrenoceptors elicits vasoconstriction in resting skeletal muscle that is blunted during exercise in an intensity-dependent manner. In humans, the underlying mechanisms remain unclear. We tested the hypothesis that stimulating endothelium-dependent vasodilatory signalling will enhance the ability of contracting skeletal muscle to blunt α CONTROL: -31 ± 3% vs.; P < 0.05) and remained blunted during exercise (blockade: -15 ± 5 vs. CONTROL: -14 ± 5%). We conclude that stimulation of EDH-like vasodilatation can blunt α

Indexed as

AcetylcholineAdenosine TriphosphateAdrenergic alpha-1 Receptor AgonistsAdultEndothelium, VascularExerciseFemaleHumansMaleMuscle, SkeletalNitroprussidePhenylephrinePotassium ChlorideReceptors, Adrenergic, alphaSignal TransductionVasoconstrictionAcetylcholineAdenosine TriphosphateAdrenergic alpha-1 Receptor AgonistsNitroprussidePhenylephrinePotassium ChlorideReceptors, Adrenergic, alphaVasoconstrictor AgentsVasodilator Agentsblood flowendothelium-derived hyperpolarizationsympathetic nervous system

Identifiers

PMID27561916
PMCPMC5157062
OpenAlexW2512040991

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.