Evidence map›Paper›PMID 20807785›Full record

ArticleThe Journal of physiology2010

Regional heterogeneity of α-adrenoreceptor subtypes in arteriolar networks of mouse skeletal muscle.

Alex W Moore, William F Jackson, Steven S Segal

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 43 citations in OpenAlex.

  1. Impaired modulation of postjunctional αThe Journal of physiology · 2018
    Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Microvascular mechanisms limiting skeletal muscle blood flow with advancing age.Journal of applied physiology (Bethesda, Md. : 1985) · 2018
    Review
  8. Article
  9. AlphaPhysiological reports · 2018
    Article
  10. Article
  11. Article
  12. Attenuated rapid onset vasodilation with greater force production in skeletal muscle of caveolin-2-/- mice.American journal of physiology. Heart and circulatory physiology · 2016
    Article
  13. Article
  14. Article
  15. Functional sympatholysis in hypertension.Autonomic neuroscience : basic & clinical · 2015
    Review
  16. Article
  17. Aging alters reactivity of microvascular resistance networks in mouse gluteus maximus muscle.American journal of physiology. Heart and circulatory physiology · 2014
    Article
  18. Article
  19. Article
  20. 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

3 authors at 2 institutions in 1 country.

Alex W MooreDepartment of Biomedical Sciences, University of Missouri, Columbia, MO 65211, USA.
William F Jackson
Steven S Segal
University of Missouri · USMichigan State University · US

Funding

Microcirculation in Aging Skeletal MuscleR01HL086483 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI SEGAL, STEVEN S · 2007 to 2012
$2.4M
NHLBI NIH HHS R01 HL086483NHLBI NIH HHS R01-HL086483
6 · The paper itself

Abstract

Activation of vascular adrenoreceptors (ARs) governs the magnitude and distribution of muscle blood flow in accord with the distribution of AR subtypes. Functional studies in the rat cremaster muscle indicate that α1ARs predominate in proximal arterioles (first-order, 1A) while α2ARs predominate in distal arterioles (third-order, 3A). However, little is known of AR subtype distribution in arteriolar networks of locomotor skeletal muscles, particularly in the mouse. We tested the hypotheses that functional AR subtypes exhibit heterogeneity among branches of arteriolar networks in a locomotor muscle and that the nature of this heterogeneity can vary between muscles having diverse functions. In anaesthetized male C57BL/6J mice (3 months old), concentration-response curves (10(-9) m to 10(-5) m, 0.5 log increments) were evaluated in the gluteus maximus muscle superfused with physiological saline solution (35°C, pH 7.4; n ≥ 5 per group). Noradrenaline (NA, non-selective αAR agonist) constricted 1A, 2A and 3A with similar potency and efficacy. Phenylephrine (PE; α1AR agonist) evoked greater (P < 0.05) constriction in 3A (inhibited by 10(-8) m prazosin; α1AR antagonist) while UK 14304 (UK; α2AR agonist) evoked greater (P < 0.05) constriction in 1A (inhibited by 10(-7) m rauwolscine; α2AR antagonist). Isoproterenol (isoprenaline; βAR agonist) dilated 1A, 2A and 3A near-maximally with similar potency and efficacy; these dilatations were inhibited by 10(-7) m propranolol (βAR antagonist) which otherwise had no effect on responses to NA, PE, or UK. Complementary experiments in the mouse cremaster muscle revealed a pattern of αAR subtype distribution that, while distinct from the gluteus maximus muscle, was consistent with that reported for the rat cremaster muscle. We conclude that functional αAR subtype distribution in arteriolar networks of skeletal muscle varies with muscle function as well as vessel branch order.

Indexed as

Adrenergic alpha-1 Receptor AgonistsAdrenergic alpha-2 Receptor AgonistsAdrenergic beta-AntagonistsAnimalsArteriolesBrimonidine TartrateIsoproterenolMaleMiceMice, Inbred C57BLModels, AnimalMuscle, SkeletalNorepinephrinePhenylephrinePrazosinPropranololAdrenergic alpha-1 Receptor AgonistsAdrenergic alpha-2 Receptor AgonistsAdrenergic beta-AntagonistsBrimonidine TartrateIsoproterenolNorepinephrinePhenylephrinePrazosinPropranololQuinoxalinesReceptors, Adrenergic, alpha-1Receptors, Adrenergic, alpha-2

Identifiers

PMID20807785
PMCPMC3002455
OpenAlexW2161754170

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.