Evidence map›Paper›PMID 23247111›Full record

ArticleThe Journal of physiology2013

Ageing alters perivascular nerve function of mouse mesenteric arteries in vivo.

Erika B Westcott, Steven S Segal

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. AnFrontiers in bioengineering and biotechnology · 2024
    Article
  3. Impact of aging on vascular ion channels: perspectives and knowledge gaps across major organ systems.American journal of physiology. Heart and circulatory physiology · 2023
    Review
  4. Role of perivascular nerve and sensory neurotransmitter dysfunction in inflammatory bowel disease.American journal of physiology. Heart and circulatory physiology · 2021
    Article
  5. Aging alters spontaneous and neurotransmitter-mediated CaMicrocirculation (New York, N.Y. : 1994) · 2020
    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. Article
  10. Article
  11. Increased amplitude of inward rectifier KAmerican journal of physiology. Heart and circulatory physiology · 2017
    Article
  12. Article
  13. Advanced age decreases local calcium signaling in endothelium of mouse mesenteric arteries in vivo.American journal of physiology. Heart and circulatory physiology · 2016
    Article
  14. Article
  15. Article
  16. 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

2 authors at 1 institution in 1 country.

Erika B WestcottDepartment of Medical Pharmacology and Physiology, University of Missouri, Columbia, MO 65212, USA.
Steven S Segal
University of Missouri · US

Funding

Intercellular Coordination of Blood Flow ControlR37HL041026 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI SEGAL, STEVEN S · 2008 to 2018
$3.7M
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-HL086483NHLBI NIH HHS R37 HL041026NHLBI NIH HHS R37-HL41026
6 · The paper itself

Abstract

Abstract  Mesenteric arteries (MAs) are studied widely in vitro but little is known of their reactivity in vivo. Transgenic animals have enabled Ca(2+) signalling to be studied in isolated MAs but the reactivity of these vessels in vivo is undefined. We tested the hypothesis that ageing alters MA reactivity to perivascular nerve stimulation (PNS) and adrenoreceptor (AR) activation during blood flow control. First- (1A), second- (2A) and third-order (3A) MAs of pentobarbital-anaesthetized Young (3-6 months) and Old (24-26 months) male and female Cx40(BAC)-GCaMP2 transgenic mice (C57BL/6 background; positive or negative for the GCaMP2 transgene) were studied with intravital microscopy. A segment of jejunum was exteriorized and an MA network was superfused with physiological salt solution (pH 7.4, 37°C). Resting tone was 10% in MAs of Young and Old mice; diameters were ∼5% (1A), 20% (2A) and 40% (3A) smaller (P 0.05) in Old mice. Throughout MA networks, vasoconstriction increased with PNS frequency (1-16 Hz) but was ∼20% less in Young vs. Old mice (P 0.05) and was inhibited by tetrodotoxin (1 μm). Capsaicin (10 μm; to inhibit sensory nerves) enhanced MA constriction to PNS (P 0.05) by ∼20% in Young but not Old mice. Phenylephrine (an α1AR agonist) potency was greater in Young mice (P 0.05) with similar efficacy (∼60% constriction) across ages and MA branches. Constrictions to UK14304 (an α2AR agonist) were less (∼20%; P 0.05) and were unaffected by ageing. Irrespective of sex or transgene expression, ageing consistently reduced the sensitivity of MAs to α1AR vasoconstriction while blunting the attenuation of sympathetic vasoconstriction by sensory nerves. These findings imply substantive alterations in splanchnic blood flow control with ageing.

Indexed as

AgingSplanchnic CirculationVasoconstrictionAdrenergic alpha-1 Receptor AgonistsAdrenergic alpha-1 Receptor AntagonistsAge FactorsAnimalsConnexinsDose-Response Relationship, DrugElectric StimulationEndothelial CellsFemaleGap Junction alpha-5 ProteinGreen Fluorescent ProteinsJejunumMaleAdrenergic alpha-1 Receptor AgonistsAdrenergic alpha-1 Receptor AntagonistsConnexinsGap Junction alpha-5 ProteinGreen Fluorescent ProteinsReceptors, Adrenergic, alpha-1Vasoconstrictor Agents

Identifiers

PMID23247111
PMCPMC3607869
OpenAlexW1493784612

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.