Evidence map›Paper›PMID 40579744›Full record

ArticleMicrocirculation (New York, N.Y. : 1994)2025

Modulatory Role of Nitric Oxide on the Vasomotor Actions of NPY in Porcine Cerebral Arteries.

Gabriela Delgado, Cameron J Morse, Breanna Barlage, M Harold Laughlin, Craig A Emter, Erika M Boerman, Jaume Padilla, Corey R Tomczak, T Dylan Olver

Abstract read
In one paragraph

Article in Microcirculation (New York, N.Y. : 1994), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

9 authors.

Gabriela DelgadoDepartment of Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Cameron J MorseDepartment of Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Breanna BarlageDepartment of Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
M Harold LaughlinDepartment of Biomedical Sciences, College of Veterinary Medicine University of Missouri, Columbia, Missouri, USA.
Craig A EmterDepartment of Biomedical Sciences, College of Veterinary Medicine University of Missouri, Columbia, Missouri, USA.
Erika M BoermanDepartment of Medical Physiology and Pharmacology, University of Missouri, Columbia, Missouri, USA.ORCID 0000-0001-8103-3485
Jaume PadillaDalton Cardiovascular Research Center, University of Missouri, Columbia, Missouri, USA.
Corey R TomczakCollege of Kinesiology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
T Dylan OlverDepartment of Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

Funding

Natural Sciences and Engineering Research Council of Canada
6 · The paper itself

Abstract

Neuropeptide Y (NPY) is a sympathetic co-transmitter that mediates vasoconstriction. However, there is evidence that it may also mediate dilation through a nitric oxide (NO)-dependent mechanism.

objectiveWe used a swine model to examine how NPY influences cerebral vascular regulation and hypothesized that NPY would elicit both vasoconstrictor and vasodilatory effects, and that such effects would be modulated partially by NO signaling.

methodsBriefly, cerebral perfusion and blood pressure were monitored during intracarotid saline or NPY infusion (0.1 μg/kg) in the presence and absence of NO synthase (NOS) inhibition (N

resultsIntracarotid NPY infusions elicited transient dilation that was blocked by NOS inhibition. In isolated pial arteries, distinct populations of NPY-Y1 receptors were observed on both the vascular smooth muscle (VSM) and endothelium. Extraluminal application of NPY elicited vasoconstriction, while intraluminal delivery elicited vasodilation. NOS inhibition enhanced the magnitude of vasoconstriction in isolated pial arteries. Endothelial denudation, Y1 receptor antagonism, and NOS inhibition each blunted NPY-induced vasodilation.

conclusionThese data suggest both vasoconstrictor and vasodilatory effects of NPY are modulated partially by NO signaling.

Indexed as

Cerebral ArteriesNeuropeptide YNitric OxideVasoconstrictionVasodilationAnimalsNG-Nitroarginine Methyl EsterNitric Oxide SynthaseReceptors, Neuropeptide YSwineNeuropeptide Yneuropeptide Y-Y1 receptorNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide SynthaseReceptors, Neuropeptide Ycerebralcerebrovascularnitric oxideNPY

Identifiers

PMID40579744
PMCPMC12205166

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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.