Evidence map›Paper›PMID 32783212›Full record

ArticleJournal of anatomy2021

Distribution and morphology of sensory and autonomic fibres in the subendocardial plexus of the rat heart.

Fiona C Shenton, Thomas Campbell, James F X Jones, Susan Pyner

Open access · hybridAbstract read
In one paragraph

Article in Journal of anatomy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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

4 authors at 2 institutions in 2 countries.

Fiona C ShentonDepartment of Biosciences, Durham University, Durham, UK.ORCID 0000-0002-6876-3480
Thomas CampbellDiscipline of Anatomy, School of Medicine, University College Dublin, Dublin 4, Ireland.ORCID 0000-0001-6287-6081
James F X JonesDiscipline of Anatomy, School of Medicine, University College Dublin, Dublin 4, Ireland.ORCID 0000-0002-1997-4257
Susan PynerDepartment of Biosciences, Durham University, Durham, UK.ORCID 0000-0002-6073-6234
Durham University · GBUniversity College Dublin · IE

Funding

British Heart Foundation PG/14/53/30900
6 · The paper itself

Abstract

Cardiac reflexes originating from sensory receptors in the heart ensure blood supply to vital tissues and organs in the face of constantly changing demands. Atrial volume receptors are mechanically sensitive vagal afferents which relay to the medulla and hypothalamus, affecting vasopressin release and renal sympathetic activity. To date, two anatomically distinct sensory endings have been identified which may subserve cardiac mechanosensation: end-nets and flower-spray endings. To map the distribution of atrial receptors in the subendocardial space, we have double-labelled rat right atrial whole mounts for neurofilament heavy chain (NFH) and synaptic vesicle protein 2 (SV2) and generated high-resolution maps of the rat subendocardial neural plexus at the cavo-atrial region. In order to elucidate the nature of these fibres, double labelling with synaptophysin (SYN) and either NFH, calcitonin gene-related peptide (CGRP), choline acetyltransferase (ChAT) or tyrosine hydroxylase (TH) was performed. The findings show that subendocardial nerve nets are denser at the superior cavo-atrial junction than the mid-atrial region. Adluminal plexuses had the finest diameters and stained positively for synaptic vesicles (SV2 and SYN), CGRP and TH. These plexuses may represent sympathetic post-ganglionic fibres and/or sensory afferents. The latter are candidate substrates for type B volume receptors which are excited by stretch during atrial filling. Deeper nerve fibres appeared coarser and may be cholinergic (positive staining for ChAT). Flower-spray endings were never observed using immunohistochemistry but were delineated clearly with the intravital stain methylene blue. We suggest that differing nerve fibre structures form the basis by which atrial deformation and hence atrial filling is reflected to the brain.

Indexed as

AnimalsAutonomic Nervous SystemCalcitonin Gene-Related PeptideCholine O-AcetyltransferaseHeartImmunohistochemistryNerve FibersRatsSensory Receptor CellsSynaptophysinTyrosine 3-MonooxygenaseCalcitonin Gene-Related PeptideCholine O-AcetyltransferaseSynaptophysinTyrosine 3-Monooxygenaseatrial mechanoreceptorsatrial volume receptorscalcitonin gene-related peptidecholine acetyltransferasecomplex unencapsulated endingsend-netflower-spray endingsmechanotransductionmethylene blueneurofilamentplasma volume regulationsynaptic vesicle protein 2synaptophysintyrosine hydroxylase

Identifiers

PMID32783212
PMCPMC7754995
OpenAlexW3047306010

What OpenQuestion holds

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LicenceCC BY
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.