Evidence map›Paper›PMID 30325514›Full record

ArticleThe Journal of comparative neurology2018

Neurons with diverse phenotypes project from the caudal to the rostral nucleus of the solitary tract.

Susan Travers, Joseph Breza, Jacob Harley, JiuLin Zhu, Joseph Travers

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2018. 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
1.8field-weighted citation impact, top 16% 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, 25 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

5 authors at 1 institution in 1 country.

Susan TraversDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio.ORCID 0000-0001-8730-3618
Joseph BrezaDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio.
Jacob HarleyDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio.
JiuLin ZhuDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio.
Joseph TraversDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio.
The Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
GUSTATORY AFFERENT ORGANIZATION IN THE SOLITARY NUCLEUSR01DC000416 · NIDCD · OHIO STATE UNIVERSITY · PI TRAVERS, SUSAN P · 1992 to 2013
$2.7M
Inhibitory Modulation and Circuitry in the Rostral Solitary NucleusR01DC016112 · NIDCD · OHIO STATE UNIVERSITY · PI TRAVERS, SUSAN P · 2017 to 2021
$2.0M
Catecholaminergic Modulation of Taste Circuitry Using OptogeneticsR21DC013676 · NIDCD · OHIO STATE UNIVERSITY · PI TRAVERS, JOSEPH B · 2014 to 2015
$422k
NCI NIH HHS P30 CA016058NIDCD NIH HHS R01 DC000416NIDCD NIH HHS R01 DC016112NIDCD NIH HHS R21 DC013676
6 · The paper itself

Abstract

The nucleus of the solitary tract is a potential site for taste-visceral interactions. Connections from the caudal, visceral area of the nucleus (cNST) to the rostral, gustatory zone (rNST) have been described, but the phenotype of cells giving rise to the projection(s) and their distribution among rNST subdivisions are unknown. To determine these characteristics of the intrasolitary pathway, we injected pan-neuronal and floxed AAV viruses into the cNST of mice expressing cre in glutamatergic, GABAergic, or catecholaminergic neurons. Particular attention was paid to the terminal field distribution in rNST subdivisions by simultaneously visualizing P2X2 localized to gustatory afferent terminals. All three phenotypically identified pathways terminated in rNST, with the density greatest for glutamatergic and sparsest for catecholaminergic projections, observations supported by retrograde tracing. Interestingly, cNST neurons had more prominent projections to rNST regions medial and ventral to P2X2 staining, i.e., the medial and ventral subdivisions. In addition, GABAergic neurons projected robustly to the lateral subdivision and adjacent parts of the reticular formation and spinal trigeminal nucleus. Although cNST neurons also projected to the P2X2-rich central subdivision, such projections were sparser. These findings suggest that cNST visceral signals exert stronger excitatory and inhibitory influences on local autonomic and reflex pathways associated with the medial and ventral subdivisions compared to weaker modulation of ascending pathways arising from the central subdivision and ultimately destined for the forebrain.

Indexed as

AnimalsCatecholaminesFemalegamma-Aminobutyric AcidGlutamic AcidImmunohistochemistryMaleMiceMice, Inbred C57BLNeural PathwaysNeuronsNeurons, AfferentProsencephalonReceptors, Purinergic P2X2Solitary NucleusTasteCatecholaminesgamma-Aminobutyric AcidGlutamic AcidReceptors, Purinergic P2X2intrasolitaryrNST subdivisionsRRID: AB_10013483RRID: AB_2040054RRID: AB_221569RRID: AB_2314409RRID: AB_2315160RRID: AB_2315161RRID: AB_390204RRID: AB_90738RRID:AB_90755RRID: ISMR_JAX: 000664RRID: ISMR_JAX: 007908RRID: ISMR_JAX: 010802RRID: ISMR_JAX 016963RRID: ISMR_RBRC09645RRID MMRRC_036778-UCDtastevisceral

Identifiers

PMID30325514
PMCPMC6193849
OpenAlexW2895841545

What OpenQuestion holds

Textmetadata
LicenceTDM
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.