Evidence map›Paper›PMID 29093172›Full record

ArticleJournal of neurophysiology2018

A computational analysis of signal fidelity in the rostral nucleus of the solitary tract.

Alison Boxwell, David Terman, Marion Frank, Yuchio Yanagawa, Joseph B Travers

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neurophysiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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 3 institutions in 2 countries.

Alison BoxwellCollege of Medicine, Ohio State University , Columbus, Ohio.
David TermanDepartment of Mathematics, Ohio State University , Columbus, Ohio.
Marion FrankDepartment of Oral Health and Diagnostic Sciences, University of Connecticut Health Center , Farmington, Connecticut.
Yuchio YanagawaDepartment of Genetic and Behavioral Neuroscience, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.
Joseph B TraversDivision of Biosciences, Ohio State University, Columbus, Ohio.
The Ohio State University · USGunma University · JPUConn Health · US

Funding

Comprehensive Training in Oral &Craniofacial SciencesT32DE014320 · NIDCR · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2001 to 2022
$10.2M
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
NIDCD NIH HHS R01 DC016112NIDCD NIH HHS R21 DC013676NIDCR NIH HHS T32 DE014320
6 · The paper itself

Abstract

Neurons in the rostral nucleus of the solitary tract (rNST) convey taste information to both local circuits and pathways destined for forebrain structures. This nucleus is more than a simple relay, however, because rNST neurons differ in response rates and tuning curves relative to primary afferent fibers. To systematically study the impact of convergence and inhibition on firing frequency and breadth of tuning (BOT) in rNST, we constructed a mathematical model of its two major cell types: projection neurons and inhibitory neurons. First, we fit a conductance-based neuronal model to data derived from whole cell patch-clamp recordings of inhibitory and noninhibitory neurons in a mouse expressing Venus under the control of the VGAT promoter. We then used in vivo chorda tympani (CT) taste responses as afferent input to modeled neurons and assessed how the degree and type of convergence influenced model cell output frequency and BOT for comparison with in vivo gustatory responses from the rNST. Finally, we assessed how presynaptic and postsynaptic inhibition impacted model cell output. The results of our simulations demonstrated 1) increasing numbers of convergent afferents (2-10) result in a proportional increase in best-stimulus firing frequency but only a modest increase in BOT, 2) convergence of afferent input selected from the same best-stimulus class of CT afferents produced a better fit to real data from the rNST compared with convergence of randomly selected afferent input, and 3) inhibition narrowed the BOT to more realistically model the in vivo rNST data. NEW & NOTEWORTHY Using a combination of in vivo and in vitro neurophysiology together with conductance-based modeling, we show how patterns of convergence and inhibition interact in the rostral (gustatory) solitary nucleus to maintain signal fidelity. Although increasing convergence led to a systematic increase in firing frequency, tuning specificity was maintained with a pattern of afferent inputs sharing the best-stimulus compared with random inputs. Tonic inhibition further enhanced response fidelity.

Indexed as

Action PotentialsModels, NeurologicalAfferent PathwaysAnimalsChorda Tympani NerveGABAergic NeuronsMice, TransgenicNeural PathwaysNeuronsSolitary NucleusTasteconvergenceinhibitionmodelingtaste

Identifiers

PMID29093172
PMCPMC5899313
OpenAlexW2765842649

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.