Evidence map›Paper›PMID 18716034›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2008

Local circuit input to the medullary reticular formation from the rostral nucleus of the solitary tract.

J Nasse, D Terman, S Venugopal, G Hermann, R Rogers, J B Travers

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
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  4. Review
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  7. Response of catecholaminergic neurons in the mouse hindbrain to glucoprivic stimuli is astrocyte dependent.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    Article
  8. Review
  9. Odor-taste convergence in the nucleus of the solitary tract of the awake freely licking rat.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  10. Article
  11. Article
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  14. Activation of NPY receptors suppresses excitatory synaptic transmission in a taste-feeding network in the lower brain stem.American journal of physiology. Regulatory, integrative and comparative physiology · 2012
    Article
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  18. Article
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  20. Leptin and the systems neuroscience of meal size control.Frontiers in neuroendocrinology · 2010
    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

6 authors at 1 institution in 1 country.

J NasseCollege of Dentistry, Ohio State Univ., 305 W. 12th Ave., Columbus, OH 43201, USA.
D Terman
S Venugopal
G Hermann
R Rogers
J B Travers
The Ohio State University · US

Funding

NEURAL BASIS OF TASTE ELICITED INGESTION AND REJECTIONR01DC000417 · NIDCD · OHIO STATE UNIVERSITY · PI TRAVERS, JOSEPH B · 1989 to 2009
$2.2M
NIDCD NIH HHS DC-00417NIDCD NIH HHS R01 DC000417
6 · The paper itself

Abstract

The intermediate reticular formation (IRt) subjacent to the rostral (gustatory) nucleus of the solitary tract (rNST) receives projections from the rNST and appears essential to the expression of taste-elicited ingestion and rejection responses. We used whole cell patch-clamp recording and calcium imaging to characterize responses from an identified population of prehypoglossal neurons in the IRt to electrical stimulation of the rNST in a neonatal rat pup slice preparation. The calcium imaging studies indicated that IRt neurons could be activated by rNST stimulation and that many neurons were under tonic inhibition. Whole cell patch-clamp recording revealed mono- and polysynaptic projections from the rNST to identified prehypoglossal neurons. The projection was primarily excitatory and glutamatergic; however, there were some inhibitory GABAergic projections, and many neurons received excitatory and inhibitory inputs. There was also evidence of disinhibition. Overall, bath application of GABA(A) antagonists increased the amplitude of excitatory currents, and, in several neurons, stimulation of the rNST systematically decreased inhibitory currents. We have hypothesized that the transition from licks to gapes by natural stimuli, such as quinine monohydrochloride, could occur via such disinhibition. We present an updated dynamic model that summarizes the complex synaptic interface between the rNST and the IRt and demonstrates how inhibition could contribute to the transition from ingestion to rejection.

Indexed as

AlgorithmsAnimalsCalciumElectric StimulationElectromyographyElectrophysiologyExcitatory Amino Acid AntagonistsFemaleHypoglossal NerveImage Processing, Computer-AssistedJawMedulla OblongataMicroinjectionsModels, NeurologicalMotor NeuronsMuscle, SkeletalCalciumExcitatory Amino Acid Antagonists

Identifiers

PMID18716034
PMCPMC4073952
OpenAlexW2149550225

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.