Evidence map›Paper›PMID 28615161›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2017

High glucose increases action potential firing of catecholamine neurons in the nucleus of the solitary tract by increasing spontaneous glutamate inputs.

Brandon L Roberts, Mingyan Zhu, Huan Zhao, Crystal Dillon, Suzanne M Appleyard

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Nucleus of the solitary tract A2 neurons control feeding behaviors via projections to the paraventricular hypothalamus.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Glutamatergic plasticity within neurocircuits of the dorsal vagal complex and the regulation of gastric functions.American journal of physiology. Gastrointestinal and liver physiology · 2021
    Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Sex-steroid-dependent plasticity of brain-stem autonomic circuits.American journal of physiology. Regulatory, integrative and comparative physiology · 2020
    Review
  17. Article
  18. Article
  19. Review
  20. 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

5 authors at 1 institution in 1 country.

Brandon L RobertsDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, Washington.
Mingyan ZhuDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, Washington.
Huan ZhaoDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, Washington.
Crystal DillonDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, Washington.
Suzanne M AppleyardDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, Washington appleyas@vetmed.wsu.edu.
Washington State University · US

Funding

Integration of Peripheral and Central Appetite Signals by Brainstem NeuronsR01DK083452 · NIDDK · WASHINGTON STATE UNIVERSITY · PI APPLEYARD, SUZANNE M · 2009 to 2018
$2.9M
NIDDK NIH HHS R01 DK083452
6 · The paper itself

Abstract

Glucose is a crucial substrate essential for cell survival and function. Changes in glucose levels impact neuronal activity and glucose deprivation increases feeding. Several brain regions have been shown to respond to glucoprivation, including the nucleus of the solitary tract (NTS) in the brain stem. The NTS is the primary site in the brain that receives visceral afferent information from the gastrointestinal tract. The catecholaminergic (CA) subpopulation within the NTS modulates many homeostatic functions including cardiovascular reflexes, respiration, food intake, arousal, and stress. However, it is not known if they respond to changes in glucose. Here we determined whether NTS-CA neurons respond to changes in glucose concentration and the mechanism involved. We found that decreasing glucose concentrations from 5 mM to 2 mM to 1 mM, significantly decreased action potential firing in a cell-attached preparation, whereas increasing it back to 5 mM increased the firing rate. This effect was dependent on glutamate release from afferent terminals and required presynaptic 5-HT

Indexed as

Action PotentialsAnimalsCatecholaminesCells, CulturedExcitatory Postsynaptic PotentialsFemaleGlucoseGlutamic AcidMiceMice, Inbred C57BLMice, TransgenicNeuronsNeurotransmitter AgentsSolitary NucleusSynaptic TransmissionCatecholaminesGlucoseGlutamic AcidNeurotransmitter AgentscatecholamineglucoseNTSserotoninvagus

Identifiers

PMID28615161
PMCPMC5625278
OpenAlexW2624776509

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.