Evidence map›Paper›PMID 25220699›Full record

ArticleNeuroscience letters2014

Artemisia santolinifolia enhances glutamatergic neurotransmission in the nucleus of the solitary tract.

Katie M Vance, David M Ribnicky, Richard C Rogers, Gerlinda E Hermann

Abstract read
In one paragraph

Article in Neuroscience letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

4 authors.

Katie M VanceLaboratory of Autonomic Neuroscience, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA 70808, USA.
David M RibnickyBiotech Center, Rutgers University, New Brunswick, NJ 08901, USA.
Richard C RogersLaboratory of Autonomic Neuroscience, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA 70808, USA.
Gerlinda E HermannLaboratory of Autonomic Neuroscience, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA 70808, USA. Electronic address: gerlinda.hermann@pbrc.edu.

Funding

Pregnane and Glycosides and Obesity/llya RaskinP50AT002776 · NCCIH · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI RASKIN, ILYA · 2005 to 2019
$24.9M
Training in Botanical Approaches to Combat Metabolic SyndromeT32AT004094 · NCCIH · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI BRANTLEY, PHILLIP J, STEPHENS, JACQUELINE M · 2009 to 2024
$5.7M
Glial-Neural Interactions in Autonomic ControlR01NS060664 · NINDS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI ROGERS, RICHARD C. · 2008 to 2012
$1.6M
NCCIH NIH HHS P50 AT002776NCCIH NIH HHS P50AT002776-01NCCIH NIH HHS T32 AT004094NCCIH NIH HHS T32-AT004094NINDS NIH HHS NS60664NINDS NIH HHS R01 NS060664
6 · The paper itself

Abstract

Artemisia extracts have been used as remedies for a variety of maladies related to metabolic and gastrointestinal control. Because the vagal afferent-nucleus of the solitary tract (NST) synapse regulates the same homeostatic functions affected by Artemisia, it is possible that these extracts may have activity at the synaptic level in the NST. Therefore, we evaluated how extracts of three common medicinal Artemisia species, Artemisia santolinifolia (SANT), Artemisia scoparia (SCO), and Artemisia dracunculus L (PMI-5011), modulate the excitability of the glutamatergic vagal afferent-NST synapse. Our in vitro live cell calcium imaging data from prelabeled vagal afferent terminals show that SANT extract is a positive modulator of vagal afferent calcium levels, as the extract significantly increased the calcium signal relative to the time control. Neither SCO nor PMI-5011 extract altered the vagal calcium signals compared to the time control. Furthermore, whole cell voltage-clamp recordings from NST neurons corroborated the vagal terminal calcium data in that SANT extract also significantly increased miniature excitatory postsynaptic current (mEPSC) frequency in NST neurons. These data suggest that SANT extract could be a pharmacologically significant mediator of glutamatergic neurotransmission within the CNS.

Indexed as

Afferent PathwaysAnimalsArtemisiaCalcium SignalingExcitatory Postsynaptic PotentialsGlutamic AcidIn Vitro TechniquesMiniature Postsynaptic PotentialsNeuronsPatch-Clamp TechniquesPlant ExtractsPresynaptic TerminalsRats, Long-EvansSolitary NucleusSynaptic TransmissionVagus NerveGlutamic AcidPlant ExtractsBotanicalCalcium imagingElectrophysiologymEPSCNSTPresynaptic

Identifiers

PMID25220699
PMCPMC4229135

What OpenQuestion holds

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Registered trials

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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.