Evidence map›Paper›PMID 30502519›Full record

ArticleRespiratory physiology & neurobiology2019

The contribution of endogenous glutamatergic input in the ventral respiratory column to respiratory rhythm.

Denise R Cook-Snyder, Justin R Miller, Angela A Navarrete-Opazo, Jennifer J Callison, Robin C Peterson, Francis A Hopp, Eckehard A E Stuth, Edward J Zuperku, Astrid G Stucke

Open access · greenAbstract read
In one paragraph

Article in Respiratory physiology & neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

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  2. Current research in physiology · 2025
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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

9 authors at 4 institutions in 1 country.

Denise R Cook-SnyderDepartment of Neuroscience, Carthage College, Kenosha, WI, United States.
Justin R MillerDepartment of Biology, Carthage College, Kenosha, WI, United States.
Angela A Navarrete-OpazoDepartment of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI, United States.
Jennifer J CallisonDepartment of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI, United States.
Robin C PetersonDepartment of Neuroscience, Carthage College, Kenosha, WI, United States.
Francis A HoppZablocki VA Medical Center, Milwaukee, WI, United States.
Eckehard A E StuthDepartment of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI, United States; Children's Hospital of Wisconsin, Milwaukee, WI, United States.
Edward J ZuperkuDepartment of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI, United States; Zablocki VA Medical Center, Milwaukee, WI, United States.
Astrid G StuckeDepartment of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI, United States; Children's Hospital of Wisconsin, Milwaukee, WI, United States. Electronic address: astucke@mcw.edu.
Carthage College · USMedical College of Wisconsin · USChildren's Hospital of Wisconsin · USMilwaukee VA Medical Center · US

Funding

Age-dependent differences in opioid-induced respiratory depressionR01GM112960 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI STUCKE, ASTRID G · 2015 to 2019
$1.2M
Neuropharmacology of Pontine Control of Breathing FrequencyI01BX000721 · VA · CLEMENT J. ZABLOCKI VA MEDICAL CENTER · PI ZUPERKU, EDWARD J · 2011 to 2018
–
BLRD VA I01 BX000721NIGMS NIH HHS R01 GM112960
6 · The paper itself

Abstract

Glutamate is the predominant excitatory neurotransmitter in the ventral respiratory column; however, the contribution of glutamatergic excitation in the individual subregions to respiratory rhythm generation has not been fully delineated. In an adult, in vivo, decerebrate rabbit model during conditions of mild hyperoxic hypercapnia we blocked glutamatergic excitation using the receptor antagonists 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo[f]quinoxaline-2,3-dione (NBQX) and d(-)-2-amino-5-phosphonopentanoic acid (AP5). Disfacilitation of the preBötzinger Complex caused a decrease in inspiratory and expiratory duration as well as peak phrenic amplitude and ultimately apnea. Disfacilitation of the Bötzinger Complex caused a decrease in inspiratory and expiratory duration; subsequent disfacilitation of the preBötzinger Complex resulted in complete loss of the respiratory pattern but maintained tonic inspiratory activity. We conclude that glutamatergic drive to the preBötzinger Complex is essential for respiratory rhythm generation. Glutamatergic drive to the Bötzinger Complex significantly affects inspiratory and expiratory phase duration. Bötzinger Complex neurons are responsible for maintaining the silent expiratory phase of the phrenic neurogram.

Indexed as

RespirationAnalysis of VarianceAnimalsBrain MappingExcitatory Amino Acid AgonistsExcitatory Amino Acid AntagonistsFemaleGlutamic AcidMaleMicroinjectionsNeuronsPeriodicityPhrenic NerveRabbitsRespiratory CenterRespiratory MechanicsExcitatory Amino Acid AgonistsExcitatory Amino Acid AntagonistsGlutamic AcidBötzinger ComplexGlutamatergic disfacilitationpreBötzinger ComplexReciprocal inhibitionRespiratory rhythmVentral respiratory column

Identifiers

PMID30502519
PMCPMC6397772
OpenAlexW2902841665

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.