Evidence map›Paper›PMID 30601705›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2019

Respiratory motoneuron properties during the transition from gill to lung breathing in the American bullfrog.

Tara A Janes, Stéphanie Fournier, Simon Chamberland, Gregory D Funk, Richard Kinkead

Abstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2019. 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
0.5field-weighted citation impact, top 43% 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, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

5 authors at 3 institutions in 2 countries.

Tara A JanesDepartment of Pediatrics, Université Laval and Institut Universitaire de Cardiologie et de Pneumologie de Québec , Québec City, Québec , Canada.ORCID 0000-0002-2824-9487
Stéphanie FournierDepartment of Pediatrics, Université Laval and Institut Universitaire de Cardiologie et de Pneumologie de Québec , Québec City, Québec , Canada.
Simon ChamberlandDepartment of Neuroscience and Physiology and New York University Neuroscience Institute, New York University Langone Medical Center , New York, New York.
Gregory D FunkDepartment of Physiology, Neuroscience and Mental Health Institute, Women and Children's Health Research Institute, University of Alberta , Edmonton, Alberta , Canada.
Richard KinkeadDepartment of Pediatrics, Université Laval and Institut Universitaire de Cardiologie et de Pneumologie de Québec , Québec City, Québec , Canada.
Institut universitaire de cardiologie et de pneumologie de Québec · CANYU Langone Health · USUniversity of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amphibian respiratory development involves a dramatic metamorphic transition from gill to lung breathing and coordination of distinct motor outputs. To determine whether the emergence of adult respiratory motor patterns was associated with similarly dramatic changes in motoneuron (MN) properties, we characterized the intrinsic electrical properties of American bullfrog trigeminal MNs innervating respiratory muscles comprising the buccal pump. In premetamorphic tadpoles (TK stages IX-XVIII) and adult frogs, morphometric analyses and whole cell recordings were performed in trigeminal MNs identified by fluorescent retrograde labeling. Based on the amplitude of the depolarizing sag induced by hyperpolarizing voltage steps, two MN subtypes (I and II) were identified in tadpoles and adults. Compared with type II MNs, type I MNs had larger sag amplitudes (suggesting a larger hyperpolarization-activated inward current), greater input resistance, lower rheobase, hyperpolarized action potential threshold, steeper frequency-current relationships, and fast firing rates and received fewer excitatory postsynaptic currents. Postmetamorphosis, type I MNs exhibited similar sag, enhanced postinhibitory rebound, and increased action potential amplitude with a smaller-magnitude fast afterhyperpolarization. Compared with tadpoles, type II MNs from frogs received higher-frequency, larger-amplitude excitatory postsynaptic currents. Input resistance decreased and rheobase increased postmetamorphosis in all MNs, concurrent with increased soma area and hyperpolarized action potential threshold. We suggest that type I MNs are likely recruited in response to smaller, buccal-related synaptic inputs as well as larger lung-related inputs, whereas type II MNs are likely recruited in response to stronger synaptic inputs associated with larger buccal breaths, lung breaths, or nonrespiratory behaviors involving powerful muscle contractions.

Indexed as

Action PotentialsAnimalsCheekExcitatory Postsynaptic PotentialsGillsLungMetamorphosis, BiologicalMotor NeuronsRana catesbeianaRespiratory MusclesSynaptic TransmissionTrigeminal Nerveamphibianneurodevelopmentrespirationtrigeminal motoneuron

Identifiers

PMID30601705
PMCPMC6459380
OpenAlexW2908107963

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.