Evidence map›Paper›PMID 31631251›Full record

ArticlePflugers Archiv : European journal of physiology2019

Optogenetic analysis of respiratory neuronal networks in the ventral medulla of neonatal rats producing channelrhodopsin in Phox2b-positive cells.

Keiko Ikeda, Hiroyuki Igarashi, Hiromu Yawo, Kazuto Kobayashi, Satoru Arata, Kiyoshi Kawakami, Masahiko Izumizaki, Hiroshi Onimaru

Abstract read
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In one paragraph

Article in Pflugers Archiv : European journal of 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 41% 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, 7 citations in OpenAlex.

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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

8 authors at 6 institutions in 2 countries.

Keiko IkedaDepartment of Physiology, International University of Health and Welfare, Chiba, 286-8686, Japan.
Hiroyuki IgarashiDepartment of Physiology and Pharmacology, Schulich School of Medicine and Dentistry, Robarts Research Institute, Western University, London, ON, N6A 5B7, Canada.
Hiromu YawoThe Institute for Solid State Physics, The University of Tokyo, Kashiwa, 277-8581, Japan.
Kazuto KobayashiDepartment of Molecular Genetics, Institute of Biomedical Sciences, Fukushima Medical University School of Medicine, Fukushima, 960-1295, Japan.
Satoru ArataDepartment of Biochemistry, Faculty of Arts and Sciences, Showa University, Fujiyoshida, Yamanashi, 403-0005, Japan.
Kiyoshi KawakamiDivision of Biology, Center for Molecular Medicine, Jichi Medical University, Shimotsuke, Tochigi, 329-0498, Japan.
Masahiko IzumizakiDepartment of Physiology, Showa University School of Medicine, Tokyo, 142-8555, Japan.
Hiroshi OnimaruDepartment of Physiology, Showa University School of Medicine, Tokyo, 142-8555, Japan. oni@med.showa-u.ac.jp.
Showa University · JPFukushima Medical University · JPInternational University of Health and Welfare · JPJichi Medical University · JPThe University of Tokyo · JPWestern University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paired-like homeobox gene Phox2b is predominantly expressed in pre-inspiratory neurons in the parafacial respiratory group (pFRG) in newborn rat rostral ventrolateral medulla. To analyse detailed local networks of the respiratory centre using optogenetics, the effects of selective activation of Phox2b-positive neurons in the ventral medulla on respiratory rhythm generation were examined in brainstem-spinal cord preparations isolated from transgenic newborn rats with Phox2b-positive cells expressing channelrhodopsin variant ChRFR(C167A). Photostimulation up to 43 s increased the respiratory rate > 200% of control, whereas short photostimulation (1.5 s) of the rostral pFRG reset the respiratory rhythm. At the cellular level, photostimulation depolarised Phox2b-positive pre-inspiratory, inspiratory and respiratory-modulated tonic neurons and Phox2b-negative pre-inspiratory neurons. In contrast, changes in membrane potential of Phox2b-negative inspiratory and expiratory neurons varied depending on characteristics of ongoing synaptic connections in local respiratory networks in the rostral medulla. In the presence of tetrodotoxin, photostimulation depolarised Phox2b-positive cells, but caused no significant changes in membrane potential of Phox2b-negative cells. We concluded that depolarisation of Phox2b-positive neurons was due to cell-autonomous photo-activation and summation of excitatory postsynaptic potentials, whereas membrane potential changes of Phox2b-negative neurons depended on the network configuration. Our findings shed further light on local networks among respiratory-related neurons in the rostral ventrolateral medulla and emphasise the important role of pre-inspiratory neurons in respiratory rhythm generation in the neonatal rat en bloc preparation.

Indexed as

AnimalsAnimals, NewbornBrain StemChannelrhodopsinsFemaleHomeodomain ProteinsMaleMedulla OblongataMembrane PotentialsNeuronsOptogeneticsRatsRespirationRespiratory CenterTetrodotoxinTranscription FactorsChannelrhodopsinsHomeodomain ProteinsNBPhox proteinTetrodotoxinTranscription FactorsChannelrhodopsinOptogeneticsParafacial respiratory groupPhox2bTransgenic rat

Identifiers

PMID31631251
OpenAlexW2980757310

What OpenQuestion holds

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Read underepoch 390

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.