Evidence map›Paper›PMID 29077751›Full record

ArticlePloS one2017

Use of ferrets for electrophysiologic monitoring of ion transport.

Niroop Kaza, S Vamsee Raju, Joan M Cadillac, John A Trombley, Lawrence Rasmussen, Liping Tang, Erik Dohm, Kevin S Harrod, Steven M Rowe

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Nicotine aerosols diminish airway CFTR function and mucociliary clearance.American journal of physiology. Lung cellular and molecular physiology · 2023
    Article
  3. Article
  4. Article
  5. Article
  6. 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

9 authors at 1 institution in 1 country.

Niroop KazaDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
S Vamsee RajuDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Joan M CadillacAnimal Resources Program, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
John A TrombleyDepartment of Anesthesiology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Lawrence RasmussenDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Liping TangDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Erik DohmAnimal Resources Program, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Kevin S HarrodDepartment of Anesthesiology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Steven M RoweDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.ORCID http://orcid.org/0000-0001-9045-0133
University of Alabama at Birmingham · US

Funding

UAB CF Research and Translation Core CenterP30DK072482 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI David M. Bedwell · 2007 to 2026
$23.0M
Translational Program in CFTR-Related Airway DiseasesR35HL135816 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ROWE, STEVEN MARK · 2017 to 2022
$6.3M
Molecular Pathogenesis and Phenotype of Acquired CFTR Dysfunction in COPDR01HL105487 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ROWE, STEVEN MARK · 2011 to 2016
$2.7M
NHLBI NIH HHS R01 HL105487NHLBI NIH HHS R35 HL135816NIDDK NIH HHS P30 DK072482
6 · The paper itself

Abstract

Limited success achieved in translating basic science discoveries into clinical applications for chronic airway diseases is attributed to differences in respiratory anatomy and physiology, poor approximation of pathologic processes, and lack of correlative clinical endpoints between humans and laboratory animal models. Here, we discuss advantages of using ferrets (Mustela putorus furo) as a model for improved understanding of human airway physiology and demonstrate assays for quantifying airway epithelial ion transport in vivo and ex vivo, and establish air-liquid interface cultures of ferret airway epithelial cells as a complementary in vitro model for mechanistic studies. We present data here that establishes the feasibility of measuring these human disease endpoints in ferrets. Briefly, potential difference across the nasal and the lower airway epithelium in ferrets could be consistently assessed, were highly reproducible, and responsive to experimental interventions. Additionally, ferret airway epithelial cells were amenable to primary cell culture methods for in vitro experiments as was the use of ferret tracheal explants as an ex vivo system for assessing ion transport. The feasibility of conducting multiple assessments of disease outcomes supports the adoption of ferrets as a highly relevant model for research in obstructive airway diseases.

Indexed as

Ion TransportAnimalsBronchiCystic Fibrosis Transmembrane Conductance RegulatorElectrophysiological PhenomenaEpithelial CellsEpithelial Sodium ChannelsFerretsTracheaCystic Fibrosis Transmembrane Conductance RegulatorEpithelial Sodium Channels

Identifiers

PMID29077751
PMCPMC5659650
OpenAlexW2766732449

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.