Evidence map›Paper›PMID 25936679›Full record

ArticleRespiratory physiology & neurobiology2015

Fentanyl effects on breath generation in C57BL/6J and A/J mouse strains.

Linnea Fechtner, Mazen El Ali, Abdus Sattar, Michael Moore, Kingman P Strohl

Abstract read
In one paragraph

Article in Respiratory physiology & neurobiology, 2015. 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
0.3field-weighted citation impact, top 46% 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, 18 citations in OpenAlex.

  1. Carfentanil Depresses Inspiratory Motor Drive.Journal of substance abuse and alcoholism · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Observational
  7. Article
  8. Article
  9. Article
  10. Intranasal Leptin Prevents Opioid-induced Sleep-disordered Breathing in Obese Mice.American journal of respiratory cell and molecular biology · 2020
    Article
  11. Article
  12. 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

5 authors at 3 institutions in 1 country.

Linnea FechtnerCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Mazen El AliLouis Stokes Department of Veteran Affairs Medical Center, Cleveland, OH, USA; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Abdus SattarCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Michael MooreLouis Stokes Department of Veteran Affairs Medical Center, Cleveland, OH, USA.
Kingman P StrohlLouis Stokes Department of Veteran Affairs Medical Center, Cleveland, OH, USA; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, Case Western Reserve University, Cleveland, OH, USA. Electronic address: kpstrohl@aol.com.
Louis Stokes Cleveland VA Medical Center · USCase Western Reserve University · USUniversity School · US

Funding

Genetic Mechanisms for Central ApneasR21NS052452 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI STROHL, KINGMAN PERKINS · 2006 to 2007
$307k
Respiratory Rhythmogenesis and Chemosensitivity: A Genomic ApproachI01BX001464 · VA · LOUIS STOKES CLEVELAND VA MEDICAL CENTER · PI STROHL, KINGMAN PERKINS · 2012 to 2015
–
BLRD VA I01 BX001464NINDS NIH HHS R21 NS052452
6 · The paper itself

Abstract

We examined the effect of fentanyl on chemoresponsiveness in mouse strains divergent in the expression of spontaneous and post-hypoxic pauses. Frequency and tidal volume were recorded with plethysmography in A/J and C57BL/6J (B6) male mice. Mice selected at random received an intraperitoneal (IP) injection of either saline, low dose fentanyl (LDF = 0.04 mg/kg), or high dose fentanyl (HDF = 0.4 mg/kg) under hypoxia (8% O2) or hyperoxia (100%O2). LDF produced a decrease in frequency during hypoxia in B6, but not A/J, mice. HDF significantly decreased frequency and tidal volume in both strains under hypoxia and hyperoxia (p<0.01); naloxone, an opioid antagonist, reversed this response. The acute administration of fentanyl at any dose did not promote apneas in strains of mice exhibiting regular or irregular respiratory patterns. However, higher doses depressed respiratory frequency in both strains. The B6 mice responded with a depressive response to hypoxia that did not recover with reoxygenation, but did recover with time or naloxone.

Indexed as

Analgesics, OpioidAnimalsDose-Response Relationship, DrugFentanylHypoxiaMaleMiceMice, Inbred AMice, Inbred C57BLPlethysmographyRespirationSpecies SpecificityTidal VolumeTime FactorsAnalgesics, OpioidFentanylApneaGenetic backgroundHypoxiaVentilatory control

Identifiers

PMID25936679
PMCPMC4490006
OpenAlexW1977182632

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.