Evidence map›Paper›PMID 42387073›Full record

ArticlePsychopharmacology2026

Fentanyl decreases arterial blood oxygen saturation more than furanylfentanyl in mice due to increased apnea.

Catherine Demery, Sierra C Moore, Kelsey E Kochan, Mengchu Li, Thomas D Prince, Benjamin M Clements, Zhongqi Chen, Jessica R Whitaker-Fornek, Erica S Levitt, Jessica P Anand and 1 more

Abstract read
In one paragraph

Article in Psychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Catherine DemeryEdward F. Domino Research Center, Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109, USA.
Sierra C MooreEdward F. Domino Research Center, Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109, USA.
Kelsey E KochanEdward F. Domino Research Center, Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109, USA.
Mengchu LiEdward F. Domino Research Center, Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109, USA.
Thomas D PrinceEdward F. Domino Research Center, Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109, USA.
Benjamin M ClementsEdward F. Domino Research Center, Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109, USA.
Zhongqi ChenDepartment of Pharmaceutical Sciences, University of Michigan College of Pharmacy, 428 Church St, Ann Arbor, MI, 48109, USA.
Jessica R Whitaker-FornekEdward F. Domino Research Center, Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109, USA.
Erica S LevittEdward F. Domino Research Center, Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109, USA.
Jessica P AnandEdward F. Domino Research Center, Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109, USA. janand@umich.edu.
John R TraynorEdward F. Domino Research Center, Department of Pharmacology, University of Michigan Medical School, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109, USA. jtraynor@umich.edu.

Funding

Allosteric Modulation of the Mu-Opioid ReceptorR37DA039997 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TRAYNOR, JOHN R. · 2015 to 2024
$6.4M
NIDA Training Program in Neuroscience-Administrative SupplementT32DA007281 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Shelly Beth Flagel · 1995 to 2026
$5.7M
Michigan Chemistry-Biology Interface Training ProgramT32GM132046 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Emily E Scott, Wenjing Wang · 2019 to 2026
$4.1M
Brainstem mechanisms of opioid-induced respiratory depressionR01HL174547 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Erica Sawyer Levitt · 2024 to 2026
$1.6M
Serotonin mechanisms in fentanyl-induced respiratory depressionR01DA061320 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Erica Sawyer Levitt · 2024 to 2026
$1.4M
CTSA Postdoctoral T32 at the University of MichiganT32TR004764 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI VICKI L ELLINGROD, Steven Edward Harte · 2024 to 2026
$1.4M
Development of Long Lasting Stable Fentanyl Antagonist to Reverse Opioid OverdoseR21DA051732 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANAND, JESSICA PRIYA · 2020 to 2021
$429k
NCATS NIH HHS T32 TR 004764NHLBI NIH HHS R01 HL 174547NIDA NIH HHS R01 DA 061320NIDA NIH HHS R01 DA061320NIDA NIH HHS R21 DA051723NIDA NIH HHS R21 DA051732NIDA NIH HHS R37 DA039997NIDA NIH HHS T32 DA007281NIGMS NIH HHS T32 GM132046
6 · The paper itself

Abstract

rationaleFatal opioid overdoses involving synthetic opioids have increased >10-fold over the past 8 years. Fentanyl, a potent synthetic opioid acting at the mu-opioid receptor (MOR), has largely replaced heroin as the predominant illicit opioid available. Various analogs have been synthesized from the fentanyl scaffold, including 2-furanylfentanyl, one of the most trafficked analogs from 2019 to 2024. Despite its prevalence, the in vivo effects of furanylfentanyl are not well characterized, especially regarding respiratory depression.

objectivesTo characterize furanylfentanyl relative to fentanyl in vitro and compare the effects of both drugs in mouse models of antinociception and respiratory depression.

methodsThe affinity and potency of fentanyl and furanylfentanyl were determined in CHO cells overexpressing MOR. Male and female CD-1 mice were administered (i.p.) fentanyl or furanylfentanyl prior to measuring antinociception (warm-water tail withdrawal), respiration (whole-body plethysmography), or oxygen saturation (pulse oximetry).

resultsFuranylfentanyl behaves as a partial agonist in vitro relative to fentanyl and morphine but with similar affinity and potency at MOR. In mice, fentanyl and furanylfentanyl produced similar effects on breathing parameters (including rate and inspiration time) that were greater than those induced by morphine, yet only fentanyl caused a drastic, long-lasting depletion of blood oxygen saturation. The discrepancy between effects on breathing and oxygen saturation may be explained by a greater number of apneas induced by fentanyl.

conclusionsThese results highlight the complexity of fentanyl-induced respiratory depression and indicate that recreational use of 2-furanylfentanyl in humans may pose a greater risk of overdose than morphine but lesser than fentanyl.

Indexed as

ApneasFentanylFuranylfentanylMouseMu-opioid receptorOpioidOverdoseOxygen saturationPlethysmographyRespiratory depression

Identifiers

PMID42387073
PMCPMC13636089

What Socratic 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 Socratic graph.