Evidence map›Paper›PMID 38532262›Full record

ArticleComparative medicine2024

Binding Affinity, Selectivity, and Pharmacokinetics of the Oxytocin Receptor Antagonist L-368,899 in the Coyote (

Sara M Freeman, J Leon Catrow, James Eric Cox, Alexandra Turano, McKenna A Rich, Hillary P Ihrig, Naveena Poudyal, Cheng-Wei Tom Chang, Eric M Gese, Julie K Young and 1 more

Open access · greenAbstract read
In one paragraph

Article in Comparative medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

11 authors at 4 institutions in 1 country.

Sara M FreemanDepartment of Biology, Utah State University, Logan, Utah; sara. freeman@usu. edu.
J Leon CatrowMetabolomics, Proteomics, and Mass Spectrometry Cores, University of Utah, Salt Lake City, Utah; Department of Biochemistry, University of Utah, Salt Lake City, Utah.
James Eric CoxMetabolomics, Proteomics, and Mass Spectrometry Cores, University of Utah, Salt Lake City, Utah; Department of Biochemistry, University of Utah, Salt Lake City, Utah.
Alexandra TuranoDepartment of Biology, Utah State University, Logan, Utah.
McKenna A RichDepartment of Biology, Utah State University, Logan, Utah.
Hillary P IhrigDepartment of Biology, Utah State University, Logan, Utah.
Naveena PoudyalDepartment of Chemistry & Biochemistry, Utah State University, Logan, Utah.
Cheng-Wei Tom ChangDepartment of Chemistry & Biochemistry, Utah State University, Logan, Utah.
Eric M GeseDepartment of Wildland Resources, Utah State University, Logan, Utah; Ecology Center, Utah State University, Logan, Utah; US Department of Agriculture, Wildlife Services, National Wildlife Research Center, Predator Research Facility, Millville, Utah.
Julie K YoungDepartment of Wildland Resources, Utah State University, Logan, Utah; Ecology Center, Utah State University, Logan, Utah; US Department of Agriculture, Wildlife Services, National Wildlife Research Center, Predator Research Facility, Millville, Utah.
Aaron L OlsenAnimal Dairy and Veterinary Sciences Department, Utah State University, Logan, Utah.
Utah State University · USUniversity of Utah · USAnimal and Plant Health Inspection Service · USLife Services (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

L-368,899 is a selective small-molecule oxytocin receptor (OXTR) antagonist originally developed in the 1990s to prevent preterm labor. Although its utility for that purpose was limited, L-368,899 is now one of the most commonly used drugs in animal research for the selective blockade of neural OXTR after peripheral delivery. A growing number of rodent and primate studies have used L-368,899 to evaluate whether certain behaviors are oxytocin dependent. These studies have improved our understanding of oxytocin's function in the brains of rodents and monkeys, but very little work has been done in other mammals, and only a single paper in macaques has provided any evidence that L-368,899 can be detected in the CNS after peripheral delivery. The current study sought to extend those findings in a novel species: coyotes (

Indexed as

CamphanesCoyotesPiperazinesReceptors, OxytocinAnimalsOxytocinPrimatesVasopressinsCamphanesL 368899OxytocinPiperazinesReceptors, OxytocinVasopressins

Identifiers

PMID38532262
PMCPMC10938559
OpenAlexW4393229454

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.