Evidence map›Paper›PMID 31540585›Full record

ArticleJournal of the American Association for Laboratory Animal Science : JAALAS2019

Concentration-dependent Toxicity after Subcutaneous Administration of Meloxicam to C57BL/6N Mice (

Anna E Sarfaty, Caroline J Zeiss, Amy D Willis, Jorgen M Harris, Peter C Smith

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Association for Laboratory Animal Science : JAALAS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Grimace scale assessment duringFrontiers in veterinary science · 2023
    Article
  7. High-dose Meloxicam Provides Improved Analgesia in Female CD1 Mice: A Pharmacokinetic and Efficacy Study.Journal of the American Association for Laboratory Animal Science : JAALAS · 2023
    Article
  8. Article
  9. Mouse Behavior in the Open-field Test after Meloxicam Administration.Journal of the American Association for Laboratory Animal Science : JAALAS · 2022
    Article
  10. Toxic Effects of High-dose Meloxicam and Carprofen on Female CD1 Mice.Journal of the American Association for Laboratory Animal Science : JAALAS · 2022
    Article
  11. 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.

Anna E SarfatyDepartment of Comparative Medicine, Yale School of Medicine, New Haven, Connecticut.
Caroline J ZeissDepartment of Comparative Medicine, Yale School of Medicine, New Haven, Connecticut.
Amy D WillisDepartment of Biostatistics, University of Washington, Seattle, Washington.
Jorgen M HarrisDepartment of Economics, Cornell University, Ithaca, New York.
Peter C SmithDepartment of Comparative Medicine, Yale School of Medicine, New Haven, Connecticut.
Yale University · USCornell University · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies using the Mouse Grimace Scale have shown that for many NSAID, including meloxicam, minimal doses of at least 20 mg/kg may be necessary to achieve adequate peri- and post-operative analgesia in mice. However, more data are needed to determine whether such NSAID doses exceed the threshold for gastrointestinal ulceration or induce other relevant pathology. We administered equal volumes of saline or injectable meloxicam (1 or 5 mg/mL) at a dose of 20 mg/kg SC to 20 young adult male and female C57BL/6N mice daily for 6 d and performed necropsies on all mice on the seventh day. Mice given 5 mg/mL meloxicam subcutaneously developed significantly more severe pathology at the injection site than saline controls. Pathology was characterized by full-thickness epidermal necrosis; cavitary lesions within subcutis, muscle, or fat; steatitis; and myositis. Mice that received 1 mg/mL meloxicam subcutaneously developed lesions that were qualitatively similar but far less severe than those after 5 mg/mL. However, no pathologic lesions typically associated with NSAID toxicity, such as gastric ulceration and liver and kidney lesions, were seen. These results demonstrate that although meloxicam injected subcutaneously causes concentration-dependent skin pathology at the injection site, a dose of 20 mg/kg can be safely administered subcutaneously at a concentration of 1 mg/mL for as long as 6 d.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalDose-Response Relationship, DrugFemaleInjections, SubcutaneousLaboratory Animal ScienceMaleMeloxicamMiceMice, Inbred C57BLMice, Inbred StrainsAnti-Inflammatory Agents, Non-SteroidalMeloxicam

Identifiers

PMID31540585
PMCPMC6926403
OpenAlexW2973690254

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.