Evidence map›Paper›PMID 39025662›Full record

ArticleComparative medicine2024

Investigating the Effect of Enterally Administered Capromorelin on Body Weight in Mice (Mus musculus).

Elizabeth M Punger, Sarah L W Norris, Stephen C Stevens, Kacee H Santos, Amanda C Christy

Abstract 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
–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

1 citing paper in PubMed.

  1. The Effect of Capromorelin and Extended-Release Buprenorphine on Body Weight in Guinea Pigs (Cavia porcellus).Journal of the American Association for Laboratory Animal Science : JAALAS · 2026
    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.

Elizabeth M Punger1Veterinary Services Branch, Veterinary Medicine Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, Maryland; and.
Sarah L W Norris2Research Support Branch, Regulated Research Administration Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, Maryland.
Stephen C Stevens1Veterinary Services Branch, Veterinary Medicine Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, Maryland; and.
Kacee H Santos1Veterinary Services Branch, Veterinary Medicine Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, Maryland; and.
Amanda C Christy1Veterinary Services Branch, Veterinary Medicine Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, Maryland; and.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significant weight loss in mice (Mus musculus) is a welfare concern and can alter physiology and behavior in ways that may confound research aims. In this study, factorial design was used to investigate the effect of enterally administered capromorelin on changes in mouse body weight overall and with various research-related interventions, such as administration of analgesics, anesthesia, or surgery. BALB/c mice (n = 61 [27 males/34 females] for analysis) were randomized into 8 intervention-treatment groups with 2 treatment allocations: capromorelin (10 mg/kg) or control, and 4 intervention allocations: no intervention; buprenorphine extended-release (XR) alone; buprenorphine XR, meloxicam, and anesthesia; or surgery under anesthesia with buprenorphine XR, meloxicam, and bupivacaine administered. Mice were habituated to handling, weighing, and voluntary consumption of condensed milk, which was used as the control solution and later a vehicle for capromorelin delivery, for 5 d (days 0 to 4). Then, mice received their interventions followed by 3 days of daily treatment or control administration (days 7 to 9). Body weights were measured daily (days 8 to 11 and day 14) to compare with baseline weights (days 0 to 4 and day 7) and evaluate for treatment and intervention effects on body weight. The interventions resulted in a decrease in group body weights 3 and 4 d after the interventions were conducted. Overall, body weights increased more in mice given capromorelin compared with control, and mice treated with capromorelin returned to, or exceeded, baseline weights faster. The weight loss was mitigated by capromorelin administration in all interventions except for the buprenorphine XR-only group. It is recommended to clinically consider enterally administered capromorelin to mitigate research-induced weight loss in mice.

Indexed as

Body WeightBuprenorphineMice, Inbred BALB CAnimalsBupivacaineFemaleMaleMeloxicamMicePiperidinesPyrazolesThiazolesWeight LossBupivacaineBuprenorphineCP 424391MeloxicamPiperidinesPyrazolesThiazolesbuprenorphine XR, extended-release buprenorphineEthiqa XR, extended-release buprenorphine by Fidelis Animal HealthGhrRA, ghrelin receptor agonistsIGF-1, insulin-like growth factor 1RoE, return to or exceed [baseline weight]

Identifiers

PMID39025662
PMCPMC11524401

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.