Evidence map›Paper›PMID 39450911›Full record

ArticleShock (Augusta, Ga.)2025

HOUSING TEMPERATURE ALTERS BURN-INDUCED HYPERMETABOLISM IN MICE.

Meagan Scott Kingren, Jaycelyn Starr Hall, Taylor Joseph Ross, Mary Claire Barre, Abigail Barlow, Martin Morales, Lillie Danielle Treas, Robert Todd Maxson, Esther Teo, Craig Porter

Abstract read
In one paragraph

Article in Shock (Augusta, Ga.), 2025. 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

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

10 authors.

Meagan Scott Kingren
Jaycelyn Starr Hall
Taylor Joseph RossArkansas Children's Research Institute, Little Rock, Arkansas.
Mary Claire BarreArkansas Children's Research Institute, Little Rock, Arkansas.
Abigail BarlowArkansas Children's Research Institute, Little Rock, Arkansas.
Martin MoralesArkansas Children's Research Institute, Little Rock, Arkansas.
Lillie Danielle TreasArkansas Children's Research Institute, Little Rock, Arkansas.
Robert Todd Maxson
Esther Teo

Funding

The Role of the Mitochondrion in the Metabolic Stress Response to Burn TraumaP20GM109096 · NIGMS · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI BORSHEIM, ELISABET · 2016 to 2025
$20.7M
Supplement for Google cloud build-outR24GM137786 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI Alan Tackett · 2020 to 2026
$15.4M
The Role of the Mitochondrion in the Metabolic Stress Response to Burn TraumaR35GM142744 · NIGMS · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI PORTER, CRAIG · 2021 to 2025
$2.0M
NIGMS NIH HHS P20 GM109096NIGMS NIH HHS R24 GM137786NIGMS NIH HHS R35 GM142744
6 · The paper itself

Abstract

abstractMice used in biomedical research are typically housed at ambient temperatures (22°C-24°C) below thermoneutrality (26°C-31°C). This chronic cold stress triggers a hypermetabolic response that may limit the utility of mice in modeling hypermetabolism in response to burns. To evaluate the effect of housing temperature on burn-induced hypermetabolism, mice were randomly assigned to receive sham, small, or large scald burns. Mice recovered for 21 days in metabolic phenotyping cages at 24°C or 30°C. Regardless of sex or sham/burn treatment, mice housed at 24°C had greater total energy expenditure ( P < 0.001), which was largely attributable to greater basal energy expenditure when compared to mice housed at 30°C ( P < 0.001). Thermoneutral housing (30°C) altered adipose tissue mass in a sex-dependent manner. Compared to sham and small burn groups, large burns resulted in greater water vapor loss, regardless of housing temperature ( P < 0.01). Compared to sham, large burns resulted in greater basal energy expenditure and total energy expenditure in mice housed at 24°C; however, this hypermetabolic response to large burns was blunted in female mice housed at 30°C, and absent in male mice housed at 30°C. Locomotion was significantly reduced in mice with large burns compared to sham and small burn groups, irrespective of sex or housing temperature ( P < 0.05). Housing at 30°C revealed sexual dimorphism in terms of the impact of burns on body mass and composition, where males with large burns displayed marked cachexia, whereas females did not. Collectively, this study demonstrates a sex-dependent role for housing temperature in influencing energetics and body composition in a rodent model of burn trauma.

Indexed as

BurnsEnergy MetabolismHousing, AnimalTemperatureAnimalsFemaleMaleMiceMice, Inbred C57BL

Identifiers

PMID39450911
PMCPMC12173143

What Socratic holds

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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 Socratic graph.