Evidence map›Paper›PMID 41256455›Full record

ArticlebioRxiv : the preprint server for biology2025

Changes in muscle strength and moderators of protein turnover in a rodent model of anorexia nervosa and recovery.

Megan E Rosa-Caldwell, Lauren Breithaupt, Ursula B Kaiser, Ruqaiza Muhyudin, Seward B Rutkove

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

5 authors.

Megan E Rosa-CaldwellEnergy Availability and Muscle Metabolism Laboratory, Exercise Science Research Center, Department of Health Human Performance and Recreation, University of Arkansas, Fayetteville, AR 72701.ORCID 0000-0002-3829-1021
Lauren BreithauptDepartment of Psychiatry, Harvard Medical School, Eating Disorders Clinical and Research Program, Massachusetts General Hospital, Boston, MA 02114.ORCID 0000-0002-2439-6519
Ursula B KaiserDivision of Endocrinology, Diabetes and Hypertension, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115.
Ruqaiza MuhyudinCachexia Research Laboratory, Exercise Science Research Center, Department of Health Human Performance and Recreation, University of Arkansas, Fayetteville, AR 72701.
Seward B RutkoveBeth Israel Deaconess Medical Center and Harvard Medical School, Department of Neurology, Boston, MA 02215.

Funding

Hormones/Genes in Women's Health: From Bench to BedsideK12HD051959 · NICHD · BRIGHAM AND WOMEN'S HOSPITAL · PI GOLDSTEIN, JILL M, REXRODE, KATHRYN M · 2005 to 2023
$8.8M
NICHD NIH HHS K12 HD051959
6 · The paper itself

Abstract

Anorexia nervosa (AN) is a psychiatric disorder characterized by severe caloric restriction, leading to health complications. In addition to fat loss, AN also results in profound skeletal muscle loss, yet molecular pathways underlying these musculoskeletal complications or how long-lasting these musculoskeletal consequences may be are currently unknown. The purpose of this study was to investigate the effects of AN and subsequent weight recovery on muscle strength, size, and moderators of protein turnover in a rat model of AN. Female Sprague Dawley rats (n=11/group, 8 weeks of age) underwent 30 days of simulated AN (50-60% food restriction) followed by varying recovery periods. Muscle mass, strength, and protein synthesis/degradation pathways were assessed. AN led to substantial reductions in muscle mass and strength. While muscle mass recovered within 30 days, muscle strength remained depressed in rats with a prior history of AN, suggesting alterations to muscle quality. Moreover, moderators of protein synthesis (Igf1, Redd1, Deptor) remained altered following 30 days of AN and subsequent recovery. These findings suggest muscle impairments in AN may be longer-lasting than previously thought and may contribute to increased health complications and reduced quality of life in those with a history of AN.

Indexed as

eating disordergastrocnemiusprotein degradationprotein synthesisstarvation

Identifiers

PMID41256455
PMCPMC12621927

What OpenQuestion holds

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LicenceCC BY
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.