Evidence map›Paper›PMID 40622971›Full record

ArticlePloS one2025

Improved physical performance in obesity-resistant rats compared to obesity-prone rats: Effects of different diets and metabolic analysis.

Daniel Sesana da Silva, Matheus Corteletti Dos Santos, Lucas Furtado Domingos, Jóctan Pimentel Cordeiro, Kiany Miranda, Maria Gabriela Siqueira Tavares, Késsia Cristina Carvalho Santos, Ana Paula Lima-Leopoldo, André Soares Leopoldo

Abstract readComparative Study
In one paragraph

Article in PloS one, 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

9 authors.

Daniel Sesana da SilvaPostgraduate Program in Physiological Sciences, Center of Health Sciences, Federal University of Espírito Santo, Vitória, Espírito Santo, Brazil.ORCID https://orcid.org/0000-0002-1901-8951
Matheus Corteletti Dos SantosPostgraduate Program in Physiological Sciences, Center of Health Sciences, Federal University of Espírito Santo, Vitória, Espírito Santo, Brazil.ORCID https://orcid.org/0009-0001-7891-7105
Lucas Furtado DomingosPostgraduate Program in Nutrition and Health, Center of Health Sciences, Federal University of Espírito Santo, Vitória, Espírito Santo, Brazil.ORCID https://orcid.org/0000-0001-5033-8104
Jóctan Pimentel CordeiroCenter of Physical Education and Sports, Federal University of Espírito Santo, Vitória, Espírito Santo, Brazil.
Kiany MirandaPostgraduate Program in Physiological Sciences, Center of Health Sciences, Federal University of Espírito Santo, Vitória, Espírito Santo, Brazil.
Maria Gabriela Siqueira TavaresPostgraduate Program in Physiological Sciences, Center of Health Sciences, Federal University of Espírito Santo, Vitória, Espírito Santo, Brazil.
Késsia Cristina Carvalho SantosPostgraduate Program in Nutrition and Health, Center of Health Sciences, Federal University of Espírito Santo, Vitória, Espírito Santo, Brazil.ORCID https://orcid.org/0000-0001-8634-4127
Ana Paula Lima-LeopoldoPostgraduate Program in Nutrition and Health, Center of Health Sciences, Federal University of Espírito Santo, Vitória, Espírito Santo, Brazil.
André Soares LeopoldoPostgraduate Program in Physiological Sciences, Center of Health Sciences, Federal University of Espírito Santo, Vitória, Espírito Santo, Brazil.ORCID https://orcid.org/0000-0001-5999-2671

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animal models, such as high-fat diet-induced obese (DIO) rats, have been used to understand its pathophysiology. These models reveal differences between obesity-prone (OP) and obesity-resistant (OR) phenotypes. Thus, OR exhibit lower body mass gain and higher levels of physical activity, suggesting a more efficient energy metabolism. This study evaluated the metabolic adaptations and physical performance of OP and OR rats. Wistar rats (30 days old) were subjected to 23-week obesity exposure protocols. Initially, rats were randomized into two groups: a) SD: fed a standard diet (n = 39) and b) HFD: fed a high-fat diet (n = 39). Subsequently, animals were characterized as OP and OR on their respective diets: SD-OR (n = 13); SD-OP (n = 13); HFD-OP (n = 13); HFD-OR (n = 13). Nutritional, metabolic, and adiposity parameters were analyzed. Basal metabolism assessment was performed using indirect calorimetry. Physical performance and aerobic capacity were determined through treadmill exercise tests with gas analyzers for maximal oxygen consumption (VO2). OR animals had lower body mass compared to OP animals, despite consuming the same caloric intake under both diets. HFD-OP rats gained 30.5% more weight than HFD-OR rats, while SD-OP rats gained 19.5% more than SD-OR rats. SD-OR rats gained 20.5% more weight than HFD-OR. No significant differences in adiposity indices were observed among groups. HFD-OR rats showed 15.6% higher VO₂max than HFD-OP rats; SD-OR rats had 12.8% higher VO₂max and 20.3% longer time to exhaustion compared to SD-OP rats. Indirect calorimetry revealed higher energy expenditure in OR animals during the dark cycle. OP animals exhibited elevated insulin and HOMA-IR levels, while OR animals had higher leptin and glucagon levels. In conclusion, OR rats showed improved physical performance and aerobic capacity compared to OP rats, even on a high-fat diet, suggesting that OR rats have adaptive mechanisms that enhance energy metabolism and endurance.

Indexed as

ObesityPhysical Functional PerformanceAdiposityAnimalsDiet, High-FatEnergy MetabolismMaleOxygen ConsumptionPhysical Conditioning, AnimalRatsRats, Wistar

Identifiers

PMID40622971
PMCPMC12233250

What Socratic holds

Textmetadata
LicenceCC BY
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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.