Evidence map›Paper›PMID 40563281›Full record

ArticleAntioxidants (Basel, Switzerland)2025

Impact of SGLT2i on Cardiac Remodeling and the Soleus Muscle of Infarcted Rats.

Lidiane Moreira Souza, Felipe Cesar Damatto, Bruna Brasil Brandão, Eder Anderson Rodrigues, Anna Clara Consorti Santos, Rafael Campos França Silva, Mariana Gatto, Luana Urbano Pagan, Paula Felippe Martinez, Gilson Masahiro Murata and 5 more

Abstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2025. 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. 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

15 authors.

Lidiane Moreira SouzaDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.ORCID 0000-0002-9726-3901
Felipe Cesar DamattoDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.
Bruna Brasil BrandãoSection of Integrative Physiology and Metabolism, Joslin Diabetes Center, Harvard Medical School, Boston, MA 02115, USA.
Eder Anderson RodriguesDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.
Anna Clara Consorti SantosDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.
Rafael Campos França SilvaDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.
Mariana GattoDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.ORCID 0000-0002-3115-0795
Luana Urbano PaganDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.
Paula Felippe MartinezIntegrated Institute of Health, Federal University of Mato Grosso do Sul-UFMS, Campo Grande 79070-900, Brazil.ORCID 0000-0001-9477-3386
Gilson Masahiro MurataLaboratory of Medical Investigation (LIM-29), Clinic Medical Department, University of Sao Paulo Medical School, Sao Paulo 05360-160, Brazil.
Leonardo Antonio Mamede ZornoffDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.
Paula Schmidt Azevedo GaiollaDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.ORCID 0000-0002-5843-6232
Inês Falcão-PiresUnIC@RISE, Department of Surgery and Physiology, Faculty of Medicine, University of Porto, 4099-002 Porto, Portugal.ORCID 0000-0003-1937-3782
Katashi OkoshiDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.ORCID 0000-0001-8980-8839
Marina Politi OkoshiDepartment of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu 18618-687, Brazil.ORCID 0000-0001-7728-4505

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior 88887.817564/2023-00 and 88887.493466/2020-00Fundação de Amparo à Pesquisa do Estado de São Paulo 2021/10923-5 and 2023/04983-0National Council for Scientific and Technological Development 307703/2022-3 and 307280/2022-5
6 · The paper itself

Abstract

Skeletal muscle changes occur in heart failure (HF). Despite the cardioprotective effects of sodium-glucose co-transporter 2 (SGLT2) inhibitors in HF, their impact on skeletal muscle remains poorly understood. We investigated the effects of the SGLT2 inhibitor empagliflozin (EMPA) on cardiac remodeling and the soleus muscle of rats with myocardial infarction (MI)-induced HF.

methodsOne week after MI induction, rats were assigned to Sham, Sham + EMPA, MI, and MI + EMPA groups. EMPA was administered (5 mg/kg/day) for 12 weeks.

resultsMI + EMPA and MI had dilated left cardiac chambers; the left atrium diameter and left ventricle end-diastolic area were smaller in MI + EMPA than MI. The ejection fraction did not differ between infarcted groups. MI + EMPA had a larger soleus cross-sectional area and higher Type II myosin heavy chain expression than MI. Carbonylated protein and malondialdehyde levels were lower and superoxide dismutase activity higher in MI + EMPA than MI. Respiratory Complex I expression was higher in MI + EMPA than MI. Metabolic enzyme activities, altered in MI, were normalized in MI + EMPA. EMPA up-regulated anabolic proteins and down-regulated catabolic proteins.

conclusionEmpagliflozin attenuates infarction-induced cardiac remodeling in rats. In soleus muscle, empagliflozin preserves cell trophism, reduces oxidative stress, normalizes muscle and mitochondrial metabolism, and positively modulates proteins involved in synthesis and degradation-related pathways.

Indexed as

energy metabolismIGF-1 pathwaymitochondrial functionmyocardial infarctionoxidative stresssoleus muscle

Identifiers

PMID40563281
PMCPMC12189243

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.