Evidence map›Paper›PMID 35270028›Full record

ArticleInternational journal of molecular sciences2022

Effect of Empagliflozin on Sphingolipid Catabolism in Diabetic and Hypertensive Rats.

Roxana Pérez-Villavicencio, Javier Flores-Estrada, Martha Franco, Bruno Escalante, Oscar Pérez-Méndez, Adriana Mercado, Rocio Bautista-Pérez

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
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

12 citing papers in PubMed, 16 citations in OpenAlex.

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  10. Role of ceramides in diabetic foot ulcers (Review).International journal of molecular medicine · 2023
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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

7 authors at 3 institutions in 1 country.

Roxana Pérez-VillavicencioDepartment of Molecular Biology, Instituto Nacional de Cardiología "Ignacio Chávez", Mexico City 14080, Mexico.
Javier Flores-EstradaDivisión de Investigación, Hospital Juárez de México, Mexico City 07760, Mexico.ORCID 0000-0002-7029-7036
Martha FrancoDepartment of Cardio-Renal Pathophysiology, Instituto Nacional de Cardiología "Ignacio Chávez", Mexico City 14080, Mexico.ORCID 0000-0003-4073-524X
Bruno EscalanteUnidad Monterrey, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Vía del Conocimiento 201, PIIT, Apodaca 66600, Mexico.
Oscar Pérez-MéndezDepartment of Molecular Biology, Instituto Nacional de Cardiología "Ignacio Chávez", Mexico City 14080, Mexico.ORCID 0000-0002-6977-1829
Adriana MercadoDepartment of Nephrology, Instituto Nacional de Cardiología "Ignacio Chávez", Mexico City 14080, Mexico.ORCID 0000-0002-6881-0160
Rocio Bautista-PérezDepartment of Molecular Biology, Instituto Nacional de Cardiología "Ignacio Chávez", Mexico City 14080, Mexico.ORCID 0000-0003-0265-668X
Instituto Nacional de Cardiología · MXHospital Juárez de México · MXInstituto Politécnico Nacional · MX

Funding

CONACyT fellowship 1000713 to Roxana Pérez Villavicencio."Project supported by the sectoral research fund for education" Grant number 219981 to M. Franco"Project supported by the sectoral research fund for education" Research Grant A1-S-9870 to Rocio Bautista-Pérez
6 · The paper itself

Abstract

The profile of sphingomyelin and its metabolites shows changes in the plasma, organs, and tissues of patients with cardiovascular, renal, and metabolic diseases. The objective of this study was to investigate the effect of empagliflozin on the levels of sphingomyelin and its metabolites, as well as on the activity of acid and neutral sphingomyelinase (aSMase and nSMase) and neutral ceramidase (nCDase) in the plasma, kidney, heart, and liver of streptozotocin-induced diabetic and Angiotensin II (Ang II)-induced hypertension rats. Empagliflozin treatment decreased hyperglycemia in diabetic rats whereas blood pressure remained elevated in hypertensive rats. In diabetic rats, empagliflozin treatment decreased sphingomyelin in the plasma and liver, ceramide in the heart, sphingosine-1-phosphate (S1P) in the kidney, and nCDase activity in the plasma, heart, and liver. In hypertensive rats, empagliflozin treatment decreased sphingomyelin in the plasma, kidney, and liver; S1P in the plasma and kidney; aSMase in the heart, and nCDase activity in the plasma, kidney, and heart. Our results suggest that empagliflozin downregulates the interaction of the de novo pathway and the catabolic pathway of sphingolipid metabolism in the diabetes, whereas in Ang II-dependent hypertension, it only downregulates the sphingolipid catabolic pathway.

Indexed as

Diabetes Mellitus, ExperimentalHypertensionAnimalsBenzhydryl CompoundsCeramidesGlucosidesHumansRatsSphingolipidsSphingomyelin PhosphodiesteraseSphingomyelinsBenzhydryl CompoundsCeramidesempagliflozinGlucosidesSphingolipidsSphingomyelin PhosphodiesteraseSphingomyelinsangiotensin II-induced hypertensionceramidediabetesempagliflozinshingosine-1-Psphingomyelinsphingosine

Identifiers

PMID35270028
PMCPMC8910883
OpenAlexW4220903369

What OpenQuestion holds

Textmetadata
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.