Evidence map›Paper›PMID 34055478›Full record

ArticlePeerJ2021

High fructose exposure modifies the amount of adipocyte-secreted microRNAs into extracellular vesicles in supernatants and plasma.

Adrián Hernández-Díazcouder, Javier González-Ramírez, Abraham Giacoman-Martínez, Guillermo Cardoso-Saldaña, Eduardo Martínez-Martínez, Horacio Osorio-Alonso, Ricardo Márquez-Velasco, José L Sánchez-Gloria, Yaneli Juárez-Vicuña, Guillermo Gonzaga and 3 more

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 93% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 5 institutions in 3 countries.

Adrián Hernández-DíazcouderPosgrado en Biología Experimental, Universidad Autónoma Metropolitana-Iztapalapa, Ciudad de México, México.
Javier González-RamírezLaboratorio de Biología Celular, Facultad de Enfermería, Universidad Autónoma de Baja California Campus Mexicali, Mexicali, Baja California, Mexico.
Abraham Giacoman-MartínezLaboratorio de Farmacología, Departamento de Ciencias de la Salud, Universidad Autónoma Metropolitana-Iztapalapa, Ciudad de México, México.
Guillermo Cardoso-SaldañaDepartamento de Endocrinología, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México.
Eduardo Martínez-MartínezLaboratorio de Comunicación Celular y Vesículas Extracelulares, Instituto Nacional de Medicina Genómica, Ciudad de México, México.
Horacio Osorio-AlonsoDepartamento de Fisiopatología Cardio-Renal, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México.
Ricardo Márquez-VelascoDepartamento de Inmunología, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México.
José L Sánchez-GloriaDepartamento de Inmunología, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México.
Yaneli Juárez-VicuñaDepartamento de Inmunología, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México.
Guillermo GonzagaDepartamento de Fisiopatología Cardio-Renal, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México.
Laura Gabriela Sánchez-LozadaDepartamento de Fisiopatología Cardio-Renal, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México.
Julio César Almanza-PérezLaboratorio de Farmacología, Departamento de Ciencias de la Salud, Universidad Autónoma Metropolitana-Iztapalapa, Ciudad de México, México.
Fausto Sánchez-MuñozDepartamento de Inmunología, Instituto Nacional de Cardiología Ignacio Chávez, Ciudad de México, México.
Instituto Nacional de Cardiología · MXUniversidad Autónoma Metropolitana · MXInstituto de Medicina Genómica · ESInstituto Nacional de Cardiologia · BRUniversidad Autónoma de Baja California · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh fructose exposure induces metabolic and endocrine responses in adipose tissue. Recent evidence suggests that microRNAs in extracellular vesicles are endocrine signals secreted by adipocytes. Fructose exposure on the secretion of microRNA by tissues and cells is poorly studied. Thus, the aim of this study was to evaluate the effect of fructose exposure on the secretion of selected microRNAs in extracellular vesicles from 3T3-L1 cells and plasma from Wistar rats.

methods3T3-L1 cells were exposed to 550 µM of fructose or standard media for four days, microRNAs levels were determined in extracellular vesicles of supernatants and cells by RT-qPCR. Wistar rats were exposed to either 20% fructose drink or tap water for eight weeks, microRNAs levels were determined in extracellular vesicles of plasma and adipose tissue by RT-qPCR.

resultsThis study showed that fructose exposure increased the total number of extracellular vesicles released by 3T3-L1 cells (

conclusionFructose exposure modifies the levels of microRNAs in extracellular vesicles in vitro and in vivo. In particular, fructose exposure increases miR-143-5p, while decreases miR-223-3p and miR-342-3p.

Indexed as

AdipocytesAdipose tissueExtracellular VesiclesFructosemicroRNA

Identifiers

PMID34055478
PMCPMC8140597
OpenAlexW3160501798

What Socratic 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 Socratic graph.