Publication:
Postprandial Circulating miRNAs in Response to a Dietary Fat Challenge.

dc.contributor.authorMantilla-Escalante, Diana C
dc.contributor.authorLópez de Las Hazas, María-Carmen
dc.contributor.authorGil-Zamorano, Judit
dc.contributor.authorDel Pozo-Acebo, Lorena
dc.contributor.authorCrespo, M Carmen
dc.contributor.authorMartín-Hernández, Roberto
dc.contributor.authorDel Saz, Andrea
dc.contributor.authorTomé-Carneiro, Joao
dc.contributor.authorCardona, Fernando
dc.contributor.authorCornejo-Pareja, Isabel
dc.contributor.authorGarcía-Ruiz, Almudena
dc.contributor.authorBriand, Olivier
dc.contributor.authorLasunción, Miguel A
dc.contributor.authorVisioli, Francesco
dc.contributor.authorDávalos, Alberto
dc.date.accessioned2024-02-10T20:01:41Z
dc.date.available2024-02-10T20:01:41Z
dc.date.issued2019-06-13
dc.description.abstractPostprandial lipemia has many physiopathological effects, some of which increase the risk of cardiovascular disease. MicroRNAs (miRNAs) can be found in almost all biological fluids, but their postprandial kinetics are poorly described. We aimed to profile circulating miRNAs in response to a fat challenge. In total, 641 circulating miRNAs were assessed by real-time PCR in plasmas from mice two hours after lipid gavage. Mice with intestine-specific loss of Dicer were screened to identify potential miRNAs released by the intestine. A total of 68 miRNAs were selected for further validation. Ten circulating miRNAs were finally validated as responsive to postprandial lipemia, including miR-206-3p, miR-543-3p, miR-466c-5p, miR-27b-5p, miR-409-3p, miR-340-3p, miR-1941-3p, miR-10a-3p, miR-125a-3p, and miR-468-3p. Analysis of their possible tissues of origin/target showed an enrichment of selected miRNAs in liver, intestine, brain, or skeletal muscle. miR-206, miR-27b-5p, and miR-409-3p were validated in healthy humans. Analysis of their predicted target genes revealed their potential involvement in insulin/insulin like growth factor (insulin/IGF), angiogenesis, cholecystokinin B receptor signaling pathway (CCKR), inflammation or Wnt pathways for mice, and in platelet derived growth factor (PDGF) and CCKR signaling pathways for humans. Therefore, the current study shows that certain miRNAs are released in the circulation in response to fatty meals, proposing them as potential novel therapeutic targets of lipid metabolism.
dc.format.number6es_ES
dc.format.volume11es_ES
dc.identifier.doi10.3390/nu11061326
dc.identifier.e-issn2072-6643es_ES
dc.identifier.journalNutrientses_ES
dc.identifier.otherhttp://hdl.handle.net/10668/14116
dc.identifier.pubmedID31200481es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/17878
dc.language.isoeng
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectCirculating miRNA
dc.subjectDiet
dc.subjectExosomes
dc.subjectFat challenge
dc.subjectPostprandial
dc.subject.meshAnimals
dc.subject.meshCirculating MicroRNA
dc.subject.meshDietary Fats
dc.subject.meshHumans
dc.subject.meshHyperlipidemias
dc.subject.meshMice
dc.subject.meshPostprandial Period
dc.subject.meshReal-Time Polymerase Chain Reaction
dc.subject.meshSignal Transduction
dc.titlePostprandial Circulating miRNAs in Response to a Dietary Fat Challenge.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication

Files