Articles producció científicaEnginyeria Electrònica, Elèctrica i Automàtica

Epigenetic programming at the Mogat1 locus may link neonatal overnutrition with long-term hepatic steatosis and insulin resistance.

  • Datos identificativos

    Identificador:  imarina:3854708
    Autores:  Ramon-Krauel, M; Pentinat, T; Bloks, VW; Cebrià, J; Ribo, S; Pérez-Wienese, R; Vilà, M; Palacios-Marin, I; Fernández-Pérez, A; Vallejo, M; Téllez, N; Rodríguez, MA; Yanes, O; Lerin, C; Díaz, R; Plosch, T; Tietge, UJF; Jimenez-Chillaron, JC
    Resumen:
    Postnatal overfeeding increases the risk of chronic diseases later in life, including obesity, insulin resistance, hepatic steatosis, and type 2 diabetes. Epigenetic mechanisms might underlie the long-lasting effects associated with early nutrition. Here we aimed to explore the molecular pathways involved in early development of insulin resistance and hepatic steatosis, and we examined the potential contribution of DNA methylation and histone modifications to long-term programming of metabolic disease. We used a well-characterized mouse model of neonatal overfeeding and early adiposity by litter size reduction. Neonatal overfeeding led to hepatic insulin resistance very early in life that persisted throughout adulthood despite normalizing food intake. Up-regulation of monoacylglycerol O-acyltransferase ( Mogat) 1 conceivably mediates hepatic steatosis and insulin resistance through increasing intracellular diacylglycerol content. Early and sustained deregulation of Mogat1 was associated with a combination of histone modifications that might favor Mogat1 expression. In sum, postnatal overfeeding causes extremely rapid derangements of hepatic insulin sensitivity that remain relatively stable until adulthood. Epigenetic mechanisms, particularly histone modifications, could contribute to such long-lasting effects. Our data suggest that targeting hepatic monoacylglycerol acyltransferase activity during early life might provide a novel strategy to improve hepatic insulin sensitivity and prevent late-onset insulin resistance and fatty liver disease.-Ramon-Krauel, M., Pentinat, T., Bloks, V. W., Cebrià, J., Ribo, S., Pérez-Wienese, R., Vilà, M., Palacios-Marin, I., Fernández-Pérez, A., Vallejo, M., Téllez, N., Rodríguez, M. À., Yanes, O., Lerin, C., Díaz, R., Plosch, T., Tietge, U. J. F., Jimenez-Chillaron, J. C. Epigenetic programming at the Mogat1 locus may link neonatal overnutrition with long-term hepatic steatosis and insulin resistance.
  • Otros:

    Enlace a la fuente original: https://faseb.onlinelibrary.wiley.com/doi/full/10.1096/fj.201700717RR
    Referencia de l'ítem segons les normes APA: Ramon-Krauel, M; Pentinat, T; Bloks, VW; Cebrià, J; Ribo, S; Pérez-Wienese, R; Vilà, M; Palacios-Marin, I; Fernández-Pérez, A; Vallejo, M; Téllez, N; (2018). Epigenetic programming at the Mogat1 locus may link neonatal overnutrition with long-term hepatic steatosis and insulin resistance.. Faseb Journal, 32(11), fj201700717RR-fj201700717RR. DOI: 10.1096/fj.201700717RR
    Referencia al articulo segun fuente origial: Faseb Journal. 32 (11): fj201700717RR-fj201700717RR
    DOI del artículo: 10.1096/fj.201700717RR
    Año de publicación de la revista: 2018-11-01
    Entidad: Universitat Rovira i Virgili
    Versión del articulo depositado: info:eu-repo/semantics/publishedVersion
    Fecha de alta del registro: 2026-05-09
    Autor/es de la URV: Rodríguez Merayo, María Araceli / Yanes Torrado, Óscar
    Departamento: Enginyeria Electrònica, Elèctrica i Automàtica
    URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
    Tipo de publicación: Journal Publications
    ISSN: 08926638
    Autor según el artículo: Ramon-Krauel, M; Pentinat, T; Bloks, VW; Cebrià, J; Ribo, S; Pérez-Wienese, R; Vilà, M; Palacios-Marin, I; Fernández-Pérez, A; Vallejo, M; Téllez, N; Rodríguez, MA; Yanes, O; Lerin, C; Díaz, R; Plosch, T; Tietge, UJF; Jimenez-Chillaron, JC
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    Áreas temáticas: Molecular biology, Medicine (miscellaneous), Genetics, General medicine, Cell biology, Biotechnology, Biology, Biodiversidade, Biochemistry & molecular biology, Biochemistry
    Direcció de correo del autor: oscar.yanes@urv.cat, oscar.yanes@urv.cat, araceli.rodriguez@urv.cat, araceli.rodriguez@urv.cat
  • Palabras clave:

    Weight-gain
    O-acyltransferase 1
    Nutritional epigenetics
    Neonatal overfeeding
    Mouse model
    Monoacylglycerol acyltransferase
    Mice
    Lipid-accumulation
    In-utero
    High-fat diet
    Glucose
    Expression
    Childhood obesity
    Biochemistry
    Biochemistry & Molecular Biology
    Biology
    Biotechnology
    Cell Biology
    Genetics
    Medicine (Miscellaneous)
    Molecular Biology
    General medicine
    Biodiversidade
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