Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
1.
J Nutr Biochem ; 112: 109240, 2023 02.
Artículo en Inglés | MEDLINE | ID: mdl-36442716

RESUMEN

Blood orange consumption presents potential health benefits and may modulate epigenetic mechanisms such as microRNAs (miRNAs) expression. MiRNAs are non-coding RNAs responsible for post-transcriptional gene regulation, and these molecules can also be used as biomarkers in body fluids. This study was designed to investigate the effect of chronic blood orange juice (BOJ) intake on the inflammatory response and miRNA expression profile in plasma and blood cells in overweight women. The study cohort was comprised of twenty women aged 18-40 years old, diagnosed as overweight, who consumed 500 mL/d of BOJ for four weeks. Clinical data were collected at baseline and after 4 weeks of juice consumption, e.g., anthropometric and hemodynamic parameters, food intake, blood cell count, and metabolic and inflammatory biomarkers. BOJ samples were analyzed and characterized. Additionally, plasma and blood cells were also collected for miRNA expression profiling and evaluation of the expression of genes and proteins in the MAPK and NFκB signaling pathways. BOJ intake increased the expression of miR-144-3p in plasma and the expression of miR-424-5p, miR-144-3p, and miR-130b-3p in peripheral blood mononuclear cells (PBMC). Conversely, the beverage intake decreased the expression of let-7f-5p and miR-126-3p in PBMC. Computational analyses identified different targets of the dysregulated miRNA on inflammatory pathways. Furthermore, BOJ intake increased vitamin C consumption and the pJNK/JNK ratio and decreased the expression of IL6 mRNA and NFκB protein. These results demonstrate that BOJ regulates the expression of genes involved in the inflammatory process and decreases NFкB-protein expression in PBMC.


Asunto(s)
Citrus sinensis , Jugos de Frutas y Vegetales , Resistencia a la Insulina , MicroARNs , Sobrepeso , Adolescente , Adulto , Femenino , Humanos , Adulto Joven , Biomarcadores , Perfilación de la Expresión Génica , Leucocitos Mononucleares/metabolismo , MicroARNs/genética , MicroARNs/metabolismo , Sobrepeso/genética , Sobrepeso/metabolismo , Transducción de Señal , Sistema de Señalización de MAP Quinasas , Resistencia a la Insulina/genética , Resistencia a la Insulina/fisiología , FN-kappa B
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA