Dietary oleanolic acid mediates circadian clock gene expression in liver independently of diet and animal model but requires apolipoprotein A1

Gabás Rivera, Clara (Universidad de Zaragoza) ; Martínez Beamonte, Roberto (Universidad de Zaragoza) ; Ríos, José L ; Navarro, María A (Universidad de Zaragoza) ; Surra, Joaquín C (Universidad de Zaragoza) ; Arnal, Carmen (Universidad de Zaragoza) ; Rodríguez Yoldi, María J (Universidad de Zaragoza) ; Osada, Jesús (Universidad de Zaragoza)
Dietary oleanolic acid mediates circadian clock gene expression in liver independently of diet and animal model but requires apolipoprotein A1
Resumen: Oleanolic acid is a triterpene widely distributed throughout the plant kingdom and present in virgin olive oil at a concentration of 57 mg/kg. To test the hypotheses that its long-term administration could modify hepatic gene expression in several animal models and that this could be influenced by the presence of APOA1-containing high-density lipoproteins (HDLs), diets including 0.01% oleanolic acid were provided to Apoe- and Apoa1-deficient mice and F344 rats. Hepatic transcriptome was analyzed in Apoe-deficient mice fed long-term semipurified Western diets differing in the oleanolic acid content. Gene expression changes, confirmed by reverse transcriptase quantitative polymerase chain reaction, were sought for their implication in hepatic steatosis. To establish the effect of oleanolic acid independently of diet and animal model, male rats were fed chow diet with or without oleanolic acid, and to test the influence of HDL, Apoa1-deficient mice consuming the latter diet were used. In Apoe-deficient mice, oleanolic acid intake increased hepatic area occupied by lipid droplets with no change in oxidative stress. Bmal1 and the other core component of the circadian clock, Clock, together with Elovl3, Tubb2a and Cldn1 expressions, were significantly
increased, while Amy2a5, Usp2, Per3 and Thrsp were significantly decreased in mice receiving the compound. Bmal1 and Cldn1 expressions were positively associated with lipid droplets. Increased Clock and Bmal1 expressions were also observed in rats, but not in Apoa1-deficient mice. The core liver clock components Clock-Bmal1 are a target of oleanolic acid in two animal models independently of the diets provided, and this compound requires APOA1-HDL for its hepatic action.

Idioma: Inglés
DOI: 10.1016/j.jnutbio.2013.07.010
Año: 2013
Publicado en: Journal of Nutritional Biochemistry 24, 12 (2013), 2100-2109
ISSN: 0955-2863

Factor impacto JCR: 4.592 (2013)
Categ. JCR: NUTRITION & DIETETICS rank: 9 / 78 = 0.115 (2013) - Q1 - T1
Categ. JCR: BIOCHEMISTRY & MOLECULAR BIOLOGY rank: 66 / 290 = 0.228 (2013) - Q1 - T1

Financiación: info:eu-repo/grantAgreement/ES/CICYT-FEDER/SAF 2010-14958
Financiación: info:eu-repo/grantAgreement/ES/DGA/B69
Financiación: info:eu-repo/grantAgreement/ES/DGA/PI025-08
Tipo y forma: Article (PostPrint)
Área (Departamento): Área Microbiología (Dpto. Microb.Med.Pr.,Sal.Públ.)
Área (Departamento): Área Fisiología (Dpto. Farmacología y Fisiolog.)
Área (Departamento): Área Producción Animal (Dpto. Produc.Animal Cienc.Ali.)
Área (Departamento): Área Bioquímica y Biolog.Mole. (Dpto. Bioq.Biolog.Mol. Celular)


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Articles > Artículos por área > Bioquímica y Biología Molecular
Articles > Artículos por área > Producción Animal
Articles > Artículos por área > Microbiología
Articles > Artículos por área > Fisiología



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