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

Banco de datos
Tipo de estudio
Tipo del documento
Asunto de la revista
País de afiliación
Intervalo de año de publicación
1.
Endocrine ; 35(2): 227-32, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19165636

RESUMEN

We have currently studied the changes induced by administration of a fructose-rich diet (FRD) to normal rats in the mass and the endocrine function of abdominal (omental) adipose tissue (AAT). Rats were fed ad libitum a standard commercial chow and tap water, either alone (control diet, CD) or containing fructose (10%, w/vol) (FRD). Three weeks after treatment, circulating metabolic markers and leptin release from adipocytes of AAT were measured. Plasma free fatty acids (FFAs), leptin, adiponectin, and plasminogen activator inhibitor-1 (PAI-1) levels were significantly higher in FRD than in CD rats. AAT mass was greater in FRD than in CD rats and their adipocytes were larger, they secreted more leptin and showed impaired insulin sensitivity. While leptin mRNA expression increased in AAT from FRD rats, gene expression of insulin receptor substrate, IRS1 and IRS2 was significantly reduced. Our study demonstrates that administration of a FRD significantly affects insulin sensitivity and several AAT endocrine/metabolic functions. These alterations could be part of a network of interacting abnormalities triggered by FRD-induced oxidative stress at the AAT level. In view of the impaired glucose tolerance observed in FRD rats, these alterations could play a key role in both the development of metabolic syndrome (MS) and beta-cell failure.


Asunto(s)
Grasa Abdominal/efectos de los fármacos , Grasa Abdominal/metabolismo , Dieta , Fructosa/administración & dosificación , Grasa Abdominal/citología , Adipocitos/química , Adipocitos/efectos de los fármacos , Adipocitos/metabolismo , Animales , Biomarcadores/sangre , Dexametasona/farmacología , Expresión Génica , Intolerancia a la Glucosa/etiología , Insulina/farmacología , Proteínas Sustrato del Receptor de Insulina/genética , Leptina/genética , Leptina/metabolismo , Masculino , Estrés Oxidativo/efectos de los fármacos , ARN Mensajero/análisis , Ratas , Ratas Wistar
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA