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Eur J Pharmacol ; 689(1-3): 233-40, 2012 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-22652429

RESUMEN

The present study investigated the early presence of inflammatory response in renal tissue of young offspring from diabetic mothers. The effect of L-arginine (L-arg) supplementation was also investigated. The offspring was divided into four groups: group CO (controls); group DO (diabetic offspring); group CA (CO receiving 2% L-arg solution) and group DA (DO receiving the 2% L-arg solution). Glycemia, arterial pressure and renal function were evaluated; gene and protein expression of pro-inflammatory cytokines were also measured. Blood pressure levels were significantly increased in 2 and 6 month-old DO rats, whereas L-arg administration caused a significant decrease in the DA group, at both ages. DO rats showed a significantly blunted glycemic response to exogenous insulin. In 2 month-old DO animals, renal protein expression of pro-inflammatory molecules was significantly increased. At six months of age, we also observed an increase in gene expression of pro-inflammatory molecules, whereas L-arg supplementation prevented this increase at both ages. Our data suggest that activation of inflammatory pathways is present early in the kidney of DO rats, and that L-arg can attenuate the expression of these markers of tissue inflammation. Our results also reinforce the concept that intrauterine environmental factors are a fundamental determinant in the development of metabolic and vascular diseases later in life.


Asunto(s)
Lesión Renal Aguda/patología , Diabetes Mellitus Experimental/patología , Mediadores de Inflamación/administración & dosificación , Complicaciones del Embarazo/patología , Efectos Tardíos de la Exposición Prenatal/patología , Lesión Renal Aguda/diagnóstico , Lesión Renal Aguda/etiología , Animales , Arginina/administración & dosificación , Arginina/toxicidad , Biomarcadores/metabolismo , Diabetes Mellitus Experimental/complicaciones , Diabetes Mellitus Experimental/diagnóstico , Diagnóstico Precoz , Femenino , Mediadores de Inflamación/toxicidad , Masculino , Embarazo , Complicaciones del Embarazo/diagnóstico , Complicaciones del Embarazo/etiología , Efectos Tardíos de la Exposición Prenatal/diagnóstico , Efectos Tardíos de la Exposición Prenatal/etiología , Distribución Aleatoria , Ratas , Ratas Wistar
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