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

Bases de datos
Tipo de estudio
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
Sci Rep ; 5: 12273, 2015 Jul 21.
Artículo en Inglés | MEDLINE | ID: mdl-26194431

RESUMEN

Nephrotic syndrome (NS) is still a therapeutic challenge. To date there is no ideal treatment. Evidence suggest that multidrug therapy has more effect than monotherapy in amelioration of renal injury. Salvianolic acid A (SAA) is the major active component of Salviae Miltiorrhizae Bunge. Previous studies have demonstrated that SAA is a multi-target agent and has various pharmacological activities. The pleiotropic properties of SAA predict its potential in the treatment of NS. The study investigated the effect of SAA on doxorubicin-induced nephropathy. The kidney function related-biochemical changes, hemorheological parameters and oxidative stress status were determined, and histological examination using light and transmission electron microcopies and western blot analysis were also performed. Results revealed that treatment with SAA alleviated histological damages, relieved proteinuria, hypoalbuminemia and hyperlipidemia, reduced oxidative stress, as well as improving hemorheology. Furthermore, SAA restored podocin expression, down-regulated the expression of NF-κB p65 and p-IκBα while up-regulating IκBα protein expression. Overall, as a multifunctional agent, SAA has a favorable renoprotection in doxorubicin-induced nephropathy. The anti-inflammation, antioxidant, amelioration of podocyte injury, improvement of hemorheology and hypolipidemic properties may constituent an important part of its therapeutic effects. All these indicate that SAA is likely to be a promising agent for NS.


Asunto(s)
Ácidos Cafeicos/uso terapéutico , Doxorrubicina/efectos adversos , Enfermedades Renales/inducido químicamente , Enfermedades Renales/tratamiento farmacológico , Lactatos/uso terapéutico , Animales , Hemorreología/efectos de los fármacos , Proteínas I-kappa B/metabolismo , Péptidos y Proteínas de Señalización Intracelular/metabolismo , Riñón/efectos de los fármacos , Riñón/patología , Riñón/ultraestructura , Enfermedades Renales/complicaciones , Masculino , Malondialdehído/metabolismo , Proteínas de la Membrana/metabolismo , Inhibidor NF-kappaB alfa , Estrés Oxidativo/efectos de los fármacos , Fosforilación , Podocitos/efectos de los fármacos , Podocitos/patología , Podocitos/ultraestructura , Proteinuria/complicaciones , Ratas Sprague-Dawley , Superóxido Dismutasa/metabolismo , Factores de Tiempo , Factor de Transcripción ReIA/metabolismo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA