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1.
Histochem Cell Biol ; 129(4): 489-501, 2008 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-18264714

RESUMEN

Dystrophic muscles suffer from enhanced oxidative stress. We have investigated whether administration of an antioxidant, epigallocatechin-3-gallate (EGCG), a component of green tea, reduces their oxidative stress and pathophysiology in mdx mice, a mild phenotype model of human Duchenne-type muscular dystrophy. EGCG (5 mg/kg body weight in saline) was injected subcutaneously 4x a week into the backs of C57 normal and dystrophin-deficient mdx mice for 8 weeks after birth. Saline was injected into normal and mdx controls. EGCG had almost no observable effects on normal mice or on the body weights of mdx mice. In contrast, it produced the following improvements in the blood chemistry, muscle histology, and electrophysiology of the treated mdx mice. First, the activities of serum creatine kinase were reduced to normal levels. Second, the numbers of fluorescent lipofuscin granules per unit volume of soleus and diaphragm muscles were significantly decreased by about 50% compared to the numbers in the corresponding saline-treated controls. Third, in sections of diaphragm and soleus muscles, the relative area occupied by histologically normal muscle fibres increased significantly 1.5- to 2-fold whereas the relative areas of connective tissue and necrotic muscle fibres were substantially reduced. Fourth, the times for the maximum tetanic force of soleus muscles to fall by a half increased to almost normal values. Fifth, the amount of utrophin in diaphragm muscles increased significantly by 17%, partially compensating for the lack of dystrophin expression.


Asunto(s)
Camellia sinensis/química , Catequina/análogos & derivados , Electrofisiología , Músculo Esquelético/efectos de los fármacos , Distrofia Muscular de Duchenne/metabolismo , Animales , Catequina/administración & dosificación , Catequina/farmacología , Creatina Quinasa/sangre , Inmunohistoquímica , Inyecciones Subcutáneas , Lipofuscina/metabolismo , Ratones , Ratones Endogámicos C57BL , Ratones Endogámicos mdx , Contracción Muscular/efectos de los fármacos , Músculo Esquelético/citología , Músculo Esquelético/metabolismo , Músculo Esquelético/patología , Distrofia Muscular de Duchenne/patología , Distrofia Muscular de Duchenne/fisiopatología , ARN Mensajero/metabolismo , Utrofina/análisis , Utrofina/metabolismo
2.
Am J Physiol Regul Integr Comp Physiol ; 290(2): R449-55, 2006 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-16179484

RESUMEN

The mdx mouse is an animal model for Duchenne muscular dystrophy. Mdx mice fed a 12% NaCl diet from birth up to 20 days of age (mdx-Na mice) had an approximately 50% reduction in serum creatine kinase (CK) activity compared with mdx mice fed a standard diet. Most notably, necrotic fibers in tibialis anterior (TA) muscle of mdx-Na mice were reduced by 99% and were similar in control mice. These mdx mice displayed significantly elevated blood Ca2+ and Na+ levels, while the total calcium content of their TA muscle was reduced to the level of control mice. In addition, mdx-Na mice had elevated zinc and magnesium contents in their TA muscle. These results suggest that elevated serum Na+ leads to Ca2+ extrusion from muscle via the Na+/Ca2+ exchanger causing a decrease in intracellular Ca2+ levels and an increase in blood Ca2+ levels. Extracellular Ca2+ and, in addition, Zn2+ and Mg2+ might also contribute to the stabilization of the cell membrane. Other possibilities explaining the surprisingly efficacious beneficial effect of dietary sodium exist and are discussed.


Asunto(s)
Modelos Animales de Enfermedad , Músculo Esquelético/efectos de los fármacos , Músculo Esquelético/patología , Distrofia Muscular de Duchenne/patología , Necrosis/prevención & control , Cloruro de Sodio/administración & dosificación , Cloruro de Sodio/farmacología , Envejecimiento , Animales , Calcio/sangre , Calcio/metabolismo , Creatina Quinasa/metabolismo , Suplementos Dietéticos , Vías de Administración de Medicamentos , Femenino , Masculino , Ratones , Ratones Endogámicos mdx , Distrofia Muscular de Duchenne/dietoterapia , Potasio/sangre , Potasio/metabolismo , Sodio/sangre , Sodio/metabolismo , Zinc/metabolismo
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