losartan-potassium has been researched along with Muscular-Dystrophy--Duchenne* in 2 studies
2 other study(ies) available for losartan-potassium and Muscular-Dystrophy--Duchenne
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Erythropoietin reduces the expression of myostatin in mdx dystrophic mice.
Erythropoietin (EPO) has been well characterized as a renal glycoprotein hormone regulating red blood cell production by inhibiting apoptosis of erythrocyte progenitors in hematopoietic tissues. EPO exerts regulatory effects in cardiac and skeletal muscles. Duchenne muscular dystrophy is a lethal degenerative disorder of skeletal and cardiac muscle. In this study, we tested the possible therapeutic beneficial effect of recombinant EPO (rhEPO) in dystrophic muscles in mdx mice. Total strength was measured using a force transducer coupled to a computer. Gene expression for myostatin, transforming growth factor-β1 (TGF-β1), and tumor necrosis factor-α (TNF-α) was determined by quantitative real time polymerase chain reaction. Myostatin expression was significantly decreased in quadriceps from mdx mice treated with rhEPO (rhEPO = 0.60 ± 0.11, control = 1.07 ± 0.11). On the other hand, rhEPO had no significant effect on the expression of TGF-β1 (rhEPO = 0.95 ± 0.14, control = 1.05 ± 0.16) and TNF-α (rhEPO = 0.73 ± 0.20, control = 1.01 ± 0.09). These results may help to clarify some of the direct actions of EPO on skeletal muscle. Topics: Animals; Disease Models, Animal; Down-Regulation; Dystrophin; Erythropoietin; Gene Expression; Male; Mice, Inbred mdx; Muscle Strength; Muscle, Skeletal; Muscular Dystrophy, Duchenne; Myostatin; Phenotype; Real-Time Polymerase Chain Reaction; Recombinant Proteins; Transforming Growth Factor beta1; Tumor Necrosis Factor-alpha | 2014 |
Diagnostic and therapeutic challenges.
Topics: Adolescent; Anemia; Anti-Inflammatory Agents; Cardiomyopathies; Epoetin Alfa; Erythropoietin; Fluorescein Angiography; Humans; Injections; Laser Coagulation; Male; Methylprednisolone; Methylprednisolone Acetate; Muscular Dystrophy, Duchenne; Recombinant Proteins; Retinal Neovascularization; Vision Disorders; Vitrectomy; Vitreous Hemorrhage | 2006 |