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Suramin attenuates dystrophin‐deficient cardiomyopathy in the mdx mouse model of duchenne muscular dystrophy
Authors:Drielen De Oliveira Moreira MSci  Juliano Alves Pereira MSci  Ana Paula Tiemi Taniguti DSci  Cíntia Yuri Matsumura DSci  Luis Alberto Ferreira Ramos MSci  Miguel Arcanjo Areas PhD  Humberto Santo Neto PhD  Maria Julia Marques PhD
Institution:Departamento de Biologia Estrutural e Funcional, Instituto de Biologia, Universidade Estadual de Campinas (UNICAMP), , Campinas, SP, 13083‐970 Brazil
Abstract:Introduction: The purpose of this study was to determine the effects of suramin, an antifibrotic agent, on cardiac function and remodeling in mdx mice. Methods: mdx mice (8 months old) received intraperitoneal injections of suramin twice a week for 3 months. Control mdx mice (8 months old) were injected with saline. Results: Suramin improved the electrocardiography profile with the main corrections seen in S‐ to R‐wave ratio, PR interval, and Q amplitude, and a significant decrease in the cardiomyopathy index. Suramin decreased myocardial fibrosis, inflammation, and myonecrosis. Conclusions: These findings suggest that suramin may be a new adjunctive therapy to help improve cardiomyopathy in DMD. Muscle Nerve 48 : 911–919, 2013
Keywords:antifibrotic drugs  cardiomyopathy  DMD  mdx  suramin
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