Duchenne muscular dystrophy progression induced by downhill running is accompanied by increased endomysial fibrosis and oxidative damage DNA in muscle of mdx mice

Author:

Lazzarin Mariana Cruz,dos Santos José Fontes,Quintana Hananiah Tardivo,Pidone Flavia Andressa Mazzuco,de Oliveira FlaviaORCID

Funder

CAPES

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,General Medicine,Physiology,Histology

Reference80 articles.

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2. Alexakis C, Partridge T, Bou-Gharios G (2007) Implication of the satellite cell in dystrophic muscle fibrosis: a self-perpetuating mechanism of collagen overproduction. Am J Physiol Cell Physiol 293(2):C661–C669. https://doi.org/10.1152/ajpcell.00061.2007

3. Allen DG, Whitehead NP, Froehner SC (2016) Absence of dystrophin disrupts skeletal muscle signaling: roles of Ca2+, reactive oxygen species, and nitric oxide in the development of muscular dystrophy. Physiol Rev 96(1):253–305. https://doi.org/10.1152/physrev.00007.2015

4. Anderson CL, De Repentigny Y, Cifelli C, Marshall P, Renaud JM, Worton RG, Kothary R (2006) The mouse dystrophin muscle promoter/enhancer drives expression of mini-dystrophin in transgenic mdx mice and rescues the dystrophy in these mice. Mol Ther 14(5):724–734. https://doi.org/10.1016/j.ymthe.2006.04.013

5. Araujo APQC, Carvalho AAS, Cavalcanti EBU, Saute JAM, Carvalho E, França MC, Junior, Martinez ARM, Navarro MMM, Nucci A, Resende MBD, Gonçalves MVM, Gurgel-Giannetti J, Scola RH, Sobreira CFDR, Reed UC, Zanoteli E (2017) Brazilian consensus on Duchenne muscular dystrophy. Part 1: diagnosis, steroid therapy and perspectives. Arq Neuropsiquiatr 75(8):104–113. https://doi.org/10.1590/0004-282x20170112

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