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Cross-talk between TRPC-1, mTOR, PGC-1 alpha and PPAR delta in the dystrophic muscle cells treated with tempol

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da Rocha, Guilherme Luiz ; Rupcic, Ian Feller ; Mizobuti, Daniela Sayuri ; Hermes, Tulio de Almeida ; Covatti, Caroline ; Mariano da Silva, Heloina Nathallie ; Araujo, Hygor Nunes ; de Lourenco, Caroline Caramano ; Silveira, Leonardo Dos Reis ; Leite Pereira, Elaine Cristina ; Minatel, Elaine
Número total de Autores: 11
Tipo de documento: Artigo Científico
Fonte: Free Radical Research; v. N/A, p. 13-pg., 2022-05-11.
Resumo

Background Ca2+ dysregulation and oxidative damage appear to have a central role in Duchenne muscular dystrophy (DMD) progression. The current study provides muscle cell-specific insights into the effect of Tempol on the TRPC 1 channel; on the positive and negative regulators of muscle cell differentiation; on the antioxidant enzymatic system; on the activators of mitochondrial biogenesis; and on the inflammatory process in the dystrophic primary muscle cells in culture. Methods: Mdx myotubes were treated with Tempol (5 mM) for 24 h. Untreated mdx myotubes and C57BL/10 myotubes were used as controls. Results: The Trypan Blue, MTT and Live/Dead Cell assays showed that Tempol (5 mM) presented no cytotoxic effect on the dystrophic muscle cells. The Tempol treated-mdx muscle cells showed significantly lower levels in the fluorescence intensity of intracellular calcium; TRPC-1 channel; MyoD; H2O2 and O-2(center dot-) production; 4-HNE levels; SOD2, CAT and GPx levels; and TNF levels. On the other hand, SOD, CAT and GR mRNA relative expression were significantly higher in Tempol treated-mdx muscle cells. In addition, higher levels of Myogenin, MHC-Slow, mTOR, PGC-1 alpha and PPAR delta were also observed in Tempol treated-mdx muscle cells. Conclusion: Our findings demonstrated that Tempol decreased intracellular calcium and oxidative stress in primary dystrophic muscle cells, promoting a cross-talk between TRPC-1, mTOR, PGC-1 alpha and PPAR delta. (AU)

Processo FAPESP: 17/01638-0 - Tempol: potencial terapia antioxidante para fibras musculares distróficas
Beneficiário:Elaine Minatel
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 14/25010-1 - Estudo morfológico comparativo entre os efeitos da vitamina E e da prednisolona em fibras musculares distróficas de camundongos mdx
Beneficiário:Ian Feller Rupcic
Modalidade de apoio: Bolsas no Brasil - Iniciação Científica