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Nutritional intervention with cyanidin hinders the progression of muscular dystrophy.
Saclier, Marielle; Bonfanti, Chiara; Antonini, Stefania; Angelini, Giuseppe; Mura, Giada; Zanaglio, Federica; Taglietti, Valentina; Romanello, Vanina; Sandri, Marco; Tonelli, Chiara; Petroni, Katia; Cassano, Marco; Messina, Graziella.
Afiliação
  • Saclier M; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
  • Bonfanti C; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
  • Antonini S; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
  • Angelini G; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
  • Mura G; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
  • Zanaglio F; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
  • Taglietti V; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
  • Romanello V; Venetian Institute of Molecular Medicine (VIMM), Department of Biomedical Sciences, University of Padova, Padova, Italy.
  • Sandri M; Venetian Institute of Molecular Medicine (VIMM), Department of Biomedical Sciences, University of Padova, Padova, Italy.
  • Tonelli C; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
  • Petroni K; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
  • Cassano M; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
  • Messina G; Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy. graziella.messina@unimi.it.
Cell Death Dis ; 11(2): 127, 2020 02 18.
Article em En | MEDLINE | ID: mdl-32071288
ABSTRACT
Muscular Dystrophies are severe genetic diseases due to mutations in structural genes, characterized by progressive muscle wasting that compromises patients' mobility and respiratory functions. Literature underlined oxidative stress and inflammation as key drivers of these pathologies. Interestingly among different myofiber classes, type I fibers display a milder dystrophic phenotype showing increased oxidative metabolism. This work shows the benefits of a cyanidin-enriched diet, that promotes muscle fiber-type switch and reduced inflammation in dystrophic alpha-sarcoglyan (Sgca) null mice having, as a net outcome, morphological and functional rescue. Notably, this benefit is achieved also when the diet is administered in dystrophic animals when the signs of the disease are seriously evident. Our work provides compelling evidence that a cyanidin-rich diet strongly delays the progression of muscular dystrophies, paving the way for a combinatorial approach where nutritional-based reduction of muscle inflammation and oxidative stress facilitate the successful perspectives of definitive treatments.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article