Flavonoids and Omega3 Prevent Muscle and Cardiac Damage in Duchenne Muscular Dystrophy Animal Model

Cells. 2021 Oct 28;10(11):2917. doi: 10.3390/cells10112917.

Abstract

Nutraceutical products possess various anti-inflammatory, antiarrhythmic, cardiotonic, and antioxidant pharmacological activities that could be useful in preventing oxidative damage, mainly induced by reactive oxygen species. Previously published data showed that a mixture of polyphenols and polyunsaturated fatty acids, mediate an antioxidative response in mdx mice, Duchenne muscular dystrophy animal model. Dystrophic muscles are characterized by low regenerative capacity, fibrosis, fiber necrosis, inflammatory process, altered autophagic flux and inadequate anti-oxidant response. FLAVOmega β is a mixture of flavonoids and docosahexaenoic acid. In this study, we evaluated the role of these supplements in the amelioration of the pathological phenotype in dystrophic mice through in vitro and in vivo assays. FLAVOmega β reduced inflammation and fibrosis, dampened reactive oxygen species production, and induced an oxidative metabolic switch of myofibers, with consequent increase of mitochondrial activity, vascularization, and fatigue resistance. Therefore, we propose FLAVOmega β as food supplement suitable for preventing muscle weakness, delaying inflammatory milieu, and sustaining physical health in patients affected from DMD.

Keywords: Duchenne muscular dystrophy; food supplement; inflammatory response; muscle homeostasis; muscle regeneration; satellite cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy / drug effects
  • Cardiomyopathy, Dilated / pathology
  • Cell Line
  • Cell Proliferation / drug effects
  • Disease Models, Animal
  • Down-Regulation / drug effects
  • Fatty Acids, Omega-3 / administration & dosage
  • Fatty Acids, Omega-3 / pharmacology*
  • Fibrosis
  • Flavonoids / administration & dosage
  • Flavonoids / pharmacology*
  • Inflammation / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred mdx
  • Muscle, Skeletal / pathology*
  • Muscular Dystrophy, Duchenne / pathology*
  • Myoblasts / drug effects
  • Myoblasts / metabolism
  • Myocardium / pathology*
  • Oxidative Phosphorylation / drug effects
  • Phenotype
  • Reactive Oxygen Species / metabolism
  • Regeneration / drug effects

Substances

  • Fatty Acids, Omega-3
  • Flavonoids
  • Reactive Oxygen Species