The Impact of Spermidine on C2C12 Myoblasts Proliferation, Redox Status and Polyamines Metabolism under H2O2 Exposure

• Published in: International journal of molecular sciences 2022-09, Vol.23 (19), p.10986
• Main Authors: Ceci, Roberta, Duranti, Guglielmo, Giuliani, Stefano, Rossi, Marianna Nicoletta, Dimauro, Ivan, Sabatini, Stefania, Mariottini, Paolo, Cervelli, Manuela
• Format: Article
• Language: English
• Subjects: Antioxidants; Apoptosis; Atrophy; Cell death; Cell number; Cell viability; Cells (biology); Gene expression; glutathione; Homeostasis; Hydrogen peroxide; Macromolecules; Metabolic disorders; Muscles; Musculoskeletal system; Myoblasts; myoblasts proliferation; Oxidation; Oxidative stress; Polyamines; polyamines homeostasis; Reactive oxygen species; redox homeostasis; Satellite cells; Skeletal muscle; Spermidine; Wounds
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms231910986

A central feature of the skeletal muscle is its ability to regenerate through the activation, by environmental signals, of satellite cells. Once activated, these cells proliferate as myoblasts, and defects in this process profoundly affect the subsequent process of regeneration. High levels of reactive oxygen species such as hydrogen peroxide (H2O2) with the consequent formation of oxidized macromolecules increase myoblasts’ cell death and strongly contribute to the loss of myoblast function. Recently, particular interest has turned towards the beneficial effects on muscle of the naturally occurring polyamine spermidine (Spd). In this work, we tested the hypothesis that Spd, upon oxidative challenge, would restore the compromised myoblasts’ viability and redox status. The effects of Spd in combination with aminoguanidine (Spd-AG), an inhibitor of bovine serum amine oxidase, on murine C2C12 myoblasts treated with a mild dose of H2O2 were evaluated by analyzing: (i) myoblast viability and recovery from wound scratch; (ii) redox status and (iii) polyamine (PAs) metabolism. The treatment of C2C12 myoblasts with Spd-AG increased cell number and accelerated scratch wound closure, while H2O2 exposure caused redox status imbalance and cell death. The combined treatment with Spd-AG showed an antioxidant effect on C2C12 myoblasts, partially restoring cellular total antioxidant capacity, reducing the oxidized glutathione (GSH/GSSG) ratio and increasing cell viability through a reduction in cell death. Moreover, Spd-AG administration counteracted the induction of polyamine catabolic genes and PA content decreased due to H2O2 challenges. In conclusion, our data suggest that Spd treatment has a protective role in skeletal muscle cells by restoring redox balance and promoting recovery from wound scratches, thus making myoblasts able to better cope with an oxidative insult.