Nitrosative Redox Homeostasis and Antioxidant Response Defense in Disused Vastus lateralis Muscle in Long-Term Bedrest (Toulouse Cocktail Study)

• Published in: Antioxidants 2021-03, Vol.10 (3), p.378
• Main Authors: Blottner, Dieter, Capitanio, Daniele, Trautmann, Gabor, Furlan, Sandra, Gambara, Guido, Moriggi, Manuela, Block, Katharina, Barbacini, Pietro, Torretta, Enrica, Py, Guillaume, Chopard, Angèle, Vida, Imre, Volpe, Pompeo, Gelfi, Cecilia, Salanova, Michele
• Format: Article
• Language: English
• Subjects: Aerospace medicine; antioxidant systems; Antioxidants; Atrophy; bedrest muscle disuse; Biochemistry, Molecular Biology; Biopsy; Confocal microscopy; Exercise; GA-binding protein; Glycolysis; Homeostasis; Life Sciences; Local anesthesia; Mass spectrometry; Metabolism; Mitochondria; Musculoskeletal system; Myogenesis; Nitrogen; Oxidative phosphorylation; Oxidative stress; Pharmaceutical sciences; Pharmacology; Phosphorylation; Physical fitness; Placebos; Polyphenols; Protein folding; Protein synthesis; Proteins; Reactive nitrogen species; Reactive oxygen species; RNS in cell signaling; Ryanodine receptors; sarcopenia; Scientific imaging; Selenium; Signal transduction; Skeletal muscle; skeletal muscle redox homeostasis; Tricarboxylic acid cycle; Vitamin E
• ISSN: 2076-3921; 2076-3921
• DOI: 10.3390/antiox10030378

Increased oxidative stress by reactive oxygen species (ROS) and reactive nitrogen species (RNS) is a major determinant of disuse-induced muscle atrophy. Muscle biopsies (thigh vastus lateralis, ) obtained from healthy male subjects enrolled in the Toulouse Cocktail bedrest (BR) study were used to assess efficacy of an antioxidant cocktail (polyphenols, omega-3, vitamin E, and selenium) to counteract the increased redox homeostasis and enhance the antioxidant defense response by using label-free LC-MS/MS and NITRO-DIGE (nitrosated proteins), qPCR, and laser confocal microscopy. Label-free LC-MS/MS indicated that treatment prevented the redox homeostasis dysregulation and promoted structural remodeling (TPM3, MYH7, MYBPC, MYH1, MYL1, HRC, and LUM), increment of RyR1, myogenesis (CSRP3), and skeletal muscle development (MUSTN1, LMNA, AHNAK). These changes were absent in the Placebo group. Glycolysis, tricarboxylic acid cycle (TCA), oxidative phosphorylation, fatty acid beta-oxidation, and mitochondrial transmembrane transport were normalized in treated subjects. Proteins involved in protein folding were also normalized, whereas protein entailed in ion homeostasis decreased. NITRO-DIGE analysis showed significant protein nitrosylation changes for CAT, CA3, SDHA, and VDAC2 in Treatment vs. Placebo. Similarly, the nuclear factor erythroid 2-related factor 2 (Nrf-2) antioxidant response element (Nrf-2 ARE) signaling pathway showed an enhanced response in the Treatment group. Increased nitrosative redox homeostasis and decreased antioxidant defense response were found in post-BR control (Placebo, = 10) vs. the antioxidant cocktail treated group (Treatment, = 10). Taken together, increased nitrosative redox homeostasis and muscle deterioration during BR-driven physical inactivity were prevented, whereas decreased antioxidant nitrosative stress defense response was attenuated by Treatment suggesting positive effects of the nutritional intervention protocol in bedrest.