4.6 Article

Effects of Omega-3 and Antioxidant Cocktail Supplement on Prolonged Bed Rest: Results from Serum Proteome and Sphingolipids Analysis

Journal

CELLS
Volume 11, Issue 13, Pages -

Publisher

MDPI
DOI: 10.3390/cells11132120

Keywords

bed rest; S-nitrosylation; RONS; antioxidant; omega-3; serum apolipoproteins; iodoTMT; TMT; serum lipid profile; sphingolipids

Categories

Funding

  1. Federal Department of Economy and Energy (BMWi) through Deutsches Zentrum fuer Luft-und Raumfahrt (DLR e.V., Bonn-Oberkassel, Germany) [50WB1421/1718, 50WB2116]
  2. Agenzia Spaziale Italiana (ASI) [2018-9-U.O STOPBROS]
  3. ASI [2021-21-U.O ASTRONEMUS]

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Physical inactivity or prolonged bed rest can lead to muscle deconditioning and increased cardiovascular disease risk. Nutritional interventions, such as an antioxidant cocktail, have been found to preserve lipemic and reactive oxidative and nitrosative stress (RONS) homeostasis. This study investigated the effects of an antioxidant cocktail on serum molecules in healthy male subjects enrolled in a 60-day bed rest protocol.
Physical inactivity or prolonged bed rest (BR) induces muscle deconditioning in old and young subjects and can increase the cardiovascular disease risk (CVD) with dysregulation of the lipemic profile. Nutritional interventions, combining molecules such as polyphenols, vitamins and essential fatty acids, can influence some metabolic features associated with physical inactivity and decrease the reactive oxidative and nitrosative stress (RONS). The aim of this study was to detect circulating molecules correlated with BR in serum of healthy male subjects enrolled in a 60-day BR protocol to evaluate a nutritional intervention with an antioxidant cocktail as a disuse countermeasure (Toulouse COCKTAIL study). The serum proteome, sphingolipidome and nitrosoproteome were analyzed adopting different mass spectrometry-based approaches. Results in placebo-treated BR subjects indicated a marked decrease of proteins associated with high-density lipoproteins (HDL) involved in lipemic homeostasis not found in the cocktail-treated BR group. Moreover, long-chain ceramides decreased while sphingomyelin increased in the BR cocktail-treated group. In placebo, the ratio of S-nitrosylated/total protein increased for apolipoprotein D and several proteins were over-nitrosylated. In cocktail-treated BR subjects, the majority of protein showed a pattern of under-nitrosylation, except for ceruloplasmin and hemopexin, which were over-nitrosylated. Collectively, data indicate a positive effect of the cocktail in preserving lipemic and RONS homeostasis in extended disuse conditions.

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