Antioxidant Response in Skeletal Muscle

A special issue of Antioxidants (ISSN 2076-3921). This special issue belongs to the section "Health Outcomes of Antioxidants and Oxidative Stress".

Deadline for manuscript submissions: 20 August 2024 | Viewed by 960

Special Issue Editors


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Guest Editor
Faculty of Health Sciences, University of Lomza, 18-400 Lomza, Poland
Interests: skeletal muscle; heart; exercise; metabolism; lipids

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Guest Editor
Department of Physiology, Medical University of Bialystok, 15-222 Bialystok, Poland
Interests: exercise; skeletal muscle fatigue; oxidative stress; mitochondria; branched-chain amino acids; lipid metabolism; stem cells; insulin resistance; carcinogenesis

Special Issue Information

Dear Colleagues,

The high oxygen consumption and metabolic rate of muscle fibers cause them to continuously generate reactive oxygen and nitrogen species (RONS) during rest, and their production is increased during muscle contraction. However, an imbalance between the antioxidant system and the generation of RONS triggers oxidative stress, which provokes damage to molecules and affects specific functions such as excitation–contraction coupling. Skeletal muscles are equipped with various enzymatic and non-enzymatic antioxidants, including superoxide dismutase, catalase, glutathione peroxidase, γ-glutamylcysteine synthetase and heme oxygenase-1. Accumulating evidence has shown that antioxidants can achieve optimal concentrations of RONS to perform physiological signal transduction in muscle. They function as biosensors of RONS and render skeletal muscle extremely flexible in both health and disease. As an example, RONS play a very important role in protein turnover, which can promote muscle hypertrophy and regeneration.

This Special Issue aims to provide a comprehensive overview of the skeletal-muscle-focused antioxidant responses accompanying both physiological (e.g., exercise) and pathological challenges. The latter involves muscle injury, metabolic diseases, muscle dystrophy, carcinogenesis, systemic inflammation, inactivity or immobilization, to only name a few disorders capable of altering redox balance. Authors are invited to submit their latest original and innovative research findings or review articles with new insights into the association between scavenging capacity and cell signaling, muscle function and muscle metabolism in the response to stressors. Both human and animal studies are welcome.

We look forward to receiving your contribution.

Dr. Jan Górski
Dr. Elzbieta Supruniuk
Guest Editors

Manuscript Submission Information

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Keywords

  • antioxidants
  • skeletal muscle
  • exercise
  • muscle injury
  • metabolic diseases
  • muscle dystrophy
  • cancer
  • immobilization

Published Papers (1 paper)

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Research

21 pages, 2747 KiB  
Article
Nitrosative Stress in Astronaut Skeletal Muscle in Spaceflight
by Dieter Blottner, Manuela Moriggi, Gabor Trautmann, Sandra Furlan, Katharina Block, Martina Gutsmann, Enrica Torretta, Pietro Barbacini, Daniele Capitanio, Joern Rittweger, Ulrich Limper, Pompeo Volpe, Cecilia Gelfi and Michele Salanova
Antioxidants 2024, 13(4), 432; https://doi.org/10.3390/antiox13040432 - 02 Apr 2024
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Abstract
Long-duration mission (LDM) astronauts from the International Space Station (ISS) (>180 ISS days) revealed a close-to-normal sarcolemmal nitric oxide synthase type-1 (NOS1) immunoexpression in myofibers together with biochemical and quantitative qPCR changes in deep calf soleus muscle. Nitro-DIGE analyses identified functional proteins (structural, [...] Read more.
Long-duration mission (LDM) astronauts from the International Space Station (ISS) (>180 ISS days) revealed a close-to-normal sarcolemmal nitric oxide synthase type-1 (NOS1) immunoexpression in myofibers together with biochemical and quantitative qPCR changes in deep calf soleus muscle. Nitro-DIGE analyses identified functional proteins (structural, metabolic, mitochondrial) that were over-nitrosylated post- vs. preflight. In a short-duration mission (SDM) astronaut (9 ISS days), s-nitrosylation of a nodal protein of the glycolytic flux, specific proteins in tricarboxylic acid (TCA) cycle, respiratory chain, and over-nitrosylation of creatine kinase M-types as signs of impaired ATP production and muscle contraction proteins were seen. S-nitrosylation of serotransferrin (TF) or carbonic anhydrase 3 (CA3b and 3c) represented signs of acute response microgravity muscle maladaptation. LDM nitrosoprofiles reflected recovery of mitochondrial activity, contraction proteins, and iron transporter TF as signs of muscle adaptation to microgravity. Nitrosated antioxidant proteins, alcohol dehydrogenase 5/S-nitrosoglutathione reductase (ADH5/GSNOR), and selenoprotein thioredoxin reductase 1 (TXNRD1) levels indicated signs of altered redox homeostasis and reduced protection from nitrosative stress in spaceflight. This work presents a novel spaceflight-generated dataset on s-nitrosylated muscle protein signatures from astronauts that helps both to better understand the structural and molecular networks associated to muscular nitrosative stress and to design countermeasures to dysfunction and impaired performance control in human spaceflight missions. Full article
(This article belongs to the Special Issue Antioxidant Response in Skeletal Muscle)
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