Reactive Oxygen Species in Skeletal Muscle and Adipose Tissue

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: 28 February 2026 | Viewed by 52

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 Assistant
Department of Physiology, Medical University of Bialystok, 15-089 Bialystok, Poland
Interests: branched-chain amino acids; lipid metabolism; stem cells; insulin resistance; fatty acid transport
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Special Issue Information

Dear Colleagues,

Reactive oxygen species (ROS) are important signaling molecules in processes such as gene activation, cellular growth, and modulation of chemical reactions in the cell. However, at elevated levels, ROS induce oxidative damage to nucleic acids, proteins, and lipids and can cause tissue dysfunction associated with many pathological conditions.

The effect of redox environment in skeletal muscle and adipose tissue has exceptional relevance to the beneficial remodeling in response to exercise, or detrimental alterations during the development of inflammatory and metabolic diseases. The interplay between both the tissues—mediated by circulating lipids, cytokines, and myokines—modifies oxidative stress and contributes to metabolic flexibility, regulates inflammatory processes, and controls whole-body homeostasis. This Antioxidants Special Issue is dedicated to collecting original articles and reviews focusing on the crosstalk between skeletal muscle and adipose tissue, and the role of oxidative stress in that communication.

We look forward to your contribution.

Prof. Dr. Jan Górski
Guest Editor

Dr. Elzbieta Supruniuk
Guest Editor Assistant

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Keywords

  • oxidative stress
  • antioxidants
  • myokines
  • adipokines
  • skeletal muscle
  • adipose tissue

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Published Papers

This special issue is now open for submission.
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