Anabolic Strategies for ICU-Acquired Weakness. What Can We Learn from Bodybuilders?
Jakub TarnawskiMaja CzubMarta DymeckiMedha SunilMarcin FolwarskiPublished in: Nutrients (2024)
The study aimed to show the potential clinical application of supplements used among sportsmen for patients suffering from Intensive Care Unit-acquired Weakness (ICUAW) treatment. ICUAW is a common complication affecting approximately 40% of critically ill patients, often leading to long-term functional disability. ICUAW comprises critical illness polyneuropathy, critical illness myopathy, or a combination of both, such as critical illness polyneuromyopathy. Muscle degeneration begins shortly after the initiation of mechanical ventilation and persists post-ICU discharge until proteolysis and autophagy processes normalize. Several factors, including prolonged bedrest and muscle electrical silencing, contribute to muscle weakness, resulting from an imbalance between protein degradation and synthesis. ICUAW is associated with tissue hypoxia, oxidative stress, insulin resistance, reduced glucose uptake, lower adenosine triphosphate (ATP) formation, mitochondrial dysfunction, and increased free-radical production. Several well-studied dietary supplements and pharmaceuticals commonly used by athletes are proven to prevent the aforementioned mechanisms or aid in muscle building, regeneration, and maintenance. While there is no standardized treatment to prevent the occurrence of ICUAW, nutritional interventions have demonstrated the potential for its mitigation. The use of ergogenic substances, popular among muscle-building sociates, may offer potential benefits in preventing muscle loss and aiding recovery based on their work mechanisms.
Keyphrases
- intensive care unit
- mechanical ventilation
- skeletal muscle
- oxidative stress
- insulin resistance
- acute respiratory distress syndrome
- stem cells
- adipose tissue
- cell death
- prognostic factors
- physical activity
- metabolic syndrome
- climate change
- ejection fraction
- multiple sclerosis
- late onset
- end stage renal disease
- endothelial cells
- dna damage
- binding protein
- blood pressure
- polycystic ovary syndrome
- patient reported outcomes
- blood glucose
- respiratory failure