Burn-induced hypermetabolism and skeletal muscle dysfunction

Am J Physiol Cell Physiol. 2021 Jul 1;321(1):C58-C71. doi: 10.1152/ajpcell.00106.2021. Epub 2021 Apr 28.

Abstract

Critical illnesses, including sepsis, cancer cachexia, and burn injury, invoke a milieu of systemic metabolic and inflammatory derangements that ultimately results in increased energy expenditure leading to fat and lean mass catabolism. Burn injuries present a unique clinical challenge given the magnitude and duration of the hypermetabolic response compared with other forms of critical illness, which drastically increase the risk of morbidity and mortality. Skeletal muscle metabolism is particularly altered as a consequence of burn-induced hypermetabolism, as it primarily provides a main source of fuel in support of wound healing. Interestingly, muscle catabolism is sustained long after the wound has healed, indicating that additional mechanisms beyond wound healing are involved. In this review, we discuss the distinctive pathophysiological response to burn injury with a focus on skeletal muscle function and metabolism. We first examine the diverse consequences on skeletal muscle dysfunction between thermal, electrical, and chemical burns. We then provide a comprehensive overview of the known mechanisms underlying skeletal muscle dysfunction that may be attributed to hypermetabolism. Finally, we review the most promising current treatment options to mitigate muscle catabolism, and by extension improve morbidity and mortality, and end with future directions that have the potential to significantly improve patient care.

Keywords: inflammation; burn injury; hypermetabolism; muscle dysfunction.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Burns / genetics
  • Burns / metabolism
  • Burns / pathology
  • Burns / rehabilitation
  • Cachexia / drug therapy*
  • Cachexia / genetics
  • Cachexia / metabolism
  • Cachexia / pathology
  • Epigenesis, Genetic
  • Exercise
  • Human Growth Hormone / therapeutic use
  • Humans
  • Insulin / therapeutic use
  • Metformin / therapeutic use
  • Muscle Proteins / biosynthesis
  • Muscle Proteins / genetics*
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / injuries
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / physiopathology
  • Muscular Atrophy / genetics
  • Muscular Atrophy / metabolism
  • Muscular Atrophy / pathology
  • Muscular Atrophy / prevention & control*
  • Oxandrolone / therapeutic use
  • Propranolol / therapeutic use
  • Protein Biosynthesis*
  • Proteolysis
  • Sepsis / metabolism*
  • Sepsis / microbiology
  • Sepsis / pathology
  • Sepsis / rehabilitation
  • Signal Transduction
  • Wound Healing / drug effects
  • Wound Healing / physiology

Substances

  • Insulin
  • Muscle Proteins
  • Human Growth Hormone
  • Oxandrolone
  • Metformin
  • Propranolol