Oxidative stress and ageing: is ageing a cysteine deficiency syndrome?

Philos Trans R Soc Lond B Biol Sci. 2005 Dec 29;360(1464):2355-72. doi: 10.1098/rstb.2005.1770.


Reactive oxygen species (ROS) are constantly produced in biological tissues and play a role in various signalling pathways. Abnormally high ROS concentrations cause oxidative stress associated with tissue damage and dysregulation of physiological signals. There is growing evidence that oxidative stress increases with age. It has also been shown that the life span of worms, flies and mice can be significantly increased by mutations which impede the insulin receptor signalling cascade. Molecular studies revealed that the insulin-independent basal activity of the insulin receptor is increased by ROS and downregulated by certain antioxidants. Complementary clinical studies confirmed that supplementation of the glutathione precursor cysteine decreases insulin responsiveness in the fasted state. In several clinical trials, cysteine supplementation improved skeletal muscle functions, decreased the body fat/lean body mass ratio, decreased plasma levels of the inflammatory cytokine tumour necrosis factor alpha (TNF-alpha), improved immune functions, and increased plasma albumin levels. As all these parameters degenerate with age, these findings suggest: (i) that loss of youth, health and quality of life may be partly explained by a deficit in cysteine and (ii) that the dietary consumption of cysteine is generally suboptimal and everybody is likely to have a cysteine deficiency sooner or later.

Publication types

  • Review

MeSH terms

  • Aging / physiology*
  • Body Composition / drug effects
  • Cysteine / chemistry
  • Cysteine / deficiency*
  • Cysteine / metabolism*
  • Cysteine / pharmacology*
  • Dietary Supplements*
  • Glutathione / blood
  • Glutathione / metabolism
  • Humans
  • Immunity, Cellular / drug effects
  • Muscle, Skeletal / drug effects
  • Oxidative Stress / physiology*
  • Protein Tyrosine Phosphatases / antagonists & inhibitors
  • Protein Tyrosine Phosphatases / metabolism
  • Reactive Oxygen Species / metabolism*
  • Receptor, Insulin / antagonists & inhibitors
  • Receptor, Insulin / metabolism
  • Serum Albumin
  • Signal Transduction / physiology*
  • Tumor Necrosis Factor-alpha / metabolism


  • Reactive Oxygen Species
  • Serum Albumin
  • Tumor Necrosis Factor-alpha
  • Receptor, Insulin
  • Protein Tyrosine Phosphatases
  • Glutathione
  • Cysteine