Hormesis, cell death and aging

Aging (Albany NY). 2011 Sep;3(9):821-8. doi: 10.18632/aging.100380.


Frequently, low doses of toxins and other stressors not only are harmless but also activate an adaptive stress response that raise the resistance of the organism against high doses of the same agent. This phenomenon, which is known as "hormesis", is best represented by ischemic preconditioning, the situation in which short ischemic episodes protect the brain and the heart against prolonged shortage of oxygen and nutrients. Many molecules that cause cell death also elicit autophagy, a cytoprotective mechanism relying on the digestion of potentially harmful intracellular structures, notably mitochondria. When high doses of these agents are employed, cells undergo mitochondrial outer membrane permeabilization and die. In contrast, low doses of such cytotoxic agents can activate hormesis in several paradigms, and this may explain the lifespan-prolonging potential of autophagy inducers including resveratrol and caloric restriction.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aging / physiology*
  • Animals
  • Autophagy / drug effects
  • Caloric Restriction
  • Cell Death / physiology*
  • Hormesis / physiology*
  • Humans
  • Ischemic Preconditioning
  • Mitochondria / metabolism
  • Resveratrol
  • Stilbenes / pharmacology


  • Stilbenes
  • Resveratrol