Photocytotoxicity of curcumin

Photochem Photobiol. 1994 Mar;59(3):290-4. doi: 10.1111/j.1751-1097.1994.tb05036.x.

Abstract

Curcumin, bis(4-hydroxy-3-methoxyphenyl)-1,6-diene-3,5-dione, is a yellow-orange dye derived from the rhizome of the plant Curcuma longa. Curcumin has demonstrated phototoxicity to several species of bacteria under aerobic conditions (Dahl, T. A., et al., 1989, Arch. Microbiol. 151 183), denoting photodynamic inactivation. We have now found that curcumin is also phototoxic to mammalian cells, using a rat basophilic leukemia cell model, and that this phototoxicity again requires the presence of oxygen. The spectral and photochemical properties of curcumin vary with environment, resulting in the potential for multiple or alternate pathways for the exertion of photodynamic effects. For example, curcumin photogenerates singlet oxygen and reduced forms of molecular oxygen under several conditions relevant to cellular environments. In addition, we detected carbon-centered radicals, which may lead to oxidation products (see accompanying paper). Such products may be important reactants in curcumin's phototoxicity since singlet oxygen and reduced oxygen species alone could not explain the biological results, such as the relatively long lifetime (t1/2 = 27 s) of the toxicant responsible for decreased cell viability.

MeSH terms

  • Animals
  • Cell Death / drug effects
  • Cell Death / radiation effects
  • Curcumin / chemistry
  • Curcumin / pharmacokinetics
  • Curcumin / toxicity*
  • Photochemistry
  • Rats
  • Reactive Oxygen Species / chemistry
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / metabolism
  • Tumor Cells, Cultured / radiation effects

Substances

  • Reactive Oxygen Species
  • Curcumin