Can we teach an old drug new tricks?

Trends Parasitol. 2012 Jun;28(6):220-4. doi: 10.1016/j.pt.2012.02.005. Epub 2012 Mar 22.

Abstract

Although resistance to chloroquine (CQ) has relegated it from modern chemotherapeutic strategies to treat Plasmodium falciparum malaria, new evidence suggests that higher doses of the drug may exert a different killing mechanism and offers this drug a new lease of life. Whereas the established antimalarial mechanisms of CQ are usually associated with nanomolar levels of the drug, micromolar levels of CQ trigger a distinct cell death pathway involving the permeabilization of the digestive vacuole of the parasite and a release of hydrolytic enzymes. In this paper, we propose that this pathway is a promising antimalarial strategy and suggest that revising the CQ treatment regimen may elevate blood drug levels to trigger this pathway without increasing the incidence of adverse reactions.

MeSH terms

  • Animals
  • Antimalarials / adverse effects
  • Antimalarials / pharmacology*
  • Chloroquine / adverse effects
  • Chloroquine / pharmacology*
  • Dose-Response Relationship, Drug
  • Drug Resistance*
  • Humans
  • Malaria, Falciparum / drug therapy*
  • Malaria, Falciparum / parasitology
  • Plasmodium falciparum / drug effects*
  • Plasmodium falciparum / metabolism*

Substances

  • Antimalarials
  • Chloroquine