Columbin inhibits cholesterol uptake in bloodstream forms of Trypanosoma brucei-A possible trypanocidal mechanism

J Enzyme Inhib Med Chem. 2005 Aug;20(4):365-8. doi: 10.1080/14756360400028127.

Abstract

The diterpenoid furanolactone (columbin) from Aristolochia albida inhibited growth of culture forms of Trypanosoma brucei. In vitro analysis of the compound at 5-250 microg/ml showed complete lysis of the parasites within 10-20 minutes post incubation. At 50 microg/ml, columbin killed about 50% of the parasites which initially appeared swollen under phase contrast microscopy. Also the total amount of cholesterol diminished dose-dependently in the presence of 10-100 microg/ml of columbin after a 3-day incubation period. In vivo analysis of the compound in T. brucei-infected mice revealed that 25 mg/kg administered for 3 consecutive days, completely cleared the parasites from the peripheral circulation. However, columbin could not clear parasites in the cerebrospinal fluid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Movement / drug effects
  • Cholesterol / metabolism*
  • Diterpenes / pharmacology*
  • Lactones / pharmacology*
  • Mice / blood
  • Mice / parasitology
  • Microscopy, Phase-Contrast
  • Sterols / metabolism*
  • Trypanocidal Agents / pharmacology*
  • Trypanosoma brucei brucei / drug effects*
  • Trypanosomiasis / drug therapy*

Substances

  • Diterpenes
  • Lactones
  • Sterols
  • Trypanocidal Agents
  • Cholesterol
  • columbin