Na(+)-ATPase and protein kinase C are targets to 1-O-hexadecylphosphocoline (miltefosine) in Trypanosoma cruzi

Arch Biochem Biophys. 2009 Jan 1;481(1):65-71. doi: 10.1016/j.abb.2008.10.018. Epub 2008 Oct 21.

Abstract

Miltefosine has been shown to be a very active compound against Trypanosoma cruzi. Here, we evaluated the effects of miltefosine on the activity of the Na(+)-ATPase and protein kinase C (PKC) present in the plasma membrane of T. cruzi. Furosemide (2mM), a specific inhibitor of Na(+)-ATPase, abolished the growth of T. cruzi showing a crucial role of this enzyme to parasite growth. Miltefosine inhibited the Na(+)-ATPase activity with IC(50)=18+/-5 microg mL(-1). This effect was shown to be reversible, dependent on the pH and Ca(2+). The inhibition was not observed when the membranes were solubilized with 0.1% deoxycholate, suggesting that the interaction between the enzyme and membrane phospholipids might be important for the drug effect. Miltefosine also inhibited the parasite PKC activity, but through a Na(+)-ATPase-independent way. Altogether the results indicate that miltefosine inhibits T. cruzi growth through, at least in part, the inhibition of both Na(+)-ATPase and PKC activities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism
  • Cell Membrane / enzymology
  • Furosemide / pharmacology
  • Hydrogen-Ion Concentration
  • Kinetics
  • Phosphorylcholine / analogs & derivatives*
  • Phosphorylcholine / pharmacology
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / metabolism*
  • Sodium-Potassium-Exchanging ATPase / antagonists & inhibitors
  • Sodium-Potassium-Exchanging ATPase / metabolism*
  • Swine
  • Trypanocidal Agents / pharmacology*
  • Trypanosoma cruzi / drug effects*
  • Trypanosoma cruzi / enzymology
  • Trypanosoma cruzi / growth & development

Substances

  • Trypanocidal Agents
  • Phosphorylcholine
  • miltefosine
  • Furosemide
  • Protein Kinase C
  • Sodium-Potassium-Exchanging ATPase
  • Calcium