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Amiodarone has intrinsic anti-Trypanosoma cruzi activity and acts synergistically with posaconazole.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2006 Feb 09; Vol. 49 (3), pp. 892-9. - Publication Year :
- 2006
-
Abstract
- There is no effective treatment for the prevalent chronic form of Chagas' disease in Latin America. Its causative agent, the protozoan parasite Trypanosoma cruzi, has an essential requirement for ergosterol, and ergosterol biosynthesis inhibitors, such as the antifungal drug posaconazole, have potent trypanocidal activity. The antiarrhythmic compound amiodarone, frequently prescribed for the symptomatic treatment of Chagas' disease patients, has also recently been shown to have antifungal activity. We now show here for the first time that amiodarone has direct activity against T. cruzi, both in vitro and in vivo, and that it acts synergistically with posaconazole. We found that amiodarone, in addition to disrupting the parasites' Ca(2+) homeostasis, also blocks ergosterol biosynthesis, and that posaconazole also affects Ca(2+) homeostasis. These results provide logical explanations for the synergistic activity of amiodarone with azoles against T. cruzi and open up the possibility of novel, combination therapy approaches to the treatment of Chagas' disease using currently approved drugs.
- Subjects :
- Acute Disease
Amiodarone chemistry
Amiodarone therapeutic use
Animals
Calcium metabolism
Chagas Disease drug therapy
Chlorocebus aethiops
Crystallography, X-Ray
Drug Synergism
Ergosterol biosynthesis
Intramolecular Transferases antagonists & inhibitors
Intramolecular Transferases chemistry
Mice
Models, Molecular
Molecular Structure
Triazoles chemistry
Triazoles therapeutic use
Trypanocidal Agents chemistry
Trypanocidal Agents therapeutic use
Trypanosoma cruzi metabolism
Vero Cells
Amiodarone pharmacology
Triazoles pharmacology
Trypanocidal Agents pharmacology
Trypanosoma cruzi drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 0022-2623
- Volume :
- 49
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 16451055
- Full Text :
- https://doi.org/10.1021/jm050691f