Amiodarone has intrinsic anti-Trypanosoma cruzi activity and acts synergistically with posaconazole

被引:153
作者
Benaim, G
Sanders, JM
Garcia-Marchán, Y
Colina, C
Lira, R
Caldera, AR
Payares, G
Sanoja, C
Burgos, JM
Leon-Rossell, A
Concepcion, JL
Schijman, AG
Levin, M
Oldfield, E
Urbina, JA
机构
[1] Inst Venezolano Invest Cient, Lab Quim Biol, Caracas 1020A, Venezuela
[2] Inst Venezolano Invest Cient, Lab Permeabilidad Ion, Caracas 1020A, Venezuela
[3] Inst Estudios Avanzados, Caracas, Venezuela
[4] Cent Univ Venezuela, Inst Expt Biol, Caracas, Venezuela
[5] Consejo Nacl Invest Cient & Tecn, INGEGI, Lab Biol Mol Enfermedad Chagas, RA-1033 Buenos Aires, DF, Argentina
[6] Inst Cochin Genet Mol, INSERM U567, Dept Malad Infect, F-75014 Paris, France
[7] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[8] Univ Illinois, Dept Biophys, Urbana, IL 61801 USA
[9] Univ Los Andes, Dept Biol, Merida, Venezuela
关键词
D O I
10.1021/jm050691f
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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' Ca2+ homeostasis, also blocks ergosterol biosynthesis, and that posaconazole also affects Ca2+ 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.
引用
收藏
页码:892 / 899
页数:8
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