Antiproliferative synergism of azasterols and antifolates against Toxoplasma gondii

被引:20
|
作者
Dantas-Leite, L
Urbina, JA
de Souza, W
Vommaro, RC
机构
[1] Fed Univ Rio De Janeiro, Inst Biofis Carlos Chagas Filho, Lab Ultraestrutura Celular Hertha Meyer, BR-21949900 Rio De Janeiro, RJ, Brazil
[2] Inst Venezolano Invest Cient, Ctr Biofis & Bioquim, Lab Quim Biol, Caracas 1020A, Venezuela
关键词
apicomplexa; azasterols; sulphonamides; endodiogeny arrest;
D O I
10.1016/j.ijantimicag.2004.08.016
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The antiproliferative effects of two azasterols, 22,26-azasterol (20-piperidin-2-yl-5alpha-pregnan-3beta-20(R,S)-diol, AZA) and 24,25(R,S)-epiminolanosterol (EIL), in combination with sulphadiazine (SDZ) and pyrimethamine (PYR) were studied against Toxoplasma gondii tachyzoites growing in cultured mammalian cells. We had previously shown that AZA and EIL, two known inhibitors of Delta(24)((25)) sterol methyl transferase in fungi and protozoa, have a potent and selective anti-T. gondii activity, although no 24-alkyl sterols have been detected in this parasite. We now report that when these sterol analogues were used in combination with the conventional SDZ/PYR treatment, potent synergistic effects were observed, ranging from 10- to 100-fold reductions of the IC50 values in the presence of sub-optimal doses of azasterols. When exposed to these drug combinations, intracellular T. gondii parasites displayed diverse subcellular alterations, including mitochondrial swelling, the arrest of the endodiogeny process with fragmented nuclei and subsequent cell lysis. These results suggest a potential new approach for the treatment of toxoplasmosis, which could significantly lower the required levels of antifolates and thus their adverse side effects. (C) 2004 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:130 / 135
页数:6
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