Martins-Duarte Erica S, Urbina Julio A, de Souza Wanderley, Vommaro Rossiane C
Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho CCS Universidade Federal do Rio de Janeiro, 21949-900-Rio de Janeiro-RJ, Brazil.
J Antimicrob Chemother. 2006 Jul;58(1):59-65. doi: 10.1093/jac/dkl180. Epub 2006 May 15.
To study the antiproliferative effects of ER119884 and E5700, two quinuclidine-based inhibitors of squalene synthase (SQS), against Toxoplasma gondii tachyzoites in epithelial cells.
The antiproliferative effects of the quinuclidine derivatives, alone or in combination with epiminolanosterol or antifolates, were analysed, resulting in the construction of isobolograms. The ultrastructure of treated tachyzoites was analysed by transmission electron microscopy.
The quinuclidine derivatives demonstrated selective anti-T. gondii activity, arresting parasite growth with IC50 values of 0.66 and 0.23 microM for ER119884 and E5700, respectively, after 24 h of interaction and 0.44 and 0.19 microM after 48 h of interaction. Both compounds induced remarkable alterations in the parasite ultrastructure, such as mitochondrial swelling and the presence of autophagosome-like structures, after 24 h of treatment. Combination of these quinuclidine derivatives with the antifolates sulfadiazine and pyrimethamine produced a synergic effect. When epiminolanosterol was combined with E5700, the effect observed was synergic, whereas the combination with ER119884 produced no interaction.
E5700 and ER119884 demonstrated selective activity against T. gondii tachyzoites and are a possible alternative to be used in association with the current therapy. The ultrastructural alterations observed suggest a possible interference with lipid metabolism.
研究两种基于奎宁环的角鲨烯合酶(SQS)抑制剂ER119884和E5700对上皮细胞中弓形虫速殖子的抗增殖作用。
分析奎宁环衍生物单独或与表雄甾醇或抗叶酸药物联合使用时的抗增殖作用,构建等效线图。通过透射电子显微镜分析经处理的速殖子的超微结构。
奎宁环衍生物表现出对弓形虫的选择性活性,在相互作用24小时后,ER119884和E5700使寄生虫生长停滞的IC50值分别为0.66和0.23微摩尔,相互作用48小时后分别为0.44和0.19微摩尔。处理24小时后,两种化合物均引起寄生虫超微结构的显著改变,如线粒体肿胀和自噬体样结构的出现。这些奎宁环衍生物与抗叶酸药物磺胺嘧啶和乙胺嘧啶联合使用产生协同作用。当表雄甾醇与E5700联合使用时,观察到的效果是协同的,而与ER119884联合使用则没有相互作用。
E5700和ER119884对弓形虫速殖子表现出选择性活性,可能是与当前疗法联合使用的一种替代选择。观察到的超微结构改变提示可能干扰脂质代谢。