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氮杂甾醇与抗叶酸剂对刚地弓形虫的抗增殖协同作用。

Antiproliferative synergism of azasterols and antifolates against Toxoplasma gondii.

作者信息

Dantas-Leite Lucas, Urbina Julio A, de Souza Wanderley, Vommaro Rossiane C

机构信息

Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Bloco G, CCS, Universidade Federal do Rio de Janeiro, 21949-9000 Rio de Janeiro, RJ, Brazil.

出版信息

Int J Antimicrob Agents. 2005 Feb;25(2):130-5. doi: 10.1016/j.ijantimicag.2004.08.016.

Abstract

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 Delta24(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.

摘要

研究了两种氮杂甾醇,即22,26 - 氮杂甾醇(20 - 哌啶 - 2 - 基 - 5α - 孕甾 - 3β - 20(R,S) - 二醇,AZA)和24,25(R,S) - 表氨基羊毛甾醇(EIL),与磺胺嘧啶(SDZ)和乙胺嘧啶(PYR)联合使用时,对在培养的哺乳动物细胞中生长的刚地弓形虫速殖子的抗增殖作用。我们之前已经表明,AZA和EIL这两种在真菌和原生动物中已知的Δ24(25)甾醇甲基转移酶抑制剂,具有强大且选择性的抗刚地弓形虫活性,尽管在这种寄生虫中未检测到24 - 烷基甾醇。我们现在报告,当这些甾醇类似物与传统的SDZ/PYR治疗联合使用时,观察到了强大的协同作用,在次优剂量的氮杂甾醇存在下,IC50值降低了10至100倍。当暴露于这些药物组合时,细胞内的刚地弓形虫寄生虫表现出多种亚细胞改变,包括线粒体肿胀、内二殖过程停滞,细胞核碎片化以及随后的细胞裂解。这些结果提示了一种治疗弓形虫病的潜在新方法,该方法可以显著降低所需的抗叶酸药物水平,从而减少其不良副作用。

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