Maia Claudia, Attias Márcia, Urbina Julio, Gilbert Ian, Magaraci Filippo, de Souza Wanderley
Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; Instituto de Bioquímica Médica, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Biochem Biophys Res Commun. 2007 Nov 16;363(2):310-6. doi: 10.1016/j.bbrc.2007.08.174. Epub 2007 Sep 10.
The effects of sterol biosynthesis inhibitors on growth and fine structure of Giardia lamblia P1 strain cultures were analyzed. Azasterols demonstrated high efficacy in killing cells. The IC(50) values for 22,26-azasterol and 24(R,S),25-epiminolanosterol were 7muM and 170nM, respectively. Morphological analysis showed that azasterols induced changes in G. lamblia ultrastructure. The most significant alterations were: (a) considerable increase of the size of the peripheral vesicles, which are part of the parasite endosomal-lysosomal system; (b) appearance of autophagosomal structures; and (c) induction of differentiation, followed by an abnormal enlargement of encystation secretory vesicles. We propose that azasterols are effective chemotherapeutic drugs against Giardia lamblia in vitro and may have another target in cells besides sterol biosynthesis.
分析了甾醇生物合成抑制剂对蓝氏贾第鞭毛虫P1株培养物生长和精细结构的影响。氮杂甾醇在杀死细胞方面显示出高效性。22,26 - 氮杂甾醇和24(R,S),25 - 表氨基羊毛甾醇的IC(50)值分别为7μM和170nM。形态学分析表明,氮杂甾醇诱导蓝氏贾第鞭毛虫超微结构发生变化。最显著的改变是:(a) 作为寄生虫内体 - 溶酶体系统一部分的外周囊泡大小显著增加;(b) 自噬体结构的出现;以及(c) 诱导分化,随后包囊分泌囊泡异常增大。我们认为氮杂甾醇是体外抗蓝氏贾第鞭毛虫的有效化疗药物,并且除了甾醇生物合成外,可能在细胞中有另一个作用靶点。