Ramos H, Milhaud J, Cohen B E, Bolard J
Centro de Biologia Celular, Facultad de Ciencias, Universidad Central de Venezuela, Caracas.
Antimicrob Agents Chemother. 1990 Aug;34(8):1584-9. doi: 10.1128/AAC.34.8.1584.
A comparative study of the effect of the polyene antibiotic amphotericin B (AmB) on the viability of Leishmania mexicana promastigotes before and after their transformation by heat into amastigotelike forms was carried out. The kinetics of cell death were followed by spectrofluorometry with the nucleic acid-binding compound ethidium bromide. It was found that the rapid killing effect that is exerted by AmB on Leishmania promastigotes was even faster after their transformation into amastigotelike forms. Binding studies of AmB to Leishmania membranes by circular dichroism indicated that heat transformation modified it from noncooperative to cooperative binding, decreasing the amount of antibiotic that bound to the membranes. Thus, the increased rate of ethidium bromide incorporation into transformed cells was not related either to the amount of AmB bound or to an increased amount of ergosterol in the membrane (the ergosterol/phospholipid ratio was four times smaller after heat shock). An increase in the Mg2+ content of the external aqueous solution was able to prevent the AmB-induced incorporation of ethidium bromide into Leishmania promastigotes to a greater extent (Ki = 13.8 mM) than it was into heat-transformed cells (Ki = 64 mM), suggesting that there were significant changes at the Leishmania cell surface on heat transformation. The significance of these results for understanding the mechanism of action of AmB on sensitive organisms is discussed.
开展了一项比较研究,观察多烯抗生素两性霉素B(AmB)对墨西哥利什曼原虫前鞭毛体在经热转化为类无鞭毛体形式前后活力的影响。通过使用核酸结合化合物溴化乙锭的荧光分光光度法追踪细胞死亡动力学。结果发现,AmB对利什曼原虫前鞭毛体的快速杀伤作用在其转化为类无鞭毛体形式后甚至更快。通过圆二色性对AmB与利什曼原虫膜的结合研究表明,热转化使其从非协同结合转变为协同结合,减少了与膜结合的抗生素量。因此,溴化乙锭掺入转化细胞的速率增加既与结合的AmB量无关,也与膜中麦角固醇量的增加无关(热休克后麦角固醇/磷脂比率小四倍)。外部水溶液中Mg2+含量的增加能够比热转化细胞(Ki = 64 mM)更大程度地阻止AmB诱导的溴化乙锭掺入利什曼原虫前鞭毛体(Ki = 13.8 mM),这表明热转化时利什曼原虫细胞表面发生了显著变化。讨论了这些结果对于理解AmB对敏感生物体作用机制的意义。