Ishiyama Aki, Otoguro Kazuhiko, Namatame Miyuki, Nishihara Aki, Furusawa Toshiaki, Takahashi Yoko, Masuma Rokuro, Shiomi Kazuro, Omura Satoshi
J Antibiot (Tokyo). 2008 Apr;61(4):254-7. doi: 10.1038/ja.2008.38.
Simaomicin alpha shows potent antimalarial activity in vitro and is known to be a cell-cycle effector. As erythrocytic schizogony of Plasmodium correlates with cell cycle events, we investigated the effect of simaomicin alpha on stage development of the malaria parasite Plasmodium falciparum. Simaomicin alpha interferes with normal parasite development in a time and concentration dependent manner. Parasites exposed to 2.5 nM simaomicin alpha at the ring stage or trophozoite stage showed disrupted development and immature schizont-like and segmenter-like forms were observed. However, schizont stage parasites were not affected by 2.5 nM simaomicin alpha. It is unclear whether mitosis involved in sequential parasite development occurred when parasites were exposed to simaomicin alpha at the ring or trophozoite stage. At a concentration of 5.0 nM, simaomicin alpha inhibited merozoite-trophozoite development. This concentration curtails p-LDH activity at all parasite stages, although its impact on the schizont stage is delayed for 24 hours.
司马米星α在体外显示出强大的抗疟活性,并且已知是一种细胞周期效应物。由于疟原虫的红细胞裂体增殖与细胞周期事件相关,我们研究了司马米星α对恶性疟原虫疟原虫阶段发育的影响。司马米星α以时间和浓度依赖性方式干扰正常的寄生虫发育。在环状期或滋养体期暴露于2.5 nM司马米星α的寄生虫显示发育受阻,观察到不成熟的裂殖体样和节段样形式。然而,裂殖体期寄生虫不受2.5 nM司马米星α的影响。尚不清楚当寄生虫在环状期或滋养体期暴露于司马米星α时,参与寄生虫连续发育的有丝分裂是否发生。在浓度为5.0 nM时,司马米星α抑制裂殖子-滋养体发育。该浓度在所有寄生虫阶段都降低了p-LDH活性,尽管其对裂殖体阶段的影响延迟了24小时。