Wu L J, Rabbege J R, Nagasawa H, Jacobs G, Aikawa M
Institute of Parasitic Diseases, Chinese Academy of Preventive Medicine, WHO Collaborating Centre of Malaria, Shanghai.
Am J Trop Med Hyg. 1988 Jan;38(1):30-6. doi: 10.4269/ajtmh.1988.38.30.
The ultrastructural changes caused by a new antimalarial drug, pyronaridine, were investigated using mice infected with erythrocytic forms of Plasmodium berghei and P. falciparum cultivated in vitro in human erythrocytes. The first changes observed in both parasites after exposure to pyronaridine occurred in the food vacuoles. This suggests that the target organelle of this drug may be the food vacuole of malarial parasites. In addition, rapid alterations were also noted within the pellicular complex of both plasmodia.
使用感染了伯氏疟原虫红细胞内期以及在人红细胞中体外培养的恶性疟原虫的小鼠,研究了一种新型抗疟药咯萘啶引起的超微结构变化。暴露于咯萘啶后,在两种疟原虫中观察到的最初变化发生在食物泡中。这表明该药物的靶细胞器可能是疟原虫的食物泡。此外,还注意到两种疟原虫的表膜复合物内也有快速变化。