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Lysis of Plasmodium falciparum by ferriprotoporphyrin IX and a chloroquine-ferriprotoporphyrin IX complex.

机译:铁原卟啉IX和氯喹-铁原卟啉IX复合物裂解恶性疟原虫。

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摘要

Ferriprotoporphyrin IX (FP) and a chloroquine-FP complex lysed isolated Plasmodium falciparum parasites as judged by decreases in the turbidity of parasite suspensions and by ultrastructural changes. Exposure of parasite suspensions to 50 microM FP or to a complex formed from 50 microM FP and 20 MicroM chloroquine reduced the number of identifiable parasites and caused swelling and loss of internal detail in those that were identifiable. The amount of lysis was dose-dependent over the range of 10 to 50 microM FP. Formation of a chloroquine-FP complex reduced, but did not eliminate, the toxicity of FP. Since there is evidence indicating that a chloroquine-FP complex forms when chloroquine-susceptible parasites are exposed to chloroquine, we suggest that accumulation of this complex may account for the chemotherapeutic effect of chloroquine against P. falciparum.
机译:铁原卟啉IX(FP)和氯喹-FP复合物溶解了分离的恶性疟原虫寄生虫,可以通过寄生虫悬浮液的浊度降低和超微结构变化来判断。将寄生虫悬浮液暴露于50 microM FP或由50 microM FP和20 MicroM氯喹形成的复合物中会减少可识别的寄生虫的数量,并导致可识别的寄生虫肿胀和内部细节丢失。裂解量在10至50 microM FP范围内呈剂量依赖性。氯喹-FP复合物的形成减少但没有消除FP的毒性。由于有证据表明当氯喹敏感性寄生虫暴露于氯喹时会形成氯喹-FP络合物,因此我们建议该络合物的积累可能解释了氯喹对恶性疟原虫的化学治疗作用。

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