Fitch C D, Chevli R, Banyal H S, Phillips G, Pfaller M A, Krogstad D J
Antimicrob Agents Chemother. 1982 May;21(5):819-22. doi: 10.1128/AAC.21.5.819.
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.
通过寄生虫悬液浊度的降低以及超微结构变化判断,亚铁原卟啉IX(FP)和氯喹-FP复合物可裂解分离出的恶性疟原虫。将寄生虫悬液暴露于50微摩尔/升的FP或由50微摩尔/升的FP与20微摩尔/升氯喹形成的复合物中,可减少可识别寄生虫的数量,并使那些可识别的寄生虫出现肿胀且内部细节消失。在10至50微摩尔/升FP范围内,裂解量呈剂量依赖性。氯喹-FP复合物的形成降低了但并未消除FP的毒性。由于有证据表明,对氯喹敏感的寄生虫暴露于氯喹时会形成氯喹-FP复合物,我们认为该复合物的积累可能是氯喹对恶性疟原虫化疗作用的原因。