Chulay J D, Haynes J D, Diggs C L
Exp Parasitol. 1983 Feb;55(1):138-46. doi: 10.1016/0014-4894(83)90007-3.
To evaluate rapidly Plasmodium falciparum growth in Vitro, [3H]hypoxanthine was added to parasite microcultures and radioisotope incorporation was measured. When culture parameters were carefully controlled, [3H]hypoxanthine incorporation was proportional to the number of parasitized erythrocytes present. Factors affecting [3H]hypoxanthine incorporation included initial parasitemia, duration of culture, duration of radioisotope pulse, parasite stage, concentration of uninfected erythrocytes, the use of serum or plasma to supplement growth, and the concentration of a variety of purines in the culture medium. The method described can be used to measure inhibition of P. falciparum growth by immune serum and has previously been used to study antimalarial drug activity in vitro.
为了快速评估恶性疟原虫在体外的生长情况,将[3H]次黄嘌呤添加到寄生虫微培养物中,并测量放射性同位素掺入量。当培养参数得到严格控制时,[3H]次黄嘌呤掺入量与存在的被寄生红细胞数量成正比。影响[3H]次黄嘌呤掺入的因素包括初始寄生虫血症、培养持续时间、放射性同位素脉冲持续时间、寄生虫阶段、未感染红细胞的浓度、使用血清或血浆补充生长以及培养基中各种嘌呤的浓度。所描述的方法可用于测量免疫血清对恶性疟原虫生长的抑制作用,并且以前已用于体外研究抗疟药物活性。