Yeo A E, Seymour K K, Rieckmann K H, Christopherson R I
Department of Biochemistry, University of Sydney, NSW, Australia.
Ann Trop Med Parasitol. 1997 Jan;91(1):17-23. doi: 10.1080/00034983.1997.11813107.
The in-vitro effects of folinic acid on the antimalarial activities of the triazine antifolates, cycloguanil and WR99210, were compared with those of their parent biguanides, proguanil and PS-15, a dihydrofolate-reductase inhibitor, pyrimethamine, and a pyrimidine antagonist, atovaquone. It was found that the minimum inhibitory concentrations of cycloguanil and WR99210 were not affected by physiological concentrations of folic or folinic acids in human serum. Experiments with Plasmodium falciparum growing in erythrocytic culture showed that the antimalarial effect of cycloguanil is readily antagonised by folinic acid, whereas WR99210 is much more refractory. Plasmodium falciparum exposed to cycloguanil (2.5 microM, 6 h) and WR99210 (1 microM, 6 h), showed depressed levels of thymidine 5'-triphosphate (dTTP) in the absence and presence of folinic acid (25 microM and 10 microM, respectively). The decrease in dTTP may be attributed to inhibition of dihydrofolate reductase. However, as the addition of folinic acid did not restore dTTP levels in the parasites, the drugs may have an additional or different mechanism of toxicity.
将亚叶酸对三嗪类抗叶酸药(环氯胍和WR99210)抗疟活性的体外作用,与其母体双胍类药物(氯胍和二氢叶酸还原酶抑制剂PS - 15)、乙胺嘧啶(一种嘧啶拮抗剂)和阿托伐醌的作用进行了比较。研究发现,环氯胍和WR99210的最低抑菌浓度不受人血清中生理浓度叶酸或亚叶酸的影响。对在红细胞培养物中生长的恶性疟原虫进行的实验表明,亚叶酸很容易拮抗环氯胍的抗疟作用,而WR99210则更具耐药性。暴露于环氯胍(2.5微摩尔/升,6小时)和WR99210(1微摩尔/升,6小时)的恶性疟原虫,无论有无亚叶酸(分别为25微摩尔/升和10微摩尔/升),其胸苷5'-三磷酸(dTTP)水平均降低。dTTP的降低可能归因于二氢叶酸还原酶的抑制。然而,由于添加亚叶酸并未恢复寄生虫中的dTTP水平,这些药物可能具有额外的或不同的毒性机制。