Cabantchik Z I, Silfen J, Firestone R A, Krugliak M, Nissani E, Ginsburg H
Department of Biological Chemistry, Hebrew University of Jerusalem, Israel.
Biochem Pharmacol. 1989 Apr 15;38(8):1271-7. doi: 10.1016/0006-2952(89)90333-x.
Various lysosomotropic detergents were tested in this work on in vitro cultures of Plasmodium falciparum and are shown to be potent antimalarial agents. The order of antimalarial potency was similar to that of cell toxicity on mammalian cells in culture (Miller DK et al., J Cell Biol 97, 1841-51 (1983]. The most efficient agents, N-dodecyl-imidazole (NDI) and N-dodecyl morpholine (NDM) displayed IC50 values of 6.7 +/- 0.7 microM and 23 +/- 5 microM. The mechanism of action of NDI measured at IC50 concentrations displayed the following features: irreversible antimalarial effect after 15 min exposure of cells to drug; alkalinization of the parasite food vacuole; inhibition of protein synthesis; inhibition of host cell protein digestion by the parasite; lack of vacuolar membrane disruption; lack of effect on the rate of constitutive autoproteolysis. No biochemical or ultrastructural indications were found to support a detergent-like action of NDI and its structural congeners on the major acidic compartment of the parasite, the food vacuole. Rather, alkalinization of that compartment by weak-base accumulation properties of the amphiphilic drugs and ensuing protonophoric effect are likely to play a major role in the various parasite-associated properties affected by these drugs.
在这项研究中,对多种溶酶体促透性去污剂进行了恶性疟原虫体外培养试验,结果表明它们是有效的抗疟剂。抗疟效力顺序与对培养的哺乳动物细胞的细胞毒性顺序相似(Miller DK等人,《细胞生物学杂志》97, 1841 - 51 (1983])。最有效的试剂,N - 十二烷基咪唑(NDI)和N - 十二烷基吗啉(NDM)的IC50值分别为6.7±0.7微摩尔和23±5微摩尔。在IC50浓度下测定的NDI的作用机制具有以下特点:细胞暴露于药物15分钟后产生不可逆的抗疟作用;寄生虫食物泡碱化;蛋白质合成受到抑制;寄生虫对宿主细胞蛋白质消化的抑制;液泡膜未被破坏;对组成型自蛋白水解速率无影响。未发现生化或超微结构迹象支持NDI及其结构类似物对寄生虫主要酸性区室即食物泡有类似去污剂的作用。相反,两亲性药物的弱碱积累特性导致该区室碱化以及随之产生的质子载体效应可能在受这些药物影响的各种与寄生虫相关的特性中起主要作用。