Kuboki Noritaka, Yokoyama Naoaki, Kojima Naoya, Sakurai Tatsuya, Inoue Noboru, Sugimoto Chihiro
National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido 080-8555, Japan.
J Parasitol. 2006 Apr;92(2):389-93. doi: 10.1645/GE-667R.1.
We demonstrate here that dipalmitoylphosphatidylcholine (DPPC) liposome has an antitrypanosomal effect, especially against the bloodstream forms (BSFs) of African trypanosomes (Trypanosoma congolense, T. brucei rhodesiense, and T. brucei brucei). The DPPC liposome significantly decreased the in vitro percentage of viable and motile BSF African trypanosomes but only marginally reduced the percentage of viable and motile procyclic form (PCF) of trypanosomes. The DPPC liposome absorption was much more pronounced to BSF than to PCF trypanosomes. Administration of the DPPC liposome showed a slight but significant reduction in the early development of parasitemia in T. congolense-infected mice. These results suggest that parasites were killed by specific binding of the DPPC liposome to the trypanosomes. This work demonstrates for the first time that a liposome has antitrypanosomal activity.
我们在此证明,二棕榈酰磷脂酰胆碱(DPPC)脂质体具有抗锥虫作用,尤其对非洲锥虫(刚果锥虫、布氏罗得西亚锥虫和布氏布氏锥虫)的血流形式(BSF)有效。DPPC脂质体显著降低了体外存活和活动的BSF非洲锥虫的百分比,但仅略微降低了锥虫存活和活动的前循环形式(PCF)的百分比。DPPC脂质体对BSF锥虫的吸收比对PCF锥虫更为明显。给予DPPC脂质体后,感染刚果锥虫的小鼠早期寄生虫血症的发展略有但显著降低。这些结果表明,寄生虫是通过DPPC脂质体与锥虫的特异性结合而被杀死的。这项工作首次证明脂质体具有抗锥虫活性。