Földes J, Matyi A
Department of Clinical Microbiology, Albert Szent-Györgyi University Medical School, Szeged, Hungary.
Acta Microbiol Immunol Hung. 1994;41(1):73-82.
The biological activity of a new synthetic polypeptide, the MAP-1987 was proved in the rodent malaria system. The administration of 4 micrograms/kg of MAP-1987 prevents the haemolysis of the Plasmodium berghei infected erythrocytes but not the Plasmodium vinckei infected ones. The MAP-1987 given alone changes neither the survival time of the infected mice nor the rate of parasitaemia. The chloroquine given alone increases the survival time of the mice infected with P. berghei under the standardized experimental condition but later the animals die with a low rate of parasitaemia. Chloroquine administered together with MAP-1987 definitely cures the P. berghei infected animals. This activity is unique and specific and it does not apply to P. vinckei infection.
一种新的合成多肽MAP - 1987的生物活性在啮齿动物疟疾系统中得到了证实。给予4微克/千克的MAP - 1987可防止伯氏疟原虫感染的红细胞发生溶血,但对文氏疟原虫感染的红细胞无效。单独给予MAP - 1987既不改变感染小鼠的存活时间,也不改变寄生虫血症的发生率。在标准化实验条件下,单独给予氯喹可增加感染伯氏疟原虫小鼠的存活时间,但随后动物会因低寄生虫血症率而死亡。氯喹与MAP - 1987联合使用可明确治愈感染伯氏疟原虫的动物。这种活性是独特且特异的,不适用于文氏疟原虫感染。