Shanks G D, Edstein M D, Chedester A L, Smith C D, Corcoran K D, Ngampochjana M, Hansukjariya P, Sattabongkot J, Webster H K
Department of Medicine, Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand.
Am J Trop Med Hyg. 1994 May;50(5):641-5. doi: 10.4269/ajtmh.1994.50.641.
New drugs for causal prophylaxis of malaria are needed. A proguanil/sulfamethoxazole combination was investigated using a rhesus monkey model (Macaca mulatta infected with Plasmodium cynomolgi) to determine whether causal prophylaxis could be achieved. When a five-day regimen of proguanil (40 mg/kg/day) combined with sulfamethoxazole (100 mg/kg/day) was used, infection of all animals (6 of 6) was observed, with an extended prepatent period (median 40 days). Two control animals became infected on days 9 and 23 following sporozoite inoculation. Plasma concentrations indicated that proguanil and sulfamethoxazole were adequately absorbed and metabolized to cycloguanil and N4-acetylsulfamethoxazole, respectively. Analysis of liver biopsy specimens demonstrated that the drugs were present two days following sporozoite inoculation but were not detectable one week later. Proguanil plus sulfamethoxazole does not eliminate exoerythrocytic-stage parasites in the rhesus monkey--P. cynomolgi model.
需要用于疟疾病因性预防的新药。使用恒河猴模型(感染食蟹猴疟原虫的猕猴)研究了氯胍/磺胺甲恶唑组合,以确定是否可以实现病因性预防。当使用氯胍(40毫克/千克/天)与磺胺甲恶唑(100毫克/千克/天)的五日疗程时,观察到所有动物(6只中的6只)均被感染,潜伏期延长(中位数为40天)。两只对照动物在接种子孢子后的第9天和第23天被感染。血浆浓度表明,氯胍和磺胺甲恶唑被充分吸收并分别代谢为环氯胍和N4-乙酰磺胺甲恶唑。肝活检标本分析表明,接种子孢子两天后药物存在,但一周后无法检测到。在恒河猴-食蟹猴疟原虫模型中,氯胍加磺胺甲恶唑不能消除红细胞外期寄生虫。