Amodiaquine-Ciprofloxacin: a potential combination therapy against drug resistant malaria

被引:5
作者
Falajiki, Y. F. [1 ,2 ]
Akinola, O. [1 ,2 ]
Abiodun, O. O. [1 ,2 ]
Happi, C. T. [2 ,3 ]
Sowunmi, A. [1 ,2 ]
Gbotosho, G. O. [1 ,2 ]
机构
[1] Univ Ibadan, Dept Pharmacol & Therapeut, Coll Med, Ibadan, Nigeria
[2] Univ Ibadan, Inst Adv Med Res & Training, Coll Med, Malaria Res Labs, Ibadan, Nigeria
[3] Redeemer Univ Nigeria, Dept Biol Sci, Mowe, Ogun State, Nigeria
基金
英国惠康基金;
关键词
Malaria; Plasmodium berghei; amodiaquine-ciprofloxacin; drug combinations; IN-VITRO ACTIVITIES; PLASMODIUM-FALCIPARUM; CHLOROQUINE; FLUOROQUINOLONES; SUSCEPTIBILITY; NORFLOXACIN; ANTIBIOTICS; ARTEMETHER; MEFLOQUINE; PEFLOXACIN;
D O I
10.1017/S0031182015000062
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Emergence of malaria parasites resistant to artemisinin necessitates the need for development of new antimalarial therapies. Ciprofloxacin (CFX) a second generation quinolone antibiotic possesses some antimalarial activities. We investigated the in vivo antimalarial activities of CFX in combination with amodiaquine in mice infected with chloroquine-resistant Plasmodium berghei ANKA. Animals were treated orally with 80 or 160 mg kg(-1) body weight of CFX alone given twice daily or in combination with amodiaquine (AQ) 10 mg kg(-1) body weight. Parasitological activity and survival of the animals were assessed over 21 days. Peak parasitaemia in the untreated control group was 72.51%. Treatment with AQ alone resulted in clearance of parasitaemia by day 4 while treatment with CFX 80 and 160 mg kg(-1) alone suppressed parasitaemia by 13.94-54.64% and 35.6-92.7%, respectively. However, the combination of CFX with AQ significantly enhanced response of infection in the animals to treatment (P < 0.05) resulting in complete resolution of parasitaemia throughout follow up period with CFX 160 mg kg(-1), delayed recrudescence time with CFX 80 mg kg(-1) and significant increase in survival rate of the animals. The results demonstrate beneficial interaction between AQ and CFX which may provide a clinically relevant antimalarial/antibiotic therapeutic option in the management of malaria.
引用
收藏
页码:849 / 854
页数:6
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