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[喹诺酮类药物对伯氏疟原虫感染小鼠的实验性影响及其可能的治疗作用]

[Effect of quinolones on mice experimental infection by Plasmodium berghei and their possible therapeutic usefulness].

作者信息

Amato Neto V, Braz L M, Campos R, Matsubara L, Silva M de F, Pinto P L

机构信息

Laboratório de Investigação Médica (Parasitologia), Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo.

出版信息

Rev Hosp Clin Fac Med Sao Paulo. 1993 May-Jun;48(3):116-8.

PMID:8248700
Abstract

The search for new antimalarial drugs is important for many reasons, specially because of the resistance of plasmodia. Some clinical and laboratory studies have recently indicated that quinolones, currently in use for treatment of bacterial infections, have antimalarial activity. So, we evaluated the possible action of ciprofloxacin, norfloxacin, ofloxacin and pefloxacin in mice experimentally infected by Plasmodium berghei, by the oral route. Taking into account parasitemia and mortality, we came to conclusion that these drugs are not effective, as judged by the methods used.

摘要

寻找新型抗疟药物非常重要,原因有很多,特别是由于疟原虫的耐药性。最近一些临床和实验室研究表明,目前用于治疗细菌感染的喹诺酮类药物具有抗疟活性。因此,我们通过口服途径评估了环丙沙星、诺氟沙星、氧氟沙星和培氟沙星对感染伯氏疟原虫的小鼠的可能作用。考虑到疟原虫血症和死亡率,根据所使用的方法,我们得出结论,这些药物无效。

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