Tetracycline Antibiotics in Malaria

S. Briolant, T. Fusai, C. Rogier, B. Pradines
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引用次数: 18

Abstract

The emergence and rapid extension of Plasmodium falciparum resistance to various antimalarial compounds has gradually limited malaria therapeutic possibilities available to clinicians and the choice of an adapted prophylaxis to travellers specific for their destinations. In this context, doxycycline constitutes an interesting alternative apart from its counter-indications, occurring primarily in children less than eight years old and in pregnant women. Already used suc- cessfully in the treatment of malaria in association with quinine in zones of multi-resistances, doxycycline has proven to be effective and well-tolerated in the prevention of malaria. Resistance to doxycycline has not been described until now. The listed prophylactic failures are primarily dependent on an incorrect observation. The mechanisms of action of doxy- cycline on the parasite are not completely elucidated. The identification of the molecular targets of doxycycline would al- low the design of structural analogues that are more active and stable.
疟疾中的四环素类抗生素
恶性疟原虫对各种抗疟疾化合物的耐药性的出现和迅速蔓延,逐渐限制了临床医生可获得的疟疾治疗可能性,也限制了旅行者针对其目的地选择适合的预防措施。在这种情况下,强力霉素是一个有趣的替代,除了它的反适应症,主要发生在8岁以下的儿童和孕妇。强力霉素已经在多重耐药区与奎宁一起成功地用于治疗疟疾,已被证明在预防疟疾方面是有效和耐受性良好的。到目前为止,对强力霉素的耐药性还没有描述。所列的预防失败主要取决于不正确的观察。羟环素对寄生虫的作用机制尚未完全阐明。多西环素分子靶点的确定将有助于设计更有效、更稳定的结构类似物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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