Maarouf M, Adeline M T, Solignac M, Vautrin D, Robert-Gero M
University of Damascus, Faculty of Pharmacy, Dept of Biochemistry & Microbiology, Syria.
Parasite. 1998 Jun;5(2):167-73. doi: 10.1051/parasite/1998052167.
Paromomycin is an antileishmanial chemotherapeutic agent. Leishmania donovani promastigotes resistant to 800 microM of paromomycin were selected by increasing drug pressure and cloned. These promastigotes did not acquire multidrug resistance. Paromomycin resistance was stable in the absence of the drug in the culture. It remained stable also in amastigotes isolated after a passage in mice. Furthermore the resistant parasites were still infective to macrophages in vitro and for mice in vivo. A sensitive method to detect and to quantify intracellular paromomycin by HPLC was developed and allowed to show that the main mechanism of resistance seems to be due to decreased drug uptake probably as a consequence of altered membrane composition.
巴龙霉素是一种抗利什曼原虫的化疗药物。通过增加药物压力筛选出对800微摩尔巴龙霉素耐药的杜氏利什曼原虫前鞭毛体并进行克隆。这些前鞭毛体未获得多药耐药性。在培养物中无药物的情况下,巴龙霉素耐药性是稳定的。在小鼠体内传代后分离出的无鞭毛体中,耐药性也保持稳定。此外,耐药寄生虫在体外对巨噬细胞以及在体内对小鼠仍具有感染性。开发了一种通过高效液相色谱法检测和定量细胞内巴龙霉素的灵敏方法,结果表明耐药的主要机制似乎是药物摄取减少,这可能是膜成分改变的结果。