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首页> 外文期刊>International Journal for Parasitology: Drugs and Drug Resistance >Drug susceptibility testing in microaerophilic parasites: Cysteine strongly affects the effectivities of metronidazole and auranofin, a novel and promising antimicrobial
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Drug susceptibility testing in microaerophilic parasites: Cysteine strongly affects the effectivities of metronidazole and auranofin, a novel and promising antimicrobial

机译:在微需氧性寄生虫中的药物敏感性测试:半胱氨酸强烈影响甲硝唑和金诺芬(一种新颖且有希望的抗菌剂)的有效性

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The microaerophilic parasites Entamoeba histolytica , Trichomonas vaginalis , and Giardia lamblia annually cause hundreds of millions of human infections which are treated with antiparasitic drugs. Metronidazole is the most often prescribed drug but also other drugs are in use, and novel drugs with improved characteristics are constantly being developed. One of these novel drugs is auranofin, originally an antirheumatic which has been relabelled for the treatment of parasitic infections. Drug effectivity is arguably the most important criterion for its applicability and is commonly assessed in susceptibility assays using in?vitro cultures of a given pathogen. However, drug susceptibility assays can be strongly affected by certain compounds in the growth media. In the case of microaerophilic parasites, cysteine which is added in large amounts as an antioxidant is an obvious candidate because it is highly reactive and known to modulate the toxicity of metronidazole in several microaerophilic parasites.In this study, it was attempted to reduce cysteine concentrations as far as possible without affecting parasite viability by performing drug susceptibility assays under strictly anaerobic conditions in an anaerobic cabinet. Indeed, T . vaginalis and E . histolytica could be grown without any cysteine added and the cysteine concentration necessary to maintain G . lamblia could be reduced to 20%. Susceptibilities to metronidazole were found to be clearly reduced in the presence of cysteine. With auranofin the protective effect of cysteine was extreme, providing protection to concentrations up to 100-fold higher as observed in the absence of cysteine. With three other drugs tested, albendazole, furazolidone and nitazoxanide, all in use against G . lamblia , the effect of cysteine was less pronounced. Oxygen was found to have a less marked impact on metronidazole and auranofin than cysteine but bovine bile which is standardly used in growth media for G . lamblia , displayed a marked synergistic effect with metronidazole.
机译:每年需用抗寄生虫药治疗的微需氧性寄生虫组织解脂Entamoeba histolytica,阴道毛滴虫和兰氏贾第鞭毛虫均引起数亿人感染。甲硝唑是最常开处方的药物,但也正在使用其他药物,并且不断开发出具有改善特性的新型药物。这些新药中的一种是金诺芬,它最初是一种抗风湿药,已被重新标记用于治疗寄生虫感染。药物有效性可以说是其适用性的最重要标准,通常在使用给定病原体的体外培养物进行药敏试验中进行评估。但是,药物敏感性试验可能会受到生长培养基中某些化合物的强烈影响。在微需氧寄生虫的情况下,大量添加的半胱氨酸作为抗氧化剂是一个明显的候选者,因为它具有很高的反应活性,并且已知可以调节甲硝唑在几种微需氧寄生虫中的毒性。通过在严格厌氧的条件下于厌氧柜中进行药物敏感性试验,尽可能不影响寄生虫生存力。确实,T。阴道和E。溶组织酶可以不添加任何半胱氨酸和维持G所需的半胱氨酸浓度生长。兰比亚可以减少到20%。发现在半胱氨酸存在下对甲硝唑的敏感性明显降低。使用金诺芬时,半胱氨酸的保护作用极强,与不存在半胱氨酸时所观察到的浓度相比,半胱氨酸的保护作用可高达100倍。经过测试的其他三种药物,分别是针对G的阿苯达唑,呋喃唑酮和nitazoxanide。羔羊,半胱氨酸的作用不太明显。与半胱氨酸和牛胆汁相比,氧气对甲硝唑和金诺芬的影响较小,而牛胆汁通常用于G的生长培养基。兰伯利亚,与甲硝唑显示出明显的协同作用。

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