Parasitology Group, Institute of Biological, Environmental and Rural Sciences, Aberystwyth University, Aberystwyth, Ceredigion, Wales SY23 3FG, UK.
Parasitology. 2012 Aug;139(9):1205-17. doi: 10.1017/S003118201200087X. Epub 2012 Jul 10.
Anthelmintics are the cornerstone of parasitic helminth control. Surprisingly, understanding of the biochemical pathways used by parasitic helminths to detoxify anthelmintics is fragmented, despite the increasing global threat of anthelmintic resistance within the ruminant and equine industries. Reductionist biochemistry has likely over-estimated the enzymatic role of glutathione transferases in anthelmintic metabolism and neglected the potential role of the cytochrome P-450 superfamily (CYPs). Proteomic technologies offers the opportunity to support genomics, reverse genetics and pharmacokinetics, and provide an integrated insight into both the cellular mechanisms underpinning response to anthelmintics and also the identification of biomarker panels for monitoring the development of anthelmintic resistance. To date, there have been limited attempts to include proteomics in anthelmintic metabolism studies. Optimisations of membrane, post-translational modification and interaction proteomic technologies in helminths are needed to especially study Phase I CYPs and Phase III ABC transporter pumps for anthelmintics and their metabolites.
抗蠕虫药是寄生虫蠕虫控制的基石。令人惊讶的是,尽管反刍动物和马业中抗蠕虫药耐药性的全球威胁日益增加,但对寄生虫蠕虫用于解毒抗蠕虫药的生化途径的理解仍是零碎的。还原生物化学可能高估了谷胱甘肽转移酶在抗蠕虫药代谢中的酶作用,而忽视了细胞色素 P-450 超家族(CYPs)的潜在作用。蛋白质组学技术为支持基因组学、反向遗传学和药代动力学提供了机会,并为对抗蠕虫药反应的细胞机制以及鉴定用于监测抗蠕虫药耐药性发展的生物标志物组提供了综合的见解。迄今为止,在抗蠕虫药代谢研究中很少尝试包括蛋白质组学。需要对寄生虫中的膜、翻译后修饰和相互作用蛋白质组学技术进行优化,特别是要研究 I 期 CYP 和 III 期 ABC 转运泵对抗蠕虫药及其代谢物的作用。