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Erythropoietin abuse and erythropoietin gene doping : detection strategies in the genomic era.

机译:促红细胞生成素滥用和促红细胞生成素基因掺杂:基因组时代的检测策略。

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摘要

The administration of recombinant human erythropoietin (rhEPO) increases the maximum oxygen consumption capacity, and is therefore abused as a doping method in endurance sports. The detection of erythropoietin (EPO) abuse is based on direct pharmacological and indirect haematological approaches, both of which have several limitations. In addition, current detection methods cannot cope with the emerging doping strategies of EPO mimicry, analogues and gene doping, and thus novel detection strategies are urgently needed. Direct detection methods for EPO misuse can be either pharmacological approaches that identify exogenous substances based on their physicochemical properties, or molecular methods that recognise EPO transgenes or gene transfer vectors. Since direct detection with molecular methods requires invasive procedures, it is not appropriate for routine screening of large numbers of athletes. In contrast, novel indirect methods based on haematological and/or molecular profiling could be better suited as screening tools, and athletes who are suspect of doping would then be submitted to direct pharmacological and molecular tests. This article reviews the current state of the EPO doping field, discusses available detection methods and their shortcomings, outlines emerging pharmaceutical and genetic technologies in EPO misuse, and proposes potential directions for the development of novel detection strategies.
机译:重组人促红细胞生成素(rhEPO)的使用增加了最大耗氧量,因此在耐力运动中被滥用为一种兴奋剂。促红细胞生成素(EPO)滥用的检测基于直接的药理学方法和间接的血液学方法,这两种方法都有一些局限性。另外,当前的检测方法不能应对新兴的EPO模仿,类似物和基因掺杂的掺杂策略,因此迫切需要新颖的检测策略。 EPO滥用的直接检测方法可以是基于物理化学性质识别外源物质的药理方法,也可以是识别EPO转基因或基因转移载体的分子方法。由于用分子方法直接检测需要侵入性程序,因此不适合常规筛查大量运动员。相反,基于血液学和/或分子谱分析的新型间接方法可能更适合作为筛查工具,怀疑使用兴奋剂的运动员将被送交直接药理和分子检测。本文回顾了EPO掺杂领域的现状,讨论了可用的检测方法及其缺点,概述了EPO滥用中新兴的药物和遗传技术,并提出了开发新型检测策略的潜在方向。

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