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尿中苯乙胺代谢物作为运动药物检测目的的潜在标志物。

Urinary phenylethylamine metabolites as potential markers for sports drug testing purposes.

机构信息

Center for Preventive Doping Research-Institute of Biochemistry, German Sport University Cologne, Cologne, Germany.

Crop Science Division, Bayer AG, Monheim, Germany.

出版信息

Biomed Chromatogr. 2022 Feb;36(2):e5274. doi: 10.1002/bmc.5274. Epub 2021 Nov 17.

Abstract

The misuse of 2-phenylethylamine (PEA) in sporting competitions is prohibited by the World Anti-Doping Agency. As it is endogenously produced, a method is required to differentiate between naturally elevated levels of PEA and the illicit administration of the drug. In 2015, a sulfo-conjugated metabolite [2-(2-hydroxyphenyl)acetamide sulfate (M1)] was identified, and pilot study data suggested that the ratio M1/PEA could be used as a marker indicating the oral application of PEA. Within this project, the required reference material of M1 was synthesized, single and multiple dose elimination studies were conducted and 369 native urine samples of athletes were analyzed as a reference population. While the oral administration of only 100 mg PEA did not affect urinary PEA concentrations, an increase in urinary concentrations of M1 was observed for all volunteers. However, urinary concentrations of both PEA and M1 showed relatively large inter-individual differences and establishing a cut-off-level for M1/PEA proved difficult. Consequently, a second metabolite, phenylacetylglutamine, was considered. Binary logistic regression demonstrated a significant (P < 0.05) correlation of the urinary M1 and phenylacetylglutamine concentrations with an oral administration of PEA, suggesting that assessing both analytes can assist doping control laboratories in identifying PEA misuse.

摘要

2-苯乙胺(PEA)在体育竞赛中的滥用被世界反兴奋剂机构禁止。由于它是内源性产生的,因此需要一种方法来区分自然升高的 PEA 水平和非法使用该药物。2015 年,鉴定出一种磺基共轭代谢物[2-(2-羟基苯基)乙酰胺硫酸盐(M1)],初步研究数据表明,M1/PEA 比值可作为指示 PEA 口服应用的标志物。在该项目中,合成了所需的 M1 参考物质,进行了单次和多次剂量消除研究,并对 369 名运动员的原生尿液样本进行了分析作为参考人群。虽然仅口服 100mg PEA 不会影响尿液 PEA 浓度,但所有志愿者的尿液 M1 浓度均增加。然而,PEA 和 M1 的尿液浓度均显示出较大的个体间差异,并且难以确定 M1/PEA 的截止值。因此,考虑了第二种代谢物苯乙酰谷氨酰胺。二元逻辑回归表明,尿液 M1 和苯乙酰谷氨酰胺浓度与 PEA 的口服给药具有显著(P<0.05)相关性,表明评估这两种分析物可以帮助兴奋剂检测实验室识别 PEA 的滥用。

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