Hemmer Selina, Wagmann Lea, Pulver Benedikt, Westphal Folker, Meyer Markus R
Department of Experimental and Clinical Toxicology, Institute of Experimental and Clinical Pharmacology and Toxicology, Center for Molecular Signaling (PZMS), Saarland University, 66421 Homburg, Germany.
State Bureau of Criminal Investigation Schleswig-Holstein, 24116 Kiel, Germany.
Metabolites. 2022 Dec 2;12(12):1209. doi: 10.3390/metabo12121209.
Synthetic cathinones are one important group amongst new psychoactive substances (NPS) and limited information is available regarding their toxicokinetics and -dynamics. Over the past few years, nontargeted toxicometabolomics has been increasingly used to study compound-related effects of NPS to identify important exogenous and endogenous biomarkers. In this study, the effects of the synthetic cathinone PCYP (2-cyclohexyl-1-phenyl-2-(1-pyrrolidinyl)-ethanone) on in vitro and in vivo metabolomes were investigated. Pooled human-liver microsomes and blood and urine of male Wistar rats were used to generate in vitro and in vivo data, respectively. Samples were analyzed by liquid chromatography and high-resolution mass spectrometry using an untargeted metabolomics workflow. Statistical evaluation was performed using univariate and multivariate statistics. In total, sixteen phase I and one phase II metabolite of PCYP could be identified as exogenous biomarkers. Five endogenous biomarkers (e.g., adenosine and metabolites of tryptophan metabolism) related to PCYP intake could be identified in rat samples. The present data on the exogenous biomarker of PCYP are crucial for setting up analytical screening procedures. The data on the endogenous biomarker are important for further studies to better understand the physiological changes associated with cathinone abuse but may also serve in the future as additional markers for an intake.
合成卡西酮是新型精神活性物质(NPS)中的一个重要类别,关于其毒代动力学和药效动力学的信息有限。在过去几年中,非靶向毒代代谢组学越来越多地用于研究NPS的化合物相关效应,以识别重要的外源性和内源性生物标志物。在本研究中,研究了合成卡西酮PCYP(2-环己基-1-苯基-2-(1-吡咯烷基)-乙酮)对体外和体内代谢组的影响。分别使用人肝微粒体混合物以及雄性Wistar大鼠的血液和尿液来生成体外和体内数据。使用非靶向代谢组学工作流程通过液相色谱和高分辨率质谱对样品进行分析。使用单变量和多变量统计进行统计评估。总共可以鉴定出PCYP的16种I相代谢物和1种II相代谢物作为外源性生物标志物。在大鼠样品中可以鉴定出5种与PCYP摄入相关的内源性生物标志物(例如腺苷和色氨酸代谢产物)。目前关于PCYP外源性生物标志物的数据对于建立分析筛查程序至关重要。关于内源性生物标志物的数据对于进一步研究以更好地理解与卡西酮滥用相关的生理变化很重要,但未来也可能用作摄入的额外标志物。