Identification of Alexamorelin Consumption Biomarkers Using Human Hepatocyte Incubations and High-Resolution Mass Spectrometry.

IF 2.3 3区 医学 Q3 CHEMISTRY, ANALYTICAL
Elizabeth Pobee, Gloria Daziani, Prince S Gameli, Giuseppe Basile, Jeremy Carlier, Anastasio Tini
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Abstract

Alexamorelin is a synthetic peptide and growth hormone secretagogue (GHS) with potential performance-enhancing properties, making its use and abuse a topic of interest in clinical research and doping monitoring. Alexamorelin mimics the natural peptide hormone ghrelin by binding to the GHS type 1a receptor (GHS-R1a) in the pituitary gland, thereby promoting endogenous growth hormone release. Identifying alexamorelin and/or its metabolite biomarkers is crucial for effective doping controls. The purpose of this study was to determine and characterize biomarkers associated with alexamorelin intake. In silico metabolite predictions were performed using GLORYx freeware, and in vitro incubations were conducted with pooled human hepatocytes from 10 donors. Samples were analyzed using liquid chromatography-high-resolution tandem mass spectrometry (LC-HRMS/MS), with data processed through Thermo Scientific's Compound Discoverer. GLORYx predicted 21 single-reaction metabolites. N-Acetylation was identified as the primary transformation, with the highest probability score (98%), and occurring either at the C-terminal Ala or the N-terminal Lys. Other predicted transformations included N-oxidation, hydroxylation, amide hydrolysis, oxidative deamination, and phase II N-glucuronidation, with probability scores below 40%. All these transformations were predicted to occur at the two C-terminal (Ala or His) or N-terminal (D-Phe or Lys) amino acids. After 3 h of incubation with hepatocytes, only one metabolite (known as examorelin or hexarelin) was detected, resulting from the C-terminal cleavage of the Ala amino acid; this metabolic reaction is mediated by a carboxypeptidase. The alexamorelin signal decreased approximately 150-fold after 3 h, indicating significant hepatic metabolism. However, examorelin itself is a commercially available GHS secretagogue, and thus, it is not specific to alexamorelin consumption. Detecting alexamorelin remains critical to documenting its use.

利用人肝细胞培养和高分辨率质谱技术鉴定阿莱克霉素消耗生物标志物。
Alexamorelin是一种合成多肽和生长激素分泌剂(GHS),具有潜在的性能增强特性,使其使用和滥用成为临床研究和兴奋剂监测的一个感兴趣的话题。Alexamorelin通过与垂体内GHS 1a型受体(GHS- r1a)结合,从而促进内源性生长激素的释放,从而模拟天然肽激素ghrelin。鉴别阿勒麦林和/或其代谢物生物标志物对于有效的兴奋剂控制至关重要。本研究的目的是确定和表征与阿莱克莫林摄入量相关的生物标志物。使用GLORYx免费软件进行计算机代谢物预测,并使用来自10个供体的人肝细胞进行体外培养。样品使用液相色谱-高分辨率串联质谱(LC-HRMS/MS)进行分析,数据通过Thermo Scientific的Compound Discoverer进行处理。GLORYx预测了21种单反应代谢物。n -乙酰化被确定为主要转化,具有最高的概率得分(98%),并且发生在c端Ala或n端Lys。其他预测转化包括n -氧化、羟基化、酰胺水解、氧化脱胺和II期n -葡萄糖醛酸化,概率得分低于40%。预测所有这些转化都发生在两个c端(Ala或His)或n端(D-Phe或Lys)氨基酸上。与肝细胞孵育3小时后,仅检测到一种代谢物(称为examorelin或hexarelin),这是由于Ala氨基酸的c端裂解引起的;这种代谢反应是由羧肽酶介导的。3 h后alexamorelin信号下降约150倍,表明肝脏代谢显著。然而,阿霉素本身是一种市售的GHS促分泌剂,因此,它不是针对阿霉素消费的。检测阿勒莫瑞林对于记录其使用仍然至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.10
自引率
20.00%
发文量
92
审稿时长
6-12 weeks
期刊介绍: The Journal of Analytical Toxicology (JAT) is an international toxicology journal devoted to the timely dissemination of scientific communications concerning potentially toxic substances and drug identification, isolation, and quantitation. Since its inception in 1977, the Journal of Analytical Toxicology has striven to present state-of-the-art techniques used in toxicology labs. The peer-review process provided by the distinguished members of the Editorial Advisory Board ensures the high-quality and integrity of articles published in the Journal of Analytical Toxicology. Timely presentation of the latest toxicology developments is ensured through Technical Notes, Case Reports, and Letters to the Editor.
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