Laboratory of Toxicology, Department of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, Belgium.
LGC Ltd- Sport and Specialised Analytical Services, Cambridge, UK.
Arch Toxicol. 2022 Nov;96(11):2935-2945. doi: 10.1007/s00204-022-03355-6. Epub 2022 Aug 12.
Synthetic cannabinoid receptor agonists (SCRAs) pose a danger to public health. This study focused on individuals experiencing recreational drug toxicity who had used 5F-MDMB-PICA.Patient records were evaluated regarding vital signs, Glasgow Coma Scale (GCS) and clinical features. Liquid chromatography coupled to high-resolution mass spectrometry (LC-HRMS) confirmed and quantified the presence of 5F-MDMB-PICA (and/or metabolites) as the only SCRA present in the serum of 71 patients. Cannabinoid activity was evaluated by a cannabinoid receptor (CB) bioassay, to assess the relationship between serum concentrations and ex vivo human CB activation potential. Furthermore, a link with the clinical presentation was appraised.5F-MDMB-PICA and five metabolites were pharmacologically profiled in vitro, revealing theoretically possible contributions of two active in vivo metabolites to overall cannabinoid activity. Serum concentrations of 5F-MDMB-PICA were correlated to the ex vivo cannabinoid activity, revealing a sigmoidal relationship. The latter could also be predicted based on pharmacological characterization of 5F-MDMB-PICA and its metabolites and an in-depth investigation of the bioassay outcome. Clinically, the GCS showed a significant trend (decrease) with increasing ex vivo cannabinoid activity.This is the first study to evaluate possible toxic effects of 5F-MDMB-PICA in a unique large patient cohort. It allows a better understanding of 5F-MDMB-PICA and metabolites in humans, suggesting a negligible contribution by 5F-MDMB-PICA metabolites to the overall cannabinoid activity in serum. Additionally, this work shows that in vitro pharmacological characterization allows close prediction of an individual's ex vivo CB activity, the latter showing a relationship with the level of consciousness.
合成大麻素受体激动剂(SCRAs)对公共健康构成威胁。本研究关注的是因使用 5F-MDMB-PICA 而经历娱乐性药物毒性的个体。评估了患者的生命体征、格拉斯哥昏迷量表(GCS)和临床特征的记录。通过液相色谱-高分辨率质谱(LC-HRMS)证实并定量了 71 名患者血清中唯一存在的 5F-MDMB-PICA(及其代谢物)。通过大麻素受体(CB)生物测定评估了大麻素活性,以评估血清浓度与体外人 CB 激活潜能之间的关系。此外,还评估了与临床表现的关系。5F-MDMB-PICA 和五种代谢物在体外进行了药理学特征分析,揭示了两种体内活性代谢物对整体大麻素活性的理论上可能的贡献。5F-MDMB-PICA 的血清浓度与体外大麻素活性相关,呈 S 型关系。后者还可以基于 5F-MDMB-PICA 及其代谢物的药理学特征和生物测定结果的深入研究进行预测。临床上,GCS 随着体外大麻素活性的增加呈显著下降趋势。这是第一项在独特的大型患者队列中评估 5F-MDMB-PICA 可能毒性作用的研究。它使我们更好地了解 5F-MDMB-PICA 和代谢物在人体内的作用,表明 5F-MDMB-PICA 代谢物对血清中整体大麻素活性的贡献可以忽略不计。此外,这项工作表明,体外药理学特征分析可以很好地预测个体的体外 CB 活性,后者与意识水平有关。