Almeida Ana Sofia, Pinho Paula Guedes de, Remião Fernando, Fernandes Carla
Laboratório de Química Orgânica e Farmacêutica, Departamento de Ciências Químicas, Faculdade de Farmácia, Universidade do Porto, Rua Jorge Viterbo Ferreira, 228, 4050-313 Porto, Portugal.
Centro Interdisciplinar de Investigação Marinha e Ambiental (CIIMAR), Universidade do Porto, Terminal de Cruzeiros do Porto de Leixões, Avenida General Norton de Matos, s/n, 4450-208 Matosinhos, Portugal.
Molecules. 2025 Jan 13;30(2):290. doi: 10.3390/molecules30020290.
New psychoactive substances (NPSs) emerged in the 2000s as legal alternatives to illicit drugs and quickly became a huge public health threat due to their easy accessibility online, limited information, and misleading labels. Synthetic cannabinoids and synthetic cathinones are the most reported groups of NPSs. Despite NPSs being widely studied, due to their structural diversity and the constant emergence of novel compounds with unknown properties, the development of new techniques is required to clarify their mode of action and evaluate their toxicological effects. Metabolomics has been a useful tool to evaluate the metabolic effects of several xenobiotics. Herein, a systematic review was performed, following PRISMA guidelines, regarding metabolomic studies on synthetic cathinones and synthetic cannabinoids to evaluate their effects in cellular metabolism. In the studies, models were the most employed (86%) and the analysis mostly followed untargeted approaches (75%) using LC-MS techniques (67%). Both groups of NPSs seem to primarily interfere with energy metabolism-related pathways. Even though this type of study is still limited, metabolomics holds great promise as a tool to clarify mechanisms of actions, identify biomarkers of exposure, and explain the toxicological effects of NPSs.
新型精神活性物质(NPSs)于21世纪初出现,作为非法药物的合法替代品,由于其在网上易于获取、信息有限且标签具有误导性,迅速成为巨大的公共卫生威胁。合成大麻素和合成卡西酮是报告最多的NPSs类别。尽管对NPSs进行了广泛研究,但由于其结构多样性以及不断出现性质未知的新型化合物,需要开发新技术来阐明其作用模式并评估其毒理学效应。代谢组学一直是评估几种外源性物质代谢效应的有用工具。在此,按照PRISMA指南,对关于合成卡西酮和合成大麻素的代谢组学研究进行了系统综述,以评估它们在细胞代谢中的作用。在这些研究中,细胞模型使用最为频繁(86%),分析大多采用非靶向方法(75%),使用液相色谱 - 质谱技术(67%)。这两类NPSs似乎主要干扰与能量代谢相关的途径。尽管这类研究仍然有限,但代谢组学作为一种阐明作用机制、识别暴露生物标志物以及解释NPSs毒理学效应的工具,具有巨大潜力。