Kim Minjeong, Jang Won-Jun, Shakya Rupa, Choi Boyeon, Jeong Chul-Ho, Lee Sooyeun
College of Pharmacy, Keimyung University, 1095 Dalgubeoldaero, Dalseo-gu, Daegu 42601, Korea.
Metabolites. 2019 Sep 20;9(10):195. doi: 10.3390/metabo9100195.
Metabolomics is a powerful tool used in the description of metabolic system perturbations caused by diseases or abnormal conditions, and it usually involves qualitative and/or quantitative metabolome determination, accompanied by bioinformatics assessment. Methamphetamine is a psychostimulant with serious abuse potential and due to the absence of effective pharmacotherapy and a high recurrence potential, methamphetamine addiction is a grave issue. Moreover, its addiction mechanisms remain unclear, probably due to the lack of experimental models that reflect personal genetic variances and environmental factors determining drug addiction occurrence. The metabolic approach is only recently being used to study the metabolic effects induced by a variety of methamphetamine exposure statuses, in order to investigate metabolic disturbances related to the adverse effects and discover potential methamphetamine addiction biomarkers. To provide a critical overview of methamphetamine-associated metabolic changes revealed in recent years using the metabolomics approach, we discussed methamphetamine toxicity, applications of metabolomics in drug abuse and addiction studies, biological samples used in metabolomics, and previous studies on metabolic alterations in a variety of biological samples-including the brain, hair, serum, plasma, and urine-following methamphetamine exposure in animal studies. Metabolic alterations observed in animal brain and other biological samples after methamphetamine exposure were associated with neuronal and energy metabolism disruptions. This review highlights the significance of further metabolomics studies in the area of methamphetamine addiction research. These findings will contribute to a better understanding of metabolic changes induced by methamphetamine addiction progress and to the design of further studies targeting the discovery of methamphetamine addiction biomarkers and therapeutic targets.
代谢组学是一种强大的工具,用于描述由疾病或异常状况引起的代谢系统扰动,通常涉及定性和/或定量代谢组测定,并伴有生物信息学评估。甲基苯丙胺是一种具有严重滥用潜力的精神兴奋剂,由于缺乏有效的药物治疗且复发可能性高,甲基苯丙胺成瘾是一个严重问题。此外,其成瘾机制仍不清楚,可能是由于缺乏反映个人基因差异和决定药物成瘾发生的环境因素的实验模型。代谢方法直到最近才被用于研究各种甲基苯丙胺暴露状态所诱导的代谢效应,以调查与不良反应相关的代谢紊乱并发现潜在的甲基苯丙胺成瘾生物标志物。为了对近年来使用代谢组学方法揭示的与甲基苯丙胺相关的代谢变化进行批判性综述,我们讨论了甲基苯丙胺毒性、代谢组学在药物滥用和成瘾研究中的应用、代谢组学中使用的生物样本,以及之前关于动物研究中甲基苯丙胺暴露后各种生物样本(包括大脑、毛发、血清、血浆和尿液)代谢改变的研究。甲基苯丙胺暴露后在动物大脑和其他生物样本中观察到的代谢改变与神经元和能量代谢紊乱有关。本综述强调了在甲基苯丙胺成瘾研究领域进一步开展代谢组学研究的重要性。这些发现将有助于更好地理解甲基苯丙胺成瘾进展所诱导的代谢变化,并有助于设计进一步的研究,以发现甲基苯丙胺成瘾生物标志物和治疗靶点。