The Gothenburg Imaging Mass Spectrometry (Go:IMS) Platform, Gothenburg, Sweden.
Department of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg 412 96, Sweden.
ACS Chem Neurosci. 2020 Mar 4;11(5):806-813. doi: 10.1021/acschemneuro.0c00014. Epub 2020 Feb 21.
Cocaine dependence displays a broad impairment in cognitive performance including attention, learning, and memory. To obtain a better understanding of the action of cocaine in the nervous system, and the relation between phospholipids and memory, we have investigated whether phospholipids recover in the brain following cocaine removal using the fly model, . In addition, the effects of methylphenidate, a substitute medication for cocaine dependence, on fly brain lipids after cocaine abuse are also determined to see if it can rescue the lipid changes caused by cocaine. Time of flight secondary ion mass spectrometry with a (CO) gas cluster ion beam was used to detect intact phospholipids. We show that cocaine has persistent effects, both increasing and decreasing the levels of specific phosphatidylethanolamines and phosphatidylinositols. These changes remain after cocaine withdrawal and are not rescued by methylphenidate. Cocaine is again shown to generally increase the levels of phosphatidylcholines in the fly brain; however, after drug withdrawal, the abundance of these lipids returns to the original level and methylphenidate treatment of the flies following cocaine exposure enhances the reversal of the lipid level reducing them below the original control. The study provides insight into the molecular effects of cocaine and methylphenidate on brain lipids. We suggest that phosphatidylcholines could be a potential target for the treatment of cocaine abuse as well as be a significant hallmark of cognition and memory loss with cocaine.
可卡因依赖症表现出广泛的认知功能障碍,包括注意力、学习和记忆。为了更好地了解可卡因在神经系统中的作用以及磷脂与记忆之间的关系,我们使用果蝇模型研究了可卡因戒断后大脑中磷脂是否恢复。此外,还确定了可卡因滥用后利他林(一种可卡因依赖的替代药物)对果蝇大脑脂质的影响,以观察它是否可以挽救可卡因引起的脂质变化。飞行时间二次离子质谱(TOF-SIMS)采用(CO)气体团簇离子束来检测完整的磷脂。我们发现可卡因具有持续的作用,既增加又降低特定的磷脂酰乙醇胺和磷脂酰肌醇的水平。这些变化在可卡因戒断后仍然存在,而且利他林不能挽救这些变化。可卡因再次显示出在果蝇脑中普遍增加磷脂酰胆碱的水平;然而,在药物戒断后,这些脂质的丰度恢复到原始水平,而可卡因暴露后甲基苯丙胺处理增强了脂质水平的逆转,使其低于原始对照。该研究深入了解了可卡因和利他林对大脑脂质的分子影响。我们认为,磷脂酰胆碱可能是治疗可卡因滥用的一个潜在靶点,也是可卡因引起认知和记忆丧失的一个重要标志。