National Chengdu Center for Safety Evaluation of Drugs, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Collaborative Innovation Center for Biotherapy, Chengdu 610041, China; State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Collaborative Innovation Center for Biotherapy, Chengdu 610041, China.
National Chengdu Center for Safety Evaluation of Drugs, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Collaborative Innovation Center for Biotherapy, Chengdu 610041, China.
Mol Cell Neurosci. 2017 Dec;85:29-44. doi: 10.1016/j.mcn.2017.08.004. Epub 2017 Aug 19.
Lipids are predominant components of the brain and key regulators for neural structure and function. The neuropsychopharmacological effect of cocaine has been intensively investigated; however, the impact of cocaine on brain lipid profiles is largely unknown. In this study, we used a LC-MS-based lipidomic approach to investigate the impact of cocaine on brain lipidome in two mouse models, cocaine-conditioned place preference (CPP) and hyperlocomotor models and the lipidome was profoundly modified in the nucleus accumbens (NAc) and striatum respectively. We comprehensively analyzed the lipids among 21 subclasses across 7 lipid classes and found that cocaine profoundly modified brain lipidome. Notably, the lipid metabolites significantly modified were sphingolipids and glycerophospholipids in the NAc, showing a decrease in ceramide and an increase in its up/downstream metabolites levels, and decrease lysophosphatidylcholine (LPC) and lysophosphoethanolamine (LPE) and increase phosphatidylcholine (PC) and phosphatidylethanolamines (PE) levels, respectively. Moreover, long and polyunsaturated fatty acid phospholipids were also markedly increased in the NAc. Our results show that cocaine can markedly modify brain lipidomic profiling. These findings reveal a link between the modified lipidome and psychopharmacological effect of cocaine, providing a new insight into the mechanism of cocaine addiction.
脂质是大脑的主要组成部分,也是神经结构和功能的关键调节剂。可卡因的神经精神药理学作用已经得到了深入研究;然而,可卡因对大脑脂质谱的影响在很大程度上是未知的。在这项研究中,我们使用基于 LC-MS 的脂质组学方法来研究可卡因对两种小鼠模型(可卡因条件性位置偏好(CPP)和过度活跃模型)中脑脂质组的影响,结果分别在伏隔核(NAc)和纹状体中发现脂质组发生了深刻改变。我们全面分析了 7 个脂质类别中的 21 个亚类中的脂质,发现可卡因深刻地改变了脑脂质组。值得注意的是,脂质代谢物在 NAc 中发生了显著改变,鞘脂和其上下游代谢物水平降低,而溶血磷脂酰胆碱(LPC)和溶血磷脂酰乙醇胺(LPE)水平降低,同时磷酸胆碱(PC)和磷酸乙醇胺(PE)水平升高。此外,NAc 中的长链和多不饱和脂肪酸磷脂也显著增加。我们的研究结果表明,可卡因可以显著改变脑脂质组学图谱。这些发现揭示了改变的脂质组与可卡因的精神药理学作用之间的联系,为可卡因成瘾的机制提供了新的见解。