Schrantee Anouk, Tremoleda Jordi L, Wylezinska-Arridge Marzena, Bouet Valentine, Hesseling Peter, Meerhoff Gideon F, de Bruin Kora M, Koeleman Jan, Freret Thomas, Boulouard Michel, Desfosses Emilie, Galineau Laurent, Gozzi Alessandro, Dauphin François, Gsell Willy, Booij Jan, Lucassen Paul J, Reneman Liesbeth
Department of Radiology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Biological Imaging Centre, Imperial College London, White City, London, United Kingdom.
PLoS One. 2017 Feb 27;12(2):e0172776. doi: 10.1371/journal.pone.0172776. eCollection 2017.
Dexamphetamine (AMPH) is a psychostimulant drug that is used both recreationally and as medication for attention deficit hyperactivity disorder. Preclinical studies have demonstrated that repeated exposure to AMPH can induce damage to nerve terminals of dopamine (DA) neurons. We here assessed the underlying neurobiological changes in the DA system following repeated AMPH exposure and pre-treated rats with AMPH or saline (4 times 5 mg/kg s.c., 2 hours apart), followed by a 1-week washout period. We then used pharmacological MRI (phMRI) with a methylphenidate (MPH) challenge, as a sensitive and non-invasive in-vivo measure of DAergic function. We subsequently validated the DA-ergic changes post-mortem, using a.o. high-performance liquid chromatography (HPLC) and autoradiography. In the AMPH pre-treated group, we observed a significantly larger BOLD response to the MPH challenge, particularly in DA-ergic brain areas and their downstream projections. Subsequent autoradiography studies showed that AMPH pre-treatment significantly reduced DA transporter (DAT) density in the caudate-putamen (CPu) and nucleus accumbens, whereas HPLC analysis revealed increases in the DA metabolite homovanillic acid in the CPu. Our results suggest that AMPH pre-treatment alters DAergic responsivity, a change that can be detected with phMRI in rats. These phMRI changes likely reflect increased DA release together with reduced DAT binding. The ability to assess subtle synaptic changes using phMRI is promising for both preclinical studies of drug discovery, and for clinical studies where phMRI can be a useful tool to non-invasively investigate DA abnormalities, e.g. in neuropsychiatric disorders.
右旋苯丙胺(AMPH)是一种精神兴奋药物,既被用于娱乐,也被用作治疗注意力缺陷多动障碍的药物。临床前研究表明,反复接触AMPH会导致多巴胺(DA)神经元的神经末梢受损。我们在此评估了反复接触AMPH后DA系统潜在的神经生物学变化,并对大鼠进行AMPH或生理盐水预处理(4次,5mg/kg皮下注射,间隔2小时),随后有1周的洗脱期。然后我们使用药理学磁共振成像(phMRI)并进行哌甲酯(MPH)激发试验,作为一种灵敏且非侵入性的体内DA能功能测量方法。我们随后通过高效液相色谱法(HPLC)和放射自显影等方法在死后验证了DA能变化。在AMPH预处理组中,我们观察到对MPH激发试验有显著更大的血氧水平依赖(BOLD)反应,特别是在DA能脑区及其下游投射区域。随后的放射自显影研究表明,AMPH预处理显著降低了尾状核-壳核(CPu)和伏隔核中DA转运体(DAT)的密度,而HPLC分析显示CPu中DA代谢物高香草酸增加。我们的结果表明,AMPH预处理改变了DA能反应性,这种变化可以通过大鼠的phMRI检测到。这些phMRI变化可能反映了DA释放增加以及DAT结合减少。使用phMRI评估细微突触变化的能力对于药物发现的临床前研究以及临床研究都很有前景,在临床研究中,phMRI可以作为一种有用的工具来非侵入性地研究DA异常,例如在神经精神疾病中。