Pharmacology and Neuroscience Research Group, Leicester School of Pharmacy, De Montfort University, The Gateway, Leicester LE1 9BH, UK.
Worcester Biomedical Research Group, School of Science and the Environment, University of Worcester, Worcester WR2 6AJ, UK.
Int J Mol Sci. 2022 Aug 2;23(15):8588. doi: 10.3390/ijms23158588.
Methylphenidate (MPH) is among the main drugs prescribed to treat patients with attention-deficit and hyperactivity disease (ADHD). MPH blocks both the norepinephrine and dopamine reuptake transporters (NET and DAT, respectively). Our study was aimed at further understanding the mechanisms by which MPH could modulate neurotransmitter efflux, using ex vivo radiolabelled neurotransmitter assays isolated from rats. Here, we observed significant dopamine and norepinephrine efflux from the prefrontal cortex (PFC) after MPH (100 µM) exposure. Efflux was mediated by both dopamine and norepinephrine terminals. In the striatum, MPH (100 µM) triggered dopamine efflux through both sodium- and vesicular-dependent mechanisms. Chronic MPH exposure (4 mg/kg/day/animal, voluntary oral intake) for 15 days, followed by a 28-day washout period, increased the firing rate of PFC pyramidal neurons, assessed by in vivo extracellular single-cell electrophysiological recordings, without altering the responses to locally applied NMDA, via micro-iontophoresis. Furthermore, chronic MPH treatment resulted in decreased efficiency of extracellular dopamine to modulate NMDA-induced firing activities of medium spiny neurons in the striatum, together with lower MPH-induced (100 µM) dopamine outflow, suggesting desensitization to both dopamine and MPH in striatal regions. These results indicate that MPH can modulate neurotransmitter efflux in brain regions enriched with dopamine and/or norepinephrine terminals. Further, long-lasting alterations of striatal and prefrontal neurotransmission were observed, even after extensive washout periods. Further studies will be needed to understand the clinical implications of these findings.
哌醋甲酯(MPH)是治疗注意力缺陷多动障碍(ADHD)患者的主要药物之一。MPH 可同时阻断去甲肾上腺素和多巴胺再摄取转运体(NET 和 DAT)。我们的研究旨在使用从大鼠分离的体外放射性标记神经递质测定法,进一步了解 MPH 调节神经递质外排的机制。在这里,我们观察到 MPH(100µM)暴露后前额叶皮层(PFC)中多巴胺和去甲肾上腺素的明显外排。外排由多巴胺和去甲肾上腺素末梢介导。在纹状体中,MPH(100µM)通过钠离子和囊泡依赖性机制触发多巴胺外排。慢性 MPH 暴露(4mg/kg/天/动物,自愿口服)15 天后,再进行 28 天的洗脱期,通过在体细胞外单细胞电生理记录评估,增加了 PFC 锥体神经元的放电率,而不会改变通过微电泳局部应用 NMDA 的反应。此外,慢性 MPH 治疗导致纹状体中细胞外多巴胺调节 NMDA 诱导的中间神经元放电活动的效率降低,同时 MPH 诱导的(100µM)多巴胺外流减少,提示纹状体区域对多巴胺和 MPH 均产生脱敏。这些结果表明,MPH 可以调节富含多巴胺和/或去甲肾上腺素末梢的脑区中的神经递质外排。此外,即使经过长时间的洗脱期,也观察到纹状体和前额叶神经传递的持久改变。需要进一步的研究来了解这些发现的临床意义。