Clinic of Clinical Neurophysiology, Georg-August-University of Göttingen, Göttingen, Germany.
Neuropsychopharmacology. 2013 Oct;38(11):2260-7. doi: 10.1038/npp.2013.127. Epub 2013 May 17.
Serotonin modulates diverse brain functions. Beyond its clinical antidepressant effects, it improves motor performance, learning and memory formation. These effects might at least be partially caused by the impact of serotonin on neuroplasticity, which is thought to be an important foundation of the respective functions. In principal accordance, selective serotonin reuptake inhibitors enhance long-term potentiation-like plasticity induced by transcranial direct current stimulation (tDCS) in humans. As other neuromodulators have discernable effects on different kinds of plasticity in humans, here we were interested to explore the impact of serotonin on paired associative stimulation (PAS)-induced plasticity, which induces a more focal kind of plasticity, as compared with tDCS, shares some features with spike timing-dependent plasticity, and is thought to be relative closely related to learning processes. In this single-blinded, placebo-controlled, randomized crossover study, we administered a single dose of 20 mg citalopram or placebo medication and applied facilitatory- and excitability-diminishing PAS to the left motor cortex of 14 healthy subjects. Cortico-spinal excitability was explored via single-pulse transcranial magnetic stimulation-elicited MEP amplitudes up to the next evening after plasticity induction. After citalopram administration, inhibitory PAS-induced after-effects were abolished and excitatory PAS-induced after-effects were enhanced trendwise, as compared with the respective placebo conditions. These results show that serotonin modulates PAS-induced neuroplasticity by shifting it into the direction of facilitation, which might help to explain mechanism of positive therapeutic effects of serotonin in learning and medical conditions characterized by enhanced inhibitory or reduced facilitatory plasticity, including depression and stroke.
血清素调节着多样化的大脑功能。除了其临床抗抑郁的效果外,它还能改善运动表现、学习和记忆形成。这些效果至少部分归因于血清素对神经可塑性的影响,而神经可塑性被认为是这些功能的重要基础。在原则上,选择性 5-羟色胺再摄取抑制剂增强了经颅直流电刺激(tDCS)在人类中诱导的长时程增强样可塑性。由于其他神经调质对人类不同类型的可塑性有明显的影响,因此我们在这里感兴趣地探索了血清素对配对关联刺激(PAS)诱导的可塑性的影响,与 tDCS 相比,PAS 诱导的是一种更集中的可塑性,与尖峰时间依赖可塑性有一些共同特征,并且被认为与学习过程密切相关。在这项单盲、安慰剂对照、随机交叉研究中,我们给 14 名健康受试者单次服用 20mg 西酞普兰或安慰剂药物,并对左侧运动皮层施加促进性和兴奋性降低的 PAS。通过单脉冲经颅磁刺激诱发的 MEP 幅度来探索皮质脊髓兴奋性,直至诱导可塑性后的第二天晚上。与各自的安慰剂条件相比,西酞普兰给药后,抑制性 PAS 诱导的后效被消除,而兴奋性 PAS 诱导的后效呈增强趋势。这些结果表明,血清素通过将 PAS 诱导的神经可塑性向促进方向转变来调节它,这可能有助于解释在学习和以增强抑制性或降低促进性可塑性为特征的医学病症(包括抑郁症和中风)中,血清素的积极治疗效果的机制。