M. A. Nitsche: Georg-August-University, University Medical Centre, Dept Clinical Neurophysiology, Robert-Koch-Str. 40, 37099 Göttingen, Germany.
J Physiol. 2012 Oct 1;590(19):4641-62. doi: 10.1113/jphysiol.2012.232975. Epub 2012 Aug 6.
The term neuroplasticity encompasses structural and functional modifications of neuronal connectivity. Abnormal neuroplasticity is involved in various neuropsychiatric diseases, such as dystonia, epilepsy, migraine, Alzheimer's disease, fronto-temporal degeneration, schizophrenia, and post cerebral stroke. Drugs affecting neuroplasticity are increasingly used as therapeutics in these conditions. Neuroplasticity was first discovered and explored in animal experimentation. However, non-invasive brain stimulation (NIBS) has enabled researchers recently to induce and study similar processes in the intact human brain. Plasticity induced by NIBS can be modulated by pharmacological interventions, targeting ion channels, or neurotransmitters. Importantly, abnormalities of plasticity as studied by NIBS are directly related to clinical symptoms in neuropsychiatric diseases. Therefore, a core theme of this review is the hypothesis that NIBS-induced plasticity can explore and potentially predict the therapeutic efficacy of CNS-acting drugs in neuropsychiatric diseases. We will (a) review the basics of neuroplasticity, as explored in animal experimentation, and relate these to our knowledge about neuroplasticity induced in humans by NIBS techniques. We will then (b) discuss pharmacological modulation of plasticity in animals and humans. Finally, we will (c) review abnormalities of plasticity in neuropsychiatric diseases, and discuss how the combination of NIBS with pharmacological intervention may improve our understanding of the pathophysiology of abnormal plasticity in these diseases and their purposeful pharmacological treatment.
术语神经可塑性涵盖了神经元连接的结构和功能的改变。异常的神经可塑性与各种神经精神疾病有关,如肌张力障碍、癫痫、偏头痛、阿尔茨海默病、额颞叶变性、精神分裂症和脑卒中后。影响神经可塑性的药物越来越多地被用作这些疾病的治疗方法。神经可塑性首先在动物实验中被发现和探索。然而,最近的非侵入性脑刺激(NIBS)使研究人员能够在完整的人类大脑中诱导和研究类似的过程。NIBS 诱导的可塑性可以通过靶向离子通道或神经递质的药理学干预来调节。重要的是,通过 NIBS 研究的可塑性异常与神经精神疾病的临床症状直接相关。因此,本综述的一个核心主题是假设 NIBS 诱导的可塑性可以探索和潜在预测中枢神经系统作用药物在神经精神疾病中的治疗效果。我们将(a)回顾在动物实验中探索的神经可塑性的基础知识,并将这些知识与我们通过 NIBS 技术在人类中诱导的神经可塑性知识联系起来。然后,我们将(b)讨论动物和人类中可塑性的药理学调节。最后,我们将(c)回顾神经精神疾病中的可塑性异常,并讨论如何将 NIBS 与药理学干预相结合,可能改善我们对这些疾病中异常可塑性的病理生理学及其有目的的药理学治疗的理解。