Odierna G Lorenzo, Vucic Steve, Dyer Marcus, Dickson Tracey, Woodhouse Adele, Blizzard Catherine
Tasmanian School of Medicine, University of Tasmania, Hobart, TAS 7000, Australia.
Brain and Nerve Research Center, The University of Sydney, Sydney 2050, Australia.
Brain. 2024 May 3;147(5):1610-1621. doi: 10.1093/brain/awae039.
Amyotrophic lateral sclerosis is a devastating neurodegenerative disease that, at present, has no effective cure. Evidence of increased circulating glutamate and hyperexcitability of the motor cortex in patients with amyotrophic lateral sclerosis have provided an empirical support base for the 'dying forward' excitotoxicity hypothesis. The hypothesis postulates that increased activation of upper motor neurons spreads pathology to lower motor neurons in the spinal cord in the form of excessive glutamate release, which triggers excitotoxic processes. Many clinical trials have focused on therapies that target excitotoxicity via dampening neuronal activation, but not all are effective. As such, there is a growing tension between the rising tide of evidence for the 'dying forward' excitotoxicity hypothesis and the failure of therapies that target neuronal activation. One possible solution to these contradictory outcomes is that our interpretation of the current evidence requires revision in the context of appreciating the complexity of the nervous system and the limitations of the neurobiological assays we use to study it. In this review we provide an evaluation of evidence relevant to the 'dying forward' excitotoxicity hypothesis and by doing so, identify key gaps in our knowledge that need to be addressed. We hope to provide a road map from hyperexcitability to excitotoxicity so that we can better develop therapies for patients suffering from amyotrophic lateral sclerosis. We conclude that studies of upper motor neuron activity and their synaptic output will play a decisive role in the future of amyotrophic lateral sclerosis therapy.
肌萎缩侧索硬化症是一种毁灭性的神经退行性疾病,目前尚无有效治愈方法。肌萎缩侧索硬化症患者循环谷氨酸水平升高和运动皮质兴奋性过高的证据,为“顺行性死亡”兴奋性毒性假说提供了实证支持基础。该假说假定,上运动神经元激活增加会以过量谷氨酸释放的形式将病理状态传播至脊髓中的下运动神经元,从而引发兴奋性毒性过程。许多临床试验都集中在通过抑制神经元激活来靶向兴奋性毒性的疗法上,但并非所有疗法都有效。因此,“顺行性死亡”兴奋性毒性假说的证据不断增加与靶向神经元激活的疗法失败之间的矛盾日益突出。解决这些矛盾结果的一个可能办法是,在认识到神经系统的复杂性以及我们用于研究它的神经生物学检测方法的局限性的背景下,我们需要对当前证据的解释进行修正。在本综述中,我们对与“顺行性死亡”兴奋性毒性假说相关的证据进行了评估,并借此确定了我们知识中需要填补的关键空白。我们希望提供一个从兴奋性过高到兴奋性毒性的路线图,以便我们能够更好地为肌萎缩侧索硬化症患者开发治疗方法。我们得出结论,对上运动神经元活动及其突触输出的研究将在肌萎缩侧索硬化症治疗的未来中发挥决定性作用。