Pusch Michael, Gavazzo Paola
Biophysics Institute, National Research Council, 16149 Genova, Italy.
Brain Sci. 2022 May 20;12(5):673. doi: 10.3390/brainsci12050673.
The pathological basis of migraine is not fully understood. Familial hemiplegic migraines (FHM) are monogenic forms of severe migraine, caused by mutations in genes encoding various neuronal and/or astrocytic ion transporting proteins. The leading hypothesis regarding the mechanism underlying migraine in FHM is that enhanced electrical excitability leads to increased extracellular potassium levels with subsequent cortical spreading depression. In this short commentary we would like to propose an additional mechanism distinct from enhanced electrical excitability per se. Rather, we propose that FHM mutations cause substantially increased energy expenditure of neurons for re-establishing ion gradients and/or for increased synaptic activity, a mechanism we call neuronal fatigue. Such a metabolic mechanism had been proposed earlier for common migraine and has received recent experimental evidence in particular for the case of FHM3. The hypothesis could be tested in future studies of FHM related models that would need to take metabolic parameters into account.
偏头痛的病理基础尚未完全明确。家族性偏瘫性偏头痛(FHM)是严重偏头痛的单基因形式,由编码各种神经元和/或星形胶质细胞离子转运蛋白的基因突变引起。关于FHM中偏头痛潜在机制的主要假说是,增强的电兴奋性导致细胞外钾水平升高,随后出现皮层扩散性抑制。在这篇简短的评论中,我们想提出一种不同于增强电兴奋性本身的额外机制。相反,我们认为FHM突变会导致神经元为重新建立离子梯度和/或增加突触活动而大量增加能量消耗,我们将这种机制称为神经元疲劳。这种代谢机制早前已针对普通偏头痛提出,最近尤其在FHM3的案例中得到了实验证据支持。该假说可在未来与FHM相关模型的研究中进行验证,这些研究需要考虑代谢参数。