Smirnova Maria P, Pavlova Irina V, Vinogradova Lyudmila V
Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences, Butlerova Street 5A, Moscow, 117485, Russia.
J Headache Pain. 2025 Nov 11;26(1):251. doi: 10.1186/s10194-025-02199-6.
Propagation of spreading depolarization (SD), a wave of transient cellular depolarization, over the cerebral cortex drives migraine aura symptoms. Growing evidence suggests that hippocampus, brain region involved in regulation of mood and cognition, also contributes to pathogenesis of migraine. Hippocampus has highly inhomogeneous functional anatomy with strong dorsoventral difference in functional and network properties. We hypothesized that cerebral dysfunction induced by SD also varies within the hippocampus and studied characteristics and effects of SD in the dorsal and ventral hippocampus of awake animals. Given high susceptibility of the hippocampus to seizures, we focused on excitatory effects of SD.
Unilateral SD was induced by a pinprick of the dorsal hippocampus in freely behaving rats. In electrophysiological experiments, local field potentials were recorded bilaterally in different sites along the dorsoventral axis of the hippocampus; propagation patterns, electrographic manifestations and excitatory effects of SD were evaluated. In separate experiments, effect of hippocampal SD on behavior was assessed.
SD waveforms varied depending on local cytoarchitecture of hippocampal zones (CA, dentate gyrus and fiber-rich areas), irrespectively of their dorsoventral level. In the dentate gyrus, unusual double-wave SDs were recorded. Reaching ventral hippocampus, unilateral SD triggered a bilateral seizure-like discharge recruited both ipsilateral (affected by SD) and contralateral (unaffected by SD) sides. The post-SD activation of the ventral hippocampus had striking behavioral manifestation - a bout of wet dog shakes.
This is the first experimental evidence that SD can trigger seizure-like activity in particular regions of awake non-epileptic brain. We suggest that the phenomenon may be relevant to mechanisms of migraine-aura triggered seizures (migralepsy).
扩散性去极化(SD)是一种短暂的细胞去极化波,其在大脑皮层的传播会引发偏头痛先兆症状。越来越多的证据表明,参与情绪和认知调节的脑区海马体也与偏头痛的发病机制有关。海马体具有高度不均匀的功能解剖结构,在功能和网络特性上存在明显的背腹差异。我们假设SD诱导的脑功能障碍在海马体内也存在差异,并研究了清醒动物背侧和腹侧海马体中SD的特征和影响。鉴于海马体对癫痫发作的高度易感性,我们重点关注了SD的兴奋作用。
在自由活动的大鼠中,通过针刺背侧海马体诱导单侧SD。在电生理实验中,沿海马体背腹轴的不同部位双侧记录局部场电位;评估SD的传播模式、电图表现和兴奋作用。在单独的实验中,评估海马体SD对行为的影响。
SD波形因海马区(CA、齿状回和纤维丰富区)的局部细胞结构而异,与它们的背腹水平无关。在齿状回中,记录到了不寻常的双波SD。单侧SD到达腹侧海马体时,会引发双侧癫痫样放电,募集同侧(受SD影响)和对侧(未受SD影响)。腹侧海马体在SD后的激活具有明显的行为表现——一阵湿狗样抖动。
这是首个实验证据,表明SD可在清醒非癫痫性大脑的特定区域触发癫痫样活动。我们认为该现象可能与偏头痛先兆引发的癫痫(偏头痛性癫痫)机制有关。