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单侧皮质扩散性抑制是清醒大鼠听源性惊厥发作的早期标志物。

Unilateral cortical spreading depression is an early marker of audiogenic kindling in awake rats.

作者信息

Vinogradova Lyudmila V, Vinogradov Vladislav Yu, Kuznetsova Galina D

机构信息

Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences, Butlerova Street 5a, Moscow 117485, Russia.

出版信息

Epilepsy Res. 2006 Sep;71(1):64-75. doi: 10.1016/j.eplepsyres.2006.05.014. Epub 2006 Jun 27.

Abstract

Spreading depression (SD), a self-propagating wave of reversible cellular depolarization, is thought to play an important role in brain pathophysiology. SD and seizures are closely related events but little is known about involvement of SD in chronic epileptogenesis. Here we show that cortical SD is the first and highly reproducible manifestation of audiogenic kindling induced by repeated sound stimulation of WAG/Rij rats with genetic audiogenic and absence epilepsy. Repetition of sound-induced running seizures in freely moving rats led to an appearance and gradual intensification of post-running facial and forelimb clonic convulsions coupled with afterdischarge in the fronto-parietal cortex. Before the development of these traditional manifestations of audiogenic kindling, an unilateral cortical SD wave began to be triggered by audiogenic seizures. Once cortical SD appeared, it became a permanent component of subsequent seizures. SD was always recorded in the hemisphere ipsilateral to the running direction. Only at the late stages of audiogenic kindling SD developed bilaterally. To estimate the contribution of SD in postictal effects of audiogenic seizures, we compared cortical activity after seizures induced SD or not. It was found that only seizures with cortical SD were followed by postictal suppression of spontaneous spike-wave discharges displayed by WAG/Rij rats. The results show that (1) cortical SD is readily triggered by brief sensory-induced seizures in awake animals; (2) SD may be responsible for postictal changes in cortical activity; (3) unilateral initiation of SD suggests asymmetrical recruitment of the cortex into seizure network during audiogenic kindling.

摘要

扩散性抑制(SD)是一种可逆性细胞去极化的自我传播波,被认为在脑病理生理学中起重要作用。SD与癫痫发作密切相关,但关于SD在慢性癫痫发生中的作用知之甚少。在此,我们表明,皮层SD是通过对具有遗传性听源性失神癫痫的WAG/Rij大鼠反复进行声音刺激所诱发的听源性点燃的首个且高度可重复的表现。在自由活动的大鼠中,声音诱发的奔跑性癫痫发作的重复导致奔跑后面部和前肢阵挛性惊厥的出现和逐渐加剧,同时伴有额顶叶皮层的放电后电位。在这些听源性点燃的传统表现出现之前,听源性癫痫发作开始触发单侧皮层SD波。一旦皮层SD出现,它就成为后续癫痫发作的一个永久组成部分。SD总是记录在奔跑方向同侧的半球。只有在听源性点燃的后期,SD才会双侧出现。为了评估SD在听源性癫痫发作的发作后效应中的作用,我们比较了诱发或未诱发SD的癫痫发作后的皮层活动。结果发现,只有伴有皮层SD的癫痫发作后,WAG/Rij大鼠才会出现发作后自发性棘波放电的抑制。结果表明:(1)清醒动物中短暂的感觉诱发癫痫发作很容易触发皮层SD;(2)SD可能是皮层活动发作后变化的原因;(3)SD的单侧起始表明在听源性点燃过程中皮层不对称地被纳入癫痫网络。

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