Neuroscience and Behavioral Sciences Department, Ribeirão Preto School of Medicine, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Epilepsy Behav. 2012 Aug;24(4):391-8. doi: 10.1016/j.yebeh.2012.04.133. Epub 2012 Jun 16.
The role of the substantia nigra pars reticulata (SNPr) and superior colliculus (SC) network in rat strains susceptible to audiogenic seizures still remain underexplored in epileptology. In a previous study from our laboratory, the GABAergic drugs bicuculline (BIC) and muscimol (MUS) were microinjected into the deep layers of either the anterior SC (aSC) or the posterior SC (pSC) in animals of the Wistar audiogenic rat (WAR) strain submitted to acoustic stimulation, in which simultaneous electroencephalographic (EEG) recording of the aSC, pSC, SNPr and striatum was performed. Only MUS microinjected into the pSC blocked audiogenic seizures. In the present study, we expanded upon these previous results using the retrograde tracer Fluorogold (FG) microinjected into the aSC and pSC in conjunction with quantitative EEG analysis (wavelet transform), in the search for mechanisms associated with the susceptibility of this inbred strain to acoustic stimulation. Our hypothesis was that the WAR strain would have different connectivity between specific subareas of the superior colliculus and the SNPr when compared with resistant Wistar animals and that these connections would lead to altered behavior of this network during audiogenic seizures. Wavelet analysis showed that the only treatment with an anticonvulsant effect was MUS microinjected into the pSC region, and this treatment induced a sustained oscillation in the theta band only in the SNPr and in the pSC. These data suggest that in WAR animals, there are at least two subcortical loops and that the one involved in audiogenic seizure susceptibility appears to be the pSC-SNPr circuit. We also found that WARs presented an increase in the number of FG+ projections from the posterior SNPr to both the aSC and pSC (primarily to the pSC), with both acting as proconvulsant nuclei when compared with Wistar rats. We concluded that these two different subcortical loops within the basal ganglia are probably a consequence of the WAR genetic background.
黑质网状部(SNPr)和上丘(SC)网络在易发性听觉惊厥大鼠品系中的作用在癫痫学中仍未得到充分探索。在我们实验室的一项先前研究中,GABA 能药物荷包牡丹碱(BIC)和毒蕈碱(MUS)被微注射到易发性听觉惊厥大鼠(WAR)品系动物的前 SC(aSC)或后 SC(pSC)的深层,同时对 aSC、pSC、SNPr 和纹状体进行脑电图(EEG)记录。只有微注射到 pSC 的 MUS 阻断了听觉惊厥。在本研究中,我们使用逆行示踪剂 Fluorogold(FG)在前 SC 和 pSC 中微注射,并结合定量 EEG 分析(小波变换),扩展了这些先前的结果,以寻找与该近交系对声刺激易感性相关的机制。我们的假设是,与抗性 Wistar 动物相比,WAR 品系的上丘特定亚区与 SNPr 之间的连接会有所不同,并且这些连接会导致该网络在听觉惊厥期间的行为改变。小波分析表明,唯一具有抗惊厥作用的治疗方法是将 MUS 微注射到 pSC 区域,这种治疗方法仅在 SNPr 和 pSC 中诱导θ带的持续振荡。这些数据表明,在 WAR 动物中,至少存在两个皮质下环路,而与听觉惊厥易感性相关的环路似乎是 pSC-SNPr 回路。我们还发现,与 Wistar 大鼠相比,WAR 大鼠的后 SNPr 向 aSC 和 pSC 的 FG+投射数量增加(主要是向 pSC),这两个核团均作为促惊厥核团。我们得出结论,基底神经节内的这两个不同的皮质下环路可能是 WAR 遗传背景的结果。