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脚桥神经元参与颞叶癫痫点燃模型中的网络变化。

Pedunculopontine neurons are involved in network changes in the kindling model of temporal lobe epilepsy.

作者信息

Nolte Marc W, Löscher Wolfgang, Gernert Manuela

机构信息

Department of Pharmacology, Toxicology, and Pharmacy, University of Veterinary Medicine Hannover, Bünteweg 17, 30559 Hannover, Germany.

出版信息

Neurobiol Dis. 2006 Jul;23(1):206-18. doi: 10.1016/j.nbd.2006.03.003. Epub 2006 May 6.

Abstract

It is well known that epileptogenesis is associated with widespread neuronal network changes in brain regions adjacent to the seizure focus but also in remote structures including basal ganglia. Besides the superior colliculus, the pedunculopontine tegmental nucleus (PPN) is one of three main target regions of basal ganglia output activity and is reciprocally connected with the substantia nigra pars reticulata (SNr), which is critically involved in seizure propagation and manipulation. We here tested the hypothesis if, apart from the traditional view that the superior colliculus mediates seizure-gating mechanisms of the SNr, the PPN is involved in kindling-induced network changes. Rats were electrically kindled via the ipsilateral basolateral amygdala. In vivo extracellular single unit recordings of right PPN neurons were performed in kindled rats 1 day after a generalized seizure in order to examine kindling-associated rather than seizure-associated activity changes. The main findings of the study were (1) a seizure-outlasting drastically reduced firing rate of PPN neurons and (2) an increase in burst and irregular firing pattern in kindled rats compared with sham-kindled and naïve controls. These changes are likely to be caused by an altered inhibitory input from the SNr. Furthermore, kindling caused (3) the oscillation frequency of PPN neurons to shift towards lower frequencies. The kindling-induced activity changes were found to be anatomically restricted to the PPN, indicating that network changes follow distinct anatomical routes. We demonstrated that the PPN is strongly affected by the functional reorganization of neurocircuitry associated with kindling. The underlying mechanisms are discussed. The findings are relevant for a better understanding of kindling-associated network changes and might provide new targets for therapeutic manipulations in epilepsies.

摘要

众所周知,癫痫发生不仅与癫痫病灶附近脑区广泛的神经元网络变化有关,还与包括基底神经节在内的远处结构的变化有关。除上丘外,脚桥被盖核(PPN)是基底神经节输出活动的三个主要目标区域之一,并且与黑质网状部(SNr)相互连接,而SNr在癫痫传播和调控中起着关键作用。我们在此测试了一个假设,即除了传统观点认为上丘介导SNr的癫痫门控机制外,PPN是否参与点燃诱导的网络变化。通过同侧基底外侧杏仁核对大鼠进行电点燃。在大鼠全身性癫痫发作1天后,对点燃大鼠右侧PPN神经元进行体内细胞外单单位记录,以检查与点燃相关而非与癫痫发作相关的活动变化。该研究的主要发现为:(1)癫痫发作后PPN神经元的放电率急剧降低且持续时间延长;(2)与假点燃和未处理的对照相比,点燃大鼠的爆发性和不规则放电模式增加。这些变化可能是由SNr抑制性输入改变引起的。此外,点燃导致(3)PPN神经元的振荡频率向更低频率偏移。发现点燃诱导的活动变化在解剖学上局限于PPN,表明网络变化遵循不同的解剖路径。我们证明PPN受到与点燃相关的神经回路功能重组的强烈影响。对潜在机制进行了讨论。这些发现有助于更好地理解与点燃相关的网络变化,并可能为癫痫治疗提供新的靶点。

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