论文标题

癫痫的退化:过度可观的脑电路及其修复的多种途径

Degeneracy in epilepsy: Multiple Routes to Hyperexcitable Brain Circuits and their Repair

论文作者

Stöber, Tristan Manfred, Batulin, Danylo, Triesch, Jochen, Narayanan, Rishikesh, Jedlicka, Peter

论文摘要

开发针对癫痫的有效疗法仍然是一个挑战。该疾病的复杂而多方面的性质仍然引起了关于其起源的争议。在这篇观点文章中,我们认为可以通过考虑大脑的堕落来调和矛盾的假设,这在多种路线中表现出导致相似功能或功能障碍的多种途径。我们在三个不同级别的堕落中举例说明了从细胞到网络和系统级别的堕落。首先,在细胞水平上,我们描述了离子通道退化与癫痫的相关性,并讨论了其与树突形态的相互作用。其次,在网络级别上,我们提供了支持神经元网络鲁棒性的突触和内在神经元特性的堕落示例,但也导致对诱发和癫痫发作的各种反应。第三,在系统级别上,我们提供了免疫系统和神经系统之间复杂相互作用的堕落示例。最后,我们表明,包括多尺度和所谓人群神经回路模型在内的计算方法有助于解散复杂的生理和病理适应性网络。这样的模型可能有助于确定最佳的个性化多坐Multitarget策略,以将系统引导到生理状态。

Developing effective therapies against epilepsy remains a challenge. The complex and multifaceted nature of this disease still fuels controversies about its origin. In this perspective article, we argue that conflicting hypotheses can be reconciled by taking into account the degeneracy of the brain, which manifests in multiple routes leading to similar function or dysfunction. We exemplify degeneracy at three different levels, ranging from the cellular to the network and systems level. First, at the cellular level, we describe the relevance of ion channel degeneracy for epilepsy and discuss its interplay with dendritic morphology. Second, at the network level, we provide examples for the degeneracy of synaptic and intrinsic neuronal properties that supports the robustness of neuronal networks but also leads to diverse responses to ictogenic and epileptogenic perturbations. Third, at the system level, we provide examples for degeneracy in the intricate interactions between the immune and nervous system. Finally, we show that computational approaches including multiscale and so called population neural circuit models help disentangle the complex web of physiological and pathological adaptations. Such models may contribute to identifying the best personalized multitarget strategies for directing the system towards a physiological state.

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