Georgescu Elena Laura, Georgescu Ioana Antoaneta, Zahiu Carmen Denise Mihaela, Şteopoaie Alexandru Răzvan, Morozan Vlad Petru, Pană Adrian Ştefan, Zăgrean Ana-Maria, Popa Daniela
Division of Physiology and Neuroscience, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Institut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, PSL Research University, Paris, France.
Front Cell Neurosci. 2018 Nov 6;12:390. doi: 10.3389/fncel.2018.00390. eCollection 2018.
The synchronization of neuronal activity in the sensorimotor cortices is crucial for motor control and learning. This synchrony can be modulated by upstream activity in the cerebello-cortical network. However, many questions remain over the details of how the cerebral cortex and the cerebellum communicate. Therefore, our aim is to study the contribution of the cerebellum to oscillatory brain activity, in particular in the case of dystonia, a severely disabling motor disease associated with altered sensorimotor coupling. We used a kainic-induced dystonia model to evaluate cerebral cortical oscillatory activity and connectivity during dystonic episodes. We performed microinjections of low doses of kainic acid into the cerebellar vermis in mice and examined activities in somatosensory, motor and parietal cortices. We showed that repeated applications of kainic acid into the cerebellar vermis, for five consecutive days, generate reproducible dystonic motor behavior. No epileptiform activity was recorded on electrocorticogram (ECoG) during the dystonic postures or movements. We investigated the ECoG power spectral density and coherence between motor cortex, somatosensory and parietal cortices before and during dystonic attacks. During the baseline condition, we found a phenomenon of permanent adaptation with a change of baseline locomotor activity coupled to an ECoG gamma band increase in all cortices. In addition, after kainate administration, we observed an increase in muscular activity, but less signs of dystonia together with modulations of the ECoG power spectra with an increase in gamma band in motor, parietal and somatosensory cortices. Moreover, we found reduced coherence in all measured frequency bands between the motor cortex and somatosensory or parietal cortices compared to baseline. In conclusion, examination of cortical oscillatory activities in this animal model of chronic dystonia caused by cerebellar dysfunction reveals a disruption in the coordination of neuronal activity across the cortical sensorimotor/parietal network, which may underlie motor skill deficits.
感觉运动皮层中神经元活动的同步对于运动控制和学习至关重要。这种同步可由小脑 - 皮层网络中的上游活动调节。然而,关于大脑皮层和小脑如何进行通信的细节仍存在许多问题。因此,我们的目的是研究小脑对振荡性脑活动的贡献,特别是在肌张力障碍的情况下,肌张力障碍是一种与感觉运动耦合改变相关的严重致残性运动疾病。我们使用 kainic 酸诱导的肌张力障碍模型来评估肌张力障碍发作期间的大脑皮层振荡活动和连通性。我们向小鼠小脑蚓部微量注射低剂量的 kainic 酸,并检查体感皮层、运动皮层和顶叶皮层的活动。我们发现连续五天将 kainic 酸重复应用于小脑蚓部会产生可重复的肌张力障碍性运动行为。在肌张力障碍姿势或运动期间,脑电图(ECoG)上未记录到癫痫样活动。我们研究了肌张力障碍发作前和发作期间运动皮层、体感皮层和顶叶皮层之间的 ECoG 功率谱密度和相干性。在基线状态下,我们发现了一种永久适应现象,即基线运动活动发生变化,同时所有皮层的 ECoG γ 频段增加。此外,给予 kainate 后,我们观察到肌肉活动增加,但肌张力障碍迹象较少,同时 ECoG 功率谱发生调制,运动皮层、顶叶皮层和体感皮层的 γ 频段增加。此外,与基线相比,我们发现运动皮层与体感皮层或顶叶皮层之间所有测量频段的相干性降低。总之,在这种由小脑功能障碍引起的慢性肌张力障碍动物模型中对皮层振荡活动的检查揭示了跨皮层感觉运动/顶叶网络中神经元活动协调的破坏,这可能是运动技能缺陷的基础。