Carè Marta, Averna Alberto, Barban Federico, Semprini Marianna, De Michieli Lorenzo, Nudo Randolph J, Guggenmos David J, Chiappalone Michela
Rehab Technologies, Istituto Italiano di Tecnologia, 16163, Genoa, Italy.
Department of Informatics, Bioengineering, Robotics System Engineering (DIBRIS), University of Genova, 16145, Genoa, Italy.
Bioelectron Med. 2022 Feb 28;8(1):4. doi: 10.1186/s42234-022-00086-y.
Acquired brain injuries, such as stroke, are a major cause of long-term disability worldwide. Intracortical microstimulation (ICMS) can be used successfully to assist in guiding appropriate connections to restore lost sensorimotor integration. Activity-Dependent Stimulation (ADS) is a specific type of closed-loop ICMS that aims at coupling the activity of two different brain regions by stimulating one in response to activity in the other. Recently, ADS was used to effectively promote behavioral recovery in rodent models following a unilateral traumatic brain injury in the primary motor cortex. While behavioral benefits have been described, the neurophysiological changes in spared areas in response to this type of stimulation have not been fully characterized. Here we explored how single-unit spiking activity is impacted by a focal ischemic lesion and, subsequently, by an ADS treatment.
Intracortical microelectrode arrays were implanted in the ipsilesional rostral forelimb area (RFA) to record spike activity and to trigger intracortical microstimulation in the primary somatosensory area (S1) of anaesthetized Long Evans rats. An ischemic injury was induced in the caudal forelimb area through microinjections of Endothelin-1. Activity from both RFA and S1 was recorded and analyzed off-line by evaluating possible changes, either induced by the lesion in the Control group or by stimulation in the ADS group.
We found that the ischemic lesion in the motor area led to an overall increase in spike activity within RFA and a decrease in S1 with respect to the baseline condition. Subsequent treatment with ADS increased the firing rate in both RFA and S1. Post-stimulation spiking activity was significantly higher compared to pre-stimulation activity in the ADS animals versus non-stimulated controls. Moreover, stimulation promoted the generation of highly synchronized bursting patterns in both RFA and S1 only in the ADS group.
This study describes the impact on single-unit activity in ipsilesional areas immediately following a cortical infarct and demonstrates that application of ADS is effective in altering this activity.
获得性脑损伤,如中风,是全球长期残疾的主要原因。皮层内微刺激(ICMS)可成功用于辅助引导适当的连接,以恢复失去的感觉运动整合。活动依赖性刺激(ADS)是一种特定类型的闭环ICMS,旨在通过响应另一个脑区的活动而刺激一个脑区,从而耦合两个不同脑区的活动。最近,ADS被用于有效促进原发性运动皮层单侧创伤性脑损伤后啮齿动物模型的行为恢复。虽然已经描述了行为益处,但这种类型的刺激对未受损区域的神经生理变化尚未得到充分表征。在这里,我们探讨了局灶性缺血性损伤以及随后的ADS治疗如何影响单个神经元的放电活动。
将皮层内微电极阵列植入同侧吻侧前肢区域(RFA),以记录放电活动并触发麻醉的Long Evans大鼠初级体感区(S1)的皮层内微刺激。通过微量注射内皮素-1在尾侧前肢区域诱导缺血性损伤。记录RFA和S1的活动,并通过评估对照组中损伤或ADS组中刺激引起的可能变化进行离线分析。
我们发现,与基线状态相比,运动区的缺血性损伤导致RFA内的放电活动总体增加,S1内的放电活动减少。随后的ADS治疗增加了RFA和S1中的放电频率。与未刺激的对照组相比,ADS组动物刺激后放电活动明显高于刺激前活动。此外,仅在ADS组中,刺激促进了RFA和S1中高度同步爆发模式的产生。
本研究描述了皮层梗死即刻对同侧区域单个神经元活动的影响,并证明ADS的应用可有效改变这种活动。