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Spike-based analysis of brain injured anesthetized animals undergoing closed-loop intracortical stimulation

机译:基于穗的脑损伤麻醉动物分析闭环闭环刺激

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Acquired brain injuries, such as stroke, are a major cause of long-term disability worldwide. When an injury occurs within primary motor cortex (M1) there is both a loss of descending information to the spinal cord and a disruption in the communication within and between spared regions, which can lead to hemiparesis and other motor dysfunction. Recently, activity-dependent stimulation (ADS), a closed loop intracortical neurostimulation technique, was shown to significantly improve 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. In this study, we investigated how neuronal activity is modified 1) following an injury to primary motor cortex and 2) in response to an ADS protocol. Intracortical microelectrode array were inserted in the ipsilesional rostral forelimb area (RFA) to record spike activity and to trigger intracortical microstimulation in the somatosensory cortex (S1). Following a rodent (Long Evans) model of ischemic injury using endothelin-1, a potent vasoconstrictor, was injected unilaterally through the extent of the forelimb area of primary motor cortex. We found that an ischemic injury in M1 led to an overall increase in spike activity within RFA and S1. Subsequent treatment with ADS promoted the generation of synchronized patterns in both RFA and S1.
机译:获得的脑损伤,如中风,是全球长期残疾的主要原因。当初级电动机皮质(M1)内发生伤害(M1)时,对脊髓下降的下降信息既缺失,并且在施工区域内和之间的通信中的发生中断,这可能导致血管血管和其他电动机功能障碍。最近,依赖于活性刺激(ADS),闭环性脑内神经刺激技术,在初级运动皮层中单侧创伤性脑损伤后显着提高啮齿动物模型中的行为恢复。虽然已经描述了行为益处,但是,禁止区域的神经生理变化响应这种类型的刺激尚未完全表征。在该研究中,我们研究了在初级电机皮层和2)损伤后如何改变神经元活性是如何进行修饰的1))响应于ADS方案。插入Ipsilesional rostral的前肢区域(RFA)中的内电极阵列以记录穗活性并引发躯体感染术皮质中的肠道内微刺激(S1)。在啮齿动物(长evans)缺血性损伤模型之后,使用内皮素-1,通过初级电机皮质的前肢区域的程度来单方面注射效率血管收缩剂。我们发现M1中的缺血性损伤导致RFA和S1内的尖峰活动总体增加。随后用ADS治疗促进了RFA和S1中的同步模式的产生。

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