McConnell George C, Rees Howard D, Levey Allan I, Gutekunst Claire-Anne, Gross Robert E, Bellamkonda Ravi V
Wallace H Coulter Department of Biomedical Engineering, Georgia Institute of Technology/Emory University, Atlanta, 30332, USA.
J Neural Eng. 2009 Oct;6(5):056003. doi: 10.1088/1741-2560/6/5/056003. Epub 2009 Aug 21.
Prosthetic devices that are controlled by intracortical electrodes recording one's 'thoughts' are a reality today, and no longer merely in the realm of science fiction. However, widespread clinical use of implanted electrodes is hampered by a lack of reliability in chronic recordings, independent of the type of electrodes used. One major hypothesis has been that astroglial scar electrically impedes the electrodes. However, there is a temporal discrepancy between stabilization of scar's electrical properties and recording failure with recording failure lagging by 1 month. In this study, we test a possible explanation for this discrepancy: the hypothesis that chronic inflammation, due to the persistent presence of the electrode, causes a local neurodegenerative state in the immediate vicinity of the electrode. Through modulation of chronic inflammation via stab wound, electrode geometry and age-matched control, we found that after 16 weeks, animals with an increased level of chronic inflammation were associated with increased neuronal and dendritic, but not axonal, loss. We observed increased neuronal and dendritic loss 16 weeks after implantation compared to 8 weeks after implantation, suggesting that the local neurodegenerative state is progressive. After 16 weeks, we observed axonal pathology in the form of hyperphosphorylation of the protein tau in the immediate vicinity of the microelectrodes (as observed in Alzheimer's disease and other tauopathies). The results of this study suggest that a local, late onset neurodegenerative disease-like state surrounds the chronic electrodes and is a potential cause for chronic recording failure. These results also inform strategies to enhance our capability to attain reliable long-term recordings from implantable electrodes in the CNS.
如今,由记录人“思想”的皮层内电极控制的假肢装置已成为现实,不再仅仅存在于科幻领域。然而,无论使用何种类型的电极,慢性记录缺乏可靠性都阻碍了植入电极在临床上的广泛应用。一个主要假设是星形胶质瘢痕会对电极产生电阻碍。然而,瘢痕电特性的稳定与记录失败之间存在时间差异,记录失败滞后1个月。在本研究中,我们测试了对此差异的一种可能解释:即由于电极的持续存在导致的慢性炎症在电极紧邻区域引起局部神经退行性状态的假设。通过刺伤伤口、电极几何形状和年龄匹配对照来调节慢性炎症,我们发现16周后,慢性炎症水平升高的动物与神经元和树突(而非轴突)损失增加有关。与植入后8周相比,我们在植入后16周观察到神经元和树突损失增加,这表明局部神经退行性状态是渐进性的。16周后,我们在微电极紧邻区域观察到轴突病理学变化,表现为蛋白质tau的过度磷酸化(如在阿尔茨海默病和其他tau蛋白病中所见)。本研究结果表明,慢性电极周围存在局部、迟发性神经退行性疾病样状态,这是慢性记录失败的潜在原因。这些结果也为提高我们从中枢神经系统植入电极获得可靠长期记录能力的策略提供了信息。