Grennan Isaac, Perry Brook, Verghese Anna, Jones Melissa, Härmson Oliver, McNamara Colin G, Sharott Andrew
Medical Research Council Brain Network Dynamics Unit, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
Medical Research Council Brain Network Dynamics Unit, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
Brain Stimul. 2025 May-Jun;18(3):993-1003. doi: 10.1016/j.brs.2025.04.019. Epub 2025 Apr 29.
Alzheimer's disease (AD) has very limited treatment options and therapies to prevent or reverse neurodegeneration remain elusive. Deep brain stimulation (DBS), whereby high-frequency pulses of electricity are delivered continuously to a specific part of the brain, has been trialled as an experimental treatment for AD. In AD patients, continuous, high frequency DBS targeted to the fornix (fx-DBS) has been shown to be safe, but not reliably effective across patients. In movement disorders, high-frequency DBS is thought to act as a virtual lesion, disrupting pathophysiological activity. In AD, it may be more advantageous to use stimulation to reinforce or rebuild oscillatory activities that are disrupted by the disease process. A primary candidate for such a target is the hippocampal theta oscillation, which provides a temporal framework for mnemonic processing and is altered in rodent models of AD.
We applied closed-loop electrical stimulation to the fornix of rats traversing a linear track, triggered by different phases of the ongoing theta oscillation in the hippocampal local field potential (LFP) using the OscillTrack algorithm.
Stimulation at different target phases could robustly suppress or amplify the theta oscillation, and these effects were significantly larger than those caused by open-loop replay of the same stimulation pattern. Amplification of the theta oscillation could be achieved irrespective of the locomotor speed of the animal, showing that it did not result from a secondary effect of behavioural change.
Our findings demonstrate that closed-loop fx-DBS is a viable method of modulating the amplitude of hippocampal theta oscillations that could be applied in human devices to provide a constructive intervention with the potential to boost memory circuit function in AD.
阿尔茨海默病(AD)的治疗选择非常有限,预防或逆转神经退行性变的疗法仍然难以捉摸。深部脑刺激(DBS),即向大脑的特定部位持续输送高频电脉冲,已作为AD的一种实验性治疗方法进行了试验。在AD患者中,针对穹窿的持续高频DBS(fx-DBS)已被证明是安全的,但对所有患者而言并非都能可靠地产生疗效。在运动障碍中,高频DBS被认为起到了虚拟损伤的作用,破坏了病理生理活动。在AD中,使用刺激来加强或重建被疾病过程破坏的振荡活动可能更具优势。这样一个靶点的主要候选对象是海马θ振荡,它为记忆处理提供了一个时间框架,并且在AD的啮齿动物模型中发生了改变。
我们使用OscillTrack算法,根据海马局部场电位(LFP)中正在进行的θ振荡的不同相位触发,对在直线轨道上穿行的大鼠的穹窿施加闭环电刺激。
在不同目标相位进行刺激能够有力地抑制或放大θ振荡,并且这些效应明显大于相同刺激模式的开环重放所引起的效应。无论动物的运动速度如何,都能实现θ振荡的放大,这表明它并非行为变化的继发效应所致。
我们的研究结果表明,闭环fx-DBS是调节海马θ振荡幅度的一种可行方法,可应用于人体设备,以提供一种建设性干预,有可能增强AD患者的记忆回路功能。