Lujan J Luis, Chaturvedi Ashutosh, McIntyre Cameron C
Department of Biomedical Engineering, Cleveland Clinic Foundation; Cleveland, Ohio 44195, USA.
Front Biosci. 2008 May 1;13:5892-904. doi: 10.2741/3124.
Deep brain stimulation (DBS) has recently emerged as a potential treatment for medically intractable neuropsychiatric disorders. Pilot clinical studies with encouraging results have been performed with DBS of the ventral anterior internal capsule (VAIC) and subgenual cingulate white matter (Cg25WM) for the treatment of obsessive-compulsive disorder and depression. However, little is known about the underlying response of individual neurons, or the networks they are connected to, when DBS is applied to the VAIC or Cg25WM. This review summarizes current understanding of the response of axons to DBS, and discusses the general brain network architectures thought to underlie neuropsychiatric disorders. We also employ diffusion tensor imaging tractography to better understand the axonal trajectories surrounding DBS electrodes implanted in the VAIC or Cg25WM. Finally, we attempt to reconcile various data sets by presenting generalized hypotheses on potential therapeutic mechanisms of DBS for neuropsychiatric disease.
深部脑刺激(DBS)最近已成为治疗药物难治性神经精神疾病的一种潜在疗法。针对腹侧前内囊(VAIC)和膝下扣带回白质(Cg25WM)进行的DBS试点临床研究取得了令人鼓舞的结果,用于治疗强迫症和抑郁症。然而,当DBS应用于VAIC或Cg25WM时,对于单个神经元或它们所连接的网络的潜在反应知之甚少。本综述总结了目前对轴突对DBS反应的理解,并讨论了被认为是神经精神疾病基础的一般脑网络结构。我们还采用扩散张量成像纤维束示踪技术,以更好地了解植入VAIC或Cg25WM的DBS电极周围的轴突轨迹。最后,我们试图通过提出关于DBS治疗神经精神疾病潜在机制的广义假设来协调各种数据集。