Nahas Ziad, Teneback Charlotte, Chae Jeong-Ho, Mu Qiwen, Molnar Chris, Kozel Frank A, Walker John, Anderson Berry, Koola Jejo, Kose Samet, Lomarev Mikhail, Bohning Daryl E, George Mark S
Department of Psychiatry, Brain Stimulation Laboratory, Mood Disorders Program, Institute of Psychiatry, Charleston, SC 29403, USA.
Neuropsychopharmacology. 2007 Aug;32(8):1649-60. doi: 10.1038/sj.npp.1301288. Epub 2007 Jan 3.
Vagus nerve stimulation (VNS) therapy has shown antidepressant effects in open acute and long-term studies of treatment-resistant major depression. Mechanisms of action are not fully understood, although clinical data suggest slower onset therapeutic benefit than conventional psychotropic interventions. We set out to map brain systems activated by VNS and to identify serial brain functional correlates of antidepressant treatment and symptomatic response. Nine adults, satisfying DSM-IV criteria for unipolar or bipolar disorder, severe depressed type, were implanted with adjunctive VNS therapy (MRI-compatible technique) and enrolled in a 3-month, double-blind, placebo-controlled, serial-interleaved VNS/functional MRI (fMRI) study and open 20-month follow-up. A multiple regression mixed model with blood oxygenation level dependent (BOLD) signal as the dependent variable revealed that over time, VNS therapy was associated with ventro-medial prefrontal cortex deactivation. Controlling for other variables, acute VNS produced greater right insula activation among the participants with a greater degree of depression. These results suggest that similar to other antidepressant treatments, BOLD deactivation in the ventro-medial prefrontal cortex correlates with the antidepressant response to VNS therapy. The increased acute VNS insula effects among actively depressed participants may also account for the lower dosing observed in VNS clinical trials of depression compared with epilepsy. Future interleaved VNS/fMRI studies to confirm these findings and further clarify the regional neurobiological effects of VNS.
迷走神经刺激(VNS)疗法在难治性重度抑郁症的开放性急性和长期研究中已显示出抗抑郁作用。尽管临床数据表明其起效时间比传统精神药物干预更慢,但作用机制尚未完全明确。我们着手绘制由VNS激活的脑系统图谱,并确定抗抑郁治疗和症状反应的系列脑功能相关性。九名符合DSM-IV标准的单极或双相情感障碍、重度抑郁型的成年人接受了辅助VNS治疗(MRI兼容技术),并参与了一项为期3个月的双盲、安慰剂对照、系列交错VNS/功能磁共振成像(fMRI)研究以及为期20个月的开放性随访。以血氧水平依赖(BOLD)信号作为因变量的多元回归混合模型显示,随着时间推移,VNS治疗与腹内侧前额叶皮质失活相关。在控制其他变量的情况下,急性VNS在抑郁程度较高的参与者中产生了更大的右侧岛叶激活。这些结果表明,与其他抗抑郁治疗类似,腹内侧前额叶皮质的BOLD失活与对VNS治疗的抗抑郁反应相关。在积极抑郁的参与者中,急性VNS对岛叶的影响增加,这也可能解释了与癫痫相比,VNS抑郁症临床试验中观察到的较低剂量。未来需要进行交错VNS/fMRI研究以证实这些发现,并进一步阐明VNS的区域神经生物学效应。