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迷走神经刺激疗法治疗难治性抑郁症:临床证据及假定的神经生物学机制

VNS therapy in treatment-resistant depression: clinical evidence and putative neurobiological mechanisms.

作者信息

Nemeroff Charles B, Mayberg Helen S, Krahl Scott E, McNamara James, Frazer Alan, Henry Thomas R, George Mark S, Charney Dennis S, Brannan Stephen K

机构信息

Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

Neuropsychopharmacology. 2006 Jul;31(7):1345-55. doi: 10.1038/sj.npp.1301082. Epub 2006 Apr 19.


DOI:10.1038/sj.npp.1301082
PMID:16641939
Abstract

Currently available therapeutic interventions for treatment-resistant depression, including switch, combination, and augmentation strategies, are less than ideal. Observations of mood elevation during vagus nerve stimulation (VNS) therapy for pharmacoresistant epilepsy suggested a role for VNS therapy in refractory major depression and prompted clinical investigation of this neurostimulation modality. The VNS Therapy System has been available for treatment of pharmacoresistant epilepsy since 1997 and was approved by the US Food and Drug Administration for treatment-resistant depression in July, 2005. The physiology of the vagus nerve, mechanics of the VNS Therapy System, and efficacy and safety in pharmacoresistant epilepsy are reviewed. Promising results of VNS therapy for treatment-resistant depression have been forthcoming from both acute and long-term studies, evidenced in part by progressive improvements in depression rating scale scores during the 1st year of treatment with maintenance of response thereafter. VNS therapy is well tolerated in patients with either pharmacoresistant epilepsy or treatment-resistant depression. As in epilepsy, the mechanisms of VNS therapy of treatment-resistant depression are incompletely understood. However, evidence from neuroimaging and other studies suggests that VNS therapy acts via innervation of the nucleus tractus solitarius, with secondary projections to limbic and cortical structures that are involved in mood regulation, including brainstem regions that contain serotonergic (raphe nucleus) and noradrenergic (locus ceruleus) perikarya that project to the forebrain. Mechanisms that mediate the beneficial effects of VNS therapy for treatment-resistant depression remain obscure. Suggestions for future research directions are described.

摘要

目前用于治疗难治性抑郁症的治疗干预措施,包括换药、联合用药和增效策略,都不尽人意。在迷走神经刺激(VNS)治疗药物难治性癫痫期间观察到情绪改善,提示VNS治疗在难治性重度抑郁症中可能起作用,并促使对这种神经刺激方式进行临床研究。VNS治疗系统自1997年起可用于治疗药物难治性癫痫,并于2005年7月获得美国食品药品监督管理局批准用于治疗难治性抑郁症。本文综述了迷走神经的生理学、VNS治疗系统的作用机制以及在药物难治性癫痫中的疗效和安全性。VNS治疗难治性抑郁症的急性和长期研究均取得了令人鼓舞的结果,部分证据是在治疗的第1年抑郁评定量表评分逐步改善,且此后疗效得以维持。VNS治疗在药物难治性癫痫或难治性抑郁症患者中耐受性良好。与癫痫一样,VNS治疗难治性抑郁症的机制尚不完全清楚。然而,神经影像学和其他研究的证据表明,VNS治疗通过孤束核的神经支配起作用,继而投射到参与情绪调节的边缘和皮质结构,包括含有投射到前脑的5-羟色胺能(中缝核)和去甲肾上腺素能(蓝斑)核周体的脑干区域。介导VNS治疗难治性抑郁症有益作用的机制仍不清楚。文中还描述了未来研究方向的建议。

相似文献

[1]
VNS therapy in treatment-resistant depression: clinical evidence and putative neurobiological mechanisms.

Neuropsychopharmacology. 2006-7

[2]
Concomitant use of vagus nerve stimulation and electroconvulsive therapy for treatment-resistant depression.

J ECT. 2006-9

[3]
Vagus nerve stimulation for treatment-resistant depression: a randomized, controlled acute phase trial.

Biol Psychiatry. 2005-9-1

[4]
Effectiveness and safety of vagus nerve stimulation for severe treatment-resistant major depression in clinical practice after FDA approval: outcomes at 1 year.

J Clin Psychiatry. 2011-10

[5]
VNS and depression: current status and future directions.

Expert Rev Med Devices. 2004-9

[6]
Vagus nerve stimulation for depression: efficacy and safety in a European study.

Psychol Med. 2008-5

[7]
Serial vagus nerve stimulation functional MRI in treatment-resistant depression.

Neuropsychopharmacology. 2007-8

[8]
[Vagus nerve stimulation. A potential therapy for chronic/recurrent depression?].

Fortschr Neurol Psychiatr. 2002-6

[9]
Vagus nerve stimulation for medically refractory epilepsy: a long-term follow-up study.

Seizure. 2007-10

[10]
Recordings from the rat locus coeruleus during acute vagal nerve stimulation in the anaesthetised rat.

Neurosci Lett. 2005-5-13

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[3]
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[6]
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