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长期迷走神经刺激对大鼠单胺能系统的电生理和神经化学影响。

Electrophysiological and neurochemical effects of long-term vagus nerve stimulation on the rat monoaminergic systems.

机构信息

University of Ottawa Institute of Mental Health Research, Ottawa, Ontario, Canada.

出版信息

Int J Neuropsychopharmacol. 2013 Mar;16(2):459-70. doi: 10.1017/S1461145712000387. Epub 2012 Apr 17.

DOI:10.1017/S1461145712000387
PMID:22717062
Abstract

Vagus nerve stimulation (VNS) is an adjunctive treatment for resistant epilepsy and depression. Electrophysiological recordings in the rat brain have already shown that chronic VNS increases norepinephrine (NE) neuronal firing activity and, subsequently, that of serotonin (5-HT) neurons through an activation of their excitatory α1-adrenoceptors. Long-term VNS was shown to increase the tonic activation of post-synaptic 5-HT1A receptors in the hippocampus. This study was aimed at examining the effect of VNS on extracellular 5-HT, NE and dopamine (DA) levels in different brain areas using in vivo microdialysis, on NE transmission in the hippocampus, and DA neuronal firing activity using electrophysiology. Rats were implanted with a VNS device and stimulated for 14 d with standard parameters used in treatment-resistant depression (0.25 mA, 20 Hz, 500 μs, 30 s on-5 min off). The results of the present study revealed that 2-wk VNS significantly increased extracellular NE levels in the prefrontal cortex and the hippocampus and enhanced the tonic activation of post-synaptic α2-adrenoceptors on pyramidal neurons. The electrophysiological experiments revealed a significant decrease in ventral tegmental area DA neuronal firing rate after long-term VNS; extracellular DA levels were nevertheless increased in the prefrontal cortex and nucleus accumbens. Chronic VNS significantly increased extracellular 5-HT levels in the dorsal raphe but not in the hippocampus and prefrontal cortex. In conclusion, the effect of VNS in increasing the transmission of monoaminergic systems targeted in the treatment of resistant depression should be involved, at least in part, in its antidepressant properties observed in patients not responding to many antidepressant strategies.

摘要

迷走神经刺激(VNS)是耐药性癫痫和抑郁症的辅助治疗方法。大鼠大脑中的电生理记录已经表明,慢性 VNS 增加去甲肾上腺素(NE)神经元的放电活动,随后通过激活其兴奋性α1-肾上腺素受体,增加 5-羟色胺(5-HT)神经元的放电活动。长期 VNS 被证明会增加海马体中突触后 5-HT1A 受体的紧张激活。本研究旨在使用活体微透析检查 VNS 对不同脑区细胞外 5-HT、NE 和多巴胺(DA)水平的影响,使用电生理学检查海马体中 NE 传递和 DA 神经元放电活动。大鼠被植入 VNS 装置,并使用治疗耐药性抑郁症的标准参数(0.25 mA、20 Hz、500 μs、30 s ON-5 min OFF)刺激 14 天。本研究结果表明,2 周 VNS 可显著增加前额叶皮层和海马体中的细胞外 NE 水平,并增强锥体神经元突触后α2-肾上腺素受体的紧张激活。电生理实验显示,长期 VNS 后腹侧被盖区 DA 神经元放电率显著降低;然而,细胞外 DA 水平在前额叶皮层和伏隔核中增加。慢性 VNS 可显著增加背侧中缝核中的细胞外 5-HT 水平,但不在海马体和前额叶皮层中增加。总之,VNS 增加单胺能系统传递的作用,至少部分涉及到对许多抗抑郁策略无反应的患者观察到的抗抑郁特性。

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