Levkovitz Y, Grisaru N, Segal M
Department of Neurobiology, The Weizmann Institute, Rehovot, Israel.
Neuropsychopharmacology. 2001 Jun;24(6):608-16. doi: 10.1016/S0893-133X(00)00244-X.
Transcranial magnetic stimulation (TMS) has been proposed as a safe and efficient treatment of human clinical depression. Although its antidepressive mechanism of action remained unknown, our previous studies indicate that TMS has a long-lasting effect on neuronal excitability in the hippocampus. We now compare the effects of chronic TMS with those of the antidepressant drugs desipramine and mianserin. The three treatments did not affect basal conduction in the perforant path to the dentate gyrus, but markedly suppressed paired-pulse and frequency-dependent inhibition, resulting from a reduction in local circuit inhibition in the dentate gyrus. Concomitantly, these treatments enhanced the expression of long-term potentiation in the perforant path synapse in the dentate gyrus. Finally, chronic TMS as well as mianserin suppressed the serotonin-dependent, potentiating action of fenfluramine on population spike in the dentate gyrus. Thus, TMS, mianserin, and desipramine are likely to affect the same neuronal populations, which may be relevant to their antidepressant action.
经颅磁刺激(TMS)已被提议作为治疗人类临床抑郁症的一种安全有效的方法。尽管其抗抑郁作用机制尚不清楚,但我们之前的研究表明,TMS对海马体中的神经元兴奋性有持久影响。我们现在比较慢性TMS与抗抑郁药物地昔帕明和米安色林的效果。这三种治疗方法均未影响通向齿状回的穿通路径中的基础传导,但显著抑制了配对脉冲和频率依赖性抑制,这是由于齿状回局部回路抑制减少所致。同时,这些治疗方法增强了齿状回穿通路径突触中长时程增强的表达。最后,慢性TMS以及米安色林抑制了芬氟拉明对齿状回群体峰电位的5-羟色胺依赖性增强作用。因此,TMS、米安色林和地昔帕明可能影响相同的神经元群体,这可能与其抗抑郁作用有关。