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Inhibition of 5-HT neuron activity and induction of depressive-like behavior by high-frequency stimulation of the subthalamic nucleus.

机译:高频刺激丘脑底核抑制5-HT神经元活性并诱导抑郁样行为。

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摘要

Bilateral, high-frequency stimulation (HFS) of the subthalamic nucleus (STN) is the surgical therapy of choice for movement disability in advanced Parkinson's disease (PD), but this procedure evokes debilitating psychiatric effects, including depressed mood, of unknown neural origin. Here, we report the unexpected finding that HFS of the STN inhibits midbrain 5-hydroxytryptamine (5-HT) neurons to evoke depression-related behavioral changes. We found that bilateral HFS of the STN consistently inhibited (40-50%) the firing rate of 5-HT neurons in the dorsal raphe nucleus of the rat, but not neighboring non-5-HT neurons. This effect was apparent at clinically relevant stimulation parameters (> or =100 Hz, > or =30 microA), was not elicited by HFS of either neighboring or remote structures to the STN, and was still present in rat models of PD. We also found that bilateral HFS of the STN evoked clear-cut, depressive-like behavior in a widely used experimental paradigm of depression (forced swim test), and this effect was also observed in a PD model. Importantly, the depressive-like behavior elicited by HFS of the STN was reversed by a selective 5-HT-enhancing antidepressant, thereby linking the behavioral change to decreased 5-HT neuronal activity. Overall, these findings link reduced 5-HT function to the psychiatric effects of HFS of the STN observed in PD patients and provide a rational basis for their clinical management. More generally, the powerful interaction between the STN and 5-HT system uncovered here offers insights into the high level of comorbidity of basal ganglia disease and mood disorder.
机译:丘脑底核(STN)的双边高频刺激(HFS)是晚期帕金森病(PD)行动不便的首选手术治疗方法,但是这种方法引起了神经源性未知的精神衰弱,包括情绪低落。在这里,我们报告意外的发现,STN的HFS抑制中脑5-羟色胺(5-HT)神经元引起抑郁症相关的行为改变。我们发现,STN的双侧HFS始终抑制(40-50%)大鼠背沟核中5-HT神经元的放电率,但不抑制邻近的非5-HT神经元的放电率。这种效应在临床相关刺激参数(>或= 100 Hz,>或= 30 microA)下很明显,不是由STN的邻近或远端结构的HFS引起的,并且仍然存在于PD大鼠模型中。我们还发现,在广泛使用的抑郁症实验模式(强迫游泳试验)中,STN的双侧HFS引起清晰,类似抑郁的行为,并且在PD模型中也观察到了这种效果。重要的是,STN的HFS引起的抑郁样行为被选择性增强5-HT的抗抑郁药逆转,从而将行为改变与降低的5-HT神经元活性联系起来。总体而言,这些发现将5-HT功能降低与PD患者中STN的HFS的精神病学效应联系起来,并为其临床管理提供了合理的基础。更一般而言,此处发现的STN和5-HT系统之间的强大相互作用为深入了解基底神经节疾病和情绪障碍的合并症提供了见识。

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