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Dopamine Modulates Serotonin Innervation in the Drosophila Brain

机译:多巴胺调节果蝇脑中的5-羟色胺神经支配。

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摘要

Parkinson’s disease (PD) results from a progressive degeneration of the dopaminergic nigrostriatal system leading to a decline in movement control, with resting tremor, rigidity and postural instability. Several aspects of PD can be modeled in the fruit fly, Drosophila melanogaster, including α-synuclein-induced degeneration of dopaminergic neurons, or dopamine (DA) loss by genetic elimination of neural DA synthesis. Defective behaviors in this latter model can be ameliorated by feeding the DA precursor L-DOPA, analogous to the treatment paradigm for PD. Secondary complication from L-DOPA treatment in PD patients are associated with ectopic synthesis of DA in serotonin (5-HT)-releasing neurons, leading to DA/5-HT imbalance. Here we examined the neuro-anatomical adaptations resulting from imbalanced DA/5-HT signaling in Drosophila mutants lacking neural DA. We find that, similar to rodent models of PD, lack of DA leads to increased 5-HT levels and arborizations in specific brain regions. Conversely, increased DA levels by L-DOPA feeding leads to reduced connectivity of 5-HT neurons to their target neurons in the mushroom body (MB). The observed alterations of 5-HT neuron plasticity indicate that loss of DA signaling is not solely responsible for the behavioral disorders observed in Drosophila models of PD, but rather a combination of the latter with alterations of 5-HT circuitry.
机译:帕金森氏病(PD)是由多巴胺能黑质纹状体系统的逐渐退化导致运动控制下降,静息性震颤,僵硬和姿势不稳导致的。可以在果蝇果蝇中模拟PD的几个方面,包括α-突触核蛋白诱导的多巴胺能神经元变性,或通过遗传消除神经DA合成而引起的多巴胺(DA)丢失。可以通过喂入DA前体L-DOPA来改善后一种模型中的缺陷行为,类似于PD的治疗范式。 PD患者的L-DOPA治疗继发并发症与释放5-羟色胺(5-HT)的神经元中DA的异位合成有关,从而导致DA / 5-HT失衡。在这里,我们检查了在缺乏神经DA的果蝇突变体中,由于DA / 5-HT信号失衡导致的神经解剖适应。我们发现,类似于PD的啮齿动物模型,DA的缺乏会导致5-HT水平升高和特定大脑区域的乔化。相反,通过L-DOPA进食增加的DA水平会导致5-HT神经元与其蘑菇体(MB)中目标神经元的连通性降低。观察到的5-HT神经元可塑性改变表明,DA信号的丢失不仅是PD果蝇模型中观察到的行为障碍的原因,而且是后者与5-HT电路改变的组合。

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