Suppr超能文献

多巴胺调节大脑中的5-羟色胺神经支配。

Dopamine Modulates Serotonin Innervation in the Brain.

作者信息

Niens Janna, Reh Fabienne, Çoban Büşra, Cichewicz Karol, Eckardt Julia, Liu Yi-Ting, Hirsh Jay, Riemensperger Thomas D

机构信息

Molecular Neurobiology of Behavior, Johann-Friedrich-Blumenbach-Institute for Zoology and Anthropology, University of Göttingen, Göttingen, Germany.

Department of Biology, University of Virginia, Charlottesville, VA, United States.

出版信息

Front Syst Neurosci. 2017 Oct 16;11:76. doi: 10.3389/fnsys.2017.00076. eCollection 2017.

Abstract

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, , 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 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 models of PD, but rather a combination of the latter with alterations of 5-HT circuitry.

摘要

帕金森病(PD)是由多巴胺能黑质纹状体系统进行性退化导致运动控制能力下降引起的,伴有静止性震颤、僵硬和姿势不稳。PD的几个方面可以在果蝇中进行建模,包括α-突触核蛋白诱导的多巴胺能神经元退化,或通过基因消除神经多巴胺合成导致的多巴胺(DA)丧失。在后一种模型中,有缺陷的行为可以通过喂食DA前体左旋多巴(L-DOPA)来改善,这类似于PD的治疗模式。PD患者L-DOPA治疗的继发性并发症与5-羟色胺(5-HT)释放神经元中DA的异位合成有关,导致DA/5-HT失衡。在这里,我们研究了在缺乏神经DA的突变体中,DA/5-HT信号失衡导致的神经解剖学适应性变化。我们发现,与PD的啮齿动物模型类似,DA的缺乏会导致特定脑区5-HT水平和分支增加。相反,通过喂食L-DOPA增加DA水平会导致5-HT神经元与它们在蘑菇体(MB)中的靶神经元之间的连接性降低。观察到的5-HT神经元可塑性变化表明,DA信号的丧失并非PD模型中观察到的行为障碍的唯一原因,而是后者与5-HT神经回路改变的综合结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e319/5650618/6a4cfdf90f69/fnsys-11-00076-g0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验