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Opioidergic Modulation of Striatal Circuits Implications in Parkinsons Disease and Levodopa Induced Dyskinesia

机译:纹状体回路的眼皮调制对帕金森氏病和左旋多巴诱发的运动障碍的影响

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摘要

The functional organization of the dorsal striatum is complex, due to the diversity of neural inputs that converge in this structure and its subdivision into direct and indirect output pathways, striosomes and matrix compartments. Among the neurotransmitters that regulate the activity of striatal projection neurons (SPNs), opioid neuropeptides (enkephalin and dynorphin) play a neuromodulatory role in synaptic transmission and plasticity and affect striatal-based behaviors in both normal brain function and pathological states, including Parkinson's disease (PD). We review recent findings on the cell-type-specific effects of opioidergic neurotransmission in the dorsal striatum, focusing on the maladaptive synaptic neuroadaptations that occur in PD and levodopa-induced dyskinesia. Understanding the plethora of molecular and synaptic mechanisms underpinning the opioid-mediated modulation of striatal circuits is critical for the development of pharmacological treatments that can alleviate motor dysfunctions and hyperkinetic responses to dopaminergic stimulant drugs.
机译:背纹状体的功能组织是复杂的,这是由于在这种结构中会聚的神经输入的多样性及其细分成直接和间接的输出途径,核小体和基质区室。在调节纹状体投射神经元(SPNs)活性的神经递质中,阿片类神经肽(脑啡肽和强啡肽)在突触传递和可塑性中起神经调节作用,并影响正常大脑功能和病理状态(包括帕金森氏病)中基于纹状体的行为( PD)。我们审查了最近的发现,对纹状体背侧阿片神经递质的细胞类型特异性影响,重点是PD和左旋多巴引起的运动障碍的不良适应性突触神经适应。了解支持阿片类药物介导的纹状体回路调节的众多分子和突触机制,对于开发可减轻运动功能障碍和对多巴胺能刺激药物的运动过度反应的药理学治疗至关重要。

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