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帕金森病中的内源性大麻素系统。

The endocannabinoid system in Parkinson's disease.

作者信息

Di Filippo Massimiliano, Picconi Barbara, Tozzi Alessandro, Ghiglieri Veronica, Rossi Aroldo, Calabresi Paolo

机构信息

Clinica Neurologica, Ospedale S. Maria della Misericordia, Universita' di Perugia, 06156 Perugia, Italy.

出版信息

Curr Pharm Des. 2008;14(23):2337-47. doi: 10.2174/138161208785740072.

Abstract

Parkinson's disease (PD) is a chronic and progressive neurodegenerative disorder of largely unknown etiology caused by a pathological cascade resulting in the degeneration of midbrain dopaminergic neurons of the substantia nigra pars compacta (SNpc) projecting to the nucleus striatum, the main input station of the basal ganglia neuronal circuit. The components of the endocannabinoid (ECB) system are highly expressed at different levels in the basal ganglia neural circuit where they bidirectionally interact with dopaminergic, glutamatergic and GABAergic signaling systems. In particular, at synapses linking cortical and striatal neurons, endocannabinoids (ECBs) are known to critically modulate synaptic transmission and to mediate the induction of a particular form of synaptic plasticity, the long-term depression. The evidence that ECBs play a central role in regulating basal ganglia physiology and motor function and the profound modifications occurring in ECB signaling after dopamine depletion in both experimental models of PD and patients suffering from the disease, provide support for the development of pharmacological compounds targeting the ECB system as symptomatic and neuroprotective therapeutic strategies for PD.

摘要

帕金森病(PD)是一种慢性进行性神经退行性疾病,病因大多不明,由一系列病理级联反应导致黑质致密部(SNpc)向纹状体核投射的中脑多巴胺能神经元变性,纹状体核是基底神经节神经回路的主要输入站。内源性大麻素(ECB)系统的成分在基底神经节神经回路中以不同水平高度表达,在那里它们与多巴胺能、谷氨酸能和γ-氨基丁酸能信号系统双向相互作用。特别是,在连接皮质和纹状体神经元的突触处,内源性大麻素(ECB)已知能关键地调节突触传递,并介导一种特殊形式的突触可塑性——长期抑制的诱导。在帕金森病的实验模型和患病患者中,ECB在调节基底神经节生理学和运动功能中起核心作用的证据,以及多巴胺耗竭后ECB信号发生的深刻变化,为开发靶向ECB系统的药理化合物作为帕金森病的症状性和神经保护治疗策略提供了支持。

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