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Harpagide,a natural product,promotes synaptic vesicle release as measured by nanoelectrode amperometry
Authors:Yun Tang  Xiao-Ke Yang  Xin-Wei Zhang  Wen-Tao Wu  Fu-Li Zhang  Hong Jiang  Yan-Ling Liu  Christian Amatore  Wei-Hua Huang
Institution:Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072 China.; State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005 China.; PASTEUR, Departement de Chimie, Pcole Normale Superieure, PSL Research University, Sorbonne Universites, UPMC Univ. Paris 06, CNRS, 24 rue Lhomond, 75005 Paris France
Abstract:Parkinson''s disease (PD) is a neurodegenerative disorder characterized by progressive loss of dopaminergic (DAergic) neurons and low level of dopamine (DA) in the midbrain. Recent studies suggested that some natural products can protect neurons against injury, but their role on neurotransmitter release and the underlying mechanisms remained unknown. In this work, nanoelectrode electrochemistry was used for the first time to quantify DA release inside single DAergic synapses. Our results unambiguously demonstrated that harpagide, a natural product, effectively enhances synaptic DA release and restores DA release at normal levels from injured neurons in PD model. These important protective and curative effects are shown to result from the fact that harpagide efficiently inhibits the phosphorylation and aggregation of α-synuclein by alleviating the intracellular reactive oxygen level, being beneficial for vesicle loading and recycling. This establishes that harpagide offers promising avenues for preventive or therapeutic interventions against PD and other neurodegenerative disorders.

Nanoelectrode amperometry was used to monitor DA release inside single DAergic synapses, and demonstrated that harpagide effectively enhances synaptic DA release by reducing intracellular ROS generation and inhibiting α-Syn phosphorylation.
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