4.5 Review

Dopaminergic Axons: Key Recitalists in Parkinson's Disease

期刊

NEUROCHEMICAL RESEARCH
卷 47, 期 2, 页码 234-248

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11064-021-03464-1

关键词

Parkinson's disease; Axon degeneration; Mitochondrial dynamics; Synaptic homeostasis; Ca2+

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Parkinson's disease is characterized by the depletion of dopamine in the striatum due to the loss of nigrostriatal dopaminergic neurons, leading to motor dysfunction and other clinical symptoms. Protecting the substantia nigra neurons is crucial for maintaining dopamine levels. Current strategies for treating PD focus on preventing cell body death but new approaches may target axonal degeneration to prevent loss of synaptic terminals and alleviate symptomatic features.
Parkinson's disease (PD) is associated with dopamine depletion in the striatum owing to the selective and progressive loss of the nigrostriatal dopaminergic neurons, which results in motor dysfunction and secondary clinical manifestations. The dopamine level in the striatum is preserved because of the innervation of the substantia nigra (SN) dopaminergic neurons into it. Therefore, protection of the SN neurons is crucial for maintaining the dopamine level in the striatum and for ensuring the desired motor coordination. Several strategies have been devised to protect the degenerating dopaminergic neurons or to restore the dopamine levels for treating PD. Most of the methods focus exclusively on preventing cell body death in the neurons. Although advances have been made in understanding the disease, the search for disease-modifying drugs is an ongoing process. The present review describes the evidence from studies involving patients with PD as well as PD models that axon terminals are highly vulnerable to exogenous and endogenous insults and degenerate at the early stage of the disease. Impairment of mitochondrial dynamics, Ca2+ homeostasis, axonal transport, and loss of plasticity of axon terminals appear before the neuronal degeneration in PD. Furthermore, distortion of synaptic morphology and reduction of postsynaptic dendritic spines are the neuropathological hallmarks of early-stage disease. Thus, the review proposes a shift in focus from discerning the mechanism of neuronal cell body loss and targeting it to an entirely different approach of preventing axonal degeneration. The review also suggests appropriate strategies to prevent the loss of synaptic terminals, which could induce regrowth of the axon and its auxiliary fibers and might offer relief from the symptomatic features of PD.

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